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Dysphagia Following Endotracheal Intubation: Frequency, Risk Factors and
Characteristics
by
Stacey Anne Skoretz
A thesis submitted in conformity
with the requirements
for the degree of Doctor of Philosophy
Department of Speech-Language Pathology
University of Toronto
© Stacey Anne Skoretz 2015

DYSPHAGIA FOLLOWING INTUBATION
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Dysphagia Following Endotracheal Intubation: Frequency, Risk Factors and
Characteristics
Stacey Anne Skoretz
Doctor of Philosophy
Department of Speech Language Pathology University of Toronto
2015
Abstract
Oropharyngeal dysphagia following endotracheal intubation occurs frequently,
however, both the incidence and associated risk factors vary across the literature. This
dissertation is comprised of three studies that investigate the frequency, associated risk
factors and characteristics of post-extubation dysphagia along with the relation between
intubation duration and swallowing outcomes with a focus on CV surgery. First, we
conducted a systematic review in order to determine dysphagia frequency according to
patient diagnoses and the association between dysphagia and intubation time. We
conducted searches using fourteen electronic databases along with manual searching of
journals and grey literature. Our critical appraisal utilized the Cochrane Risk of Bias
Assessment and GRADE tools. Our second study assessed dysphagia frequencies
according to four intubation duration strata on consecutive patients following CV
surgery: I (≤12 h), II (>12 to ≤24 h), III (> 24 to ≤ 48 h), and IV (>48 h). We also
derived independent predictors for dysphagia across the entire sample using logistic
regression. Finally, we conducted a feasibility study with prospective consecutive
enrollment in order to determine patient tolerance of the instrumental procedures used to
assess swallowing physiology, videofluoroscopy swallowing study (VFS) and

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nasendoscopy, following prolonged intubation after CV surgery. Along with study
impact on patients and nursing workflow, we assessed other feasibility parameters
including recruitment rate, task completion durations and measurement reliability.
Findings from our systematic review, identified a range of dysphagia frequency from 3%
to 62% and intubation duration from 124.8 to 346.6 mean hours across the fourteen
included studies. The highest dysphagia frequencies, 62%, 56%, and 51%, occurred
following prolonged intubation and included patients across all diagnostic subtypes.
Overall, the quality of the evidence was low. In our second study, we reported a
dysphagia frequency of 5.6 % (51/909) across the entire sample, however, we identified
that frequency varied according to intubation group: I, 1 % (7/699); II, 8.2 % (11/134);
III, 16.7 % (6/36); and IV, 67.5 % (27/40). Across the entire sample, the independent
predictors of dysphagia included intubation duration (p < .001; odds ratio [OR] 1.93,
95 % confidence interval [CI] 1.63-2.29) according to 12-hour increments and age (p =
.004; OR 2.12, 95 % CI 1.27-3.52) according to 10-year increments. For our final study,
of the 16 eligible patients, three agreed to participate. Following a videofluoroscopy
swallowing study (VFS) completion, all patients exhibited oral and pharyngeal
swallowing impairments. VFS completion time ranged from 14 to 52 minutes with item
interrater reliability ranging from .25 (95% CI: -.10-.59) to .99 (95% CI: .98-.99).
Participants reported minimal study burden. In conclusion, our collective findings report
the frequency of dysphagia across numerous patient populations, associated risk factors
and swallowing characteristics. With this information, we provide the means to identify
at-risk patients following extubation after CV surgery. For future studies, we propose
ways to improve study enrollment as well as suggest instrumental procedures and

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interpretation methods best suited to assessing swallowing physiology in this patient
population.

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Acknowledgements
It takes a village. No kidding. I am the luckiest human on the planet to have a
community such as this. If it were not for the selfless acts of kindness, love and support
that I received; I would have never finished this marathon. The people I am about to
mention were my supports when I could not stand on my own, my foundation when
everything around me was turning to sand, and my light when all I could see was dark.
What you all have done throughout this process will never be lost on me.
For my husband Bill: thank you for sacrificing so much throughout these years
and especially during the final three as we struggled to survive, quite literally. You have
provided for our little family, taken on the role of primary caregiver more times than I
can count, and taken countless hours off of work to provide support without ever uttering
one word of complaint. Your capacity for love, tolerance and understanding is
remarkable. To my baby Grace: thank you for being such a Life Force. You always
greet the day happily and readily embrace it with vigor - there is nothing that is more
perfect than that. Thank you for adding a dimension to my life that I would not have
otherwise had. I do apologize that the first words you heard and books you read were all
surrounding deglutition. I’ve started putting away for your future therapy.
To my supervisor Dr. Rosemary Martino: I thank you mightily for your guidance,
knowledge, support, sacrifice and confidence you have in my work and in me. While
what you offer the profession is remarkable, it is second only to your kindness, integrity
and humanity. For my supervisory committee Drs. Joan Ivanov, John Granton and
Terrence Yau: thank you for your expertise, patience and support. I am honoured that
you agreed to mentor me throughout this journey. I strive for your balance of research
and clinical practice. For the Ladies-of-the-Lab: Trixie Reichardt, Dr. Heather Flowers

DYSPHAGIA FOLLOWING INTUBATION
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and Stephanie Shaw, thank you for playing such an important role in my successes both
personally and professionally. I am so happy that you are a part of my life.
Thank you for everything you have done for me Mom. I have not forgotten the
life sacrifices you have made to get me here. Without the past, there would be no
present. To my sister Cassandra, I will never forget the help you provided while we were
renovation refugees and while I was in the newborn baby haze. To my sister Mikaela:
this adventure would have been a lot less Awesome without you. From saving all your
high-school pennies to come visit Toronto to your presence during the important events
of this journey, thank you for being there. Someday I really will find you a “solar-
powered laser beam guitar”. For my aunt Hélène: thank you for understanding me. The
generosity and empathy you possess is without measure. I quite literally would not have
survived without you.
Michelle Graham, thank you for being my steadfast friend throughout these years.
Above all, you were the only person who was there by my side as I packed up my life’s
rubble to start another. Thank you. Vance Ward, you supported this adventure not only
with your time and friendship but also with your remarkable culinary skills. Thank you
for feeding my stomach and my soul. To my dear Kelly Ryan, David Rose and the rest of
the Hamilton/Grimsby gang: who wouldn’t want to have a Ph.D. with a minor in
viniculture? I will now have time to become learned in the ways of that “Rock Lobster”
thing and I have not forgotten that our off-grid life adventures wait. For Mar and Shar: I
am so grateful that our paths collided and blessed me with you, Mar-toonies and harp
strings. You have added depth and fuel for my right hemisphere. For Drs. Jim Coyle and
Joe Murray: thank you for checking in over the years and making sure that I was still

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alive. Your help and balanced wisdom really did keep things on track. For Randy
Reichardt and Megan Sui: I am eternally grateful for your mad library skills.
Lastly but certainly not least, to Dr. John Stone: without you this would have
never came to be. Thank you for giving me my very first research assistantship during
my master’s and encouraging me to pursue doctoral studies. You helped me to believe
that I was capable and had skills worthy of higher learning. Without that and all of the
kind gestures you and your wonderful wife Sandra have displayed over the years, I would
not have made it to this point. Thank you for being a role model for me in this world of
academia. Your intellect, candor, practicality and humour are something that I respect
deeply. You have shown me that there is much to be gained and to offer throughout this
process. I can only hope to have even a fraction of that same positive impact on this
Earth.
Onward…

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TABLE OF CONTENTS Abstract ............................................................................................................................. ii Acknowledgements ............................................................................................................ v Table of Contents ........................................................................................................... viii List of Tables .................................................................................................................. xii List of Figures ................................................................................................................ xiii List of Appendices ......................................................................................................... xiv List of Abbreviations ....................................................................................................... xv INTRODUCTION 1. Chapter I ......................................................................................................................... 1 I. The Swallow ............................................................................................................... 2 Normal Swallowing Physiology ................................................................................. 2 Swallowing Stages ................................................................................................. 2 The vagus nerve ......................................................................................... 5
Airway protection during the swallow ....................................................... 6 Respiration and swallowing ....................................................................... 7
Aging .......................................................................................................... 9 Diagnosing Dysphagia ............................................................................................. 10
Dysphagia Screening ........................................................................................... 10 Clinical Swallowing Evaluation .......................................................................... 13 Instrumental Swallowing Assessments ................................................................ 15 The videofluoroscopic swallow study ..................................................... 16 Fiberoptic endoscopic evaluation of the swallow .................................... 20
Fiberoptic endoscopic evaluation of the swallow with sensory testing ... 21 VFS versus FEES: Which to choose? ...................................................... 22
II. Endotracheal Intubation and Mechanical Ventilation ............................................. 24 Background ................................................................................................................ 24 Dysphagia Following Endotracheal Intubation ........................................................ 24 Dysphagia characteristics ......................................................................... 28 Consequences of dysphagia ...................................................................... 29 Etiology of Post-extubation Dysphagia .................................................................... 32 Endotracheal Intubation ........................................................................................ 32
Upper aerodigestive tract morbidities ....................................................... 33 Injury and biomechanical changes ............................................... 33 Injury etiology .............................................................................. 35
Mechanical Ventilation and the Swallow ............................................................ 36 Breathing and swallowing: Taxing an already taxed system ................... 37
Anesthesia and Upper Aerodigestive Function .................................................... 39 III. Cardiovascular Surgery .......................................................................................... 42 Heart Disease ............................................................................................................ 42 Burden of Care ..................................................................................................... 42 Heart Disease Risk Factors ................................................................................... 42 Cardiovascular Surgery Types .................................................................................. 43 Risk Factors for Dysphagia Following CV Surgery ................................................. 45

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Surgery Type ........................................................................................................ 46 Transesophageal Echocardiogram ....................................................................... 46
Cardiopulmonary Bypass ..................................................................................... 48 Stroke ................................................................................................................... 49 Recurrent Laryngeal Nerve Injury ....................................................................... 49 Prolonged Intubation Following Cardiovascular Surgery ................................... 51 Age ....................................................................................................................... 53 Dysphagia Characteristics ......................................................................................... 54 Gaps in the Literature .................................................................................................... 55 Purposes .................................................................................................................... 57 THE INCIDENCE OF DYSPHAGIA FOLLOWING ENDOTRACHEAL INTUBATION: A SYSTEMATIC REVIEW 2. Chapter II ..................................................................................................................... 59 Abstract ........................................................................................................................ 59 Introduction .................................................................................................................. 61 Materials and Methods ................................................................................................. 63 Operational Definitions ............................................................................................. 63 Search Strategy ......................................................................................................... 63 Eligibility Criteria .................................................................................................... 64 Study Selection ......................................................................................................... 64 Assessment of Methodological Quality .................................................................... 64 Data Extraction ......................................................................................................... 65 Results ...........................................................................................................................66 Literature Retrieved .................................................................................................. 66 Study Characteristics and Quality Assessment ......................................................... 69 Dysphagia Following Endotracheal Intubation ........................................................ 73 Duration of Intubation and the Frequency Dysphagia ......................................... 73 Swallowing Assessment Methods ........................................................................ 74 Frequency of Dysphagia Following Intubation ................................................... 75 Discussion .................................................................................................................... 79
DYSPHAGIA AND ASSOCIATED RISK FACTORS FOLLOWING EXTUBATION IN CARDIOVASCULAR SURGICAL PATIENTS 3. Chapter III .................................................................................................................... 83 Abstract ........................................................................................................................ 83 Introduction .................................................................................................................. 85 Patients and Methods ................................................................................................... 86 Data Abstraction ....................................................................................................... 86 Operational Definitions ............................................................................................. 87 Statistical Analyses ................................................................................................... 87 Results .......................................................................................................................... 88 Dysphagia Frequency and Criteria ............................................................................ 89 Intubation Duration Across Study Sample ............................................................... 90

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Patient Characteristics Across Study Sample ........................................................... 90 Discussion .................................................................................................................. 100 DYSPHAGIA INCIDENCE AND SWALLOWING PHYSIOLOGY FOLLOWING PROLONGED INTUBATION AFTER CARDIOVASCULAR SURGERY: A FEASIBILITY STUDY 4. Chapter IV ................................................................................................................... 104 Abstract ...................................................................................................................... 104 Introduction ................................................................................................................ 106 Methods ...................................................................................................................... 109 Participants .............................................................................................................. 109 Study Process .......................................................................................................... 109 Videofluoroscopic Swallow Study ......................................................................... 110 Imaging .............................................................................................................. 110
Videofluoroscopic Swallow Study Procedure ................................................... 110 Videofluoroscopic Swallow Study Measures ......................................................... 111 Standardized VFS Assessment Tools ................................................................ 111
Displacement Measurements ............................................................................. 113 Study Impact Questionnaires and Patient Variables ................................................ 114 Scoring and Statistical Analyses .............................................................................. 117 Results ........................................................................................................................ 118 Patient Recruitment and Characteristics ................................................................. 118 Videofluoroscopic Swallow Study ......................................................................... 120 Videofluoroscopic Measures ............................................................................. 121 Standardized VFS assessment tools ....................................................... 122 Displacement measurements .................................................................. 125 Study Impact Questionnaires .................................................................................. 127 Patient Comfort Questionnaire .......................................................................... 127
Workload Impact Questionnaires ...................................................................... 127 Discussion .................................................................................................................. 128 DISCUSSION 5. Chapter V ................................................................................................................... 137 Introduction ................................................................................................................ 137 Summary of Thesis Findings ..................................................................................... 138 Clinical Implications .................................................................................................. 144 Research Implications ................................................................................................ 146 Future Studies ............................................................................................................ 148 Limitation of the Thesis ............................................................................................. 151
Conclusions ................................................................................................................ 152

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REFERENCES 6. References .................................................................................................................. 155 APPENDICES 7. Appendices ................................................................................................................. 225

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LIST OF TABLES
Table 1.1. Description and critical appraisal of screening tools used with patients following extubation ........................................................................................................ 12
Table 2.1. Study characteristics and frequency of dysphagia according to patient diagnosis .......................................................................................................................... 70
Table 2.2. Risk of bias and methodological quality (GRADE) across studies ................ 72
Table 2.3. Intubation duration according to presence of dysphagia ................................ 74
Table 2.4a. Surgical and medical risk factor association with dysphagia ........................77
Table 2.4b. Studies either supporting or not supporting risks for dysphagia ...................78
Table 3.1. Comparing dysphagia frequency and intubation duration across intubation groups . ............................................................................................................................. 90
Table 3.2. Pre-operative demographics and presenting clinical characteristics across sample .............................................................................................................................. 92
Table 3.3. Peri-operative characteristics across sample ................................................... 95
Table 3.4. Post-operative patient outcomes across sample .............................................. 97
Table 3.5. Independent predictors of postoperative dysphagia ........................................ 99
Table 4.1. MBSImpTM© oral and pharyngeal components ............................................. 112
Table 4.2. Penetration-Aspiration Scale ........................................................................ 113
Table 4.3. Survey questions ........................................................................................... 116
Table 4.4. Patient characteristics ................................................................................... 120
Table 4.5. Task completion time and interrater reliability according to VFS measure . 122
Table 4.6. Hyoid displacement measurements according to patient .............................. 126

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LIST OF FIGURES
Figure 2.1. Study selection process .................................................................................. 68
Figure 4.1. Study enrollment ......................................................................................... 119
Figure 4.2a. MBSImpTM© oral components across patients .......................................... 123
Figure 4.2b. MBSImpTM© pharyngeal components across patients ............................... 124
Figure 4.3. Pharyngeal constriction ratio by patient according to bolus texture and volume
......................................................................................................................................... 127

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LIST OF APPENDICES Appendix A – CHEST Licenses .....................................................................................225
Appendix B – Systematic Review Proposal ...................................................................237
Appendix C – Study Selection Form ..............................................................................240
Appendix D – Cochrane Collaboration’s Risk of Bias Assessment ...............................241
Appendix E – Data Extraction Form ..............................................................................242
Appendix F – Explanatory Meta-Analyses .....................................................................243
Appendix G – Search Strategies Across Databases ........................................................247
Appendix H – Non-English Articles ...............................................................................248
Appendix I – Handsearched Journals and Reference Yield ............................................249
Appendix J – Dysphagia Licenses ..................................................................................250
Appendix K – Data Abstraction Manual ........................................................................254
Appendix L – Medical Record Review Form .................................................................258
Appendix M – Retrospective Study Sample Size Estimation .........................................260
Appendix N – Characteristics of Intubation Stratum I ...................................................261
Appendix O – Characteristics of Intubation Stratum II ..................................................265
Appendix P – Characteristics of Intubation Stratum III .................................................269
Appendix Q – Characteristics of Intubation Stratum IV ................................................273

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LIST OF ABBREVIATIONS
APACHE Acute Physiology and Chronic Health Evaluation ASHA American Speech-Language and Hearing Association CABG Coronary artery bypass grafting CI Confidence interval CN Cranial nerve COPD Chronic Obstructive Pulmonary Disease CPAP Continuous positive airway pressure CPB Cardiopulmonary bypass CSE Clinical swallow evaluation CV Cardiovascular CVA Cerebral vascular accident DREP Dysphagia Risk Evaluation Protocol ETT Endotracheal tube FEES Fiberoptic Endoscopic Evaluation of the Swallow FEESST Fiberoptic Endoscopic Evaluation of the Swallow with Sensory
Testing GBP Pound sterling GCS Glasgow Coma Score GERD Gastro-esophageal reflux disease GI Gastrointestinal GRADE Grading of Recommendation, Assessment, Development, and
Evaluation hrs Hours IABP Intra-aortic balloon pump ICC Intraclass correlation coefficient ICU Intensive care unit inSLN Internal branch of the superior laryngeal nerve IQR Interquartile range LAR Laryngeal adductor response LCR Laryngeal cough reflex LOS Length of stay LP Laryngopharyngeal LV Left ventricular MBSImpTM© Modified Barium Swallow Measurement Tool for Swallow
Impairment Profile MBS Modified barium swallow MI Myocardial infarction min Minute N/A Not applicable NG/NGT Nasogastric feeding tube NPO Nil per os NT Not tested NYHA New York Heart Association OI Overall impairment PA Pharyngeal area

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PAS Penetration Aspiration Scale PEG Percutaneous endoscopic gastronomy tube PMV Prolonged mechanical ventilation PC Pressure control PCR Pharyngeal constriction ratio PS Pressure support PV Pressure ventilation RLN Recurrent laryngeal nerve SD Standard deviation SLP Speech-language pathologist TEE Transesophageal echocardiography TIA Transient ischemic attack TWH Toronto Western Hospital US United States of America USD United States dollar VF Videofluoroscopic VFS Videofluoroscopic swallow study yrs Years

1
CHAPTER I
INTRODUCTION
Swallowing is a physiological act necessary for species viability. Swallowing
food and/or fluid is often taken for granted until it is rendered dysfunctional. In the
words of George Bernard Shaw: “there is no love sincerer than the love of food” (Shaw,
1903/2012, Act I, p. 74).
Oropharyngeal dysphagia, herein referred to as dysphagia, is an upper
aerodigestive tract abnormality secondary to impaired swallowing physiology (Martino et
al., 2005). It impairs one’s ability to safely engage in deglutition thereby leading to
potential malnutrition (Smithard, O'Neill, Parks, & Morris, 1996; Westergren, Ohlsson,
& Rahm Hallberg, 2001), respiratory complications (Cabré et al., 2014; Kwok, Davis,
Cagle, Sue, & Kaups, 2013; Martino et al., 2005) and even death (Cabré et al., 2010;
Macht et al., 2011). In the United States (US) during 2004 and 2005, dysphagia
prevalence in the acute care setting was estimated at 0.4% of all hospitalizations (Altman,
Yu, & Schaefer, 2010) and in those following mechanical ventilation, an incidence as
high as 84% (Macht et al., 2011). The disorder is an economic burden leading to $547
million annually in additional hospitalization costs in the US alone (Altman et al., 2010;
Cichero & Altman, 2012). Post-extubation dysphagia also contributes to increased
pneumonia, reintubation, and mortality (Macht et al., 2011). Those patients with
dysphagia following extubation incur triple the healthcare costs as compared to those
without (Ferraris, Ferraris, Moritz, & Welch, 2001).
This introductory chapter will provide background information for the research
studies that follow, which focus on dysphagia following endotracheal intubation in
general and following cardiovascular surgery more specifically. It is comprised of three

INTRODUCTION
2
major sections: I. The Swallow; II. Endotracheal Intubation and Mechanical Ventilation;
and III. Cardiovascular (CV) Surgery. Together these sections review: normal swallow
physiology and the current methods available by which to assess it; how the swallow may
be impacted by endotracheal intubation, mechanical ventilation, and anesthesia in
general; and finally how the swallow may be impacted in the CV surgical population.
I. The Swallow
Normal Swallowing Physiology
Swallowing stages. The swallow is a complex process involving 30 muscles
located throughout the oral cavity, larynx and pharynx which are controlled by six cranial
nerves (CN V, VII, IX-XII), three cervical nerve roots (C1-C3) and multiple cortical,
subcortical and brainstem regions (Miller, Bieger, & Conklin, 1997; Shaw & Martino,
2013). Traditionally, the entire swallowing act was considered involuntary or reflexive
and mitigated primarily through the infratenorium via a central pattern generator housed
within the medulla oblongata (Miller, Bieger, & Conklin, 1997; Shaw & Martino, 2013).
With the advancement of imaging technologies it is now accepted that aspects of the
swallow are governed by either the supratentorium or the infratentorium (Hamdy, Aziz,
Thompson, & Rothwell, 2001; Hamdy et al., 1999; Martin, Goodyear, Gati, & Menon,
2001; Michou et al., 2014; Shaw & Martino, 2013).
The act of swallowing is a continuous and dynamic sequence of events, which
integrates the movement of multiple muscles and structures (Perlman & Christensen,
1997; Shaw & Martino, 2013). For descriptive purposes, it is traditionally divided into
discrete stages: oral, pharyngeal and esophageal (Perlman & Christensen, 1997). The
oral stage is further sub-divided into two phases: the oral preparatory and oral transport
phases (Perlman & Christensen, 1997). These oral phases are primarily under volitional

INTRODUCTION
3
or supratentorial control (Hamdy et al., 1999; Humbert & Robbins, 2007; Martin,
Goodyear, Gati, & Menon, 2001; Palmer, Hiiemae, Matsuo, & Haishima, 2007), whereas
the pharyngeal and esophageal stages are considered reflexive or involuntary and
governed by the infratentorium (Diamant, 1995; Diamant, 1996; Ertekin, 2011; Ertekin &
Aydogdu, 2003; Michou et al., 2014; Miller, 1982; Miller, 1993). Historically, only
volitional swallowing events were considered modifiable (Hamdy et al., 1999; Humbert
& Robbins, 2007; Martin, Goodyear, Gati, & Menon, 2001; Palmer, Hiiemae, Matsuo, &
Haishima, 2007). Now, there is emerging evidence that those swallowing acts governed
by the infratentorium, once considered purely reflexive, may too be altered (Michou et
al., 2014). While their event sequence may not be modifiable, the response amplitude
and timing may be altered through intervention (Michou et al., 2014).
During the oral preparatory phase, the bolus is navigated throughout the oral
cavity onto the dental surfaces and throughout the lateral cheek sulci as needed (Palmer et
al., 2007; Palmer, Rudin, Lara, & Crompton, 1992). Once bolus preparation is complete,
the intrinsic tongue muscles create a trough-like furrow in order to contain the bolus
between the dorsal tongue surface and hard palate readying the bolus for transport into
the oropharynx (Cook et al., 1989; Curtis, Cruess, & Dachman, 1985; Dodds, Stewart, &
Logemann, 1990; Dodds et al., 1989; Taniguchi, Tsukada, Ootaki, Yamada, & Inoue,
2008). The pressure within the oropharynx increases with the tongue creating wave-like
movements transporting the bolus from the oral cavity posteriorly into the pharynx (Cook
et al., 1989; Curtis et al., 1985; Dantas et al., 1990; Dodds et al., 1989; McConnel, 1988;
Santander, Engelke, Olthoff, & Völter, 2013; Taniguchi et al., 2008).
The purpose of the pharyngeal stage, lasting approximately one second, is to
move the bolus towards the upper esophageal sphincter (Cassiani, Santos, Parreira, &

INTRODUCTION
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Dantas, 2011; Cook et al., 1989; Curtis, Cruess, Dachman, & Maso, 1984; Kahrilas,
1993; Logemann et al., 2000; Logemann, Pauloski, Rademaker, & Kahrilas, 2002;
McConnel, 1988). It is initiated with the depression of the posterior tongue and the
closure or the continued closure of multiple “valves” or “ports” throughout the upper
aerodigestive tract (Curtis et al., 1985; Olthoff, Zhang, Schweizer, & Frahm, 2014;
Shaker, Dodds, Dantas, Hogan, & Arndorfer, 1990). The resultant increased pressure,
sequential tongue movements along with the initiation of a sphincter-like motion of the
lateral and posterior pharyngeal walls assist with posterior bolus movement (Curtis et al.,
1985; Ekberg & Nylander, 1982; Kahrilas, Logemann, Lin, & Ergun, 1992; McConnel,
1988; Olthoff et al., 2014; Palmer, Tanaka, & Ensrud, 2000). The upper esophageal
sphincter begins to relax (Jacob, Kahrilas, Logemann, Shah, & Ha, 1989) while the hyo-
laryngeal complex, which includes the hyoid bone and larynx, begin an anterior and
superior ascent (Cook et al., 1989; Curtis et al., 1985; Logemann et al., 1992; Logemann
et al., 2000; Logemann et al., 2002; Olthoff et al., 2014). As the true and false vocal
folds close, the epiglottis begins to retroflex passively while covering the adducted
arytenoid cartilages (Curtis et al., 1985; Ekberg & Sigurjónsson, 1982; Inamoto et al.,
2013; Logemann et al., 1992; Ohmae, Logemann, Kaiser, Hanson, & Kahrilas, 1995;
Shaker et al., 1990). At this time, an obligatory apneic period commences which
typically lasts less than one second (Martin, Logemann, Shaker, Dodds, & Trammell,
1994; Martin-Harris, Brodsky, et al., 2005; Martin-Harris, Brodsky, Price, Michel, &
Walters, 2003; Selley, Flack, Ellis, & Brooks, 1989a). As the bolus begins its descent
through the UES, the esophageal stage commences and lasts between 8 and 13 seconds
(De Vincentis et al., 1984). Esophageal peristalsis moves the bolus through the distal and
proximal areas of the esophagus, through the lower esophageal sphincter and into the

INTRODUCTION
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stomach (Goyal & Chaudhury, 2008; Lin et al., 2014). As the bolus enters the UES, the
posterior tongue, epiglottis, and hyolaryngeal complex return to their rest positions
(Perlman & Christensen, 1997; Yoon, Park, Park, & Jung, 2014) with the UES closing
after the passing of the bolus tail (Jacob et al., 1989; Lin et al., 2014; Yoon et al., 2014).
The true and false vocal folds abduct, the soft palate lowers and respiration resumes
completing the swallowing act (Perlman & Christensen, 1997; Zemlin, 1998).
The vagus nerve. The swallow is executed via six cranial nerves, of which the
vagus nerve is central to swallow function (Miller et al., 1997; Zemlin, 1998). Its
relevance to the integrity of the swallow is exemplified in those patients experiencing
endotracheal intubation and/or CV surgery due to its anatomical location and injury risk
during these interventions (Benouaich, Porterie, Bouali, Moscovici, & Lopez, 2012;
Cavo, 1985; Dimarakis & Protopapas, 2004; Gibbin & Egginton, 1981; Hamdan,
Moukarbel, Farhat, & Obeid, 2002; Ishimoto et al., 2002; Itagaki, Kikura, & Sato, 2007;
Murty & Smith, 1989; Myssiorek, 2004; Shafei, el-Kholy, Azmy, Ebrahim, & al-
Ebrahim, 1997; Tewari & Aggarwal, 1996). The vagus nerve has multiple branches of
which we will discuss two in detail: the internal branch of the superior laryngeal nerve
(inSLN) and the recurrent laryngeal nerve (RLN). The inSLN passes through the thyroid
cartilage with smaller branches innervating the ipsilateral hemilaryngeal mucosa (Rueger,
1972; Stephens, Wendel, & Addington, 1999) including the epiglottis, aryepiglottic folds,
glottis (true and false vocals folds), arytenoid mucosa and subglottic mucosa (Rueger,
1972; Stephens et al., 1999). These branches are primarily afferent and integral for the
elicitation of various protective reflexes including the laryngeal adductor response (LAR)
and laryngeal cough reflex (LCR) (Bradley, 2000; Sulica, 2004; Yoshida, Tanaka,
Hirano, & Nakashima, 2000). In contrast, the RLN has two branches, the right and left,

INTRODUCTION
6
each with differing courses and both with afferent and efferent fibers (Benouaich et al.,
2012). The right branch courses caudally to the right common carotid and subclavian
artery then towards the larynx (Benouaich et al., 2012; Moreau et al., 1998; Zemlin,
1998). The left courses inferiorly making a loop under the lower aortic arch before it
moves superiorly between the trachea and esophagus with termination at the larynx
(Benouaich et al., 2012; Moreau et al., 1998; Zemlin, 1998). Together, the two RLN
branches innervate all intrinsic laryngeal muscles (except the cricothyroid) and subglottal
mucosa (Benouaich et al., 2012; Moreau et al., 1998; Zemlin, 1998) and are key in the
movement of glottal structures during swallowing (Cavo, 1985; Gibbin & Egginton,
1981).
Airway protection during the swallow. The upper airway is protected through
the movement of laryngeal structures and their reflexive responses, including the LAR
and LCR, as moderated by their respective laryngeal nerve branches (Bradley, 2000;
Sulica, 2004; Yoshida et al., 2000). Laryngeal structural movements, specifically
retroflexion of the epiglottis, the adduction of the true vocal folds (Medda et al., 2003)
and medialization of the aryepiglottic and false vocal folds act as a multi-layered valving
system protecting the airway from prandial aspiration (Benouaich et al., 2012; Cavo,
1985; Gibbin & Egginton, 1981). These laryngeal reflexes are moderated primarily by
the inSLN (Rueger, 1972; Stephens et al., 1999) as initiated through mechanoreceptor
stimulation in the areas of the tongue base, epiglottis, pyriform sinuses and supraglottic
larynx (Bradley, 2000; Rueger, 1972; Stephens et al., 1999; Sulica, 2004; Yoshida et al.,
2000). Both the LAR and LCR help to prevent unwanted material from entering and
therefore compromising the airway. The LAR is a rapid adduction of the vocal folds due
to stimulation of the laryngeal mucosa (Ambalavanar, Tanaka, Selbie, & Ludlow, 2004)

INTRODUCTION
7
thereby quickly closing off access to the upper trachea. The LCR is a cough reflex also
triggered by mechanical stimulation of the larynx or trachea (Bradley, 2000; Rueger,
1972; Stephens et al., 1999; Sulica, 2004; Yoshida et al., 2000). When the LCR is
elicited in normal subjects, it results in involuntary coughing and breathing pattern
alterations (Nishino, Tagaito, & Isono, 1996; Yoshida et al., 2000). When the LAR or
LCR is absent or require higher than normal thresholds to elicit a response, the risk of
aspiration is also higher (Aviv, 1997; Aviv et al., 1997; Cunningham, Halum, Butler, &
Postma, 2007; Setzen et al., 2003; Tabaee et al., 2006). Ultimately, these reflexes can be
affected by disease processes or interventions that interrupt their afferent control
including gastroesophageal reflux (Mendell & Logemann, 2002; Phua, McGarvey, Ngu,
& Ing, 2005), chronic obstructive pulmonary disease (COPD) (Tsuzuki et al., 2012),
stroke (Park, Kim, Ko, & McCullough, 2010), endotracheal intubation and anesthesia
(Hasegawa & Nishino, 1999). Impairment to either the LAR or LCR is a decreased or
delayed glottal closure (Mendell & Logemann, 2002; Park et al., 2010), which can lead to
airway compromise (Aviv et al., 2002; Tabaee et al., 2006).
Respiration and swallowing. The upper respiratory and deglutitive systems are
biomechanically interdependent requiring precise coordination due to their shared
anatomy and neurophysiological regulation (Miller, 1982; Sumi, 1963). A typical
respiration-swallow cycle is as follows: expiration, swallow initiation, swallow apnea,
swallow and then resumption of expiration (Martin-Harris, Brodsky, et al., 2005).
During restful respiration, the true vocal folds abduct facilitating relatively unimpeded air
passage throughout the upper and lower airways (Zemlin, 1998). In contrast, during the
swallow, a momentary respiratory cessation occurs in concert with the medialization of
the true and false vocal folds and epiglottic retroflexion (McFarland & Lund, 1995;

INTRODUCTION
8
Nishino, 2012). The duration of the apneic period ranges from 0.5 - 1.0s (Martin,
Logemann, et al., 1994; Martin-Harris, Brodsky, et al., 2005; Martin-Harris et al., 2003).
At this same time, an alteration in respiratory cycling ensures that expiration occurs after
swallow completion providing added protection for the upper and lower respiratory tracts
from prandial aspiration (McFarland & Lund, 1995; Nishino, 2012).
Respiration will always take biological precedence over deglutition (Selley, Ellis,
Flack, & Brooks, 1990) and in order to minimize airway compromise, respiration will
adapt when in relative proximity to deglutitive acts (Martin-Harris et al., 2003; Preiksaitis
& Mills, 1996; Selley et al., 1990; Selley et al., 1989a). Even as food or fluid approaches
the mouth, respiratory cycling is reorganized in order to ensure expiration occurs
following the completion of the swallow (Palmer & Hiiemae, 2003; Selley et al., 1989a).
The swallow apneic period occurs consistently after expiration commences in healthy
individuals (Martin, Logemann, et al., 1994; Preiksaitis, Mayrand, Robins, & Diamant,
1992; Preiksaitis & Mills, 1996). It is postulated that this resumption of exhalation
following bolus passage into the esophagus (Martin, Logemann, et al., 1994; Selley et al.,
1989a; Smith, Wolkove, Colacone, & Kreisman, 1989) is a protective mechanism that
facilitates the expulsion of pharyngeal residue following the swallow with an outward
flow of air (Selley et al., 1989a; Smith et al., 1989). Similarly, the cessation of
respiration during the swallow apneic period also serves a protective purpose and it too
may be altered by medical and environmental circumstances (Issa & Porostocky, 1994;
Martin, Logemann, et al., 1994; Martin-Harris, Brodsky, et al., 2005; Martin-Harris et al.,
2003; Preiksaitis et al., 1992; Preiksaitis & Mills, 1996). The duration of the apneic
period is typically bolus size dependent (Issa & Porostocky, 1994; Martin, Logemann, et
al., 1994; Martin-Harris, Brodsky, et al., 2005; Martin-Harris et al., 2003; Preiksaitis et

INTRODUCTION
9
al., 1992; Preiksaitis & Mills, 1996). However, during feeding paradigms that mimic
meals, increasing bolus sizes do not increase the apneic period duration; therefore, some
paradigms have the potential to compromise airway protection in specific patient
populations (Preiksaitis & Mills, 1996). Environmental changes notwithstanding,
respiratory cycling and swallow apneic periodicity can be affected by medical
interventions, particularly secondary to endotracheal intubation and mechanical
ventilation as will be discussed in section II.
Aging. Aging influences the swallow through physiological alterations, sensory
changes and attenuation of protective airway reflexes. In general when comparing
healthy elderly subjects to a younger cohort, there is an overall prolongation in swallow
duration (Robbins, Hamilton, Lof, & Kempster, 1992; Shaw et al., 1995) characterized
by increased oral transit time (Shaw et al., 1995; Yoshikawa et al., 2005), pharyngeal
transit time and pharyngeal dwell time (Cook et al., 1994; Yoshikawa et al., 2005). Oral
stage changes include increased mastication cycles and piecemeal deglutition
(Yoshikawa et al., 2005) resulting in multiple swallows to clear a single bolus, inefficient
lingual movements, and inadequate bolus formation (Frederick, Ott, Grishaw, Gelfand, &
Chen, 1996). Pharyngeal differences, when compared to younger cohorts, include
delayed initiation of hyolaryngeal elevation (Robbins et al., 1992), increased pharyngeal
residue (Cook et al., 1994; Frederick et al., 1996) and increased prevalence of airway
penetration (Frederick et al., 1996; Yokoyama, Mitomi, Tetsuka, Tayama, & Niimi,
2000; Yoshikawa et al., 2005). Swallowing sensory changes associated with aging have
also been explored (Aviv, 1997; Pontoppidan & Beecher, 1960). When conducting
airway sensory testing, Aviv and colleagues (1997) demonstrated higher than normal
thresholds for sensory discrimination and reduced laryngopharyngeal (LP) sensitivity

INTRODUCTION
10
(Aviv, 1997), confirming the progressive loss of protective airway reflexes with age
(Pontoppidan & Beecher, 1960). Other oral and pharyngeal sensory perception affected
by age is the perception of fluid viscosity (Smith, Logemann, Burghardt, Zecker, &
Rademaker, 2006). As a result, regardless of their medical diagnosis, the elderly are a
demographic at increased risk of dysphagia.
Diagnosing Dysphagia
Dysphagia screening. Dysphagia screening is used to identify at-risk patients
(Martino et al., 2005; Martino, Pron, & Diamant, 2000). In the event of screening failure,
they are referred for further assessment and a more accurate detailing of the nature and
severity of their dysphagia if present (Martino et al., 2005). While many swallowing
screening tools have been validated for use with stroke patients (Martino, Flowers, Shaw,
& Diamant, 2013; Schepp, Tirschwell, Miller, & Longstreth, 2012), at present no
screening tools have been properly psychometrically validated for use in patients
following extubation (Macht, Wimbish, Bodine, & Moss, 2013) and as a result, their
ability to predict dysphagia is currently unknown. The three screening methods which
have been used to screen patients for dysphagia following extubation include: 1) the 3-
Ounce Water Swallow Challenge (Leder, Suiter, Warner, & Kaplan, 2011; Suiter &
Leder, 2008) originally used for screening for swallowing impairment following stroke
(DePippo, Holas, & Reding, 1992), 2) the Preliminary Assessment Protocol (Mangilli,
Moraes, & Medeiros, 2012; Padovani, Moraes, Sassi, & de Andrade, 2013) and 3) gag
reflex testing (DeVita & Spierer-Rundback, 1990). Please see Table 1.1. Of these three,
the 3-Ounce Water Swallow Challenge is the only screening tool that has been tested on
extubated patients while using an instrumental criterion reference test (FEES) (Suiter &
Leder, 2008). This study was limited by its retrospective design and restrictive definition

INTRODUCTION
11
of dysphagia while exhibiting a high bias risk with unclear patient enrollment and a lack
of assessor blinding.

12
Table 1.1.
Description and critical appraisal of swallowing screening methods used with patients following extubation.
Screening Criterion Reference Testing
Method Description Validity Reliability Likelihood
Ratio (95% CI)
Etiology Test Blinding Design and Enrolment
Sensitivity Specificity Intrarater Interrater
3-oz. Water Swallow Challenge a
Patient to drink three ounces of water from cup without interruption
95.5% 49.1% NR NR 1.88 (1.61-2.20)
Mixed acute care patients
FEES
The same assessor conducted criterion test and screen concurrently
Retrospective, unclear (referred for swallowing assessment)
Preliminary Assessment Protocol (PAP)
Thirteen clinical conditions b screened for presence and/or impairment severity
NR NR NR NR NR
Prolonged mechanical ventilation (>48 h)
NR NR Prospective, consecutive
Gag reflex testing c
Stimulation of one or both faucial pillars in order to elicit gag
47-87% 48-57% NR NR 1.0 (0.9-2.3)
to 2.1 (1.1-4.7)
Stroke VFS NR Prospective, consecutive
Note. CI = confidence interval; NR = not reported; FEES = fiberoptic endoscopic evaluation of swallowing; VFS = videofluoroscopic swallowing study. a Study included heterogeneous acute care patients with results reported herein for cardiothoracic patients only (Suiter & Leder, 2008). b PAP clinical conditions include: tube feeding, breathing pattern, breathing and speech coordination, dysphonia, gag reflex, cough reflex, laryngeal elevation, oxygen saturation, supplemental oxygen, speech intelligibility, saliva, dentition and orofacial motor ability (Mangilli et al., 2012). c Psychometric values reported as a range based on a metaanalyses including stroke patients (Martino et al., 2000) as values unknown for recently extubated patients.

13
A recent nationwide survey was sent to all speech-language pathologists in the US
caring for patients who are or were mechanically ventilated (Macht et al., 2012). The
goal of this survey was to report on SLP practice patterns providing service for this
particular patient population (Macht et al., 2012). Of the respondents, only 41% of
hospitals screen for dysphagia following extubation (Macht et al., 2012). While informal
screening methods are utilized by clinicians who provide medical services for recently
extubated patients (Macht et al., 2012), all dysphagia screening tools have been validated
on patient populations whose etiologies are primarily neurogenic in nature (Martino et
al., 2013; Schepp et al., 2012; Wilkinson, Burns, & Witham, 2012) and as a result, the
predictive value of screening for dysphagia in other populations, including those
following extubation, remains to be determined (Wilkinson et al., 2012).
Clinical swallowing evaluation (CSE). The practice patterns of the speech-
language pathologists conducting the CSE throughout the continuum of care were
surveyed and results found little use of standardized methods (Martino, Pron, & Diamant,
2004), little consensus on assessment task importance (McCullough, Wertz, Rosenbek, &
Dinneen, 1999) and practice patterns varied widely (Martino et al., 2004). With only one
standardized assessment tool available for clinical swallowing evaluations (Mann
Assessment of Swallowing Ability [MASA]; Mann, 2002), which was validated with
stroke patients, clinicians need to rely on an informal approach.
Components of the CSE vary across clinicians and their reliability has been
questioned (McCullough et al., 2000). Regardless, some CSE components have shown
diagnostic value across different patient groups. They include: 1) detailed clinical,
medical and medication history (Castell & Donner, 1987; McCullough & Martino, 2013),
2) oral motor evaluation (Mann & Hankey, 2001; McCullough & Martino, 2013; Murray,

INTRODUCTION
14
1999), 3) laryngeal function assessment including volitional cough (Daniels, Ballo,
Mahoney, & Foundas, 2000; Horner, Brazer, & Massey, 1993; Schroeder, Daniels,
McClain, Corey, & Foundas, 2006) and voice assessment (Linden, Kuhlemeier, &
Patterson, 1993; McCullough, Wertz, & Rosenbek, 2001), 4) assessment of secretion
management (Langmore et al., 1998; Murray, Langmore, Ginsberg, & Dostie, 1996) and
lastly, 5) the inclusion of trial swallows if deemed clinically appropriate (McCullough &
Martino, 2013). In reference to recently extubated patients in particular, clinicians focus
their CSE to include: case history along with patient interview, dentition, secretion
management, oral motor function, and clinical assessment of oral (efficiency, lip seal)
and pharyngeal (delay, vocal quality) function using food and fluid trials consisting of
multiple textures (Macht et al., 2012).
Following a nationwide survey on practice patterns of SLPs providing service for
mechanically ventilated patients, only 3% of the respondents report that they receive CSE
referrals for all recently extubated patients with 29% reporting that dysphagia referral
guidelines exist for these patients in their respective hospitals (Macht et al., 2012).
Following extubation, SLPs reported waiting a median time of 24 hours prior to
conducting a CSE with 60% of the respondents reporting that a CSE was the primary
diagnostic method for determining post-extubation dysphagia (Macht et al., 2012).
Similar to dysphagia screening, the only standardized CSE have been validated on the
stroke population (Mann, 2002) with a standardized protocol yet to be psychometrically
validated for use with patients following exutbation. In Brazil, the Dysphagia Risk
Evaluation Protocol (DREP) (Padovani, Moraes, Mangili, & de Andrade, 2007) in
conjunction with the Prelimary Assessment Protocol and oral feeding trials are being
utilized as a full clinical swallowing assessment for recently extubated patients (Padovani

INTRODUCTION
15
et al., 2013) however, their psychometric properties are yet to be determined. Hence,
adjunct examination of the swallow by way of objective instrumentation is warranted
particularly for patients at high risk of pharyngeal impairments with or without silent
aspiration (McCullough, Wertz, & Rosenbek, 2001; Noordally, Sohawon, De Gieter,
Bellout, & Verougstraete, 2011) such as those who have experienced prolonged
intubation.
Instrumental swallowing assessments. Instrumental methods of assessing
swallow function include the videofluoroscopic swallow study (VFS) (Logemann, 1993,
1997) and fiberoptic endoscopic evaluation of the swallow (FEES) (Langmore, Schatz, &
Olsen, 1988; Langmore, Schatz, & Olson, 1991). Not only is instrumentation used to
discern the integrity of the swallow and to ascertain potential cause of airway
compromise, it also affords clinicians the opportunity to assess any possible benefit from
interventions such as those involving bolus texture, volume, and administration
modifications and/or compensatory strategies (Martin-Harris, Logemann, McMahon,
Schleicher, & Sandidge, 2000).
The instrumentation most widely available to SLPs providing service to
mechanically ventilated patients is videofluoroscopy (98%) followed by endoscopy
(41%) (Macht et al., 2012). Where available, the VFS is used to assess dysphagia in
approximately 40% of referred patients following extubation (Macht et al., 2012) as
compared to a slightly lower utilization with neurological patients at 36% (Martino et al.,
2004). Hospitalized patients requiring mechanical ventilation, with or without
tracheotomy, have an increased risk of silent aspiration thereby necessitating more
careful inspection of airway compromise with instrumental assessment (Davis &
Thompson Stanton, 2004; Elpern, Scott, Petro, & Ries, 1994; Tolep et al., 1996). While

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both VFS and FEES provide a comprehensive assessment of swallow function and
determine the efficacy of therapeutic strategies, each offer a unique diagnostic
perspective (Aviv, 2000b; Hiss & Postma, 2003; Kidder, Langmore, & Martin, 1994;
Langmore, 2003; Logemann, 1993; Logemann, Rademaker, Pauloski, Ohmae, &
Kahrilas, 1998). The following sections describe each method along with their relative
advantages and weaknesses.
The videofluoroscopic swallow study. The widely accepted gold standard for
instrumental swallowing evaluations of the oral, pharyngeal and upper esophageal phases
of the swallow is the VFS (Martin-Harris et al., 2000; McCullough et al., 2005). Using
videofluoroscopy, Dr. Jeri Logemann adapted the original radiographic swallowing
assessment, barium cineradiography (Donner & Siegel, 1965; Ramsey, Watson, Gramiak,
& Weinberg, 1955), with her procedure and protocol still used routinely (Logemann,
1993, 1997). The VFS affords a dynamic and continuous view of the structures involved
in the swallow (Dodds et al., 1990; Logemann, 1993, 1997). The procedure typically
involves a speech-language pathologist, radiologist and x-ray technician while taking
place in a diagnostic imaging suite outfitted with a fluoroscopy unit (Logemann, 1993).
A regulated amount of food and fluid mixed with barium contrast is given to the patient
while the fluoroscopy unit captures its movement from the oral cavity to beyond the
upper esophageal sphincter (Logemann, 1993). Two views can be obtained during the
VFS, lateral and anterior-posterior, and whether one or both views are conducted is
dependent upon the mobility of the patient, the accommodation of the equipment and the
assessment goals of the VFS (Logemann, 1993, 1997). With the current digital
fluoroscopic technologies, capture rates using a pulse of 30 frames per second with high
resolution recording are recommended (Bonilha et al., 2013).

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Serial radiographic images of the oral cavity, pharynx, upper airway and proximal
esophagus are captured in sequence while the patient swallows barium-contrasted food
and/or liquid (Dodds et al., 1990; Logemann, 1993, 1997). The clinician conducting the
study may espouse either a regimented (Lazarus et al., 1993; Logemann, 1993) or more
patient-led approach (Linden & Siebens, 1983) with bolus textures, volume and order of
presentation are at their discretion. Regardless, protocol components vary across
institutions particularly regarding the textures (Martino et al., 2004) and the barium
concentrations used (Stokely, Molfenter, & Steele, 2014). In addition, the reliability of
videofluoroscopic swallowing interpretation has long been described as poor
(McCullough, Wertz, Rosenbek, et al., 2001; Stoeckli, Huisman, Seifert, & Martin-
Harris, 2003) including poor interrater reliability for airway compromise ratings with
intraclass correlation coefficients ranging from 0.01 to 0.65 (McCullough et al., 2001) .
However, efforts are being made to standardize the procedural protocol (Lazarus et al.,
1993; Logemann, 1993, 1997; Martin-Harris et al., 2008; Martin-Harris et al., 2000) and
its interpretation (Leonard, Kendall, McKenzie, Goncalves, & Walker, 2000; Martin-
Harris et al., 2008; Rosenbek, Robbins, Roecker, Coyle, & Wood, 1996).
Two recent approaches have targeted interpretation objectivity and rater
reliability, namely: 1) through the use of rating scales or scoring systems (Eisenhuber et
al., 2002; Martin-Harris et al., 2008; Molfenter & Steele, 2013; Pearson, Molfenter,
Smith, & Steele, 2013; Rosenbek et al., 1996) or 2) through the digital measurement of
structural movements during the swallow (Allen, White, Leonard, & Belafsky, 2010;
Leonard, Rees, Belafsky, & Allen, 2009; Leonard et al., 2000; Steele et al., 2011).
Individually, each method assesses different aspects of the swallow. The VFS rating
scales or scoring systems each evaluate a different aspect of the swallow using

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18
videofluoroscopic (VF) images (Eisenhuber et al., 2002; Martin-Harris et al., 2008;
Molfenter & Steele, 2013; Pearson et al., 2013; Rosenbek et al., 1996) ranging from
rating structural movement involved in all stages of the swallow (Martin-Harris et al.,
2008), to more specific aspects such as airway protection (Rosenbek et al., 1996) or the
quantification of oropharyngeal residue (Eisenhuber et al., 2002; Molfenter & Steele,
2013; Pearson et al., 2013). Of these methods, two are psychometrically validated: the
Modified Barium Swallow Measurement Tool for Swallow Impairment (MBSImpTM©,
Northern Speech Services, Gaylord, MI) (Martin-Harris et al., 2008) and the Penetration-
Aspiration Scale (PAS)(Rosenbek et al., 1996). The MBSImpTM© is comprised of 17
different components that together describe oral, pharyngeal and esophageal function.
The PAS is an 8-point interval scale that describes the degree to which material has
invaded the airway and whether the material has been ejected. Together, the
MBSImpTM© and PAS quantify swallowing impairment severity and airway protection
respectively.
The MBSImpTM© is the first and only swallowing impairment rating tool of its
kind which has been psychometrically validated (Martin-Harris et al., 2008). Its aim is to
assist the clinician with the interpretation of the underlying swallowing physiology
thereby assisting with intervention approaches (Martin-Harris et al., 2008). The tool’s
authors confirm construct and external validity through their confirmatory factor analysis
and validation against external surrogate measures of swallowing and nutrition along
with high (>80%) intra- and interrater concordance for blinded ratings of the VFS
(Martin-Harris et al., 2008). During the validation study for the MBSImpTM©, the chosen
patient eligibility criteria and the VFS protocol closely aligned with the patients and
protocols seen in clinical practice (Martin-Harris et al., 2008). While the MBSImpTM©

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provides information regarding the physiology underlying the potential airway
compromise, it does not elaborate on the degree of airway invasion or the patient’s
response (Martin-Harris et al., 2008). As a result, the authors of the MBSImpTM© suggest
using the PAS (Rosenbek et al., 1996) in concert with the MBSImpTM© (Martin-Harris et
al., 2008).
The PAS is used to quantify airway invasion using VF images (Rosenbek et al.,
1996). In their seminal study, the authors reported average interjudge intraclass Kappa
coefficients ranging from 0.35 to 0.88 with intrajudge coefficients ranging from 0.21 to
1.0 (Rosenbek et al., 1996). Following its development using stroke, head and neck
cancer patients as well as healthy subjects, it was validated using four judges on multiple
swallows recorded from healthy older subjects along with stroke patients (Rosenbek et
al., 1996). The scale has been utilized widely in both research and clinical practice and
with numerous patient populations (Allen et al., 2010; Bhattacharyya, Kotz, & Shapiro,
2003; Colodny, 2002; Cvejic et al., 2011; Hutcheson et al., 2012; Martin-Harris et al.,
2008; Molfenter & Steele, 2013; Troche, Brandimore, Okun, Davenport, & Hegland,
2014).
While the MBSImpTM© and PAS provide a rating for aspects of the patient’s
swallow, they do not objectively measure structural movement during the swallow.
Individual VF images can be extracted from the VFS and used to conduct image-based
measurements of various structures involved in swallowing (Perlman, VanDaele, &
Otterbacher, 1995) including hyoid bone displacement (Leonard, 2007; Leonard et al.,
2000; Molfenter & Steele, 2014; Perlman et al., 1995; Steele et al., 2011) and pharyngeal
wall constriction (Leonard, 2007; Leonard et al., 2000). Adequate hyoid elevation (Jacob
et al., 1989; Kim & McCullough, 2008; Leonard, 2007; Steele et al., 2011) and

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pharyngeal constriction (Leonard, Kendall, & McKenzie, 2004; Leonard, 2007; Leonard
et al., 2009; Leonard et al., 2000; Setzen et al., 2003; Yip, Leonard, & Belafsky, 2006)
are associated with successful propulsion of food or fluid through the pharynx into the
esophagus thereby preventing laryngeal penetration, tracheal aspiration and/or
pharyngeal residue. There are numerous methods to measure hyoid excursion (Molfenter
& Steele, 2012; Molfenter & Steele, 2014) and one published method to measure
pharyngeal constriction (Leonard et al., 2004; Leonard, 2007; Leonard et al., 2009;
Leonard et al., 2000). Two of the most recently published methods for measuring
anterior and superior hyoid excursion include reporting: 1) the displacement as a
trajectory in absolute units (Leonard, 2007; Leonard et al., 2000) or alternatively 2) the
movement with an anatomical scalar as a reference (Molfenter & Steele, 2014; Steele et
al., 2011). Pharyngeal constriction is measured by way of a ratio that compares the area
of the pharynx at rest with that of it at its most constricted during the swallow (Leonard et
al., 2004; Leonard, 2007; Leonard et al., 2009; Leonard et al., 2000). These displacement
measures may in turn assist in determining possible treatment approaches in order to
remediate specific swallow deficiencies.
Fiberoptic endoscopic evaluation of the swallow. Fiberoptic endoscopic
evaluation of the swallow (FEES) was first published as a dysphagia assessment method
in 1988 (Langmore et al., 1988). Presently it is receiving increasing acceptance as a
viable alternative to the VFS (Hiss & Postma, 2003; Langmore, 2003; Macht et al.,
2012). It typically involves a speech-language pathologist along with an otolaryngologist
or physician trained in the procedure (Langmore, 2003; Langmore et al., 1988). The SLP
and physician have complementary responsibilities during the procedure with the

INTRODUCTION
21
physician rendering pertinent medical diagnoses and the SLP diagnosing and managing
the dysphagia (ASHA, 2000).
FEES utilizes flexible nasendoscopy where the scope is passed through the
nasopharynx and is suspended above the epiglottis (Langmore et al., 1988). It provides a
direct view of the hypopharynx and larynx along with the superior aspects of the upper
trachea and upper esophageal sphincter (Langmore et al., 1988; Langmore et al., 1991;
Murray et al., 1996). Similar to the VFS protocol, the patient is given a variety of bolus
sizes and textures including both solid and liquid depending upon patient tolerance
(Langmore et al., 1988). Different from VFS, the feeding trials are not mixed with a
radiopaque medium, rather food colouring in order to differentiate the bolus from the
surrounding mucosa (Langmore et al., 1988; Langmore et al., 1991). While the use of
coloured dye in enteral tube feeding has had detrimental health effects (Maloney & Ryan,
2002; Maloney et al., 2002), the limited quantity utilized throughout the FEES procedure
has not resulted in any documented medical complications.
Several protocols and scoring systems have been developed for FEES (Langmore,
2011; Murray, 1999). Parameters assessed include the adequacy of structural movement
in relation to bolus position, secretions, airway protection and mucosal integrity
(Langmore, 2011; Murray, 1999). Currently, there are no psychometrically validated
tools for the interpretation of FEES.
Fiberoptic endoscopic evaluation of the swallow with sensory testing. The
FEES procedure may also be expanded to include a sensory testing component (Aviv,
2000a; Aviv et al., 2000; Aviv, Kim, Sacco, et al., 1998; Aviv, Kim, Thomson, et al.,
1998; Aviv et al., 2002). Laryngopharyngeal sensory thresholds are assessed using
measured air pulses as delivered through a nasendoscopy scope equipped with a separate

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22
air channel (Aviv, 2000a; Aviv et al., 2000; Aviv, Kim, Sacco, et al., 1998; Aviv, Kim,
Thomson, et al., 1998; Aviv et al., 2002). These are delivered to the aryepiglottic folds in
an attempt to elicit the laryngeal adductor reflex (LAR) (Aviv, 2000a; Aviv et al., 2000;
Aviv, Kim, Sacco, et al., 1998; Aviv, Kim, Thomson, et al., 1998; Aviv et al., 2002). The
greater air pressure required to elicit the LAR, the greater the laryngeal sensory loss
(Aviv, 1997; Aviv, Kim, Sacco, et al., 1998; Aviv et al., 1997; Aviv et al., 2002). The
normal sensory threshold in order to elicit the LAR is <4.0 mmHg (Aviv et al., 2000;
Aviv, Kim, Thomson, et al., 1998; Aviv et al., 2002). Apart from sensory threshold
testing on neurogenic and mixed patient populations (Aviv et al., 2000; Aviv et al.,
1997), no study has determined sensory thresholds in patients following extubation and
its relationship to their airway protection and swallowing physiology.
VFS versus FEES: which to choose? The instrumental tool of choice is often
based on the diagnostic needs of the clinician, the medical status of the patient or
equipment accessibility (Hiss & Postma, 2003; Langmore, 2003; Langmore et al., 1988;
Langmore et al., 1991). While patients can be managed equally well with either VFS or
FEES (Aviv, 2000b), when compared to VFS, FEES contributes different information
regarding swallow physiology which may provide diagnostic and therapeutic value for
certain populations (Hiss & Postma, 2003; Kelly, Drinnan, & Leslie, 2007; Kelly, Leslie,
Beale, Payten, & Drinnan, 2006; Langmore, 2003; Langmore et al., 1988; Murray et al.,
1996; Wu, Hsiao, Chen, Chang, & Lee, 1997). This is particularly true for patients who
have undergone medical interventions, such as endotracheal intubation, that may affect
their upper airway structural integrity and physiology. In addition, FEES may be more
appropriate for particular clinical situations for example when assessing patients with
restricted mobility or for those unable to leave their care unit due to medical fragility,

INTRODUCTION
23
recent extubation or critical illness (Ajemian, Nirmul, Anderson, Zirlen, & Kwasnik,
2001; Leder, Cohn, & Moller, 1998; Noordally et al., 2011). When compared to VFS,
FEES is arguably a more sensitive tool for identifying airway penetration, aspiration,
and/or residue (Kelly et al., 2007; Kelly et al., 2006; Wu et al., 1997) along with
assessing retained pharyngeal secretions (Murray et al., 1996) or mucosal abnormalities
(Langmore et al., 1988; Langmore et al., 1991). When comparing the influence of
instrumental assessment method on the interpretation of penetration, aspiration and
residue using raters blinded to each other and clinical information, scores were
significantly higher for FEES examinations when compared to VFS (Kelly et al., 2007;
Kelly et al., 2006). Since FEES does not involve radiation exposure, it can be conducted
for as long as the patient will tolerate scope placement (Hiss & Postma, 2003; Langmore,
2003; Leder, 1998). As a result, this procedure may evaluate fatigue or practice effects
over the course of a meal or completed serially in order to evaluate swallow recovery
(Hiss & Postma, 2003; Langmore, 2011; Langmore, 2003; Langmore et al., 1988;
Langmore et al., 1991; Murray, 1999). When comparing costs, FEES is more economic
when compared to VFS due to comparatively lower equipment and personnel costs (Aviv
et al., 2001). However, VFS is recommended if the goals either individually or in
combination are to 1) assess oral and pharyngeal physiology in concert (Logemann et al.,
1998), 2) use standardized methods of interpretation (Martin-Harris et al., 2008;
Rosenbek et al., 1996), or 3) conduct structural displacement measurements (Leonard,
2007; Leonard et al., 2000).

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II. Endotracheal Intubation and Mechanical Ventilation
Background
In 2000, approximately 250,000 patients in the US required prolonged mechanical
ventilation (PMV) for durations exceeding 96 hours during acute illness (Zilberberg, de
Wit, Pirone, & Shorr, 2008). In Ontario by the year 2026, it is projected that the number
requiring PMV will increase by 80% when compared to the incidence in 2006 (Needham
et al., 2005). PMV is a medical necessity and in 2003, its usage in the US accrued costs
of over $16 billion annually, accounting for nearly two-thirds of all healthcare costs
(Zilberberg & Shorr, 2008). Following discharge from acute care, those requiring PMV
continue to have functional disability necessitating ongoing medical care (Chelluri et al.,
2004; Garland et al., 2004; Herridge et al., 2011; Myhren, Ekeberg, & Stokland, 2010).
As a result, early diagnosis of the comorbidities that occur following PMV, such as
dysphagia (Ajemian et al., 2001; Barker, Martino, Reichardt, Hickey, & Ralph-Edwards,
2009; Leder, Cohn, et al., 1998; Tolep et al., 1996), will minimize complications and
improve patient outcomes (Needham et al., 2005).
Dysphagia Following Endotracheal Intubation
It is widely accepted that dysphagia is prevalent in a variety of medical conditions
including stroke (Martino et al., 2005), head and neck cancer (Ward, Bishop, Frisby, &
Stevens, 2002), closed head injuries (Lazarus & Logemann, 1987), spinal cord injuries
(Abel, Ruf, & Spahn, 2004; Kirshblum, Johnston, Brown, O'Connor, & Jarosz, 1999;
Wolf & Meiners, 2003) or cervical spine surgery (Lee, Bazaz, Furey, & Yoo, 2007;
Smith-Hammond et al., 2004; Tervonen et al., 2007). While dysphagia has been
reported to occur in as many as 84% of patients following mechanical ventilation (Macht
et al., 2011), when compared to other patient populations, relatively little has been

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published in this area (Ajemian et al., 2001; Atkins et al., 2010; Atkins et al., 2007;
Barker et al., 2009; Barquist, Brown, Cohn, Lundy, & Jackowski, 2001; Bordon et al.,
2011; Brodsky et al., 2014; Brown et al., 2011; de Larminat, Montravers, Dureuil, &
Desmonts, 1995; de Medeiros, Sassi, Mangilli, Zilberstein, & de Andrade, 2014; DeVita
& Spierer-Rundback, 1990; El Solh, Okada, Bhat, & Pietrantoni, 2003; Elpern et al.,
1994; Ferraris et al., 2001; Hafner, Neuhuber, Hirtenfelder, Schmedler, & Eckel, 2008;
Harrington et al., 1998; Keeling et al., 2007; Kwok et al., 2013; Leder, Cohn, et al., 1998;
Macht, King, et al., 2013; Macht et al., 2011; Messina et al., 1991; Murty & Smith, 1989;
Padovani, Moraes, de Medeiros, de Almeida, & de Andrade, 2008; Rousou et al., 2000;
Tolep et al., 1996). Though the adverse effect of artificial airways on swallowing
function is debatable (Barquist et al., 2001; Leder & Ross, 2000), swallowing
impairments have been documented following prolonged oral endotracheal intubation
(Ajemian et al., 2001; Barker et al., 2009; El Solh et al., 2003; Hogue et al., 1995;
Rousou et al., 2000), tracheotomy (Bonanno, 1971; DeVita & Spierer-Rundback, 1990)
and mechanical ventilation (DeVita & Spierer-Rundback, 1990; Elpern et al., 1994;
Macht et al., 2011; Tolep et al., 1996).
Dysphagia frequency following endotracheal intubation varies widely in the
literature from 3% (Ferraris et al., 2001) to greater than 80% (Macht et al., 2011; Tolep et
al., 1996). Post-extubation dysphagia has been documented across various diagnostic
groups including critical illness (Ajemian et al., 2001; Barquist et al., 2001; Brodsky et
al., 2014; de Larminat et al., 1995; de Medeiros et al., 2014; DeVita & Spierer-Rundback,
1990; El Solh et al., 2003; Hafner et al., 2008; Macht et al., 2011; Padovani et al., 2008;
Partik et al., 2000; Tolep et al., 1996), trauma (Bordon et al., 2011; Brown et al., 2011;
Kwok et al., 2013; Leder, Cohn, et al., 1998), organ transplantation (Atkins et al., 2010;

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Atkins et al., 2007; Helenius-Hietala et al., 2013; Murty & Smith, 1989; Skoretz,
Graham, Kamitomo, & Martino, 2010), thoracic surgery (Davis & Cullen, 1974; Keeling
et al., 2007), orthopedics (Stanley, Bastianpillai, Mulcahy, & Langton, 1995), neurogenic
diseases (Macht, King, et al., 2013; Padovani et al., 2007), and cardiovascular surgery
(Barker et al., 2009; Burgess, Cooper, Marino, Peuler, & Warriner, 1979; Ferraris et al.,
2001; Harrington et al., 1998; Hogue et al., 1995; Messina et al., 1991; Partik et al., 2003;
Rousou et al., 2000; Skoretz & Rebeyka, 2009; Skoretz, Yee, & Martino, 2012). Few
studies are prospective (Barquist et al., 2001; Brodsky et al., 2014; Brown et al., 2011;
Burgess et al., 1979; Davis & Cullen, 1974; El Solh et al., 2003; Hogue et al., 1995;
Kwok et al., 2013; Stanley et al., 1995) with some basing dysphagia frequency on a
heterogeneous patient subset referred for swallowing assessments (de Medeiros et al.,
2014; Hafner et al., 2008; Macht, King, et al., 2013; Macht et al., 2011; Moraes, Sassi,
Mangilli, Zilberstein, & de Andrade, 2013). Intubation times have been reported in few
studies (Ajemian et al., 2001; Barker et al., 2009; Barquist et al., 2001; El Solh et al.,
2003; Hogue et al., 1995; Leder, Cohn, et al., 1998; Rousou et al., 2000) and a variety of
diagnostic methods are utilized across studies with many conducting assessments at
undeclared time intervals following extubation (Barker et al., 2009; Brodsky et al., 2014;
Ferraris et al., 2001; Hogue et al., 1995; Macht, King, et al., 2013; Macht et al., 2011;
Rousou et al., 2000). We will discuss each of these limitations in turn.
Studies reporting on post-extubation dysphagia are limited by their patient sample
and their failure to declare intubation durations across the population. The studies often
include heterogeneous patient populations (Ajemian et al., 2001; Barquist et al., 2001;
Bordon et al., 2011; Brown et al., 2011; Davis & Cullen, 1974; de Larminat et al., 1995;
Keeling et al., 2007; Kwok et al., 2013; Leder, Cohn, et al., 1998; Padovani et al., 2008)

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with diagnoses commonly known to cause dysphagia (Abel et al., 2004; Kirshblum et al.,
1999; Lazarus & Logemann, 1987; Martino et al., 2005; Ward et al., 2002; Wolf &
Meiners, 2003). For example, many studies have included patients with neurogenic
diagnoses (Bordon et al., 2011; Brown et al., 2011; Hafner et al., 2008; Kwok et al.,
2013; Macht, King, et al., 2013; Tolep et al., 1996), head and/or neck malignancies
(Keeling et al., 2007) and in-situ tracheostomies (Bordon et al., 2011; Brown et al., 2011;
DeVita & Spierer-Rundback, 1990; Hafner et al., 2008; Harrington et al., 1998; Hogue et
al., 1995; Macht, King, et al., 2013; Tolep et al., 1996). In addition, few studies declare
intubation durations across their patient sample (Ajemian et al., 2001; Barker et al., 2009;
Barquist et al., 2001; El Solh et al., 2003; Hogue et al., 1995; Leder, Cohn, et al., 1998;
Rousou et al., 2000). As a result, dysphagia frequency estimates following extubation
according to diagnosis are likely imprecise and the relation between intubation duration
and dysphagia remains unclear.
Methods utilized by SLPs in order to assess swallowing impairments vary (Macht
et al., 2012; Martino et al., 2004), particularly when assessing swallowing following
mechanical ventilation (Macht et al., 2012). At present, screening and clinical
swallowing evaluation tools have yet to be psychometrically validated on patients
following extubation and as a result, standardized practice is lacking (Macht et al., 2012).
In the published literature, the diagnostic methods used to assess patients’ swallowing
following extubation ranges from swallowing screening, clinical swallowing assessments
(Bordon et al., 2011; Brodsky et al., 2014; Brown et al., 2011; de Medeiros et al., 2014;
Kwok et al., 2013; Macht, King, et al., 2013; Macht et al., 2011; Moraes et al., 2013) to
instrumental assessments including chest radiographs (Burgess et al., 1979; Davis &
Cullen, 1974; Stanley et al., 1995), barium cineradiography (Hogue et al., 1995; Rousou

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et al., 2000), FEES (Ajemian et al., 2001; Barquist et al., 2001; El Solh et al., 2003;
Hafner et al., 2008; Leder, Cohn, et al., 1998), VFS (Barker et al., 2009; Ferraris et al.,
2001; Keeling et al., 2007) and swallowing latency measurements (de Larminat et al.,
1995). In some studies, multiple assessment methods are utilized (Barker et al., 2009;
Barquist et al., 2001; Ferraris et al., 2001; Harrington et al., 1998; Hogue et al., 1995;
Tolep et al., 1996) with many of the utilized methods, such as static radiographs (Burgess
et al., 1979; Davis & Cullen, 1974) and latency measurements (de Larminat et al., 1995),
lacking in sensitivity and specificity. The timing of dysphagia assessment across studies
varies from immediately following extubation (Burgess et al., 1979; de Larminat et al.,
1995) to assessment upon discharge (Brodsky et al., 2014). Some studies do not declare
assessment timing in relation to extubation timing (Barker et al., 2009; Ferraris et al.,
2001; Hogue et al., 1995; Rousou et al., 2000). Due to rapid change in the patient’s
status following extubation (de Larminat et al., 1995), consistent assessment timing is
crucial. Without consistent assessment methods with adequate precision (Whiting,
Rutjes, Reitsma, Bossuyt, & Kleijnen, 2003; Whiting et al., 2006) or timing of post-
extubation evaluations, the accuracy of reported dysphagia frequency is questionable.
Dysphagia characteristics. Swallowing physiology following mechanical
ventilation is described in the literature using various methods. From impairment based
on clinical observation (de Medeiros et al., 2014; Macht, King, et al., 2013; Macht et al.,
2011; Moraes et al., 2013; Padovani et al., 2007) to limited dysphagia descriptions
following the use of instrumentation (Hafner et al., 2008; Leder, Cohn, et al., 1998), no
study to date has described both oral and pharyngeal post-extubation swallowing
physiology using psychometrically validated measures. Following clinical assessment,
dysphagia severity following extubation has been rated as moderately-severe in the

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majority of patients (Macht, King, et al., 2013; Macht et al., 2011) with primary clinical
signs including post-swallow coughing (de Medeiros et al., 2014; Kwok et al., 2013;
Padovani et al., 2007) and voice change (de Medeiros et al., 2014; Kwok et al., 2013).
Reporting dysphagia characteristics based solely on clinical assessment can be
questionable (McCullough et al., 2000). For example, one study reports the frequency of
silent aspiration and pharyngeal residue without the use of instrumentation (Kwok et al.,
2013), both of which are impossible to confirm based on clinical observation alone.
Following instrumental assessments, many studies define dysphagia primarily as
penetration or aspiration (Burgess et al., 1979; Davis & Cullen, 1974; Ferraris et al.,
2001; Hafner et al., 2008; Stanley et al., 1995) with aspiration frequencies ranging from
45% (Leder, Cohn, et al., 1998) to 90% (Hogue et al., 1995). Even with instrumentation,
most dysphagia is characterized using general descriptions that are not operationally
defined (de Larminat et al., 1995; Ferraris et al., 2001; Leder, Cohn, et al., 1998; Rousou
et al., 2000). For example, the swallowing impairment is characterized with nonspecific
terms such as delay (de Larminat et al., 1995) or oral and/or pharyngeal abnormalities
(Ferraris et al, 2001). As a result, it is difficult to understand post-extubation swallowing
physiology, the mechanisms underlying dysphagia and possible methods of remediation.
Consequences of dysphagia. The medical status of patients following extubation
is often tenuous (Blackwood et al., 2011) and when present, dysphagia and its sequelae
can lead to higher rates of mortality (Cabré et al., 2010; DeVita & Spierer-Rundback,
1990; Macht, King, et al., 2013; Macht et al., 2011), increased hospitalization costs
(Altman et al., 2010; Cichero & Altman, 2012; Ferraris et al., 2001; Semenov, Starmer,
& Gourin, 2012; Starmer et al., 2014) and poor patient outcomes (Barker et al., 2009;
Brown et al., 2011; Macht, King, et al., 2013; Macht et al., 2011; Rashkin & Davis,

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1986). In-hospital mortality for those with severe post-extubation dysphagia is
significantly higher when compared to those without the disorder (Macht et al., 2011).
Regardless of the underlying diagnosis, mortality at 1 year following hospital discharge is
28% higher in those with dysphagia as opposed to those without (Cabré et al., 2010).
Post-extubation dysphagia impacts a patient’s nutritional status by delaying resumption
of oral intake (Barker et al., 2009; Ferraris et al., 2001; Hafner et al., 2008; Macht, King,
et al., 2013; Macht et al., 2011) and hospital discharge (Barker et al., 2009; Brown et al.,
2011; Macht, King, et al., 2013; Macht et al., 2011). These prolonged hospitalizations
due to dysphagia incur greater costs (Altman et al., 2010; Cichero & Altman, 2012;
Ferraris et al., 2001; Semenov et al., 2012; Starmer et al., 2014). In the US, it is
estimated the increased length of stay secondary to dysphagia alone incurs $547 million
of additional care charges annually (Altman et al., 2010). Poor patient outcomes
associated with post-extubation dysphagia include increased rates of pneumonia (Brown
et al., 2011; Kwok et al., 2013; Macht, King, et al., 2013), reintubation (Barker et al.,
2009; Kwok et al., 2013; Macht, King, et al., 2013; Macht et al., 2011), and aspiration
(Ajemian et al., 2001; Harrington et al., 1998; Hogue et al., 1995; Leder, Cohn, et al.,
1998). Whether the etiology of aspiration is prandial in nature (Lundy et al., 1999;
Smith, Logemann, Colangelo, Rademaker, & Pauloski, 1999) or of contaminated oral
secretions (Marik, 2001, 2006; Marik, 2011; Marik & Kaplan, 2003; Murray et al., 1996),
it can increase a patient’s risk of developing pneumonia (Loeb, McGeer, McArthur,
Walter, & Simor, 1999; Lundy et al., 1999; Martino et al., 2005; Starmer et al., 2014).
Dysphagia, particularly in the presence of other medical comorbidities, is a
significant predictor for aspiration pneumonia (Cabré et al., 2014; Hibberd, Fraser,
Chapman, McQueen, & Wilson, 2013; Langmore et al., 1998; Marik & Kaplan, 2003;

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Martin, Corlew, et al., 1994). According to the US National Hospital Discharge Survey,
the relative risk of aspiration pneumonia in patients with dysphagia is approximately nine
times greater when compared to those who do not have the disorder (Altman et al., 2010).
Following stroke, the risk of developing pneumonia is eleven times greater in patients
who aspirate compared to similar patients who do not (Martino et al., 2005). Aspiration
pneumonia also increases readmissions to the intensive care unit (Kozlow, Berenholtz,
Garrett, Dorman, & Pronovost, 2003) and hospital (Cabré et al., 2014) and is associated
with increased hospitalization durations and care costs (Kozlow et al., 2003). Following
surgery, aspiration pneumonia increases the average hospital length of stay by five times
(25 days versus 5 days) and hospitalization costs by four times ($58,000 USD versus
$14,000) (Kozlow et al., 2003). In Canada, the mean healthcare costs of aspiration
pneumonia per patient can run as high as $94,000 (Sutherland, Hamm, & Hatcher, 2010).
Aspiration and its adverse outcomes impacts the recovery of the critically ill (Cameron,
Mitchell, & Zuidema, 1973; Christ et al., 2006; Shifrin & Choplin, 1996) particularly
those who have undergone mechanical ventilation (Almirall, Cabré, & Clavé, 2012;
DeVita & Spierer-Rundback, 1990; Elpern et al., 1994; Kozlow et al., 2003; Spray,
Zuidema, & Cameron, 1976; Tolep et al., 1996). Therefore early multi-disciplinary
involvement with this patient group is essential (Marsh, Bertanou, Suominen, &
Venkatachalam, 2010; Starks & Harbert, 2011).
In an attempt to mitigate the ill-effects of aspiration pneumonia, specifically the
increased cost of care, hospital protocols now include speech-language pathology led
assessments and interventions (Marsh et al., 2010; Starks & Harbert, 2011). There is
emerging evidence that the frequency of pneumonia following CV surgery has been
reduced with SLP-lead protocol targeting oral care and mandatory swallowing

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assessments following extubation (Starks & Harbert, 2011). In Great Britain alone these
SLP led initiatives have reduced annual hospitalization costs incurred by iatrogenic
respiratory infections from 48.2 million GBP to 26.1 million (Marsh et al., 2010).
Etiology of Post-extubation Dysphagia
Endotracheal intubation. Endotracheal intubation, particularly of prolonged
durations, is an independent predictor of dysphagia (Barker et al., 2009; Bordon et al.,
2011; Brodsky et al., 2014; Hogue et al., 1995; Kwok et al., 2013; Macht, King, et al.,
2013). In trauma patients, the odds of dysphagia following extubation increased nearly
three-fold with every additional day of mechanical ventilation (Kwok et al., 2013).
While some studies dispute the relation between dysphagia and mechanical ventilation
duration (Barquist et al., 2001) or the use of artificial airways (Leder & Ross, 2000),
there is general consensus, albeit based on only a few studies, that increasing intubation
durations increase the frequency of dysphagia (Barker et al., 2009; Bordon et al., 2011;
Brodsky et al., 2014; Hogue et al., 1995; Kwok et al., 2013; Macht, King, et al., 2013).
Despite this, there is little consensus, either in the mechanical ventilation or dysphagia
literature regarding the cutpoint that defines prolonged intubation.
The durations that define prolonged intubation vary widely across both the
intubation (Macewen, 1880; Vogelhut & Downs, 1979) and dysphagia literature
(Ajemian et al., 2001; de Larminat et al., 1995; Tolep et al., 1996). The earliest record
of prolonged endotracheal intubation, published in 1880, included patients who were
intubated for 24 hours or more (Macewen, 1880). In contrast, other authors have defined
prolonged intubation as greater than seven days (Vogelhut & Downs, 1979). In the
dysphagia literature, prolonged intubation has been defined as greater than 24 hours (de
Larminat et al., 1995), 48 hours (Ajemian et al., 2001; Barker et al., 2009; Barquist et al.,

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2001; Bordon et al., 2011; Brodsky et al., 2014; El Solh et al., 2003; Leder, Cohn, et al.,
1998; Padovani et al., 2008) or 8 days (Tolep et al., 1996). This lack of consistency
makes comparisons across studies difficult.
Upper aerodigestive tract morbidities. Regardless of the medical necessity that
precipitated the need for endotracheal intubation, injuries to the upper aerodigestive tract
following endotracheal tube placement are recognized complications (Cook, Scott, &
Mihai, 2010; Domino, Posner, Caplan, & Cheney, 1999). Injuries to the larynx and
pharynx following endotracheal intubation account for over half of all closed anesthesia
claims in the US (Domino et al., 1999). Post-extubation upper aerodigestive tract
morbidities include structural and sensory changes which can lead to biomechanical
alterations that disrupt the structural coordination necessary for deglutition and airway
protection (Burns, Dayal, Scott, van Nostrand, & Bryce, 1979; DeVita & Spierer-
Rundback, 1990; El Solh et al., 2003; Medda et al., 2003; Santos, Afrassiabi, &
Weymuller, 1994; Sellery, Worth, & Greenway, 1978).
Injury and biomechanical changes. Nearly all intubated patients experience some
degree of pharyngeal, laryngeal and/or subglottal damage (Colice, Stukel, & Dain, 1989;
Santos et al., 1994; Stauffer, Olson, & Petty, 1981; Thomas et al., 1995), which
ultimately affects glottal competence and airway protection. Clinically observable
symptoms range from mild cases of vocal hoarseness to more serious complications
including aphonia (Hamdan, Sibai, Rameh, & Kanazeh, 2007; Santos et al., 1994) and
stridor (Grillo, 1979; Grillo & Donahue, 1996; Macchiarini, Verhoye, Chapelier, Fadel,
& Dartevelle, 2001; Tadié et al., 2010). Post-extubation stridor as a result of inadequate
glottal opening can be potentially fatal precipitating the need for reintubation (Tadié et
al., 2010) and/or surgical intervention either by way of an emergent tracheotomy or

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surgical repair (Grillo, 1979; Grillo & Donahue, 1996; Macchiarini et al., 2001). Other
post-extubation vocal fold pathologies include: arytenoid subluxation (Talmi, Wolf, Bar-
Ziv, Nusem-Horowitz, & Kronenberg, 1996), edema, ulceration (Burns et al., 1979;
Colice et al., 1989; Santos et al., 1994; Tadié et al., 2010), tissue granulation (Colice et
al., 1989; Colton House, Noordzij, Murgia, & Langmore, 2011; Lundy, Casiano, Shatz,
Reisberg, & Xue, 1998; Mencke et al., 2003; Santos et al., 1994; Tadié et al., 2010),
abnormal vocal fold mobility (Burns et al., 1979; Colton House et al., 2011; Lundy et al.,
1998; Peppard & Dickens, 1983; Santos et al., 1994; Tadié et al., 2010), and vocal fold
hematomas (Mencke et al., 2003; Peppard & Dickens, 1983). Increased swelling
throughout the oropharynx may also occur, negatively affecting respiration by increased
laryngeal resistance (Tanaka, Isono, Ishikawa, Sato, & Nishino, 2003) and/or work of
breathing (Ishaaya, Nathan, & Belman, 1995). This edema may also affect swallowing
sensory integration due to the high density of afferent receptors throughout the area
including the pharyngeal mucosa, base of tongue and faucial pillars (DeVita & Spierer-
Rundback, 1990; Miller, 1982). Resolution of some LP injuries may occur in the weeks
following extubation (Colice, 1992; Colice et al., 1989; Peppard & Dickens, 1983; Santos
et al., 1994), with others having delayed onset and a more protracted recovery course
(Santos et al., 1994). As a result, LP injuries can affect the integrity of the swallow at
any time following extubation.
To our knowledge, only one study has evaluated the relation between intubation
duration and the co-occurrence of dysphagia and LP abnormalities (Postma et al., 2007).
The authors retrospectively evaluated the FEES examinations of 100 hospitalized patients
referred for swallowing assessments. They found a high incidence of glottal edema
(33%), granuloma formation (31%), and vocal fold paresis (24%) in those patients with

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dysphagia. While those who were intubated had significantly higher incidence of LP
anomalies, nearly two thirds of the cohort who were not intubated also presented LP
anomalies, thus, highlighting the importance of structural integrity for adequate
swallowing mechanics.
Injury etiology. The etiologies of LP morbidities following intubation are
typically mechanical in nature (Arts, Rettig, de Vries, Wolfs, & in't Veld, 2013; Combes
et al., 2001; Dubick & Wright, 1978; Grillo, 1979; Grillo & Donahue, 1996; Hamdan et
al., 2007; Honeybourne, Costello, & Barham, 1982; Lundy et al., 1998; Macchiarini,
Verhoye, Chapelier, Fadel, & Dartevelle, 2000; Macchiarini et al., 2001; Stauffer et al.,
1981; Tanaka et al., 2003) and are not necessarily a result of traumatic, difficult (Asai,
Koga, & Vaughan, 1998) or prolonged intubations (Heffner, 2010; Lundy et al., 1998).
Though debated throughout the literature (Braz, Volney, Navarro, Braz, & Nakamura,
2004; Colton House et al., 2011), LP injury location and severity is often dependent upon
an oral versus nasal approach (Dubick & Wright, 1978), endotracheal tube type (Tanaka
et al., 2003), cuff volume (Combes et al., 2001; Honeybourne et al., 1982), and cuff
pressure (Arts et al., 2013; Combes et al., 2001; Hamdan et al., 2007). For example,
when comparing oral versus nasal intubation, the incidence of laryngeal morbidity such
as impaired glottis closure, laryngeal edema and ulceration was higher with an oral
approach (Dubick & Wright, 1978). Injuries related to cuff location and volume include
subglottic stenosis and tracheoesophageal fistula (Grillo, 1979; Grillo & Donahue, 1996;
Lundy et al., 1998; Macchiarini et al., 2000, 2001; Stauffer et al., 1981).
The recurrent laryngeal nerve may be damaged due to intubation (Cavo, 1985;
Dimarakis & Protopapas, 2004; Gibbin & Egginton, 1981; Hamdan et al., 2002; Ishimoto
et al., 2002; Shafei et al., 1997). More specifically, the anterior branch of the RLN can

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be injured due to the insertion or alternatively, the presence of the endotracheal tube
(Brandwein, Abramson, & Shikowitz, 1986; Itagaki et al., 2007; Myssiorek, 2004; Stout,
Bishop, Dwersteg, & Cullen, 1987). Injury severity is often related to endotracheal tube
cuff position, volume (Brandwein et al., 1986; Itagaki et al., 2007; Myssiorek, 2004;
Stout et al., 1987), size, or placement duration (Inada, Fujise, & Shingu, 1998; Itagaki et
al., 2007; Myssiorek, 2004; Stout et al., 1987). Kikura and colleagues (2006) reported a
two-fold increase in the odds of vocal fold injury with intubations of three to six hours
compared to a fifteen-fold increase in RLN injury in those patients intubated for 15 hours
or more (Kikura, Suzuki, Itagaki, Takada, & Sato, 2007). As a result, those with post-
operative vocal cord paralysis should be treated with an interdisciplinary approach and
undergo early diagnosis and management in order to minimize post-operative
complications (Schneider et al., 2003), such as dysphagia, which may contribute to
respiratory decompensation or even death.
Mechanical ventilation and the swallow. Patients requiring mechanical
ventilation comprise a diagnostic subgroup with a tenuous respiratory system and unique
respiratory physiology (Aliverti et al., 2011; Blackwood et al., 2011; Capdevila et al.,
1998; Esteban et al., 2002; Habib, Zacharias, & Engoren, 1996; Herridge et al., 2011;
Ishaaya et al., 1995; Zhu, Lee, & Chee, 2012). Those requiring mechanical ventilation
often need respiratory support due to pathological processes that decrease lung
compliance, pulmonary elasticity and respiratory muscle strength as well as contribute to
alveolar derecruitment and impaired muccociliary clearance (Ashbaugh, Bigelow, Petty,
& Levine, 1967; Crimi & Slutsky, 2004; Fan, Needham, & Stewart, 2005; Habib et al.,
1996; Petty & Ashbaugh, 1971; Zhu et al., 2012). Because of their underlying respiratory
physiology, these patients are at an intrinsic disadvantage in their ability to overcome any

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respiratory complications secondary to dysphagia (Cvejic et al., 2011; Gross, Atwood,
Ross, Olszewski, & Eichhorn, 2009; Harding, 2002; Martin-Harris, Michel, & Castell,
2005; Nishino, 2012). When compared to other patient groups, the recently extubated
patient differs in more ways. The decision to proceed with extubation is based on many
clinical and pulmonary factors (Blackwood et al., 2011; Fan et al., 2005; Yang & Tobin,
1991) including breathing patterns, work of breathing and respiratory physiology
(Blackwood et al., 2011; Capdevila et al., 1998; Ishaaya et al., 1995; Khamiees, Raju,
DeGirolamo, Amoateng-Adjepong, & Manthous, 2001; Leitch, Moran, & Grealy, 1996;
Mehta, Nelson, Klinger, Buczko, & Levy, 2000). Although breathing patterns and
respiratory function are often similar for patients both before and shortly following
extubation, it differs from that of healthy subjects (Krieger, Chediak, Gazeroglu,
Bizousky, & Feinerman, 1988). As we will discuss in the subsequent sections, these
respiratory variations from normal (Nishino, 2012) along with changes in the swallowing
reflex and apneic period following mechanical ventilation (Hasegawa & Nishino, 1999),
increases a patient’s risk for dysphagia and its sequelae (Martin, Logemann, et al., 1994;
Martin-Harris, Michel, et al., 2005; Nilsson, Ekberg, Bülow, & Hindfelt, 1997).
Breathing and swallowing: Taxing an already taxed system. Mechanical
ventilation has an immediate and sometimes lasting effect on the coordination of
swallowing and respiration (Elpern et al., 1994; Hasegawa & Nishino, 1999; Nishino,
2012; Nishino, Sugimori, Kohchi, & Hiraga, 1989). Abnormal breathe-swallow
coordination has been observed in numerous patient populations (Hadjikoutis,
Pickersgill, Dawson, & Wiles, 2000; Hirst, Ford, Gibson, & Wilson, 2002; Nilsson et al.,
1997; Selley, Flack, Ellis, & Brooks, 1989b) including those following mechanical
ventilation (Aliverti et al., 2011; Capdevila et al., 1998; Elpern et al., 1994; Hasegawa &

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38
Nishino, 1999; Nishino, 2012). This discoordination often increases the frequency of
airway penetration and/or aspiration (Nilsson et al., 1997) predisposing patients to
pulmonary complications (Martin, Logemann, et al., 1994; Martin-Harris, Michel, et al.,
2005). Healthy subjects enact a protective mechanism that involves a spontaneous phase
resetting of the inhalation-exhalation respiratory pattern when they are about to engage in
a swallowing act (Paydarfar, Gilbert, Poppel, & Nassab, 1995; Terzi et al., 2007).
Following mechanical ventilation, patients often initiate their swallow during inspiration
(Hadjikoutis et al., 2000; Nishino, 2012; Nishino & Hiraga, 1991) even though their
breathe-swallow cycle still remains coupled (Nishino & Hiraga, 1991). In addition, their
airway may be compromised further due to temporal and apneic period alterations during
swallowing (Hasegawa & Nishino, 1999; Paydarfar et al., 1995).
Patients who are tachypneic, hypercapneic or hypoxemic are at increased risk of
aspiration when compared to those who are not (Boden et al., 2009; Gross et al., 2009;
Matsuo, Hiiemae, Gonzalez-Fernandez, & Palmer, 2008; Nishino, Hasegawa, Ide, &
Isono, 1998). Following extubation, patients often exhibit compensatory respiratory
mechanics as a result of their altered lung volumes (Habib et al., 1996; Zhu et al., 2012)
leading to increased work of breathing and respiratory rates (Ishaaya et al., 1995; Mehta
et al., 2000). These increases can result in a shortening of the obligatory apneic period
during swallowing (Boden et al., 2009; Martin, Logemann, et al., 1994; Nilsson et al.,
1997; Nishino et al., 1998). In addition, these patients may also engage in suboptimal
ventilation (Blackwood et al., 2011; Habib et al., 1996; Zhu et al., 2012). The net effect
of these respiratory alterations results in decreased glottic closure durations with a higher
likelihood of an unprotected airway while the bolus passes through the pharynx (Boden et
al., 2009; Gross, Atwood, Grayhack, & Shaiman, 2003; Nishino et al., 1998).

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Altered respiratory physiology and its adverse effect on the swallow has also been
demonstrated in healthy subjects (Gross et al., 2003; Nishino et al., 1998). In an
experimental paradigm illustrating the effect of altered lung volumes, healthy subjects
with normal swallows were given oral trials at three randomized and artificially-induced
lung volumes: total lung capacity, function residual capacity and residual volume (Gross
et al., 2003). The duration of pharyngeal activity was significantly shorter in the latter
two lung volume paradigms with more frequent airway compromise (Gross et al., 2003).
Similar findings were reported in an earlier study (Nishino et al., 1998). When
hypercapnea was induced, the subjects’ swallowing rate decreased, breathing and
swallowing became discoordinated, and swallow timing was altered (Nishino et al.,
1998). The hypercapneic condition induced more frequent clinical instances of aspiration
and those who exhibiting these clinical signs, often initiated swallowing during the
inhalatory phase (Nishino et al., 1998). Throughout the study, no clinical instances of
aspiration occurred during the expiratory phase (Nishino et al., 1998). These studies
support the premise that although recently extubated patients are able to sustain
respiration unsupported, their dysphagia risk is greater than that of healthy subjects for
numerous reasons including an inability to sustain adequate airway protection during
swallowing due to alterations with their: respiratory pattern, breathe-swallow
coordination, respiratory rate and the timing of swallowing activities.
Anesthesia and upper aerodigestive function. Drug regimens utilized for
general anesthesia can have a sedating and lasting effect (Chia, Lee, & Liu, 2008;
d'Honneur et al., 1992; Isono, Ide, Kochi, Mizuguchi, & Nishino, 1991; Mencke et al.,
2014; Nishino & Hiraga, 1991; Park et al., 2011; Rimaniol, D'Honneur, & Duvaldestin,
1994; Sauer, Stahn, Soltesz, Noeldge-Schomburg, & Mencke, 2011) impairing airway

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40
protection capabilities (Cedborg et al., 2014; Chia et al., 2008; Isono et al., 1991; Mencke
et al., 2003; Sundman et al., 2001). Although these regimens minimize upper airway
complications by allowing for ease of intubation, subsequent induction and eventual
extubation (Chia et al., 2008; Honarmand & Safavi, 2008; Mazzarella et al., 1987;
Mencke et al., 2014; Park et al., 2011), higher frequencies of LP impairments have been
reported with some drug regimens when compared to others (Mencke et al., 2006) along
with lasting laryngeal effects even after reversal (Sauer et al., 2011). In healthy
volunteers, Sundman and colleagues (2001) evaluated the effect of various anesthesia
medications on airway competence while assessing swallowing with videoradiography
and pharyngeal manometry (Sundman et al., 2001). Airway penetration and impaired
pharyngeal constriction persisted even as subhypnotic doses of propofol, isoflurane or
sevoflurane were weaned and/or reversed (Sundman et al., 2001). Similarly, in another
study with healthy subjects, swallowing became progressively impaired with decreased
airway protection during partial neuromuscular blockade (Cedborg et al., 2014). While
the half-life and residual effects of many anesthesia medications are relatively short
ranging from 20 minutes to approximately two hours (d'Honneur et al., 1992; d'Honneur
et al., 1996), the effect of anesthesia can be unique and longer lasting in various muscle
groups (d'Honneur et al., 1992; d'Honneur et al., 1996; Hwang, St John, & Bartlett, 1983;
Nishino, Shirahata, Yonezawa, & Honda, 1984).
Some induction medications have a more pronounced effect on upper
aerodigestive musculature (d'Honneur et al., 1996). Those muscles involved in
swallowing and airway patency recover more slowly following induction when compared
to those involved in respiration (d'Honneur et al., 1996; Hwang et al., 1983; Nishino et
al., 1984). For example, in animal studies the cranial nerve (CN) that innervates the

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41
intrinsic lingual muscles (CN XII) is more sensitive to general anesthetics than the vagus
and phrenic nerves (Hwang et al., 1983; Nishino et al., 1984). The recovery time of
laryngeal muscles following anesthesia also differs when compared to those in the hand
(Donati, Meistelman, & Plaud, 1991; Plaud, Debaene, Lequeau, Meistelman, & Donati,
1996). This differential sensitivity and recovery time is of particular importance during
the period following anesthesia and extubation (Isono et al., 1991). Oral feeding is
typically considered at this time as the patient is breathing spontaneously; however,
swallowing can be impaired following anesthesia even if respiration is unassisted
(Cedborg et al., 2014; Isono et al., 1991). As a result, it is still not clear when oral
feeding can be initiated following extubation (Kerz & Wahlen, 2004).

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III. Cardiovascular Surgery
Heart Disease
Burden of care. Approximately 1.3 million Canadians have heart disease (Heart
and Stroke Foundation of Canada, 2003; Lee et al., 2009; Public Health Agency of
Canada, 2009). Heart disease accounts for 20% of all Canadian hospitalizations and is
the leading cause of death in Canada (Heart and Stroke Foundation of Canada, 2003; Lee
et al., 2009; Public Health Agency of Canada, 2009). In 2000, cardiovascular disease
incurred over $22 billion in costs to the Canadian healthcare system (Heart and Stroke
Foundation of Canada, 2003; Public Health Agency of Canada, 2009) and continues to
impart substantial economic burden by incurring millions of dollars in long-term
disability annually (Heart and Stroke Foundation of Canada, 2003). At a cost of $3,400
per patient per hospitalization (Heart and Stroke Foundation of Canada, 2003; Public
Health Agency of Canada, 2009), heart disease-related hospital admissions are the
highest incurring cost category across all medical diagnoses (Heart and Stroke
Foundation of Canada, 2003; Public Health Agency of Canada, 2009). While the
mortality rate for all cardiovascular diseases dropped by 56% between the years of 1969-
1999 and continues to do so (Heart and Stroke Foundation of Canada, 2003), heart
disease prevalence is rising with nearly 40% of adults having three or more of its risk
factors (Public Health Agency of Canada, 2009).
Heart disease risk factors. Heart disease risk factors differ for coronary vessel
and valve disease. Risk factors for vessel disease are primarily attributed to remediable
lifestyle or environmental factors (Greenland et al., 2003; Heart and Stroke Foundation of
Canada, 2003; Public Health Agency of Canada, 2009; Rosengren et al., 2004; Yusuf et
al., 2005; Yusuf et al., 2004). The large INTERHEART study, including 226 coronary

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43
care facilities across 52 countries, identified a risk factor set that was attributable for 90%
of coronary vessel disease (Yusuf et al., 2004). These lifestyle or environmental related
factors included: abnormal lipids, smoking, hypertension, diabetes, abdominal obesity
(Yusuf et al., 2005; Yusuf et al., 2004), psychosocial factors (i.e., a combination of home,
work related or financial stresses and/or anxiety and/or depression) (Rosengren et al.,
2004; Yusuf et al., 2004), limited consumption of fruits and vegetables, regular
consumption of alcohol, and limited physical activity (Yusuf et al., 2005; Yusuf et al.,
2004). Risk factors for cardiac valve dysfunction include congenital anomalies, systemic
disease and/or degenerative processes (Bakir, Onan, Onan, Gul, & Uslu, 2013; Bolling et
al., 2010; Boudoulas et al., 2013; David, Armstrong, McCrindle, & Manlhiot, 2013;
David, Ivanov, Armstrong, Christie, & Rakowski, 2005; Lio et al., 2014; Modi, Hassan,
& Chitwood, 2008; Rankin et al., 2013) for example; endocarditis, rheumatic heart
disease (Bakir et al., 2013; Boudoulas et al., 2013; Yau, El-Ghoneimi, Armstrong,
Ivanov, & David, 2000), and myocardial ischemia (Boudoulas et al., 2013; Lio et al.,
2014; Rankin et al., 2013). When medical management is no longer sufficient for
remediating cardiac-related illnesses, cardiovascular surgery is often required (Heart and
Stroke Foundation of Canada, 2003; Public Health Agency of Canada, 2009).
Cardiovascular Surgery Types
In 2005 alone, over 32,000 coronary artery bypass and/or heart valve surgeries
were performed in Canada (Heart and Stroke Foundation of Canada, 2003; Public Health
Agency of Canada, 2009). The most frequent age demographic undergoing valve and/or
bypass surgery were patients between 65-80 years of age (Heart and Stroke Foundation
of Canada, 2003; Public Health Agency of Canada, 2009). Across all hospitalizations in
the US, coronary artery bypass grafting and cardiac valve surgery is the most common

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surgical intervention with total hospital costs ranging from $7, 054 to $46, 317 per patient
(Kilic et al., 2014).
Cardiovascular surgeries, including coronary artery bypass and/or valve surgery,
are life sustaining procedures given the roles of the heart, major coronary arteries and the
tricuspid, mitral, pulmonic and aortic valves (Hillis et al., 2011; Nishimura et al., 2014).
Coronary arteries supply the myocardium with blood (Hillis et al., 2011) while the
cardiac valves aid in the prevention of regurgitant blood flow throughout the heart
chambers (Nishimura et al., 2014). Coronary artery bypass grafting is a surgical
procedure where one or multiple constricted coronary arteries are bypassed using
autologous arteries or veins serving to improve blood supply to the myocardium (Hillis et
al., 2011). In 1960, the first successful bypass procedure was performed by Dr. Goetz in
the US (Goetz, Rohman, Haller, Dee, & Rosenak, 1961). Subsequently in 1964, Dr.
Kolesov completed the first successful bypass using a suture closure in Russia (Kolesov
& Potashov, 1965). Either with or without coronary artery bypass grafting, cardiac valve
surgery consists of repair or replacement of any of the one or more heart valves
(Boudoulas et al., 2013; Nishimura et al., 2014). Cardiac valves are repaired or replaced
if they have a primary congenital pathology (Sarris, Comas, Tobota, & Maruszewski,
2012) or exhibit either regurgitation or stenosis (Bakir et al., 2013; Boodhwani & El
Khoury, 2014; David et al., 2013; Nishimura et al., 2014; Yau et al., 2000). Valve
surgery can include either the rebuilding or reshaping of a valve leaflet (annuloplasty) or
a complete valve replacement with a mechanical or biological valve (Bolling et al., 2010;
Boodhwani & El Khoury, 2014; David et al., 2013; David, Bos, & Rakowski, 1992;
David et al., 2005; Denti, Maisano, & Alfieri, 2014; Nishimura et al., 2014).

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These cardiac surgeries can be conventional (Hillis et al., 2011; Nishimura et al.,
2014), minimally invasive (Bravata et al., 2007; Cheng et al., 2011; Modi et al., 2008;
Rosengart et al., 2008) and/or robot-assisted (Chitwood et al., 2008; Mohr, Falk,
Diegeler, & Autschback, 1999). Often, the method that is utilized dependent on
numerous surgical, medical and patient variables (Boodhwani & El Khoury, 2014;
Bravata et al., 2007; David et al., 2013; David et al., 2005; Hillis et al., 2011; Liebrich et
al., 2013; Nishimura et al., 2014; Ralph-Edwards, Robinson, Gordon, & Ivanov, 1999).
Although the medical outcomes (Bravata et al., 2007; Hill et al., 2004; Ivanov, Borger,
Tu, Rao, & David, 2008; Modi et al., 2009; Wan et al., 2013) and cost efficiency of
newer approaches are continuously debated (Awad, Mathur, Baldock, Oliver, & Kennon,
2014; Hill et al., 2004; Sellke et al., 2005; Vassileva et al., 2013), the evolution of CV
surgery to include off-pump procedures (Sedrakyan, Wu, Parashar, Bass, & Treasure,
2006) or minimally invasive interventions (Bravata et al., 2007; Cheng et al., 2011; Modi
et al., 2008) have resulted in favorable clinical outcomes with a reduction in adverse
events for some populations. Fortunately these and other modern surgical approaches
have resulted in declining mortality rates (Cheng et al., 2011; Heart and Stroke
Foundation of Canada, 2003; Ivanov et al., 2008; Liebrich et al., 2013; Modi et al., 2008;
Public Health Agency of Canada, 2009); however, as the number of survivors increase so
does the risk and frequency of post-operative morbidities (David et al., 2013; Ralph-
Edwards et al., 1999; Rao et al., 1996; Song et al., 2009; Takagi, Tanabashi, Kawai, &
Umemoto, 2007).
Risk Factors for Dysphagia Following CV Surgery
The manifestation of dysphagia following CV surgery has been associated with
surgical, medical and patient-specific factors (Burgess et al., 1979; Ferraris et al., 2001;

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Hogue et al., 1995; Messina et al., 1991; Partik et al., 2003; Rousou et al., 2000). Across
the CV surgical population, the incidence of dysphagia approximates 3-4% (Ferraris et
al., 2001; Hogue et al., 1995; Rousou et al., 2000). Following intubation durations of
greater than 48 hours, the frequency increases to approximately 51% (Barker et al.,
2009). Other risk factors for dysphagia include surgery type (Barker et al., 2009; Ferraris
et al., 2001), peri-operative TEE use (Hogue et al., 1995; Rousou et al., 2000), operative
time (Rousou et al., 2000), age (Ferraris et al., 2001; Harrington et al., 1998; Hogue et al.,
1995) and vocal fold immobility (Joo, Duarte, Ghadiali, & Chhetri, 2009). However,
their association with dysphagia is not consistently supported in the literature (Hogue et
al., 1995; Messina et al., 1991; Rousou et al., 2000). It is yet unknown whether the
discrepancies in these reported risks are due to differences in study design and/or
methodological quality.
Surgery type. Patients undergoing valve surgery reportedly experience post-
operative dysphagia more frequently as compared to patients undergoing other cardiac
procedures (Barker et al., 2009; Ferraris et al., 2001), however, this finding is not
consistent (Hogue et al., 1995; Rousou et al., 2000). To date, no study has evaluated the
impact of surgical methods on swallowing physiology therefore; the biological
plausibility underlying the higher incidence of dysphagia following valvular surgery is
still unknown.
Transesophageal echocardiogram. Transesophageal echocardiogram (TEE), a
cardiac imaging tool which aids in surgical and clinical decision-making, is used intra-
operatively as a means for gathering real-time anatomic and physiological information
regarding cardiac function, valvular competence, and arterial patency (Bergquist,
Bellows, & Leung, 1996; Bergquist, Leung, & Bellows, 1996; Eltzschig et al., 2008;

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Enriquez-Sarano et al., 1999; Kihara et al., 2009; le Polain de Waroux et al., 2007; Van
Dyck, Watremez, Boodhwani, Vanoverschelde, & El Khoury, 2010). Operative
outcomes are improved with the use of TEE (Bergquist, Bellows, et al., 1996; Bergquist,
Leung, et al., 1996; Enriquez-Sarano et al., 1999; le Polain de Waroux et al., 2007; Van
Dyck et al., 2010) and TEE-associated morbidities or mortalities are rare <0.2% (Daniel
et al., 1991; Kallmeyer, Collard, Fox, Body, & Shernan, 2001; Min et al., 2005; Piercy,
McNicol, Dinh, Story, & Smith, 2009).
The peri-operative TEE probe is passed through the pharynx, the esophagus and
into the stomach and as a result, adverse events may include complications to the upper
aerodigestive tract (Côté & Denault, 2008; Daniel et al., 1991; Owall, Ståhl, &
Settergren, 1992; Piercy et al., 2009). A systematic review on transesophageal-related
complications by Cote and colleagues (2008) identified primary regions for these
complications including: oropharyngeal (odynophagia, dental injury, vocal fold paralysis,
dysphagia), pulmonary (bronchospasm, endotracheal tube malposition) and upper
gastrointestinal (GI) (upper GI hemorrhage, esophageal abrasion, esophageal perforation
(Côté & Denault, 2008). Although these regions are intrinsic in the execution of a safe
swallow, the occurrence of TEE-related swallowing morbidity is rare (Kallmeyer et al.,
2001). For example, in a study of 7200 TEE cases (Kallmeyer et al., 2001), the incidence
of swallowing related post-operative morbidity was small: odynophagia (.1%), dysphagia
(.01%), esophageal abrasions (.06%) and dental injury (.03%).
Despite the rare occurrence of TEE-related dysphagia, TEE use has been reported
as an independent predictor of the disorder (Hogue et al., 1995; Rousou et al., 2000).
Due to the location of the TEE probe intra-operatively, some authors have suggested that
post-TEE dysphagia is secondary to RLN injury (Sakai et al., 1999). Sakai and

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colleagues (1999) reported significantly greater post-TEE RLN palsy occurring in
females as compared to males (Sakai et al., 1999). This finding has been corroborated by
other others (Piercy et al., 2009) suggesting that the smaller female upper aerodigestive
tract is at greater risk of compression-related injuries. However, contradictory findings
have also been published (Kawahito, Kitahata, Kimura, Tanaka, & Oshita, 1999; Messina
et al., 1991; Owall et al., 1992). In a study comparing RLN injury and TEE usage, no
significant differences between sexes were noted (Kawahito et al., 1999). Rather than
TEE, these authors implicated surgery type, surgical time and intubation duration as
predictive factors in RLN injury (Kawahito et al., 1999). Patients requiring prolonged
TEE often have more severe illness and require prolonged surgical times (Hogue et al.,
1995), thereby confounding the relation between TEE use and dysphagia.
Cardiopulmonary bypass. Conventional cardiopulmonary bypass (CPB), or
extracorporeal circulation, is a peri-operative necessity for many cardiovascular
surgeries; however, due to its unnatural processes which include the exposure of blood
elements to nonintimal structures, nonpulsatile flow, abnormal homeostasis and increased
coagulation activation, its use often precipitates and/or compounds the patient’s
protective inflammatory response (Laffey, Boylan & Cheng, 2002; Warren et al.,2009).
These inflammatory responses manifest clinically in many ways including neurological
morbidity (Lee et al., 2003; Lev-Ran et al., 2005; Mack et al., 2004), stroke (Borger et
al., 1998; Borger, Ivanov, Weisel, Rao, & Peniston, 2001; Hogue, Murphy, Schechtman,
& Dávila-Román, 1999; Likosky et al., 2003; Rao et al., 1995) and/or neurocognitive
deficits (Djaiani et al., 2004; Doganci, Gunaydin, Kocak, Yilmaz, & Demirkilic, 2013;
Floyd et al., 2006; Newman et al., 2001; Zanatta et al., 2013) . Nissinen and colleagues
(2009) evaluated the impact of cardiopulmonary bypass duration along with aortic cross-

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clamp time during cardiovascular surgery. They reported that increasing time intervals of
both aortic cross clamping and cardiopulmonary bypass increased the odds of post-
operative morbidity, particularly stroke, by 1.2 and 1.5 respectively (Nissinen, 2009).
Stroke. While majority of patients with stroke have dysphagia irrespective of
other medical comorbidities (Martino et al., 2005), stroke following CV surgery is a rare
occurrence ranging from 1.3% - 4.6% (Borger et al., 2001; Bucerius et al., 2003; Hogue
et al., 1999; Likosky et al., 2003; Salazar et al., 2001). Despite this, overall patient
outcomes associated with stroke following CV surgery are significantly poorer than those
without stroke with the majority of patients facing long-term moderate to severe deficits
along with lower survival rates at one and five years post-surgery (Salazar et al., 2001).
Risk factors for peri-operative stroke include age (Rao et al., 1995), pre-operative stroke
(Bucerius et al., 2003; Rao et al., 1995; Ricotta, Faggioli, Castilone, & Hassett, 1995),
carotid stenosis >50%, reoperation, cardiopulmonary bypass and valve surgery (Bucerius
et al., 2003; Ricotta et al., 1995). While the majority of those with stroke have dysphagia
(Martino et al., 2005), only one study has reported stroke as an independent predictor of
dysphagia following CV surgery (Rousou et al., 2000). Others have reported that neither
pre- nor peri-operative strokes are associated with its development (Barker et al., 2009;
Ferraris et al., 2001; Hogue et al., 1995).
Recurrent laryngeal nerve injury. Recurrent laryngeal nerve injury is a known
outcome secondary to both heart disease (Camishion, Gibbon, & Pierucci, 1966; Morgan
& Mourant, 1980; Victoria, Graham, Karnell, & Hoffman, 1999) as well as
cardiovascular surgery (Benouaich et al., 2012; Dimarakis & Protopapas, 2004; Hamdan
et al., 2002; Ishimoto et al., 2002; Murty & Smith, 1989; Myssiorek, 2004; Tewari &
Aggarwal, 1996). The frequency of vocal fold immobility, either unilateral or bilateral

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paralysis or paresis, following CV surgery is rare <2% (Dimarakis & Protopapas, 2004;
Itagaki et al., 2007; Shafei et al., 1997) however this post-operative outcome can greatly
reduce a patient’s quality of life (Zumtobel, End, Bigenzahn, Klepetko, & Schneider,
2006) and increase their dysphagia risk (Joo et al., 2009; Leder & Ross, 2005; Leder,
Suiter, Duffey, & Judson, 2012; Rosenthal, Benninger, & Deeb, 2007). Recovery of the
RLN injury depends upon the rate of axonal neuroregeneration as well as the etiology of
the RLN injury (Zealear & Billante, 2004). The injury, regardless of etiology, may be
temporary, resolving within 6 months following surgery (Joo et al., 2009) or take longer
to recover if at all (Ishimoto et al., 2002).
In both non-surgical and surgical cardiac patients, the etiology and severity of
RLN injury depends on anatomical, mechanical and surgical variables (Camishion et al.,
1966; Morgan & Mourant, 1980; Victoria et al., 1999). In patients with heart disease, the
RLN may be injured by way of compression secondary to an enlarged left atrium
(Camishion et al., 1966; Morgan & Mourant, 1980). In rare cases, RLN injury occurs
following cardioversion for atrial fibrillation (Victoria et al., 1999). Due to the aortic and
subclavian course of the RLN (Benouaich et al., 2012), injury may occur due to
sternotomy, sternal retraction and the mediastinal operating site location (Benouaich et
al., 2012; Dimarakis & Protopapas, 2004; Murty & Smith, 1989; Myssiorek, 2004;
Tewari & Aggarwal, 1996). Intra-operative factors potentially causing RLN damage
include myocardial cooling (Dimarakis & Protopapas, 2004; Hamdan et al., 2002; Tewari
& Aggarwal, 1996), aortic manipulation (Ishimoto et al., 2002; Itagaki et al., 2007), and
central venous catheterization (Martin-Hirsch & Newbegin, 1995). Etiology
notwithstanding, patients with post-operative vocal fold immobility present a diagnostic

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subgroup at increased risk for dysphagia (Joo et al., 2009; Leder et al., 2012; Rosenthal et
al., 2007).
Post-operative vocal fold immobility increases a patient’s risk of dysphagia
primarily due to airway protection impairment (Leder & Ross, 2005; Leder et al., 2012;
Rosenthal et al., 2007). This may contribute to respiratory morbidity (Leder & Ross,
2005; Leder et al., 2012; Rosenthal et al., 2007) and even death (Cavo, 1985; Gibbin &
Egginton, 1981). In a retrospective cohort study, all patients with either unilateral or
bilateral vocal fold paralysis following CV surgery exhibited hoarseness, weak cough and
dysphagia for thin fluids (Joo et al., 2009). In another study exploring vocal fold
immobility across hospitalized patients, over a third of the patients exhibited airway
penetration with nearly a quarter exhibiting aspiration (Bhattacharyya et al., 2003).
Prolonged intubation following cardiovascular surgery. All patients
undergoing cardiovascular (CV) surgery require endotracheal intubation and mechanical
ventilation as part of standard surgical intervention; however, the duration of intubation
after surgery varies (Cislaghi, Condemi, & Corona, 2009; Reddy, Grayson, Griffiths,
Pullan, & Rashid, 2007). Fast-tracked extubation, which is typically defined as
extubation within six to eight hours post-operatively (Cheng, 1998), is now considered
standard care worldwide (Silbert & Myles, 2009; Zhu et al., 2012). Historically, the
duration that defined a fast-tracked extubation was reportedly arbitrary with no
physiological basis (Zhu et al., 2012). This fast-tracking however has resulted in
improved patient outcomes, including improved respiratory and circulatory outcomes
(Cheng et al., 1996; Ingersoll & Grippi, 1991) and a marked reduction in hospitalization
costs (Arom, Emery, Petersen, & Schwartz, 1995; Cheng, 1998; Hawkes, Dhileepan, &
Foxcroft, 2003; Rashid, Sattar, Dar, & Khan, 2008).

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Similar to the time period that defines early or fast-tracked extubation following
CV surgery (Zhu et al., 2012), the intubation period that constitutes a prolonged duration
is also arbitrary (Cheng et al., 1996; Christian, Engel, & Smith, 2011; Cislaghi et al.,
2009; Cohen et al., 2000; Habib et al., 1996; Légaré, Hirsch, Buth, MacDougall, &
Sullivan, 2001; Pappalardo et al., 2004; Reddy et al., 2007; Trouillet et al., 2009;
Widyastuti, Stenseth, Pleym, Wahba, & Videm, 2012; Yende & Wunderink, 2002). In
the CV surgery literature, prolonged intubation has been defined as greater than: eight
hours (Yende & Wunderink, 2002); 12 hours (Cheng et al., 1996; Cislaghi et al., 2009),
24 hours (Habib et al., 1996; Légaré et al., 2001; Widyastuti et al., 2012), 48 hours
(Cohen et al., 2000; Reddy et al., 2007), 72 hours (Christian et al., 2011; Trouillet et al.,
2009), seven days (Pappalardo et al., 2004) or 14 days (Combes et al., 2003). The
dysphagia literature is similarly inconsistent with prolonged intubations defined as
greater than: 24 hours (de Larminat et al., 1995), 48 hours (Ajemian et al., 2001; Barker
et al., 2009; El Solh et al., 2003; Leder, Cohn, et al., 1998) or eight days (Tolep et al.,
1996). Regardless of these cutpoints, ultimately the patient’s medical status determines
how long endotracheal intubation and mechanical ventilation are needed (Branca,
McGaw, & Light, 2001; Christian et al., 2011; Cislaghi et al., 2009; Habib et al., 1996; Ji
et al., 2010; Légaré et al., 2001; Reddy et al., 2007; Suematsu et al., 2000; Widyastuti et
al., 2012; Yende & Wunderink, 2002).
Prolonged intubation has been consistently reported as an independent predictor
of dysphagia following CV surgery (Barker et al., 2009; Hogue et al., 1995; Rousou et
al., 2000). When compared to the overall incidence of dysphagia (approximately 3%)
following CV surgery using cumulative intubations across the sample (Ferraris et al.,
2001; Hogue et al., 1995; Rousou et al., 2000), the frequency of dysphagia increases over

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ten-fold following durations exceeding 48 hours to approximately 51% (Barker et al.,
2009). While relatively few studies have reported on dysphagia following CV surgery
(Barker et al., 2009; Burgess et al., 1979; Ferraris et al., 2001; Harrington et al., 1998;
Hogue et al., 1995; Messina et al., 1991; Partik et al., 2003; Rousou et al., 2000), most
report cumulative dysphagia frequencies regardless of intubation duration (Ferraris et al.,
2001; Hogue et al., 1995; Rousou et al., 2000), with only two (Barker et al., 2009;
Burgess et al., 1979) focusing on specific intubation times: greater than 48 hours (Barker
et al., 2009) and from eight to 28 hours (Burgess et al., 1979). As a result, dysphagia
frequencies following durations of less than 24 hours or between 24 to 48 hours are
unknown providing uncertainty as to which patients are at the greatest risk.
Age. Age itself is an independent predictor of dysphagia following CV surgery
(Barker et al., 2009; Hogue et al., 1995); however, it remains to be determined if
advanced age alone or the combination of age and other age-associated post-operative
morbidities are causative factors in the development of dysphagia. According to the
United Nations report on World Aging published in 2013, by the year 2050, there will be
2 billion people worldwide over the age of 60 as compared to 841 million in 2013
(United Nations, 2013). Due to the effects of aging and degenerative disease processes on
the cardiovascular system, this will increase the need for cardiac interventions
exponentially (Ferrari, Radaelli, & Centola, 2003; Scott, Seifert, Grimson, & Glass,
2005). While the elderly population has similar outcomes for isolated cardiac
interventions when compared to a younger cohort (Vasques, Messori, Lucenteforte, &
Biancari, 2012), age in itself remains a risk for significant post-operative morbidities
(Barnett et al., 2003; Fremes et al., 1989; Scott et al., 2005; Vasques, Lucenteforte,
Paone, Mugelli, & Biancari, 2012), which may increase a patient’s risk for dysphagia.

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54
As patients age, surgeries are often more complex requiring multiple interventions,
prolonged aortic cross clamp time and therefore prolonged CPB (Tjang, van Hees,
Körfer, Grobbee, & van der Heijden, 2007; Vasques, Lucenteforte, et al., 2012). As a
result, the elderly face an increased risk of reperfusion injury, systemic inflammatory
response (Cremer et al., 1996; Nissinen et al., 2009) and microemboli (Djaiani et al.,
2004; Doganci et al., 2013; Floyd et al., 2006; Zanatta et al., 2013). The elderly have
higher rates of post-operative stroke (Vasques, Lucenteforte, et al., 2012), longer
durations of endotracheal intubation (Barnett et al., 2003; Scott et al., 2005), and death
(Barnett et al., 2003; Fremes et al., 1989; Tjang et al., 2007; Vasques, Lucenteforte, et al.,
2012).
Dysphagia Characteristics
Dysphagia has been characterized following CV surgery primarily through case
studies (Adkins, Maples, Graham, Witt, & Davies, 1986; Cappell, 1991, 1995; Chesshyre
& Braimbridge, 1971; Dines & Anderson, 1966; Galvin et al., 1988; Morgan & Mourant,
1980; Skoretz & Rebeyka, 2009; Skoretz et al., 2012; Tekin et al., 2000). Only two
studies with samples greater than ten have provided more extensive dysphagia
descriptions following CV surgery (Hogue et al., 1995; Partik et al., 2003). All case
studies but two (Skoretz & Rebeyka, 2009; Skoretz et al., 2012) describe the dysphagia
as primarily esophageal as a result of cardiac-related esophageal compression (Cappell,
1991; Chesshyre & Braimbridge, 1971; Dines & Anderson, 1966; Morgan & Mourant,
1980; Tekin et al., 2000). One case series including only adults with aortic arch
malformations described general oropharyngeal dysphagia signs and symptoms (Adkins
et al., 1986). All but four studies (Hogue et al., 1995; Partik et al., 2003; Skoretz &
Rebeyka, 2009; Skoretz et al., 2012), two case studies (Skoretz & Rebeyka, 2009;

INTRODUCTION
55
Skoretz et al., 2012) and two with larger samples (Hogue et al., 1995; Partik et al., 2003),
described dysphagia using diagnostic methods ill-equipped to assess both oral and
pharyngeal aspects of the swallow.
The four studies, which described oral and pharyngeal aspects of the swallow
following CV surgery, utilized radiographic methods specifically developed to assess
dysphagia including barium cineradiography (Hogue et al., 1995) and videofluoroscopy
(Partik et al., 2003; Skoretz & Rebeyka, 2009; Skoretz et al., 2012). In both case studies,
Skoretz and colleagues described the swallowing impairments as primarily pharyngeal in
nature with airway compromise characterized by both penetration and aspiration (Skoretz
& Rebeyka, 2009; Skoretz et al., 2012). Hogue and colleagues (1995) confirmed
dysphagia in 4% (n=34, N=869) of their patients and reported on a variety of oral and
pharyngeal functions. Neither the case studies nor the study by Hogue and colleagues
provided operational definitions of the swallowing impairment. In contrast, Partik and
colleagues (2003) enrolled a mixed pediatric and adult symptomatic patient sample
(N=22). They described the swallowing function using operationally defined
terminology for various oral and pharyngeal aspects. While these studies are the first to
provide some characterization of the swallowing impairment following CV surgery, no
study to date has analyzed swallowing physiology following CV surgery using
standardized rating scales or objective physiological measurements. As a result, the
mechanisms underlying dysphagia in this population are largely undetermined as are the
best methods by which to assess and treat the disorder.
Gaps in the Literature
The frequency of dysphagia following intubation varies widely across the
literature (Ferraris et al., 2001; Tolep et al., 1996) with an overall paucity of studies

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56
focusing on post-extubation dysphagia (Ajemian et al., 2001; Atkins et al., 2010; Atkins
et al., 2007; Barker et al., 2009; Barquist et al., 2001; Bordon et al., 2011; Brodsky et al.,
2014; Brown et al., 2011; de Larminat et al., 1995; de Medeiros et al., 2014; DeVita &
Spierer-Rundback, 1990; El Solh et al., 2003; Elpern et al., 1994; Ferraris et al., 2001;
Hafner et al., 2008; Harrington et al., 1998; Keeling et al., 2007; Kwok et al., 2013;
Leder, Cohn, et al., 1998; Macht, King, et al., 2013; Macht et al., 2011; Messina et al.,
1991; Murty & Smith, 1989; Padovani et al., 2008; Rousou et al., 2000; Tolep et al.,
1996). While it is generally accepted that artificial airways interfere with the ability to
execute a safe swallow, the evidence surrounding the relation between intubation
duration and swallow function is still undetermined across patients with varying
diagnoses. Discrepancies exist in the literature regarding both incidence and risk factors
particularly following CV surgery with little consensus on predictive risk factors for
dysphagia in general. It still remains to be determined how frequently dysphagia occurs
following extubation and how to maximize positive patient outcomes.
The definition of prolonged intubation varies throughout the dysphagia (Ajemian
et al., 2001; Barker et al., 2009; de Larminat et al., 1995; El Solh et al., 2003; Tolep et al.,
1996) and CV surgery literature (Cheng et al., 1996; Christian et al., 2011; Cislaghi et al.,
2009; Cohen et al., 2000; Habib et al., 1996; Légaré et al., 2001; Pappalardo et al., 2004;
Reddy et al., 2007; Trouillet et al., 2009; Widyastuti et al., 2012; Yende & Wunderink,
2002). While prolonged intubation is a risk factor for dysphagia following CV surgery
(Barker et al., 2009; Hogue et al., 1995; Rousou et al., 2000), most studies report
cumulative dysphagia frequencies regardless of intubation period (Ferraris et al., 2001;
Hogue et al., 1995; Rousou et al., 2000). No study to date has reported dysphagia
frequency according to specific intubation durations following both coronary artery

INTRODUCTION
57
bypass grafting and valve surgery. In particular, dysphagia frequencies following
intubation durations of less than 24 hours or between 24 to 48 hours have yet to be
determined and as a result, it is still unknown as to which patients are at greatest risk of
the disorder following CV surgery.
The number of studies that focus on dysphagia following CV surgery are few
(Barker et al., 2009; Burgess et al., 1979; Ferraris et al., 2001; Harrington et al., 1998;
Hogue et al., 1995; Messina et al., 1991; Partik et al., 2003; Rousou et al., 2000), with the
majority reporting on dysphagia associated risk factors rather than systematically
characterizing the swallowing impairment (Barker et al., 2009; Ferraris et al., 2001;
Hogue et al., 1995; Messina et al., 1991; Rousou et al., 2000). Many studies are limited
by their dysphagia descriptions (Burgess et al., 1979; Harrington et al., 1998; Hogue et
al., 1995), assessment methods (Burgess et al., 1979; Harrington et al., 1998), and
inclusion criteria (Partik et al., 2003). At present, no study to date has analyzed
swallowing physiology using standardized rating scales or objective physiological
measurement and as a result, the mechanisms underlying dysphagia following CV
surgery have yet to be determined.
Purposes
The overarching goal of this body of research was to determine which patients are
at greatest risk of dysphagia following CV surgery and in so doing, elucidate the relation
between the duration of endotracheal intubation and dysphagia. We conducted three
studies in order to meet this goal, with a focus on the cardiovascular surgical population,
while addressing the discrepancies in both the incidence of post-extubation dysphagia as
well as its associated risk factors. Our primary objectives were to determine: 1) the
incidence of dysphagia following endotracheal intubation across diagnostic groups with a

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focus on the cardiovascular surgical population, 2) the patient characteristics associated
with dysphagia following CV surgery and 3) the feasibility of determining dysphagia
incidence and swallowing physiology prospectively following CV surgery using a
homogeneous, consecutive patient sample.
Our first study protocol addressed the first two primary objectives. We conducted
a systematic review in order to evaluate the literature regarding the incidence of
dysphagia following endotracheal intubation along with its associated risk factors across
a variety of patient diagnostic groups. In addition, we investigated the relationship of
endotracheal intubation duration and dysphagia in the published literature. Our second
study protocol also addressed the first two primary objectives, however, this time using a
homogeneous cardiovascular surgical patient population and a retrospective design. In
this study, we stratified the patients according to intubation duration in order to determine
dysphagia frequencies according to each stratum. Across the entire patient sample, we
also investigated the risk factors associated with dysphagia following CV surgery.
Together, these objectives satisfied the goal of determining those at greatest risk of
dysphagia following CV surgery and provide the foundation for our third study. Our
third study objective described the feasibility of: 1) determining the incidence of
dysphagia prospectively and 2) describing swallowing physiology of consecutively
enrolled patients following CV surgery after prolonged intubation. In this study, we
evaluated the impact and tolerability on patients and nurses of conducting instrumental
swallowing assessments. The results of this study would ultimately inform a future large-
scale protocol which will systematically determine dysphagia incidence and patient’s
swallowing physiology following prolonged intubation after CV surgery using
prospective enrollment.

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CHAPTER II
THE INCIDENCE OF DYSPHAGIA FOLLOWING ENDOTRACHEAL INTUBATION: A SYSTEMATIC REVIEW
This chapter has been previously published in the journal Chest (Skoretz,
Flowers, & Martino, 2010). The format and references for this chapter have been revised
to conform to the requirements set forth by the School of Graduate Studies at the
University of Toronto. Permission was obtained from the American College of Chest
Physicians to reproduce this copyrighted material in this format (license numbers:
2891530934800, 2891531334875, 2891561082923, 2891561216033; Appendix A).
Abstract
Hospitalized patients are often at increased risk of oropharyngeal dysphagia
following prolonged endotracheal intubation. While reported incidence can be high, it
varies widely. We conducted a systematic review to determine the: 1) incidence of
dysphagia following endotracheal intubation, 2) association between dysphagia and
intubation time and 3) patient characteristics associated with dysphagia. Fourteen
electronic databases were searched, using keywords dysphagia, deglutition disorders and
intubation, along with manual searching of journals and grey literature. Two reviewers,
blinded to each other, selected and reviewed articles at all stages according to our
inclusion criteria: adult participants who underwent intubation and clinical assessment for
dysphagia. Exclusion criteria were case series (n<10), dysphagia determined by patient
report, patients with tracheostomies, esophageal dysphagia, and/or diagnoses known to
cause dysphagia. Critical appraisal utilized the Cochrane Risk of Bias assessment and
GRADE tools. A total of 1,489 citations were identified, of which 288 articles were
reviewed and 14 met inclusion criteria. The studies were heterogeneous in design,

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swallowing assessment and study outcome therefore we present findings descriptively.
Dysphagia frequency ranged from 3% to 62% and intubation duration from 124.8 to
346.6 mean hours. The highest dysphagia frequencies, 62%, 56%, and 51%, occurred
following prolonged intubation and included patients across all diagnostic subtypes. All
studies were limited by design and risk of bias. Overall quality of the evidence was very
low. This review highlights the poor available evidence for dysphagia following
intubation and hence the need for high quality prospective trials.

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Introduction
Endotracheal intubation and ventilatory support are life-sustaining procedures
often required during the course of a patient’s hospitalization, but their presence can
complicate resumption of oral intake (DeVita & Spierer-Rundback, 1990; Tolep et al.,
1996). Artificial airways often have negative effects on laryngeal competence and overall
swallowing physiology (DeVita & Spierer-Rundback, 1990; Tolep et al., 1996). It
remains to be determined whether oropharyngeal dysphagia, if present, is attributed to the
artificial airway alone or in part to the underlying medical conditions that precipitated its
placement. Notwithstanding this uncertainty, patients on prolonged ventilation comprise
a diagnostic group at increased risk of oropharyngeal dysphagia (Ajemian et al., 2001;
DeVita & Spierer-Rundback, 1990; El Solh et al., 2003; Tolep et al., 1996).
Oropharyngeal dysphagia, also referred to as dysphagia or disordered swallowing,
is an abnormality of the swallow physiology of the upper aerodigestive tract. It occurs
frequently in patients with structural or neurological disruption to the head and neck area
from diseases such as stroke (Martino et al., 2005), head and neck cancer (Ward et al.,
2002) and/or necessary medical treatments including cervical spine surgery (Smith-
Hammond et al., 2004), prolonged intubation (Ajemian et al., 2001; El Solh et al., 2003),
tracheotomy (Bonanno, 1971; DeVita & Spierer-Rundback, 1990) and mechanical
ventilation (DeVita & Spierer-Rundback, 1990; Elpern et al., 1994; Tolep et al., 1996).
While dysphagia is itself not a disease but rather a symptom of another medical condition
and/or the interventions required to treat the condition, it can lead to a variety of medical
complications. Common consequences of dysphagia include dehydration, malnutrition
(Smithard et al., 1996; Westergren et al., 2001), aspiration of oral secretions (Murray et
al., 1996), food or fluid (Lundy et al., 1999; Smith, Logemann, Colangelo, Rademaker, &

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Pauloski, 1999) and eventually death (Smithard et al., 1996). Aspiration often leads to
pneumonia (Holas, DePippo, & Reding, 1994; Johnson, McKenzie, & Sievers, 1993;
Loeb et al., 1999; Lundy et al., 1999; Martino et al., 2005). In fact, the risk of developing
pneumonia is 11 times greater in patients who aspirate compared to similar patients with
no aspiration (Martino et al., 2005).
Although the literature reports a high incidence of dysphagia following
intubation, these reports vary widely from 3% (Ferraris et al., 2001) to 83% (Tolep et al.,
1996). Studies have also shown that prolonged intubation can be an independent
predictor of dysphagia (Barker et al., 2009; Hogue et al., 1995). Artificial airways
increase the risk of upper airway injury and concomitant laryngeal pathologies (Sellery et
al., 1978; Stauffer et al., 1981; Sue & Susanto, 2003), which in turn affect upper airway
mechanics, aerodynamics and protective reflexes (DeVita & Spierer-Rundback, 1990;
Tolep et al., 1996). These laryngeal pathologies include, but are not limited to,
epithelial/mucosal abrasions, tracheo-esophageal fistula formation, tracheal stenosis and
granulation tissue (Stauffer et al., 1981; Sue & Susanto, 2003). Multiple ventilation
cycles can further exacerbate the dysphagia by disrupting the delicate synchrony between
swallowing and breathing, leading to aspiration (Elpern et al., 1994). While the cause of
dysphagia in these patients is multifactorial and perhaps debatable (Leder & Ross, 2000;
Terk, Leder, & Burrell, 2007), it is clear from the available literature that artificial
airways interfere with the ability to execute an efficient and safe swallow. What is not yet
known is how frequently dysphagia occurs and how to avoid its ill effects.
In order to evaluate the available evidence and attempt to resolve these
uncertainties, we conducted a systematic review to assess a) the incidence of dysphagia
following intubation across various patient diagnostic groups, b) the association between

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dysphagia and the duration of endotracheal intubation and c) patient characteristics
associated with dysphagia.
Materials and Methods
A detailed protocol directed the various stages of our search and appraisal of the
literature on dysphagia and endotracheal intubation (see Appendix A).
Operational Definitions
We operationalized relevant terms a priori. Endotracheal intubation was defined
as the presence of an endotracheal tube in the oropharynx. Oropharyngeal dysphagia was
defined as any impairment or abnormality of the oral, pharyngeal or upper esophageal
stage of deglutition. The presence of oropharyngeal dysphagia was identified by either a
clinical bedside swallow evaluation (CSE) or instrumental assessment, including
videofluoroscopic swallow study (VFS) or fiberoptic endoscopic evaluation of the
swallow (FEES).
Search Strategy
From the start of online availability to May 2009, we searched for eligible
citations in 14 electronic databases (MEDLINE [1950-] EMBASE [1980-], CINAHL
[1982-], PsycINFO [1960-], AMED [1985-], HealthSTAR [1966-], BIOSIS Previews
[1980-], Cochrane DSR [1988-], ACP Journal Club [1991-], DARE [1991-], CCTR
[1991-], CMR [1995-], HTA [2001-], and NHSEED [1995-]) using the search terms
deglutition disorders, swallowing disorders, dysphagia, swallowing and intubation. In
addition, we manually searched for relevant citations in twenty content related journals
between 1988 and May 2009, conference proceedings, and grey/unpublished literature
(GrayLIT Network, GreySource, OpenSigle, and ProQuest Dissertations). We also

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reviewed citations from the accepted articles. A complete list of manually searched
journals and conference proceedings is available.
Eligibility Criteria
Of the identified citations, we included only articles with abstracts and those
reporting the presence or absence of oropharyngeal dysphagia in adult patients (>18 years
old) who underwent endotracheal intubation during their hospitalization. We accepted
retrospective or prospective study designs using only consecutive enrollment, provided
that the sample size exceeded ten. We included articles published in any language.
Specific to this study, we defined swallowing assessment method to be clinical or
instrumental assessment. In order to avoid overestimating dysphagia incidence secondary
to endotracheal intubation, we excluded articles with patients at high risk for dysphagia
secondary to their primary diagnosis. These included patients with neurogenic or head
and neck diagnoses as well as tracheostomized patients. Articles using only patient report
to identify dysphagia were also excluded.
Study Selection
The first two authors, blinded to each other’s results, reviewed all citations,
abstracts and articles to determine eligibility for inclusion using a form designed a priori
(Appendix B). If the reviewers could not determine inclusion/exclusion based on the
abstract alone, the citation was accepted. Articles of all accepted citations were retrieved
and reviewed to determine the final studies for inclusion. Disagreements at all stages of
the selection process were resolved by consensus.
Assessment of Methodological Quality
The same two reviewers, once again blinded to each other’s results, assessed the
included studies for risk of bias and quality using the Risk of Bias Assessment tool

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(Appendix C) and the GRADE approach (Grading of Recommendations, Assessment,
Development and Evaluation) as recommended by the Cochrane Collaboration (Higgins,
Green, & Cochrane Collaboration., 2008). All disagreements were resolved by
consensus.
The Risk of Bias Assessment tool (Higgins et al., 2008) included sequence
generation, allocation concealment, blinding, consecutive enrollment, and the
completeness of outcome reporting. Study quality using the GRADE approach gave the
highest rating (high level evidence) to randomized trials while observational studies were
rated as low in quality as suggested by the Cochrane Collaboration (Higgins et al., 2008).
Anticipating a large number of observational studies, we modified this Cochrane quality
rating by downgrading in the presence of certain factors including limitations in study
design, indirectness of evidence (e.g., indirect population or study’s main outcomes),
unexplained heterogeneity, or the imprecision of results. Conversely, study quality was
upgraded if study design and results suggested little to no evidence of bias.
Data Extraction
One reviewer, using a form determined a priori, extracted data regarding study
design, sample size, patient diagnoses, incidence of dysphagia, method of dysphagia
assessment, intubation duration, and patient co-morbidities (Appendix D). A second
reviewer checked all extracted data for accuracy. Due to the heterogeneity of patient
diagnoses, study methodology and outcomes across accepted studies; we summarized
results descriptively (see Appendix E for exploratory meta-analyses). Risk of bias
analyses were conducted using the Cochrane Collaboration software program Review
Manager (RevMan, version 5.0.20; The Nordic Cochrane Centre; Copenhagen,

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Denmark). Quality assessment ratings were adapted from GRADEprofiler©
(GRADEpro©, version 3.2.2; available from http://www.gradeworkinggroup.org).
Results
Literature Retrieved
We retrieved a total of 1,489 citations through database (Appendix F) and manual
searching (Figure 2.1). Of these, 351 did not have abstracts and were eliminated. We
reviewed the remaining 1,138 titles and abstracts. An additional 848 abstracts were
eliminated because they: were case series with sample sizes of less than 10, did not enroll
patients consecutively, included pediatric patients, did not report swallowing outcomes,
and included patients following tracheotomy. Two articles were not retrievable (Sarroca
et al., 2003; Vasilev, Germanova, Tzaner, Shwabe, & Karadimov, 2005). We retrieved
and reviewed the full text articles of the remaining 288 citations. Of these, 14 languages
were represented including English (Appendix G). Following full article review, 274
articles were eliminated because they did not meet our inclusion criteria. Of those, 58
articles used only patient report of dysphagic symptoms, 31 articles included patients
with esophageal diagnoses, 27 articles included patients with primary diagnoses of head
and neck cancer and/or neurogenic diagnoses (e.g., stroke, traumatic brain injury, and
neurosurgical patients) and 8 articles did not describe their method for assessing the
swallow. Other article eliminations included: 3 duplicate publications (de Larminat,
Dureuil, Montravers, & Desmonts, 1992; de Larminat, Montravers, Dureuil, &
Desmonts, 1991; Laryea & Ajemian, 2006) using patients from studies accepted for this
review (Ajemian et al., 2001; de Larminat et al., 1995), 2 articles (Leder, Sasaki, &
Burrell, 1998; Leder & Suiter, 2008) with study samples based on only patients referred
for suspected dysphagia and 1 article (Partik et al., 2000) that enrolled only patients with

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confirmed dysphagia. A total of 50 citations, 45 articles and 5 abstracts, were retrieved
from manual searches (Appendix H). Six studies were accepted following manual
searching: 3 articles (Barker et al., 2009; Ferraris et al., 2001; Keeling et al., 2007) from
content related journals, 2 articles (Burgess et al., 1979; Stanley et al., 1995) from the
bibliographic references of accepted studies and 1 article (Padovani et al., 2008) from
review of grey literature databases. In the end, a total of 14 articles were accepted and
underwent further analysis (Table 2.1). A comprehensive list of articles not accepted for
full review is available from the authors on request.

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.
Figure 2.1. Study selection process.
1,489 citations recovered by database and manual searches
351 eliminated (citations without abstracts)
848 eliminated (abstracts not meeting inclusion criteria)
288 full text articles retrieved and reviewed
144 eliminated (articles not meeting inclusion criteria)
2 eliminated (articles not retrievable)
1,138 titles and abstracts reviewed
3 eliminated (duplicate publications)
58 eliminated (patient report of dysphagia symptoms)
31 eliminated (esophageal diagnoses)
27 eliminated (head/neck cancer and neurogenic diagnoses)
3 eliminated (confirmed or suspected dysphagia)
8 eliminated (dysphagia assessment method not described)
14 articles accepted for review

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Study Characteristics and Quality Assessment
Of the 14 accepted articles (Table 2.1), 11 were prospective including 2
randomized trials (Barquist et al., 2001; Stanley et al., 1995), 3 cohort studies (Burgess et
al., 1979; Davis & Cullen, 1974; El Solh et al., 2003), 1 case-control study (de Larminat
et al., 1995) and 5 case-series (Ajemian et al., 2001; Ferraris et al., 2001; Hogue et al.,
1995; Keeling et al., 2007; Leder, Cohn, et al., 1998). Of the retrospective studies: 2
articles (Barker et al., 2009; Rousou et al., 2000) were case-series and 1 article (Padovani
et al., 2008) was a cohort design. Patient diagnoses varied across studies. A total of eight
studies (Barker et al., 2009; Burgess et al., 1979; Davis & Cullen, 1974; Ferraris et al.,
2001; Hogue et al., 1995; Keeling et al., 2007; Rousou et al., 2000; Stanley et al., 1995)
enrolled surgical patients, and of these, 5 articles (Barker et al., 2009; Burgess et al.,
1979; Ferraris et al., 2001; Hogue et al., 1995; Rousou et al., 2000) enrolled
cardiovascular surgery patients and the remaining 3 articles (Davis & Cullen, 1974;
Keeling et al., 2007; Stanley et al., 1995) enrolled patients with mixed surgical diagnoses.
Three other studies (de Larminat et al., 1995; El Solh et al., 2003; Padovani et al., 2008)
enrolled patients with mixed medical diagnoses. An additional 3 studies (Ajemian et al.,
2001; Barquist et al., 2001; Leder, Cohn, et al., 1998) enrolled patients with a variety of
both medical and surgical diagnoses.

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Table 2.1 Study characteristics and frequency of dysphagia according to patient diagnosis
Study Study Design Na Swallowing Assessment Method Timing of
Assessment Post-extubation
Dysphagia Frequency
Surgical – cardiovascular only Barker et al (2009) Case-series 254 Screening, CSE and/or VFS NR
130/254 (51%)
Burgess et al (1979) Cohort 64 Chest x-rayb Immediately to 8h 13/64 (20%)c
Ferraris et al (2001) Case-series 1,042 Screening, VFS NR 31/1042 (3%)d
Hogue et al (1995) Case-series 844 Screening, Barium cineradiography NR 28/844 (3%)d
Rousou et al (2000) Case-series 838 Screening, Barium cineradiography NR 23/838 (3%)d Surgical - mixede
Davis & Cullen (1974)
Cohort 26 Chest x-rayb 10 and 15 min 9/26 (35%)c Keeling et al (2007) Case-series 133 CSE, VFS Within 48h 19/133 (14%)c
Stanley et al (1995) Randomized 40 Chest x-rayb NR 1/40 (3%)c
Mixed - medicalf deLarminat et al (1995) Case-control 34 Swallow latency measurements Immediately 21/3 (62%)g
El Solh et al (2003) Cohort 84 FEES Within 48h 37/84 (44%)c
Padovani et al (2008) Cohort 23 CSE 1-5 days 8/23 (35%) Mixed – medical and surgicalh
Ajemian et al (2001) Case-series 48 FEES Within 48h 27/48 (56%)c Barquist et al (2001) Randomized 70 CSE and FEES 48±2hi, 24±2hj 7/70 (10%)c
Leder et al (1998) Case-series 20 FEES 24±2h 9/20 (45%)c
Note. CSE = clinical swallowing evaluation; VFS = videofluoroscopic swallowing study; FEES = Fiberoptic endoscopic evaluation of the swallow; NR = not reported. a Includes only patients meeting inclusion criteria for this review. b With administration of oral contrast agent. c Dysphagia defined as aspiration only. d Instrumental assessment conducted with only those patients failing dysphagia screening. e Includes limb arthroplasty, thorocotomy or pulmonary resection, abdominal or vascular surgery. f Includes patients with respiratory illnesses, sepsis, liver failure and/or other medical illness. g Dysphagia defined as swallowing latency on day 0. h Includes surgical/medical intensive care patients, critically ill trauma, burns, and/or elective surgical patients. i CSE only. j FEES only.

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According to Cochrane methodology (Higgins et al., 2008), we assessed each study for
risk of bias and poor study design to generate a quality GRADE (Table 2.2). Of the 14 included
studies, one study (Leder, Cohn, et al., 1998) had the lowest risk of bias with only one area
receiving a rating of unclear. Of the two randomized trials, 1 study (Barquist et al., 2001) had
adequate sequence generation and allocation concealment. Only one other study (Stanley et al.,
1995) declared blinding. All 14 studies accounted for their outcomes but only 8 specifically
declared consecutive enrollment (Ajemian et al., 2001; Barker et al., 2009; El Solh et al., 2003;
Ferraris et al., 2001; Hogue et al., 1995; Keeling et al., 2007; Leder, Cohn, et al., 1998; Rousou
et al., 2000). Outcomes were operationally defined in 4 studies (Barker et al., 2009; Barquist et
al., 2001; El Solh et al., 2003; Leder, Cohn, et al., 1998) while only 8 studies (Ajemian et al.,
2001; Burgess et al., 1979; Davis & Cullen, 1974; de Larminat et al., 1995; El Solh et al., 2003;
Leder, Cohn, et al., 1998; Padovani et al., 2008; Stanley et al., 1995) conducted the same
swallow assessment for all study enrollees. All studies received a high or unclear risk of bias
rating in at least one area. Additionally, each study had factors that decreased the quality of the
evidence such as i) insensitive swallowing assessment measures (Burgess et al., 1979; Davis &
Cullen, 1974; de Larminat et al., 1995; Stanley et al., 1995), ii) small sample size of less than 50
enrollees (Ajemian et al., 2001; Davis & Cullen, 1974; de Larminat et al., 1995; Leder, Cohn, et
al., 1998; Padovani et al., 2008; Stanley et al., 1995) and iii) different types of swallowing
assessment for enrollees (Barker et al., 2009; Ferraris et al., 2001; Hogue et al., 1995; Keeling et
al., 2007; Rousou et al., 2000). As a result, each study in this review was assigned a GRADE of
very low.

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72 Table 2.2 Risk of bias and methodological quality (GRADE) across studies
Study Sequence Generation
Allocation Concealment Blinding Consecutive
Enrollment
All Outcomes Addressed
Outcomes Operationally
Defined
Consistent Assessment
for All Enrollees
GRADE
Ajemian et al (2001) N/A N/A Unclear Yes Yes Unclear Yes Very Low
Barker et al (2009) N/A N/A Unclear Yes Yes Yes No Very Low Barquist et al
(2001) Yes Yes No N/A Yes Yes N/A Very Low
Burgess et al (1979) Unclear Unclear Unclear Unclear Yes No Yes Very Low
Davis & Cullen (1974) N/A N/A Unclear Unclear Yes No Yes Very Low
deLarminat et al (1995) N/A N/A Unclear Unclear Yes No Yes Very Low
El Solh et al (2003) N/A N/A No Yes Yes Yes Yes Very Low
Ferraris et al (2001) N/A N/A Unclear Yes Yes No Unclear Very Low
Hogue et al (1995) N/A N/A No Yes Yes No Unclear Very Low Keeling et al
(2007) N/A N/A Unclear Yes Yes No No Very Low
Leder et al (1998) N/A N/A Unclear Yes Yes Yes Yes Very Low Padovani et al
(2008) N/A N/A Unclear Unclear Yes No Yes Very Low
Rousou et al (2000) N/A N/A Unclear Yes Yes No Unclear Very Low
Stanley et al (1995) Unclear Unclear Yes Unclear Yes No Yes Very Low
Note. GRADE = Grading of Recommendations, Assessment, Development and Evaluation; N/A = not applicable.

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Dysphagia Following Endotracheal Intubation
Duration of intubation and the frequency dysphagia. Seven of the included studies
(Ajemian et al., 2001; Barker et al., 2009; Barquist et al., 2001; El Solh et al., 2003; Hogue et al.,
1995; Leder, Cohn, et al., 1998; Rousou et al., 2000) reported mean durations of intubation in
those with and without dysphagia (Table 2.3). Leder and his colleagues (1998) reported the
lengthiest intubation duration in the dysphagic patients (mean, 346.6 h ± 298.6) with a dysphagia
frequency of 45%. Ajemian and his colleagues (2001) reported the highest dysphagia frequency
with a mean intubation duration of 192.0h in patients with dysphagia. One study (Barquist et al.,
2001) reported longer intubation durations in patients without dysphagia (mean, 288.0h ± 235.2)
compared to those with dysphagia (mean, 254.4h ± 175.2). Five of these studies (Ajemian et al.,
2001; Barker et al., 2009; Barquist et al., 2001; El Solh et al., 2003; Leder, Cohn, et al., 1998)
included only enrollees with prolonged intubation defined as greater than 48h.

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Table 2.3 Intubation duration according to presence of dysphagia
Study
Targeted Intubation
Time (h)
Intubation Duration (h, mean ± SDa) Dysphagia
Frequency Dysphagia No Dysphagia
Leder et al (1998) >48 346.6 ± 298.6 283.7 ± 192.0 45%
Barquist et al (2001) >48 254.4 ± 175.2 288.0 ± 235.2 10%
Rousou et al (2000) NR 200.9 ± 75.0 15.3 ± 1.6 3%
El Solh et al (2003)b >48 223.2 ± 156.0 184.8 ± 112.8 36%
Ajemian et al (2001) >48 192.0 184.8 56%
El Solh et al (2003)c >48 187.2 ± 165.6 148.8 ± 127.2 52%
Barker et al (2009) >48 142.4 ± 63.0 87.1 ± 43.3 51%
Hogue et al (1995 NR 124.8 ± 40.8 50.4 ± 4.8 3%
Note. h = hour; SD = standard deviation; NR = not reported. a Where reported. b Young age cohort (<65 years old). c Elderly age cohort (>65 years old).
Swallowing assessment methods. The methods used to assess swallowing function were
variable. All studies but one (Padovani et al., 2008) used instrumental methods to determine the
presence or absence of dysphagia and/or aspiration. Seven studies (Ajemian et al., 2001; Burgess
et al., 1979; Davis & Cullen, 1974; de Larminat et al., 1995; El Solh et al., 2003; Leder, Cohn, et
al., 1998; Stanley et al., 1995) conducted instrumentation on all study enrollees. Three studies
(Ajemian et al., 2001; El Solh et al., 2003; Leder, Cohn, et al., 1998) used fiberoptic endoscopic
evaluation of swallowing (FEES), three studies (Burgess et al., 1979; Davis & Cullen, 1974;
Stanley et al., 1995) used chest radiography following administration of an oral contrast agent,
and one study (de Larminat et al., 1995) measured swallowing latency via submental

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electromyography. Three studies (Ferraris et al., 2001; Hogue et al., 1995; Rousou et al., 2000)
used videofluoroscopic swallowing studies (VFS) or barium cineradiography only on those
patients who failed swallowing screening. Clinical swallowing evaluation (CSE) was the sole
method to assess dysphagia in one study (Padovani et al., 2008) while another study (Barquist et
al., 2001) utilized either CSE and FEES depending on the arm of their randomized trial.
Across studies, swallowing assessments were conducted at various time periods
following extubation. Five studies (Ajemian et al., 2001; Barquist et al., 2001; El Solh et al.,
2003; Keeling et al., 2007; Leder, Cohn, et al., 1998) conducted their swallowing assessment
between 24 and 48 hours following extubation. Studies using chest radiographs (Burgess et al.,
1979; Davis & Cullen, 1974; Stanley et al., 1995) administered oral contrast at various time
points with radiographs taken at two minutes (Stanley et al., 1995), 30 minutes (Burgess et al.,
1979) and 1 hour (Davis & Cullen, 1974) following the contrast ingestion. The study using
electromyography (de Larminat et al., 1995) measured swallow latency immediately (day 0), and
at 1, 2, and 7 days following extubation. One study (Padovani et al., 2008) assessed swallowing
between days 1 and 5 following extubation. For another five studies (Barker et al., 2009; Ferraris
et al., 2001; Hogue et al., 1995; Rousou et al., 2000; Stanley et al., 1995) the timing of
swallowing assessment was not reported.
Frequency of dysphagia following intubation. The incidence of dysphagia across
studies included in this review ranged widely from 3% (Ferraris et al., 2001; Hogue et al., 1995;
Rousou et al., 2000; Stanley et al., 1995) to 62% (de Larminat et al., 1995). Those studies
reporting the highest dysphagia frequencies (Ajemian et al., 2001; Barker et al., 2009; de
Larminat et al., 1995; El Solh et al., 2003; Leder, Cohn, et al., 1998), between 44% and 62%, had
prolonged intubation periods. Three studies (Ferraris et al., 2001; Hogue et al., 1995; Rousou et

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al., 2000) reporting the lowest dysphagia frequency did not report findings from screening and/or
CSE and only reported dysphagia in those patients with abnormal VFS or barium
cineradiography. One study (Barker et al., 2009) utilized either CSE or VFS to determine
dysphagia frequency but did not stratify according to assessment method.
Swallowing impairment as an outcome was defined differently across studies, either as
any level of dysphagia severity (Barker et al., 2009; Ferraris et al., 2001; Hogue et al., 1995;
Padovani et al., 2008; Rousou et al., 2000), only aspiration (Ajemian et al., 2001; Barquist et al.,
2001; Burgess et al., 1979; Davis & Cullen, 1974; El Solh et al., 2003; Keeling et al., 2007;
Leder, Cohn, et al., 1998; Stanley et al., 1995) or only swallowing latency (de Larminat et al.,
1995). Regardless of definition, the dysphagia frequencies varied widely. Studies reporting on
any level of dysphagia severity (Barker et al., 2009; Ferraris et al., 2001; Hogue et al., 1995;
Padovani et al., 2008; Rousou et al., 2000) had frequencies ranging from 3% (Ferraris et al.,
2001; Hogue et al., 1995; Rousou et al., 2000) to 51% (Barker et al., 2009). Those studies
reporting only aspiration also had wide ranging frequencies from 3% (Stanley et al., 1995) to
56% (Ajemian et al., 2001).
Several of the included studies identified patient risk factors, surgical and/or medical,
associated with dysphagia (Table 2.4). Some risks were consistently associated with dysphagia
while others were consistently not associated (Table 2.4a). In contrast, some studies reported
association with several risk factors, while others reported no association for the same risk
factors (Table 2.4b).

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Table 2.4a. Surgical and medical risk factor association with dysphagia
Associated with dysphagia Not associated with dysphagia
Congestive heart failurea,b Functional statusc Increased hospital LOSa-e Hypercholesterolemiaa Increased ICU LOSc,d Multiple intubationsb Increased operative timee Peri-operative TEEd,e Sepsisb
APACHE scoresc,f COPDa, b, d, g Circulatory shocka, b Elevated CPB timea,d,e GERDg Hypertensiona,b,d ICU readmissionb Myocardial infarctionb,d NYHA >2 a,b Peripheral vascular diseasea Pre-operative CVAa,b,d Smokingb Surgery urgencyb
Note. APACHE = Acute Physiology and Chronic Health Evaluation; COPD = chronic obstructive pulmonary disease; CPB = cardiopulmonary bypass; GERD = gastro-esophageal reflux disease; LOS = length of stay; ICU = intensive care unit; NYHA = New York Heart Association staging (heart failure); TEE = trans-esophageal echocardiography; vascular accident; CVA = cerebral. a Ferraris et al., 2001. b Barker et al., 2009. c El Solh et al., 2003. d Hogue et al., 1995. e Rousou et al., 2000. f deLarminat et al., 1995. g Ajemian et al., 2001.

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Table 2.4b Studies either supporting or not supporting risks for dysphagia
Risk Factors Association with Dysphagia
Supporting Not Supporting
Age Barquist et al (2001) Ferraris et al (2001) Hogue et al (1995)
Ajemian et al (2001) deLarminat et al (1995)
Leder et al (1998) Rousou et al (2000)
Decreased cardiac output Hogue et al (1995) Barker et al (2009)
Diabetes mellitus Ferraris et al (2001) Ajemian et al (2001) Barker et al (2009) Hogue et al (1995)
Intubation duration Barker et al (2009) Hogue et al (1995) Rousou et al (2000)
Ajemian et al (2001) Barquist et al (2001)
deLarminat et al (1995) El Solh et al (2003) Leder et al (1998)
Left ventricle ejection fraction Rousou et al (2000) Hogue et al (1995)
Peri-operative CVA Rousou et al (2000) Barker et al (2009) Hogue et al (1995)
Post-operative pulmonary complications Hogue et al (1995) Leder et al (1998)
Pre-op/post-op IABP Hogue et al (1995)a Barker et al (2009)
Renal risks Ferraris et al (2001) Barker et al (2009) Hogue et al (1995)
Surgery type Barker et al (2009)b Ferraris et al (2001)c
Hogue et al (1995) Rousou et al (2000)
Tube feeding Barker et al (2009) Ajemian et al (2001) El Solh et al (2003) Leder et al (1998)
Note. CVA = cerebral vascular accident; IABP = intra-aortic balloon pump. a Post-operative IABP only. b Coronary artery bypass. c Non-coronary procedures.

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Discussion
This systematic review verifies that reported dysphagia frequency following endotracheal
intubation is variable, ranging from 3% (Ferraris et al., 2001; Hogue et al., 1995; Rousou et al.,
2000; Stanley et al., 1995) to 62% (de Larminat et al., 1995). Over half of the studies (Ajemian
et al., 2001; Barker et al., 2009; Burgess et al., 1979; Davis & Cullen, 1974; de Larminat et al.,
1995; El Solh et al., 2003; Leder, Cohn, et al., 1998; Padovani et al., 2008) reported a dysphagia
frequency exceeding 20%. The highest dysphagia frequencies of 62% (de Larminat et al., 1995),
56% (Ajemian et al., 2001) and 51% (Barker et al., 2009) included patients experiencing
prolonged intubation (>24 hours) across all diagnostic subtypes, mixed medical, mixed medical-
surgical and cardiovascular surgical groups respectively. Hence, no single diagnosis appeared to
be associated with greater risk of dysphagia. The wide range of dysphagia frequency identified in
this review is more likely attributed to variations in study design, such as method and timing of
swallowing assessment. Many studies were observational and few declared blinding or
operational definitions. Together, design variability and poor quality resulted in studies with a
high risk of bias; thereby weakening the available evidence on dysphagia frequency following
endotracheal intubation.
Across all studies, poor study quality and high risk of bias likely led to either under or
over reporting of dysphagia. Oddly, studies reporting the longest intubation duration did not
report the highest dysphagia frequencies (Barquist et al., 2001; Leder, Cohn, et al., 1998; Rousou
et al., 2000). However, their large standard deviations (Barquist et al., 2001; Leder, Cohn, et al.,
1998), coupled with failure to use the same instrumental assessments for all enrollees (Rousou et
al., 2000), seriously questions the accuracy of these frequency estimates. In contrast, three
studies reporting the lowest dysphagia frequencies had the largest sample sizes (Ferraris et al.,

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2001; Hogue et al., 1995; Rousou et al., 2000). We also question the accuracy of these frequency
estimates as they appeared to include patients with relatively short intubation durations and
consequently not expected to have dysphagia. Across studies, the timing of swallowing
assessments ranged from immediately (Burgess et al., 1979; de Larminat et al., 1995) to five
days (Padovani et al., 2008) following extubation. In general, one would expect the highest
dysphagia frequency in patients with prolonged intubation durations and assessments conducted
immediately following extubation. However, due to the poor study quality and variability of the
included studies our findings could not corroborate this premise.
A wide assortment of swallowing assessment methods, including screening, clinical
swallowing evaluations and a variety of instrumental assessments, were included in the accepted
studies. Dysphagia frequency varied regardless of assessment type. Although heterogeneity
across studies did not permit a statistical association of dysphagia frequency and swallow
assessment, studies using FEES on all enrollees reported some of the highest frequencies of
dysphagia from 44% (El Solh et al., 2003) to 56% (Ajemian et al., 2001). In contrast, other
studies assessing the swallow with static chest radiographs (Burgess et al., 1979; Davis &
Cullen, 1974; Stanley et al., 1995) or clinical measures (Padovani et al., 2008) detected a lower
incidence of dysphagia, from 3% (Stanley et al., 1995) to 35% (Davis & Cullen, 1974; Padovani
et al., 2008). When compared with other swallowing assessment methods, direct visualization of
pharyngeal and laryngeal swallowing structures (e.g. FEES) may be a more sensitive measure
(Kelly et al., 2007; Kelly et al., 2006).
Studies varied in how swallowing outcomes were defined. Over half of the included
studies (Ajemian et al., 2001; Barquist et al., 2001; Burgess et al., 1979; Davis & Cullen, 1974;
El Solh et al., 2003; Keeling et al., 2007; Leder, Cohn, et al., 1998; Stanley et al., 1995) used

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aspiration as their main swallowing outcome. Aspiration is only one aspect across the spectrum
of swallowing impairments. While aspiration is considered dysphagia in its most severe form,
defining dysphagia as such would limit diagnostic scope and potentially miss other significant
swallowing findings. For example, one study (Barquist et al., 2001) reporting a low incidence of
dysphagia (10%) also commented on other pharyngeal aspects of the swallow. These findings
were reported only qualitatively thereby explaining, in part, their low reported frequency.
Although we used stringent selection criteria and rigorous methodology while excluding
confounding diagnoses for dysphagia, this review is limited by many factors. Most limitations
were imposed by the design, quantity and quality of the original research. The few included
studies were heterogeneous, differing in regard to their outcomes, study design and patient
diagnoses. Consequently, instead of combining outcome data with a meta-analysis, we chose to
employ descriptive methods. We found insufficient evidence to: 1) calculate the relative risk of
dysphagia following a range of intubation durations and 2) to determine effect of intubation
duration on the frequency of dysphagia across all studies. We propose that using sensitive
swallow assessments on all enrollees, while reporting on all aspects of swallowing function,
would best represent the frequency and characteristics of dysphagia following extubation.
Future research endeavours should include homogeneous patient populations or larger sample
sizes and rigorous methodology. This research is necessary to permit clinicians to identify
patients who are at greater risk of dysphagia and enable more appropriate interventions.
In conclusion, there are relatively few studies with specific outcomes focusing on
dysphagia following intubation. The majority of identified studies are of very low quality with
high risk of bias. Although variable, most studies with prolonged intubation durations and those
that conducted instrumental assessments on the entire study population reported higher

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frequencies of dysphagia. Given the high likelihood of serious medical complications of
dysphagia, particularly pneumonia, we recommend that swallowing assessments should be
conducted on patients undergoing prolonged intubation durations. In the meantime, we call for
high quality studies using homogeneous patient populations to assess the influence of prolonged
intubation on dysphagia and to determine whether select medical comorbidities put patients at
greater risk.

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CHAPTER III
DYSPHAGIA AND ASSOCIATED RISK FACTORS FOLLOWING EXTUBATION IN CARDIOVASCULAR SURGICAL PATIENTS
This chapter has been previously published in the journal, Dysphagia (Skoretz, Yau,
Ivanov, Granton, & Martino, 2014). The format and references for this chapter have been
revised to conform to the requirements set forth by the School of Graduate Studies at the
University of Toronto. Permission was obtained from the publisher, Springer, to reproduce this
copyrighted material in this format (license number: 3493380167372, Appendix J).
Abstract
Following cardiovascular (CV) surgery, prolonged mechanical ventilation >48 h
increases dysphagia frequency over tenfold: 51 % in compared to 3-4 % across all durations.
Our primary objective was to identify dysphagia frequency following CV surgery with respect to
intubation duration. Our secondary objective was to explore characteristics associated with
dysphagia across the entire sample. Using a retrospective design, we stratified all consecutive
patients who underwent CV surgery in 2009 at our institution into intubation duration groups
defined a priori: I (≤12 h), II (>12 to ≤24 h), III (> 24 to ≤ 48 h), and IV (>48 h). Eligible
patients were >18 years old who survived extubation following coronary artery bypass alone or
cardiac valve surgery. Patients who underwent tracheotomy were excluded. Two blinded
reviewers extracted pre-, peri- and postoperative patient variables from a pre-existing database
and medical charts. Disagreements were resolved by consensus. Across the entire sample,
multivariable logistic regression analysis determined independent predictors of dysphagia.
Across the entire sample, dysphagia frequency was 5.6 % (51/909) but varied by group: I, 1 %
(7/699); II, 8.2 % (11/134); III, 16.7 % (6/36); and IV, 67.5 % (27/40). Across the entire sample,

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the independent predictors of dysphagia included intubation duration in 12-h increments
(p < .001; odds ratio [OR] 1.93, 95 % confidence interval [CI] 1.63-2.29) and age in 10-year
increments (p = .004; OR 2.12, 95 % CI 1.27-3.52). Patients had a twofold increase in their odds
of developing dysphagia for every additional 12 h with endotracheal intubation and for every
additional decade in age. These patients should undergo post-extubation swallow assessments in
order to minimize complications.

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Introduction
Dysphagia is a recognized complication following extubation that can lead to increased
morbidity, mortality (Macht et al., 2011), and hospital costs (Ferraris et al., 2001). While a
patient’s dysphagia risk increases following prolonged periods of mechanical ventilation, no
study to date has reported dysphagia frequencies across stratified intubation durations following
both coronary artery bypass grafting and cardiac valve surgery (Skoretz, Flowers, et al., 2010).
All patients undergoing cardiovascular (CV) surgery require endotracheal intubation and
mechanical ventilation as part of standard surgical intervention; however, the duration of
intubation after surgery varies (Cislaghi et al., 2009; Reddy et al., 2007). When intubation
duration exceeds 48 h following CV surgery, the frequency of swallowing impairments
(dysphagia) is 51 % (Barker et al., 2009), approximately ten times greater than that of the CV
surgical population as a whole (Ferraris et al., 2001; Hogue et al., 1995; Rousou et al., 2000).
The number of studies that focus on dysphagia following CV surgery are few (Barker et
al., 2009; Burgess et al., 1979; Ferraris et al., 2001; Harrington et al., 1998; Hogue et al., 1995;
Messina et al., 1991; Partik et al., 2003; Rousou et al., 2000) and the evidence surrounding the
relation between intubation duration and dysphagia in this population is limited (Skoretz,
Flowers, et al., 2010). In particular, most studies addressing intubation duration report
cumulative dysphagia frequencies regardless of intubation periods (Ferraris et al., 2001; Hogue
et al., 1995; Rousou et al., 2000), with only two (Barker et al., 2009; Burgess et al., 1979)
focusing on specific intubation durations: >48 h (Barker et al., 2009) and from 8 to 28 h (Burgess
et al., 1979). As a result, dysphagia frequencies following intubation durations of <24 h or
between 24 and 48 have yet to be reported. In addition to the limitations in the CV surgery
literature, discrepancies also exist regarding the definition of prolonged intubation in other

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diagnostic groups (Ajemian et al., 2001; de Larminat et al., 1995; Leder, Cohn, et al., 1998;
Tolep et al., 1996). In those studies prolonged intubation is defined as >24 h (de Larminat et al.,
1995), >48 h (Ajemian et al., 2001; Leder, Cohn, et al., 1998) or as long as 8 days (Tolep et al.,
1996). Overall, dysphagia following extubation regardless of the diagnostic group requires
further investigation (Skoretz, Flowers, et al., 2010).
Our primary goal was to report the frequency of dysphagia according to varying
intubation duration following coronary artery bypass grafting and/or cardiac valve surgery.
Furthermore, we also sought to explore the characteristics associated with dysphagia across this
CV surgical population thereby determining those at greatest risk for dysphagia.
Patients and Methods
Following institutional ethics board approval, we retrospectively reviewed the medical
records of all consecutive patients who underwent CV surgery in a 12-month period (January-
December 2009) at a single institution. We included adult patients (>18 years of age) who
survived their final extubation following coronary artery bypass alone or valve replacements
and/or repairs as their primary procedure. We excluded patients who underwent cardiac
transplantation, implantation of ventricular assist devices, repair of adult congenital heart defects,
and other complex procedures. Patients who underwent a pre- or postoperative tracheotomy
were also excluded.
Data Abstraction
Demographic, clinical, and operative patient data from electronic medical charts and the
existing CV surgery database were utilized for this study.
The electronic chart review was conducted in accordance with a data abstraction manual
that we developed and finalized a priori (Appendix K). Two raters (SAS and a research

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assistant), blinded to each other, reviewed the electronic charts of all patients who met the
study’s inclusion criteria. The reviewers recorded data regarding (1) extubation dates and times,
(2) perioperative transesophageal echocardiography, and (3) medical orders and nursing staff
documentation pertaining to tube feeding, assessment by speech-language pathology (SLP), and
dietary texture modifications. Data were recorded using a pre-established form (Appendix L).
Disagreements between raters were resolved by consensus.
The CV surgery database is completed prospectively for all patients who undergo CV
surgery at our institution (Rao et al., 1996). Trained CV surgery research nurses collect and
enter the data. Their reliability is regularly monitored through internal chart audits. Only the
variables of interest were extracted for this study, including those pertaining to demographics as
well as preoperative, perioperative, and postoperative outcomes.
Operational Definitions
Both intubation duration strata and oropharyngeal dysphagia were defined a priori.
Specifically, intubation durations were grouped into four strata: I (≤12 h), II (>12 to ≤24 h), III
(>24 to ≤48 h), and IV (>48 h). Dysphagia was defined as any abnormality of the oral,
pharyngeal, or upper esophageal stage of deglutition resulting in impairment in swallowing.
Impairment was identified by any one of the following medical orders that occurred within 96 h
following the patient’s final extubation: (1) enteral feeding, (2) swallowing assessment order
recommending enteral feeding, modified-texture diet, or nil per os (NPO), or (3) modified
texture diet order as written by a speech-language pathologist or medical staff.
Statistical Analyses
We reported data as frequency, mean with standard deviation (SD), and median with
interquartile range (IQR) as appropriate. The frequency of dysphagia was summarized

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descriptively. Comparisons were made between those with and those without dysphagia across
the entire study sample, using Mann-Whitney or unpaired 2-sided t-tests for continuous variables
and Pearson’s χ2 test or Fisher’s exact test for proportions. Missing variables were imputed with
the median. Variables for our main-effect regression model were selected using a backward
stepwise bootstrapping method (n = 1,000, inclusion threshold p < .05). In order to avoid
colinearity, predictor variables that were deemed clinically redundant were not entered into the
bootstrap. We considered variables occurring in >10 % of the bootstrapping resamples for our
final model. Our final regression was conducted using a backward stepwise method. For the
purposes of the bootstrap and regression, the following variables were dichotomized and/or
defined as: (1) moderate left ventricular (LVEF <40 %) dysfunction, (2) New York Heart
Association (NYHA) class IV symptoms, (3) myocardial infarction within 30 days
preoperatively, and (4) a nonelective surgical procedure.
Bivariate analyses were conducted using IBM® SPSS© v19.0 for Mac OS X (IBM®,
Armonk, NY, USA). Bootstrap and regression modeling were conducted using SAS v9.1 for
Windows (SAS Institute Inc., Cary, NC, USA). We determined statistical significance by a 2-
tailed p < .05.
Results
A total of 1,480 patients underwent CV surgery between January 1 and December 31,
2009, at our institution. Of those, 944 patients underwent coronary artery bypass grafting or
valve repairs and/or replacements as their primary procedures. Of the 944 patients, a total of 35
patients were excluded: 17 patients died while intubated, 17 underwent a tracheotomy, and one
patient had no recorded intubation time. The remaining 909 patients were then stratified
according to intubation duration: I (≤12 h) included 699 patients (76.9 % of total), II (>12 to ≤24

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h) 134 patients (14.7% of total), III (>24 to ≤48 h) 36 patients (4.0% of total), and IV (>48 h) 40
patients (4.4 % of total). This sample size met a total sample required to meet expected event
rate in our intubation groups (see Appendix M for sample size calculation).
Dysphagia Frequency and Criteria
Dysphagia frequency was 5.6% (51/909) across the entire study sample but varied across
intubation groups: I, 1.0 % (7/699); II, 8.2 % (11/134); III, 16.7 % (6/36); and IV, 67.5 % (27/40)
(Table 3.1). Of the 51 patients with dysphagia, 47 (92 %) patients met two or more of our criteria
for dysphagia, with nearly half (25/51, 49 %) meeting all three. Four patients (8 %) met only one
of our dysphagia criteria. All four of these patients required enteral feeding as their primary
form of nutrition and had a Glasgow Coma Score (GCS) of 14 or higher. The first dysphagia
criterion was met within 24 h following extubation for 19 patients (37 %), within 48 h for 18
patients (35 %), within 72 h for nine patients (18 %) and within 96 h for 5 (10 %) patients.

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Table 3.1 Comparing dysphagia frequency and intubation duration across intubation groups
Intubation group
Dysphagia frequency
Total (n = 909)
Without dysphagia (n = 858)
With dysphagia (n = 51)
Ia 699 (76.9) 692 (80.7) 7 (13.7)
IIb 134 (14.7) 123 (14.3) 11 (21.6)
IIIc 36 (4.0) 30 (3.5) 6 (11.8)
IVd 40 (4.4) 13 (1.5) 27 (52.9)
Note. Values are n (%); h = hours. a I, ≤ 12.0 h; b II, >12.0 h and ≤24.0 h ; c III, >24.0 h and ≤48.0 h; d IV, >48.0 h.
Intubation Duration Across Study Sample
Median intubation duration [IQR] for all patients was 6.9 h [6.2]. Across the entire
sample, those with dysphagia had significantly longer median intubation duration than those
without (68.8 h [93.7] vs. 6.8 h [5.2]; p < .001).
Patient Characteristics Across Study Sample
Demographic variables and preoperative clinical characteristics are presented in Table
3.2. Across the sample, the mean (±SD) age was 65.9 years (±12.0). Those with postoperative
dysphagia were significantly older than those without (74.3 ± 8.7 vs. 65.4 ± 12.0 years; p <
.001), with proportionately more having at least moderate chronic kidney disease (58.8 vs. 19.9
%; p < .001). Cardiovascular surgical risk factors differed between those with and those without

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dysphagia, including NYHA symptom class (p = .008), congestive heart failure (41.2 vs. 16.9 %,
p < .001), preoperative atrial fibrillation (17.6 vs. 5.6 %, p = .003) and preoperative stroke or
transient ischemic attack (25.5 vs. 8.7 %, p = .001). Some patient characteristics were not
discriminatory, including diabetes, preoperative myocardial infarction, hypertension and
respiratory risks such as a history of smoking. Of the entire study sample (n = 909), there was
missing data from 1 to 11 patients (0.1-1.2 %) for the following variables: family history of heart
disease (1.0 %), diabetes (0.1 %), LV grade (0.4 %), NYHA symptom class (1.2 %),
hyperlipidemia (0.2 %), smoking history (0.2 %) and chronic kidney disease (0.1 %) (Table 3.2).

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Table 3.2 Pre-operative demographics and presenting clinical characteristics across sample
Variable
All patients
(n = 909)
Without dysphagia (n = 858)
With dysphagia
(n = 51)
p-value
Age, mean yrs (SD) 65.9 (12.0) 65.4 (12.0) 74.3 (8.7) < .001 median yrs (IQR) 67.0 (17.0) 67.0 (17.0) 76.0 (12.0) < .001 Male, n (%) 649 (71.4) 612 (71.3) 37 (72.5) .876 Family history of heart diseasea, n (%)
476 (52.9) 449 (52.8) 27 (54.0) .885
Diabetes Risksb Diabetesc, n (%) 309 (34.0) 292 (34.0) 17 (33.3) 1.00 Cardiovascular Surgical Risks Circulatory shock, n (%) 10 (1.1) 9 (1.0) 1 (2.0) .440 Non-Q-wave infarction, n (%) 127 (14.0) 124 (14.5) 3 (5.9) .097
Q-wave infarction, n (%) 15 (1.7) 14 (1.6) 1 (2.0) .582
LV graded .042
1, n (%) 582 (64.3) 556 (65.1) 26 (51.0) 2, n (%) 207 (22.9) 193 (22.6) 14 (27.5) 3, n (%) 107 (11.8) 98 (11.5) 9 (17.6) 4, n (%) 9 (1.0) 7 (0.8) 2 (3.9)
NYHA classificatione .008
I, n (%) 131 (14.6) 130 (15.3) 1 (2.0) II, n (%) 189 (21.0) 183 (21.6) 6 (12.0) III, n (%) 295 (32.9) 273 (32.2) 22 (44.0) IV, n (%) 283 (31.5) 262 (30.9) 21 (42.0)
Congestive heart failure, n (%)
166 (18.3) 145 (16.9) 21 (41.2) <.001
Hypertensive, n (%) 655 (72.1) 616 (71.8) 39 (76.5) .524

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Variable
All patients
(n = 909)
Without dysphagia (n = 858)
With dysphagia
(n = 51)
p-value
Diet or medically treated hyperlipidemiaf, n (%)
658 (72.5)
620 (72.4)
38 (74.5)
.753
Previous stroke or TIA, n (%) 88 (9.7) 75 (8.7) 13 (25.5) .001 Heart block / pacemaker, n (%) 18 (2.0) 17 (2.0) 1 (2.0) 1.000 Atrial fibrillation or flutter, n (%) 57 (6.3) 48 (5.6)
9 (17.6) .003
Left main artery stenosis, n (%) 209 (23.0) 197 (23.0) 12 (23.5) 1.00 Respiratory Risks Current or past smokerg, n (%)
529 (58.3) 498 (58.0) 31 (63.3) .552
Renal Risks
Chronic kidney diseaseh n (%) 201 (22.1) 171 (19.9) 30 (58.8) <.001
Note. yrs = years; LV = left ventricular; NYHA = New York Heart Association; TIA = transient ischemic attack. a Missing data: 8 patients without dysphagia, 1 patient with dysphagia (total: 1.0%). b Missing data: 1 patient without dysphagia (total: 0.1%). c Includes diet controlled, orally medicated and insulin dependent diabetics. d Missing data: 4 patients without dysphagia (total: 0.4%). e Missing data: 10 patients without dysphagia, 1 patient with dysphagia (total: 1.2%). f Missing data: 2 patients without dysphagia (total: 0.2%). g Missing data: 2 patients with dysphagia (total: 0.2%), h At least moderate chronic kidney disease as defined by an estimated creatinine clearance <60mL/min; missing data: 1 patient without dysphagia (total: 0.1%).

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Of 909 patients, 567 (62.4 %) underwent coronary artery bypass as their primary
surgery, with the remaining patients (342/909, 37.6 %) undergoing valve repair and/or
replacement. Many operative characteristics and perioperative complications
distinguished those with and without dysphagia (Table 3.3). More patients with
dysphagia underwent valve repair and/or replacement as compared to coronary artery
bypass grafting (60.8 vs. 39.2 %, p = .001) and also required a perioperative
transesophageal echocardiogram (74.5 vs. 44.3 %, p < .001). Patients with dysphagia
also had more perioperative strokes, sepsis, and low output syndrome. Lastly, more
patients with dysphagia required intra-aortic balloon pump placement (15.7 vs. 2.9 %,
p < .001) and/or inotropic support (54.9 vs. 39.5 %, p = .039) than patients without.

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Table 3.3 Peri-operative characteristics across sample
Variable
All patients (n = 909)
Without dysphagia (n = 858)
With dysphagia
(n = 51) p-value
Procedure .001 CABG, [n (%)] 567 (62.4) 547 (63.8) 20 (39.2) Valve, [n (%)] 342 (37.6) 311 (36.2) 31 (60.8)
Urgency .701 Elective, [n (%)] 574 (63.1) 543 (63.3) 31 (60.8) Inpatient, [n (%)] 263 (28.9) 245 (28.6) 18 (35.3) Urgent, [n (%)] 59 (6.5) 57 (6.6) 2 (3.9) Emergent, [n (%)] 13 (1.4) 13 (1.5) 0 (0.0)
CPB usage 826 (90.9) 783 (91.3) 43 (84.3) .126 CPB duration, [median (IQR)] (min)
85.0 (41.0) 84.0 (41.0) 94.0 (82.0) .014
TEE, [n (%)] 418 (46.0) 380 (44.3) 38 (74.5) <.001 Perioperative Complications
Strokea, [n (%)] 10 (1.1) 4 (0.5) 6 (11.8) <.001 Sepsisb, [n (%)] 8 (0.9) 5 (0.6) 3 (5.9) .008 Use of dopamine in ICU, [n (%)]
367 (40.4) 339 (39.5) 28 (54.9) .039
MI, [n (%)] 13 (1.4) 10 (1.2) 3 (5.9) .032 Low-output syndromec, [n (%)]
20 (2.2) 13 (1.5) 7 (13.7) <.001
IABP usage 33 (3.6) 25 (2.9) 8 (15.7) <.001
Note. CABG = coronary artery bypass graft; CPB = cardiopulmonary bypass; IQR = interquartile range; min = minutes; ICU = intensive care unit; MI = myocardial infarction; TEE = transesophageal echocardiogram utilized peri-operatively; IABP = intra-aortic balloon pump placement either pre-, peri- or post-operatively. a Evidence of persistent neurological deficit. b Positive blood culture. c Use of inotrope or mechanical devices for more than 30 minutes to maintain a blood pressure > 90mmHg with a C.I.< 2.2 l/m/m2.

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Postoperative outcomes also differed between those with and without dysphagia
(Table 3.4). In addition to longer intubation durations, those with dysphagia had
significantly higher frequencies of reintubation (p = < .001), reoperation (p = < .001) and
postoperative atrial fibrillation (p = .002). While patients with dysphagia had longer
stays in the intensive care unit (p = < .001), they were not readmitted to the intensive care
unit at a greater rate (p = .108). For descriptive data of intubation strata I, II, III, and IV
refer to Appendices N, O, P and Q respectively.

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Table 3.4 Post-operative patient outcomes across sample
Variable
All patients (n = 909)
Without Dysphagia (n = 858)
With Dysphagia
(n = 51) p-value
Intubation duration, [median (IQR)] (hours)
6.9 (6.2)
6.8 (5.2)
68.8 (93.7)
<.001
Reintubation, [n (%)] 25 (2.8) 13 (1.5) 12 (23.5) <.001 Number of intubations <.001
1, [n (%)] 884 (97.2) 845 (98.5) 39 (76.5) 2, [n (%)] 23 (2.5) 13 (1.5) 10 (19.6) 3, [n (%)] 1 (0.1) 0 (0.0) 1 (2.0)
4, [n (%)] 1 (0.1) 0 (0.0) 1 (2.0) Re-operation, [n (%)] 35 (3.9) 27 (3.1) 8 (15.7) <.001 Atrial fibrillation, [n (%)]
342 ( 37.6) 312 ( 36.4) 30 (58.8) .002
Post-extubation repeat ICU admission, [n (%)]
21 (2.3)
18 (2.1)
3 (5.9)
.108
ICU stay [median (IQR)] (h)
40.8 (50.2) 28.3 (46.8) 142.9 (97.5) <.001
Preoperative hospital stay [median (IQR)] (days)
1.0 (1.0) 1.0 (1.0) 1.0 (3.0) .001
Postoperative hospital stay, [median (IQR)] (days)
7.0 (3.0) 7.0 (3.0) 15.0 (10.0) <.001
Total inpatient stay, [median (IQR)] (days)
8.0 (5.0) 8.0 (4.0) 16.0 (10.0) <.001
Note. ICU = intensive care unit; IQR = interquartile range.

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After exclusion of clinically redundant predictor variables, 26 variables were
entered into the bootstrapping selection model. Of those, 13 were included in >10 % of
the bootstrap resamples and were subsequently entered into the multivariate model (Table
3.5). Findings from logistic regression analysis identified the following independent
predictors of dysphagia: intubation duration (p < .001; OR 1.93, 95 % CI 1.63–2.29) for
every 12-h increment, age (p = .004; OR 2.12, 95 % CI 1.27–3.52) for every 10-year
increment, and the occurrence of postoperative sepsis (p = .01; OR 14.03, 95 % CI 1.78–
110.72) with a model c-statistic of 0.94.

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Table 3.5
Independent predictors of postoperative dysphagia
Variable p-value Odds Ratio 95% CI
Demographics
Age 0.004 2.12a 1.27–3.52
Male 0.13 2.08 0.81–5.34
Pre-operative Characteristics
Atrial fibrillationb 0.38 1.75 0.51–6.06
Chronic kidney diseasec 0.09 2.15 0.90–5.13
Congestive heart failure 0.51 1.41 0.51–3.89
Hypertension 0.44 0.69 0.27–1.78
Left main artery stenosis 0.33 1.62 0.62–4.26
Left ventricular dysfunction 0.62 1.32 0.44–3.95
Peri-/Post-operative Characteristics
Intubation duration <.001 1.93d 1.63–2.29
MIe 0.23 0.44 0.12–1.66
Sepsisf 0.01 14.03 1.78–110.72
Strokeg 0.13 4.37 0.66–29.05
Valve surgery 0.36 1.57 0.59–4.15
Note. CI = confidence interval. a Point estimate based on ten year increments. b Preoperative atrial fibrillation or atrial flutter. c At least moderate chronic kidney disease as defined by estimated creatinine clearance of <60mL/min. d point estimate based on 12 hour increments. e preoperative myocardial infarction including Q-wave and Non-Q-wave infarctions. f peri/post-operative sepsis as defined by positive blood cultures. g peri/post-operative stroke.

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Discussion
This study is the first to report dysphagia frequency across stratified intubation
durations after both coronary artery bypass and cardiac valve surgery. We determined
that dysphagia frequency (1) is highest following intubation exceeding 48 h, (2) is
negligible in those patients intubated for ≤12 h and (3) exceeds the cumulative population
incidence previously reported (Ferraris et al., 2001; Hogue et al., 1995; Rousou et al.,
2000) in those intubated between 12 and 48 h. Most notably, our findings are the first to
determine that the odds of a patient having dysphagia increase by a factor of 2 for every
additional 12 h of endotracheal intubation or for every additional decade of age.
Similar to previous work, this study identified many pre- and perioperative risk
factors associated with dysphagia as well as three independent predictors: advanced age
(Hogue et al., 1995), prolonged intubation (Barker et al., 2009; Hogue et al., 1995), and
sepsis (Barker et al., 2009). While we also found that both pre- and perioperative stroke
(Barker et al., 2009; Rousou et al., 2000) as well as TEE use (Hogue et al., 1995; Rousou
et al., 2000) were more common in those presenting with dysphagia, neither variable
proved to be independently predictive of dysphagia in our study. Although TEE use was
not predictive of dysphagia in our study, the frequency of dysphagia was more common
in those patients who underwent valve surgery than those who underwent bypass. While
some studies have reported higher gastrointestinal complications, including
gastrointestinal ischemia and hemorrhage, following valve surgery (Bolcal et al., 2005;
D'Ancona et al., 2003), to our knowledge no study has compared the occurrence of
oropharyngeal dysphagia in those who underwent bypass versus valve surgery. Although
comparing the frequency of dysphagia between these two patient groups (valve vs.

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bypass) is outside the scope of this current study, we feel that it does warrant
investigation in the future. While only speculative, this difference is likely multifactorial
and may be related to the type of surgery or any number of other factors such as baseline
cardiac function, pre-existing medical comorbidities, perioperative stroke,
cardiopulmonary bypass time, inotropic support, or intubation duration.
The frequency of dysphagia across our entire sample is similar to that reported
previously (Ferraris et al., 2001; Hogue et al., 1995; Rousou et al., 2000). Specifically,
our results also confirm previously reported low frequencies for patients intubated ≤12 h
(Burgess et al., 1979). In addition, we confirmed that those patients intubated for >48 h
were at the greatest risk of developing dysphagia; our dysphagia frequency for that
intubation group was 67.5 %, a much higher frequency than previously reported (Barker
et al., 2009). Although the study by Barker and colleagues was conducted at the same
institution, patients in our study who had intubations >48 h were older and had greater
NYHA symptom class, suggesting a population at increased risk of complications.
Establishing the cause of dysphagia following endotracheal intubation is a
challenge often due to patients’ medical complexity and their comorbidities. While
determining causation is outside the scope of our current study, some have reported
structural and mechanical alterations to the upper airway following extubation in those
patients with dysphagia (Postma et al., 2007; Tolep et al., 1996). In addition, various
intubation techniques and induction medication can either positively or negatively affect
protective airway reflexes (Mencke et al., 2003).
Our study had limitations that were inherent in its retrospective nature. We were
unable to investigate baseline swallowing status as well as rule out all pre-existing

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medical conditions that may predispose a patient to dysphagia such as neurological
disorders (Martino et al., 2005). Our postoperative definition of dysphagia was also
limited to bedside speech-language pathology assessment findings as well as surrogate
nutrition variables such as modified texture diets or tube feeding as few patients received
instrumental swallowing assessments. However, our identification of those with
dysphagia was conservative. Specifically, we limited initial identification of dysphagia to
within 96 h of final extubation, and most patients met multiple criteria for the presence of
dysphagia. The dysphagic patients had adequate consciousness as assessed by the GCS
scores and/or nursing records. We were unable to fully assess the presence of delirium as
formal delirium screening scores were not recorded and they could not be derived from
the available data. Finally, our data were limited to a single large, quaternary-care
cardiac center serving a broad multiethnic demographic, suggesting but not proving that
our findings would be applicable to similar centers. Limitations notwithstanding, we
attempted to maintain methodological rigor, maximize generalizability and minimize bias
in several ways: (1) developing a priori operational definitions of dysphagia and our
descriptive intubation strata, (2) including a homogeneous patient sample typical of many
CV surgery centers, and (3) maintaining blinding throughout our data collection.
In conclusion, our description of dysphagia frequency, according to varying
intubation durations in a CV surgery population, demonstrated that the highest risk of
dysphagia occurs in patients intubated for more than 48 h. We identified risk factors
associated with dysphagia as well as its independent predictors across the entire study
sample. In general, older patients, those with perioperative sepsis, and longer intubation
had the greater dysphagia risk. While further prospective studies are needed to determine

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perioperative or comorbid factors that affect dysphagia severity and/or recovery, the
present findings will serve as an important first step in the identification of at-risk
patients following extubation.

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CHAPTER IV
DYSPHAGIA INCIDENCE AND SWALLOWING PHYSIOLOGY FOLLOWING PROLONGED
INTUBATION AFTER CARDIOVASCULAR SURGERY: A FEASIBILITY STUDY
Abstract
Dysphagia incidence following prolonged intubation after cardiovascular (CV)
surgery, although common (>50%), has never been determined prospectively with the
population’s swallowing physiology largely unknown. As a first step, our primary
objective was to assess feasibility and patient acceptance of tests used to evaluate
swallowing physiology following prolonged intubation after cardiovascular surgery.
From July-October 2011, all consecutive adults undergoing CV surgery at our institution
who were intubated >48 hours were approached to participate. Patients with
tracheostomies were excluded. Enrolled patients underwent a videofluoroscopic
swallowing study (VFS) and nasendoscopy within 48 hours after extubation. VFSs were
interpreted using ratings scales (Modified Barium Swallow Measurement Tool for
Swallow ImpairmentTM© and Penetration Aspiration Scale) and objective physiological
measurements (hyoid displacement and pharyngeal constriction ratio). Two independent
raters blinded to clinical data completed physiological measurements. Feasibility
parameters included: recruitment rate, patient participation, task completion durations and
the inter-rater reliability of VFS measures. Upon study completion, participants
completed self-administered impact questionnaires. Of the 39 patients intubated for >48h,
16 met eligibility criteria. Three were enrolled and completed the VFS. All refused
nasendoscopy. VFS completion time ranged from 14 minutes to 52 minutes with item
interrater reliability ranging from .25 (95% CI: -.10-.59) to .99 (95% CI: .98-.99).
Participants reported minimal study burden. Oral and pharyngeal swallow abnormalities

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were observed across all patients. This study design was not feasible. Recruitment was
slow, few patients participated and no patient agreed to all procedures. We discuss
necessary methodological changes and lessons learned for future research.

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Introduction
Dysphagia occurs in approximately half of all patients who are intubated for 48
hours or more following cardiovascular (CV) surgery (Barker et al., 2009; Skoretz et al.,
2014). Not only does post-extubation dysphagia increase hospitalization costs (Ferraris
et al., 2001); patients with the disorder are at greater risk of pneumonia, reintubation, and
death (Macht et al., 2011).
What is known about dysphagia frequency and swallowing physiology following
prolonged intubation after CV surgery is limited by study design and the quality of the
available literature (Skoretz, Flowers, et al., 2010). The reported dysphagia incidence is
questionable given these intrinsic study limitations which include retrospective design,
variable diagnostic methods, inconsistent use of instrumental assessments across
enrollees and lack of assessor blinding (Skoretz, Flowers, et al., 2010). In addition, while
most studies report on dysphagia associated risk factors (Skoretz, Flowers, et al., 2010),
the few that have characterized the swallowing impairment (Barker et al., 2009; Burgess
et al., 1979; Ferraris et al., 2001; Harrington et al., 1998; Hogue et al., 1995; Partik et al.,
2003) have done so using: instrumental assessment methods with low sensitivity and
specificity (Burgess et al., 1979; Harrington et al., 1998), general dysphagia terminology
(Barker et al., 2009; Ferraris et al., 2001; Harrington et al., 1998), assessments focusing
on only aspiration (Burgess et al., 1979; Harrington et al., 1998), a mixed adult and
pediatric patient sample (Partik et al., 2003) or without using operationally defined
swallowing outcomes (Hogue et al., 1995). To date two studies have reported on
swallowing characteristics beyond aspiration and general pharyngeal impairment (Hogue
et al., 1995; Partik et al., 2003), yet no study has analyzed the swallowing physiology

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using standardized rating scales or objective physiological measurements. Hence, the
mechanisms underlying dysphagia in this population are yet to be determined.
Presently, there are two psychometrically validated tools designed to rate the
swallow captured on videofluoroscopy: the Modified Barium Swallow Measurement
Tool for Swallow Impairment (Martin-Harris et al., 2008) (MBSImpTM©, Northern
Speech Services, Gaylord, MI) and the Penetration-Aspiration Scale (Rosenbek et al.,
1996) (PAS). The MBSImpTM© is comprised of 17 different components that collectively
describe oral, pharyngeal and esophageal function. The PAS is an 8-point interval scale
that describes the degree to which material has invaded the airway and whether the
material has been ejected. Together, the MBSImpTM© and PAS quantify swallowing
impairment severity and airway protection respectively.
While the MBSImpTM© and PAS rate aspects of the patient’s swallow, they do not
objectively measure structural movement during the swallow. Individual
videofluoroscopic images can be extracted from the videofluoroscopic swallow study
(VFS) and used to conduct targeted objective physiological measurements such as hyoid
bone displacement (Leonard, 2007; Leonard et al., 2000; Molfenter & Steele, 2014;
Steele et al., 2011) and pharyngeal constriction (Leonard, 2007; Leonard et al., 2000).
Adequate hyoid elevation (Jacob et al., 1989; Kim & McCullough, 2008; Leonard, 2007;
Steele et al., 2011) and pharyngeal constriction (Leonard, 2007; Leonard et al., 2009;
Setzen et al., 2003; Yip et al., 2006) are associated with successful propulsion of food or
fluid through the pharynx into the esophagus thereby preventing laryngeal penetration,
tracheal aspiration and/or pharyngeal residue. Recently extubated patients are at
increased risk of reduced hyoid elevation as well as impaired pharyngeal constriction due

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to the relative inactivity of oropharyngeal musculature during endotracheal intubation and
at present this has never been investigated. In addition, these displacement measures are
useful to clinicians when designing treatment programs for patients with dysphagia.
While the VFS is widely accepted as a gold standard instrumental technique to
assess the swallow, it is not the diagnostic tool of choice when ruling out oropharyngeal
and laryngeal pathologies. Regardless of the underlying medical etiology, intubation and
presence of the artificial airway can lead to mucosal abnormalities, laryngeal edema,
granulomas and vocal fold immobility which can affect the anatomical integrity and
physiology of the swallow (DeVita & Spierer-Rundback, 1990; Postma et al., 2007;
Thomas et al., 1995; Tolep et al., 1996). Nasendoscopy provides a direct view of the
hypopharynx and larynx, along with the superior aspects of the upper trachea and upper
esophageal sphincter, providing diagnostic information not otherwise acquired with
videofluoroscopy (Langmore et al., 1988; Langmore et al., 1991; Murray et al., 1996).
Together, these diagnostic techniques provide a comprehensive assessment of the
swallow and the structures involved; however, these tests are lengthy, invasive and may
not be tolerated by this patient population. As a result, the feasibility of using these
instrumental approaches on patients following prolonged intubation after CV surgery
needs to be determined.
Our primary objective was to determine the feasibility of using these instrumental
assessments in order to assess swallowing and upper airway physiology prospectively on
consecutively enrolled CV surgery patients following prolonged intubation. Our
secondary objective was to explore the tolerability and impact of this study on patients
and nursing. These findings will be used to inform a future large-scale study to

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systematically evaluate the incidence of dysphagia and formally assess the swallowing
physiology of this patient population.
Methods Participants
From July 1 to October 31 2011, all consecutive patients intubated for >48 hours
following CV surgery at our institution were approached for study participation. Eligible
patients included those >18 years of age who were extubated within the previous 48
hours. We excluded patients with a history of dysphagia, tracheotomy, head/neck cancer,
or neurological disorders including stroke or seizures. Also excluded were patients
deemed inappropriate for study participation by the attending medical team, including
those with reduced consciousness, medical instability or who were nil per os (NPO) due
to gastroenterologic complications. Our institutional research ethics board approved this
study and all participants provided written informed consent prior to participation. If the
patient was unable to provide research consent, the patient’s surrogate decision maker
was approached for consent on the patient’s behalf.
Study Process
Within 48 hours from time of extubation, the patient’s swallow was assessed
using a VFS conducted by a speech-language pathologist blinded to all clinical data. In
addition, these patients were given the option to undergo flexible nasendoscopy by
otolaryngology. At the completion of instrumental testing, we invited the patient and
attending nurse to provide anonymous feedback on the study process using a self-
administered impact questionnaire. We measured feasibility throughout the study using
process and resource parameters including: recruitment rate, number of eligible patients,

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losses to enrollment, patient participation with the instrumental protocols, task
completion times and the inter-rater reliability of the VFS measures.
Videofluoroscopic Swallow Study
Imaging. Fluoroscopy was conducted using a Toshiba Ultimax System MDX-
8000A (Toshiba America Medical Systems Inc., Tustin, CA) in the lateral position.
Using continuous pulse, the image was captured in uncompressed form using a TIMS
2000 DICOM system (Forest Imaging, Chelmsford, MA) at a rate of 30 frames per
second. Image collimation allowed for views of the anterior lip margins, superior aspect
of the nasal passages, posterior margins of the cervical vertebrae, and cervical esophagus.
A visible scalar with known dimensions (a quarter) was placed submentally in the image
field for calibration of image magnification.
Videofluoroscopic swallow study procedure. Each patient was presented with
various fluid and food textures combined with E-Z-EM barium contrast agents (E-Z-EM
Inc., Lake Success, NY) according to institutional standard practice and preparation. The
trials were presented as follows: 1) thin liquid with diluted liquid Polibar Plus barium
sulfate suspension (47% w/v; 3 x 5-ml boluses by spoon, 2 x 15-ml boluses by cup), 2)
applesauce mixed with powdered barium (28% w/w; 3 x 5-ml boluses by spoon), 3) ½
Peak Frean digestive cookie coated with barium paste (60% w/w) and 4) sequential cup
sips of the thin liquid barium dilution (47% w/v; 100-ml maximum). This sequence was
discontinued as soon as patient safety was a concern. For all trials, except for sequential
cup sipping, a cue-swallow command was used with instruction to hold the bolus in the
oral cavity and then swallow on command.

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Videofluoroscopic Swallow Study Measures
Following VFS completion, we conducted two types of analyses: i. standardized
VFS assessment tools and ii. objective physiological displacement measurements.
Standardized VFS assessment tools. Each VFS was scored in its entirety using
two standardized, validated and reliable tools: the Modified Barium Swallow Impairment
Profile (MBSImpTM©, Northern Speech Services, Gaylord, MI) (Martin-Harris et al.,
2008) and the Penetration Aspiration Scale (PAS) (Rosenbek et al., 1996).
One rater (SAS), while blinded to clinical data, completed the MBSImpTM© for
each bolus administration. The MBSImpTM© is a standardized tool used to quantify
severity of oral and pharyngeal impairment through assessment of 17 physiologic
components. Each component has a rank-ordered scoring system, ranging from a three to
five point scale, with increasing scores indicating greater impairment. A priori we
excluded two components, pharyngeal constriction and esophageal clearance, the former,
as it requires an anterior posterior fluoroscopic view, which cannot be obtained from this
patient population given their restricted mobility at the time of testing, and the latter as it
was beyond the scope of this study. Table 4.1 summarizes the components included in
this study along with their scoring ranges. The MBSImpTM© rater completed the
MBSImpTM© certification process. This process included a minimum of 21 training hours
and subsequently required a minimum of 80% reliability during accuracy testing of the
MBSImpTM© physiologic components.

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Table 4.1.
MBSImpTM© oral and pharyngeal componentsa
Component Scale Abbreviation
Oral 1 Lip closure (0-4) LipC 2 Tongue control during bolus hold (0-3) TC 3 Bolus preparation/mastication (0-3) BP 4 Bolus transport/lingual motion (0-4) BT 5 Oral residue (0-4) OR 6 Initiation of pharyngeal swallow (0-4) IPS Pharyngeal 7 Soft palate elevation (0-4) SPE 8 Laryngeal elevation (0-3) LE 9 Anterior hyoid excursion (0-2) HM 10 Epiglottic movement (0-2) EM 11 Laryngeal vestibule closure (0-2) LVC 12 Pharyngeal stripping wave (0-2) PSW 14 Pharyngoesophageal segment opening (0-3) PESO 15 Tongue base retraction (0-4) TBR 16 Pharyngeal residue (0-4) PR
Note. a Components 13 (Pharyngeal constriction) and 17 (Esophageal clearance) excluded a priori.
Two independent raters (SAS and RM) blinded to each other and all clinical data
conducted PAS scoring for each bolus administration. The PAS (Rosenbek et al., 1996)
is an 8-point scale that scores the depth of airway invasion by the fluid or food bolus,
whether it is expelled from the airway as well as any patient reaction (Table 4.2).

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Table 4.2. Penetration-Aspiration Scale (Rosenbek et al., 1996)
Score Description
1 Material does not enter the airway
2 Material enters the airway, remains above the vocal folds, and is ejected from the airway
3 Material enters the airway, remains above the vocal folds, and is not ejected from the airway
4 Material enters the airway, contacts the vocal folds, and is ejected from the airway
5 Material enters the airway, contacts the vocal folds, and is not ejected from the airway
6 Material enters the airway, passes below the vocal folds and is ejected into the larynx or out of the airway
7 Material enters the airway, passes below the vocal folds, and is not ejected from the trachea despite effort
8 Material enters the airway, passes below the vocal folds, and no effort is made to eject
Displacement measurements. Two independent raters (SAS and RM) blinded to
each other and all clinical data, conducted frame selection and displacement
measurements for each 5-ml and 15-ml bolus using ImageJ (National Institutes of Health,
Bethesda, MD) focusing on two domains: hyolaryngeal excursion and pharyngeal
constriction.
Hyoid excursion during each swallow was calculated according to two
techniques: 1) as an absolute trajectory measurement in millimeters (mm) quantifying the
anterior-superior displacement of the hyoid bone from its rest position (Leonard, 2007;

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Leonard et al., 2000) and 2) as an internally scaled calculation of separate anterior and
superior hyoid movement using the patient’s cervical vertebrae as a reference (Steele;
Steele et al., 2011). We utilized two fluoroscopy images per bolus for each technique:
one with the hyoid at rest and one at maximal anterior-superior displacement. The hyoid
“rest” frame was defined differently for each: 1) during bolus hold prior to swallow
initiation for the absolute measurements and 2) during lowest hyoid position following
swallow completion for the scaled measurements. Frame selection, anatomical tracing
specifications, and displacement calculations for both techniques were completed
according to previously published methods (Leonard, 2007; Leonard et al., 2000; Steele;
Steele et al., 2011).
We measured pharyngeal constriction during the swallow using ImageJ through a
pharyngeal constriction ratio calculation (PCR)(Leonard, 2007; Leonard et al., 2009;
Leonard et al., 2000). For this measurement, we defined the bolus hold frame (PAHOLD)
as the hold during the 5-ml thin liquid bolus. The maximum pharyngeal contraction
frames (PAMAX) were defined as the frame with maximal pharyngeal contraction during
each of the following: 5-ml and 15-ml thin liquid and 5-ml pureed boluses. Following
pharyngeal space tracing for each frame, we calculated the pharyngeal constriction ratio
by dividing the pharyngeal area (cm2) of the selected frames (PAMAX/PAHOLD)(Leonard,
2007; Leonard et al., 2009; Leonard et al., 2000).
Study Impact Questionnaires and Patient Variables
Following VFS completion, the patient and attending nurse were asked to
complete study impact questionnaires. The questionnaires (Table 4.3) utilized a 5-point
Likert scale rating patient comfort, study impact on nursing workload and perceived

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study value while providing an open-ended section for comments. Once completed, we
instructed the patient and/or nurse to deposit their questionnaire in a locked box on the
hospital unit. Following unblinding, the first author (SAS) recorded patient variables such
as demographics (age, gender) and operative information (surgery type, intubation
duration).

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Table 4.3.
Survey questions
Respondent Question Rating Scale
A. Patient
How did you find the x-ray swallow test? Easy
Somewhat easy Adequate Somewhat
difficult Very
difficult
Overall, how was your experience with this research?
Easy
Somewhat easy Adequate Somewhat
difficult Very
difficult
How was this form to complete? Easy
Somewhat easy
Adequate Somewhat difficult
Very difficult
B. Nurse
In your opinion, to what degree did this study affect the delivery of patient care? Not at all Very little A little Somewhat A lot
How did the participation of this study fit into your daily tasks? Easily Somewhat
easily Adequately With difficulty
With great difficulty
How were you able to accommodate being part of the videofluoroscopic swallow study? Easily Somewhat
easily Adequately With difficulty
With great difficulty
How was this form to complete? Easy Somewhat easy Adequate Somewhat
difficult Very
difficult

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Scoring and Statistical Analyses
For each patient, we scored each bolus administration individually with both the
MBSImpTM© and PAS according to published guidelines (Martin-Harris et al., 2008;
Rosenbek et al., 1996), if a texture or bolus volume was not administered to a patient
secondary to safety concerns, the patient received the highest, thereby most impaired,
MBSImpTM© and PAS score for that trial (Martin-Harris et al., 2008). For each patient,
we derived overall impression scores (OI) for each of the MBSImpTM© components
according to published standards, namely using the patient’s worst score for each
component regardless of texture or volume (Martin-Harris et al., 2008). We derived the
total oral impairment (components 1-6) and total pharyngeal impairment (components 7-
12, 14-16) scores for each patient by the summation of each OI score from the
appropriate oral and pharyngeal components. We dichotomized PAS scores as either
normal (PAS scores < 2) or abnormal (PAS scores ≥ 3) for each bolus administration
(Allen et al., 2010; Daggett, Logemann, Rademaker, & Pauloski, 2006) and summarized
these data as frequency counts.
We reported displacement measurements as medians and interquartile ranges
(IQR) according to bolus volume and texture. We calculated the single measures inter-
observer agreement using absolute agreement two-way mixed intraclass correlation
coefficient (ICC) for both frame selection and displacement measurements. We reported
the approximate duration in minutes for patient transport, patient study participation and
task completion (VFS preparation, study archiving, frame selection, displacement
measurements, MBSImpTM© and PAS scoring). We summarized questionnaire responses
descriptively and according to frequency counts. Statistical analyses were conducted

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using IBM SPSS version 22 (IBM Corporation, Armonk, NY). Radar plots were created
using OriginPro 9.1 (OriginLab Corporation, Northampton, MA) and scatter plots were
created using GraphPad Prism 6 (GraphPad Software Inc., La Jolla, CA).
Results
Patient Recruitment and Characteristics
During the four-month study period, 39 patients required intubation for more than
48 hours (Figure 4.1). Of those, 16 met the inclusion criteria with three patients agreeing
to participate for an approximate recruitment rate of one patient every five weeks. Of the
remaining 13 patients, six declined participation, six were not approached for
participation due to institutional and operational restrictions (i.e., weekend extubation and
diagnostic imaging suite downtime), and one was transferred off-service.

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Figure 4.1. Study enrollment.
Intubated >48h: N = 39
Did not meet inclusion criteria: n = 23 • Exclusion diagnoses: n = 10 • Expired: n = 6 • Tracheotomy: n = 7
Unable to enroll: n = 13 • Imaging restrictions: n = 2 • Weekend extubation: n = 4 • Patient transfer: n = 1 • Declined participation: n = 6
Enrolled: N = 3

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Our consecutive case series consisted of two males and one female aged 71, 37,
and 71 years respectively. Intubation durations ranged from 49 to 82 hours with all
patients undergoing an atraumatic intubation and extubation as documented by the
attending anaesthesiologist. Participant characteristics are summarized in Table 4.4. At
the time of study participation, all patients were in intensive care requiring 24-hour one-
to-one nursing care. All enrolled patients refused the nasendoscopy procedure.
Table 4.4.
Patient characteristics
Case Demographics Operative Variables
Sex Age (yrs)
Surgery type Intubation duration
(h)
P1 M 71 Heart transplant 53.3
P2 M 37 Aortic valve replacement Tricuspid valve repair
49.3
P3 F 71 Coronary artery bypass 82.5
Note. yrs = years; h = hours.
Videofluoroscopic Swallow Study
The videofluoroscopic swallow study (VFS) was completed 30, 25, and 37 hours
following extubation on patients 1, 2, and 3 respectively. All consistencies and volumes
were administered to patients 1 and 2, with patient 2 requiring two mouthfuls for the ½
digestive cookie. For patient 3, the VFS protocol was discontinued following two of the
three pureed (5-ml) boluses. Patients 1 and 3 were administered an additional thin fluid

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(5-ml) bolus secondary to technical difficulties. For these patients, the first thin fluid
bolus (5-ml) was not included in the analyses. After this exclusion, total of 11, 10, and 5
boluses were included in the analyses for patients 1, 2, and 3 respectively. All patients
were NPO prior to the VFS. Artifacts on the radiographic image included a central line
(patients 1 and 2) and an in-situ nasogastric feeding tube (patient 3).
For each VFS, patient preparation and transport to and from the fluoroscopy suite
ranged from 30 to 60 minutes. Prior to patient arrival, room and equipment preparation
required an average of ten minutes. While in the imaging suite, patient setup and the
VFS were completed within 15 minutes. Following the completion of each VFS, data
transfer and study archiving took approximately one hour. A total of three study
personnel were involved in the VFS directly: an x-ray technician, a speech-language
pathologist (SAS) and a research coordinator. The patient’s nurse and clinical speech-
language pathologist were also in attendance.
Videofluoroscopic measures. Videofluoroscopic measurements were completed
for all 3 patients. The time to complete frame selection and measurement for each
method ranged from less than two minutes to six minutes per bolus administration. The
total time to complete each measurement ranged from 14 minutes to 52 minutes for each
VFS. Each VFS measure and its corresponding task completion time and inter-rater
reliability (as applicable) are summarized in Table 4.5.

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Table 4.5.
Task completion time and interrater reliability according to VFS measure
VFS Measure Completion Time (min) ICC (95% CI)
Per bolus administration Per VFS Frame
selection Measurement
MBSImpTM© 6 52
N/A
N/A
PAS <2 17 N/A .92 (.83-.96)
Absolute hyoid displacementa 5 35 .99 (.98-.99) .90 (.76-.96)
Scaled hyoid displacementa <2 14 .98 (.96-.99) .26 (-.05-.52)
Pharyngeal constrictiona 5 35 .99 (.98-.99) .25 (-.10-.59)
Note. VFS = videofluoroscopic swallow study; min = minutes; CI = confidence interval; MBSImpTM© = Modified Barium Swallow Impairment Profile; N/A = not applicable; PAS = Penetration Aspiration Scale. a displacement measurements conducted on 5-ml and 15-ml bolus volumes only.
Standardized VFS assessment tools. Patient 3 received the maximum overall
impression (OI) score across all individual MBSImpTM© oral and pharyngeal components
(Figures 4.2a and 4.2b). As a result, patient 3 received the highest total oral and total
adjusted pharyngeal scores of 22 and 26 respectively, exhibiting the most severe
swallowing impairment of all patients in our case series. Of the two remaining patients,
patient 1 received a total oral impairment score of nine as compared to three for patient 2,
with greater impairment on: lip closure, bolus preparation, bolus transport and the
initiation of the pharyngeal swallow. Conversely, patient 2 received a total pharyngeal
impairment score of six as compared to five for patient 1, with greater impairment on

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laryngeal vestibule closure and pharyngeal stripping wave components. Of the remaining
pharyngeal components, patients 1 and 2 differed only on tongue base retraction with OI
scores of two and one respectively. Of the oral components, all three patients exhibited
impairment on oral residue and initiation of the pharyngeal swallow. Additionally, all
patients exhibited impairment on the following pharyngeal components:
pharyngoesophageal segment opening, tongue base retraction and pharyngeal residue.
Figure 4.2a. MBSImpTM© oral components across patients.
Patient 1 Patient 2 Patient 3

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Figure 4.2b. MBSImpTM© pharyngeal components across patients
Regardless of texture, volume or paradigm (i.e. cued versus spontaneous
swallow), patients 1 and 2 had normal airway protection on all swallows (a PAS score of
≤ 2). We observed abnormal airway protection across all bolus administrations with
patient 3 (a PAS score of ≥ 3). Clinically, patients 1 and 2 began regular texture diets
following VFS completion while patient 3 remained NPO with enteral feeding via
nasogastric feeding tube.
Patient 1 Patient 2 Patient 3

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Displacement measurements. Hyoid displacements are presented in Table 4.6.
Patient 3 presented with the smallest median (IQR) absolute hyoid displacement
(Leonard, 2007; Leonard et al., 2000): 8.3mm (2.3) and 8.3mm (1.7) with thin (5-ml) and
pureed (5-ml) textures respectively. For the same bolus textures and volume, patient 1
had the largest median (IQR) displacements: 12.7mm (1.7) and 14.8mm (2.1)
respectively. Absolute displacement median values increased with both increasing
volume as well as increasing texture viscosity for patients 1 and 2 whereas median values
for patient 3 remained consistent regardless of stimulus change. Scaled anterior and
superior hyoid displacement measurements (%C2C4 units) (Steele et al., 2011) were
similarly patterned with: 1) smallest median values regardless of texture for patient 3 and
2) largest median values for patient 1 with thin fluid boluses.

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Table 4.6.
Hyoid displacement measurements according to patient
Case Absolute Hyoid Displacement (mm)
Scaled Hyoid Displacement (%C2-C4 units)
Anterior hyoid displacement Superior hyoid displacement
Thin liquid Pureed Thin liquid Pureed Thin liquid Pureed
5ml 15ml 5ml 5ml 15ml 5ml 5ml 15ml 5 ml P1 12.7 (1.7) 14.2 (3.2) 14.8 (2.1) 41.6 (18.7) 52.4 (6.0) 40.8 (30.7) 18.5 (25.8) 31.0 (10.9) 36.9 (25.9) P2 9.8 (1.8) 9.8 (1.6) 9.9 (2.1) 23.1 (41.0) 27.4 (8.1) 24.3 (9.4) 27.9 (57.8) 33.6 (17.0) 36.7 (30.8) P3 8.3 (2.3) NT 8.3 (1.7) 17.9 (12.2) NT 22.5 (5.8) 13.9 (14.5) NT 17.8 (9.5) Note. Values are reported as median (IQR), mm = millimeter; ml = milliliter; NT = not tested; IQR = interquartile range.

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When comparing PCR measurements across patients according to bolus texture and
volume (Figure 4.3), we measured the smallest median (IQR) pharyngeal constriction ratio with
thin fluid boluses (5-ml) for patient 1 (.02 [.03]) and the largest with patient 3 (.09 [.09]) for the
same bolus texture and volume. Within patients across bolus texture and volumes, PCR values
decreased with increasing viscosity for patients 2 and 3 with the inverse measured for patient 1.
Figure 4.3. Pharyngeal constriction ratio by patient according to bolus texture and volume. Study Impact Questionnaires
Patient comfort questionnaires. One patient completed the patient comfort
questionnaire. Ratings were “adequate” for VFS and overall study participation and “easy” for
questionnaire completion. This patient would have preferred more information during the
consent process about the instrumental assessment. Of the two remaining patients, one was
medically incapable of completing the questionnaire and one was discharged prior to
questionnaire completion.
Workload impact questionnaires. All attending nurses, three CVICU nurses and one
nursing student, completed the workload impact questionnaire. All nurses reported the study fit

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well with daily tasks and the majority felt VFS accommodation was “easy” or “adequate”. Half
of the nurses reported the study’s impact on patient care delivery was minimal. Nursing
suggestions for study modifications included: 1) further advance notice regarding the procedure
timing in order to allow ample time to ready the patient for transport and 2) regular confirmation
with nursing staff regarding the patient’s hemodynamic stability and inotropic support
requirements prior to scheduling transport.
Discussion
Our study as designed was not feasible. As a result, this experience has afforded us the
opportunity to revisit our methodology prior to conducting a larger study. While we were able to
enroll participants prospectively with the aim to conduct an instrumental swallowing assessment
within 48 hours after extubation following cardiovascular surgery, the rate of enrollment was low
and none of the enrolled patients agreed to all procedures. We had poor response rates on patient
impact questionnaires. In contrast, all nurses completed their impact questionnaires. They rated
our study protocol as “easy to accommodate” and without significant impact on workflow. Also,
all enrolled patients underwent the VFS procedure, therefore making our study the first to
describe swallowing physiology on consecutively enrolled, recently extubated patients following
CV surgery using psychometrically validated and objective measures.
We took great lengths to maximize the methodological rigor of this study. We recognize
that this may have negatively impacted patient enrollment and study feasibility, but it permitted
us to contrast our study with previous work which may have favored ease of study conduct over
maximized rigor. We minimized bias risk through: consecutive enrollment, conducting the same
instrumental assessment on all patients, and assessor blinding both to each other and clinical data
throughout the study. Our findings have shown us that for a successful future large-scale study

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with the objectives of determining dysphagia incidence prospectively and assessing swallowing
physiology, it will be important to consider changes in design. Following our experiences, we
propose diagnostic methods and interpretation measures more suited to investigating swallowing
physiology in this population with the goals of increasing enrollment rate and minimizing impact
on patients while ensuring study rigor.
Although we enrolled a limited number of patients during the study’s four-month
duration, we were able to target the patient group at the highest risk of developing dysphagia
(Barker et al., 2009; Skoretz et al., 2014). In order to meet a hypothetical sample size of 100
patients however, it would take over ten years to complete the study at this enrollment rate at a
single institution. Increasing the number of eligible patients can be met through: 1) including
patients intubated for durations greater than 24 rather than 48 hours, 2) reducing the number of
patients lost to enrollment and 3) expanding the study to include multiple centers. First,
expanding the prolonged intubation definition to include durations exceeding 24 hours would
continue to capture at-risk patients (Skoretz et al., 2014). In a recent study conducted at the same
institution stratifying patients following CV surgery according the various intubation durations
(Skoretz et al., 2014), the authors demonstrated that dysphagia frequencies following intubation
durations of 24-48 hours were the second highest, approximately 17%, second only to those
intubated for more than 48 hours. Second, eligible patients extubated over the weekend
accounted for 25% of our losses to enrollment. These losses could be minimized through
increasing research staff availability over weekends or increasing the post-extubation
instrumental assessment window from 48 to 72 hours. Third, including other centres similar to
ours would increase the number of available patients meeting our eligibility criteria.

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These study changes are not without caveats. While including multiple sites or
conducting weekend assessments would require additional research staff thereby accruing
additional study costs, increasing the post-extubation instrumental assessment window could be
problematic for study objectives namely 1) determining dysphagia incidence and 2) comparing
swallow outcomes across the sample. First, swallowing physiology changes rapidly following
extubation and as a result, there may be great variability across the sample. Two studies have
reported on serial swallowing examinations following extubation: one reporting swallowing
latencies in critical care patients (de Larminat et al., 1995) and the other on aspiration frequency
following coronary artery bypass grafting (Burgess et al., 1979). De Larminat and colleagues
(de Larminat et al., 1995) found swallowing delays resolved within 48 hours. Similarly, Burgess
and colleagues (Burgess et al., 1979) reported decreasing aspiration frequency from 33% to 20%
to <1% following assessments conducted immediately, at four hours and eight hours post-
extubation respectively. Second, prior to swallowing outcome comparisons, a broader range in
post-extubation assessment times would require patient stratification according to assessment
completion time. As a result, a larger sample size may be required.
Although all nursing staff responded to our impact questionnaires, only one patient
completed theirs. This limits our ability to make inferences regarding patient impact, however,
we will use the respondent`s data to improve the consenting process. In addition, all patients
refused nasendoscopy. This suggests altering the study protocol to include only one instrumental
procedure. The research ethics board disallowed enquiry regarding participant refusal rationale
throughout the study, therefore we are unable to determine if patients would still enroll if
nasendoscopy were a stand-alone assessment. In regards to the nursing respondents, all felt
study participation fit well with their daily tasks. However they were equally divided on the

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degree to which study participation impacted the delivery of patient care. Their comments
focused on timing issues with regards to patient preparation for and transport to radiology.
These issues may be resolved through an instrumental swallowing assessment conducted at the
bedside.
Even though all patients refused nasendoscopy in a paradigm that also included VFS, an
instrumental swallowing assessment that can be conducted in the ICU (e.g., fiberoptic
endoscopic evaluation of swallowing [FEES]) may be more appealing to both patients and
nurses. It may reduce the study’s impact on patients, nurses and operational resources as it
would: 1) eliminate patient transport outside of ICU, 2) reduce the number of staff required to
complete the instrumental assessment and 3) eliminate the use of a diagnostic imaging suite.
Since FEES is conducted at the bedside, it may be easier to schedule the procedure around other
diagnostic procedures that patients must undergo while in the ICU. It can be conducted solely by
a speech-language pathologist trained in the procedure with an otolaryngologist present or with
them reviewing the recorded assessment at a later date. Not only does FEES involve fewer staff
than VFS, it is arguably more sensitive in identifying events such as aspiration and pharyngeal
residue (Kelly et al., 2007; Kelly et al., 2006). While this procedure offers the added benefit of
direct visualization of oropharyngeal and laryngeal mucosa and secretions (Langmore et al.,
1988; Langmore et al., 1991; Murray et al., 1996), FEES also has its limitations. Due to the
position of the scope in the oropharynx, this technique eliminates an oral functional assessment.
In addition, the view of the larynx and upper trachea is obliterated during the swallow due to soft
palate elevation and pharyngeal constriction. As a result, airway penetration or aspiration
occurring at that time cannot be observed. Currently, it also lacks psychometrically validated
methods for interpretation or objective kinematic measurement techniques.

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Previously unreported for this patient population, the MBSImpTM© and PAS together
provided a thorough standardized description of swallow function for each patient in our case
series. Commensurate with the detailed impairment information acquired while using the
MBSImpTM© for each patient, we found the certification process and scoring method in our study
required a substantial time commitment. While this time commitment may be reasonable for our
research objectives, conducting MBSImpTM© component scoring for each bolus administration
may not be clinically feasible.
According to the MBSImpTM©, all three patients exhibited some degree of impairment in
the areas of oral and pharyngeal clearance, pharyngeal swallow initiation, tongue base retraction
and pharyngoesophageal segment opening. In addition, two of the three patients also showed
impairment on the following: lip closure, bolus preparation, bolus transport, pharyngeal stripping
wave and laryngeal vestibule closure. Similar impairments have been reported in other studies
(Hogue et al., 1995; Partik et al., 2003). For example, Hogue and colleagues (1995) reported
impaired oral function in 22% of patients along with impaired swallowing reflex in 67% and
decreased pharyngeal peristalsis in 56%. In a study by Partik and colleagues (2003), they
described tongue impairment in 27% of patients, along with impaired pharyngeal reflex trigger
and/or pharyngeal weakness in 46% and upper esophageal sphincter dysfunction in 14%. In
contrast, airway compromise occurred infrequently in our study when compared to previous
publications. Only one of the three patients exhibited abnormal airway protection in our study
whereas the number of patients aspirating ranged from 59% (Partik et al., 2003) to 90% (Hogue
et al., 1995) previously.
To the best of our knowledge, we are the first to report on swallowing kinematics on
recently extubated patients following CV surgery. The time required to complete the

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displacement measurements ranged from 14 to 35 minutes for each VFS. Of all the
measurements, scaled hyoid displacement required the least time to complete. By virtue of using
scaled units when comparing measurements across patients, this method mitigates possible
confounds such as sex and “size-of-system” differences (Molfenter & Steele, 2014). Therefore,
if significant differences are found using this technique, they may be more likely due to differing
physiology. As a result, this method may prove to be beneficial when investigating what factors
influence physiological differences in this patient population. When comparing interrater
agreement across all displacement measures, the reliability for frame selection across all
measures and absolute hyoid displacement measurement was excellent (Shrout & Fleiss, 1979).
In contrast, the reliability was poor for both scaled hyoid displacement measurement as well as
pharyngeal constriction ratio. Due to the anatomical location of a radiographic artifact on each
patient either along the cervical spine (i.e., central line) or in the pharynx (i.e., nasogastric tube),
it is likely that these measures were most susceptible to their presence thereby accounting for the
high variability between raters. While the published intra- and interrater reliabilities for these
methods are good to excellent (Leonard et al., 2000; Molfenter & Steele, 2014; Steele et al.,
2011), it is likely that these displacement measurement methods were designed and tested
primarily using subjects other than those in intensive care. Regardless, it is our opinion that
hyoid displacement and pharyngeal constriction measures are necessary for this population due
to the relative inactivity of the pharyngeal and laryngeal musculature during intubation and its
potential effect on swallow function (DeVita & Spierer-Rundback, 1990; Postma et al., 2007;
Thomas et al., 1995; Tolep et al., 1996). Ultimately, the reliability will need to be addressed
prior to their implementation in a larger study.

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Although we were unable to conduct any inferential statistical analyses due to our small
study sample, we were able to observe swallowing performance patterns across patients and VFS
measures. For example, the patient exhibiting the highest score on the PAS presented with the
smallest median hyoid displacement measurements with both the absolute and scaled measures
and largest median pharyngeal constriction ratios. Similarly in other populations, patients
exhibiting abnormal airway protection have reduced hyoid displacement measurements (Steele et
al., 2011) and a greater pharyngeal constriction ratio (Yip et al., 2006). Another pattern was
observed. Across patients, increasing MBSImpTM© impairment ratings on the anterior hyoid
displacement, pharyngeal stripping and laryngeal vestibule closure components corresponded
with smaller hyoid displacement, larger PCR measurements and abnormal airway protection
respectively. For example, the patient with the most impairment on the anterior hyoid
displacement MBSImpTM© component had the smallest hyoid displacement measurement.
Similarly, the patient with the highest impairment on the pharyngeal stripping wave component
had the largest PCR measurement. However due to our limited enrollment and poor inter-rater
reliability on some measures, our swallowing outcomes are unlikely to representative of this
patient population and must be interpreted with caution.
This feasibility study, which by definition is descriptive and exploratory in nature, has
several limitations. Not only was this study conducted for a very limited duration, it was
conducted at a single institution with limited enrollment thereby restricting generalizability of
our findings to other clinical sites. Due to our limited enrollment, we were unable to report
dysphagia frequency, and the swallowing characteristics we explored are unlikely to be
representative of this population as whole. In addition our small sample size precluded statistical
comparisons of our VFS measures both within and across patients. While our study exclusions

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restricted etiologies that may cause pre-operative dysphagia, our patients’ pre-surgical
swallowing function was unknown. Although we analyzed our VFS using objective and
validated measures, our methodological differences throughout our VFS protocol, including
bolus volume, barium concentrations, and a bolus-hold swallowing paradigm, made comparisons
to normative data impossible.
Our patients’ acuity further restricted our VFS assessments in many ways. First, we had
to limit the number of boluses given during our VFS. While we recognize the physiological
differences that occur during swallowing when using cued rather than spontaneous swallowing
paradigms (Daniels, Schroeder, DeGeorge, Corey, & Rosenbek, 2007; Nagy et al., 2013), we had
to balance our chosen measurement methodologies that primarily utilize a bolus-hold with
minimizing patient burden by limiting the number of bolus administrations. Second, all of our
patients presented with either a central line or a nasogastric feeding tube. While we ensured the
external portions of these radiographic artifacts were out of the image as much as possible, these
items were likely a large contributor to our poor interrater reliability and will continue to pose
challenges during the measurement processes in future acute-care studies. Finally, although the
impact of nasogastric feeding tubes on swallowing is debatable (Huggins, Tuomi, & Young,
1999; Leder & Suiter, 2008; Wang, Wu, Chang, Hsiao, & Lien, 2006), we cannot determine
what, if any, affect it had on the VFS measures.
While we were able to conduct VFSs successfully on consecutive patients shortly after
extubation following CV surgery, the enrollment rate was such that it would not be feasible to
conduct this study as presented on a larger scale. We were unable to successfully execute our
study protocol with no patients agreeing to all procedures. The lessons learned throughout the
process have assisted with study changes prior to future implementation. Future prospective

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studies should include patients intubated for 24 hours or more while allowing for instrumental
swallowing assessments throughout the week. Patient burden is minimized while using one
instrumental procedure and ideally, swallowing physiology should be documented using
standardized tools and objective physiological measurements in order to most reliably
characterize the swallow function of these patients. Due to the patient’s acuity, specifically
while in intensive care, FEES may be the most appropriate instrumental procedure. It can be
conducted at the bedside and is more conducive to: ruling out oropharyngeal and laryngeal
pathologies, serial examination allowing for documentation of swallowing recovery, and can be
expanded to include upper airway sensory testing. The benefits of using FEES however, must be
weighed against the limited interpretation tools currently available. The swallowing physiology
of recently extubated patients is so under-researched at this time, that it warrants investigation of
all swallowing kinematics, temporal measures, and event sequences. As a result, VFS may be
the instrumentation of choice if reporting physiology is the primary objective. Although
dysphagia incidence and swallowing physiology of this population still remains elusive, our
study provides the necessary foundation for successful conduct of future studies aiming to
determine dysphagia frequency and characteristics in post-extubation patients.

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CHAPTER V
DISCUSSION
Introduction
The series of three studies that comprise this dissertation make novel contributions to the
dysphagia literature while focusing on the recently extubated as well as cardiovascular surgical
patients. For our initial study, we were the first to conduct a systematic review of the literature
focusing on endotracheal intubation and dysphagia (Skoretz, Flowers, et al., 2010). We
ascertained that longer intubation durations are associated with higher dysphagia frequencies.
However, the evidence was limited by an overall paucity in the literature, poor study quality and
a high risk of bias. Using this information, we designed and executed our two subsequent studies
with sound methodology to minimize bias risk and characterize swallow physiology.
Specifically, our second study was the first to report dysphagia frequency according to stratified
intubation durations after both coronary artery bypass and cardiac valve surgery (Skoretz et al.,
2014). We identified independent predictors of dysphagia while clarifying the intubation
durations that posed the greatest risk for post-operative dysphagia. We used this intubation
duration for our prospective and final study, aimed at assessing the feasibility and patient
acceptance of instrumental swallowing assessments after CV surgery following prolonged
intubation. We gathered feasibility data on several patient and study parameters. This study
provided the first interpretation of videofluoroscopic swallow studies using standardized rating
scales and kinematic measurements on consecutively enrolled patients following prolonged
intubation after CV surgery. Although the recruitment was slow, proving our study was not
feasible as designed, this study also provided numerous lessons regarding patient eligibility
criteria, study impact on patient and nursing along with swallowing instrumentation and

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interpretation methods. In sum, all three studies offer value to the clinical community and
inform future studies. The findings from this research will provide the foundation for future
large-scale prospective research that will properly validate the findings herein related to
dysphagia incidence, swallowing physiology and identifying those with dysphagia after
cardiovascular (CV) surgery following prolonged intubation.
Summary of Thesis Findings
Our systematic review was the first to evaluate all of the existing post-extubation
dysphagia literature thereby providing an up-to-date summary of the evidence (Skoretz, Flowers,
et al., 2010). Due to study heterogeneity in the existing literature, we were unable to conduct a
meta-analysis and instead, provided a descriptive report of our findings. We confirmed that
dysphagia incidence varies across diagnostic groups, ranging from three to 62% (de Larminat et
al., 1995; Ferraris et al., 2001; Hogue et al., 1995; Rousou et al., 2000; Stanley et al., 1995), with
no particular diagnosis associated with greater dysphagia risk. Regardless of etiology, the
highest dysphagia frequencies occurred following prolonged intubation durations (Ajemian et al.,
2001; Barker et al., 2009; de Larminat et al., 1995).
As a whole, the available evidence espoused poor study quality and high risk of bias
primarily due to study design. Many of the included studies were either retrospective
observational studies (Barker et al., 2009; Ferraris et al., 2001; Padovani et al., 2008; Rousou et
al., 2000) or failed to declare whether enrollment was consecutive (Burgess et al., 1979; Davis &
Cullen, 1974; de Larminat et al., 1995; Padovani et al., 2008; Stanley et al., 1995). In addition,
there were many variations in study design particularly regarding the timing (Ajemian et al.,
2001; Barquist et al., 2001; Burgess et al., 1979; Davis & Cullen, 1974; de Larminat et al., 1995;
El Solh et al., 2003; Keeling et al., 2007; Leder, Cohn, et al., 1998) and type of swallowing

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assessments (Ajemian et al., 2001; Barker et al., 2009; Barquist et al., 2001; Burgess et al., 1979;
Davis & Cullen, 1974; de Larminat et al., 1995; El Solh et al., 2003; Ferraris et al., 2001; Hogue
et al., 1995; Keeling et al., 2007; Leder, Cohn, et al., 1998; Padovani et al., 2008; Rousou et al.,
2000; Stanley et al., 1995). These variations likely influenced the wide range of reported
dysphagia frequencies and other study outcomes identified by our review.
Dysphagia assessment methods varied across included studies (Ajemian et al., 2001;
Barker et al., 2009; Barquist et al., 2001; Burgess et al., 1979; Davis & Cullen, 1974; de
Larminat et al., 1995; El Solh et al., 2003; Ferraris et al., 2001; Hogue et al., 1995; Keeling et al.,
2007; Leder, Cohn, et al., 1998; Padovani et al., 2008; Rousou et al., 2000; Stanley et al., 1995)
with only one declaring blinding (Stanley et al., 1995). However, even in studies with similar
assessment methods, dysphagia frequencies were inconsistent. Despite this, some general trends
were noted. Specifically, those studies reporting the highest frequencies used FEES on all
enrollees (Ajemian et al., 2001; El Solh et al., 2003). In contrast, the studies reporting the lowest
dysphagia frequencies used debatably less sensitive methods to diagnose dysphagia including
clinical assessments (Padovani et al., 2008) or static chest radiographs following the ingestion of
radio-opaque contrast (Burgess et al., 1979; Davis & Cullen, 1974; Stanley et al., 1995). The
majority of the included studies limited their outcome to aspiration (Ajemian et al., 2001;
Barquist et al., 2001; Burgess et al., 1979; Davis & Cullen, 1974; El Solh et al., 2003; Keeling et
al., 2007; Leder, Cohn, et al., 1998; Stanley et al., 1995) with only a few declaring an operational
definition for dysphagia (Barker et al., 2009; Barquist et al., 2001; El Solh et al., 2003; Leder,
Cohn, et al., 1998). Across all included studies, no psychometrically validated tools measuring
both oral and pharyngeal function were utilized nor were any kinematic measurements

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conducted. Additionally, none of the studies used validated tools for screenings, assessments, or
interpretation methods for all patients.
Our systematic review revealed other gaps in the literature, specifically with regards to
dysphagia research following CV surgery. With this population, most studies reported dysphagia
frequency for cumulative intubation durations across the entire study sample (Ferraris et al.,
2001; Hogue et al., 1995; Rousou et al., 2000) or for durations greater than 48 hours (Barker et
al., 2009). As a result, dysphagia frequencies for patients intubated for less than 48 hours for
both coronary artery bypass grafting and valve surgery was essentially unknown.
Our second study was designed to address the noted deficiencies from our systematic
review. Given that no previous study had targeted the relation between intubation duration and
corresponding dysphagia frequencies, we incorporated this as our main objective (Skoretz et al.,
2014). Specifically, our second study assessed dysphagia frequencies according to the following
intubation strata: ≤12.0 hours, >12.0 to ≤24.0 hours, >24.0 to ≤48 hours and greater than 48
hours. We were the first to document that dysphagia occurs most frequently in those intubated
for greater than 48 hours when compared to lesser intubation times (Skoretz et al., 2014). Also,
we were the first to confirm that dysphagia is in fact, negligible in patients intubated for ≤12
hours (Skoretz et al., 2014). Although, our dysphagia frequency across our entire sample was
similar to previously published work (Ferraris et al., 2001; Hogue et al., 1995; Rousou et al.,
2000), we were the first to report that dysphagia frequencies exceed the cumulative population
incidence for durations between 12 and 48 hours (Skoretz et al., 2014).
Not only did this study identify those at greatest risk of dysphagia relative to intubation
duration, but we also identified independent predictors and associated risk factors for dysphagia
in this population (Skoretz et al., 2014). We corroborated previous work reporting similar

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independent predictors for dysphagia including: advanced age (Hogue et al., 1995), prolonged
intubation (Barker et al., 2009; Hogue et al., 1995) and sepsis (Barker et al., 2009). Our
findings, however, were the first to report that the odds of a patient having dysphagia increase by
a factor of two for every additional twelve hours of endotracheal intubation or for every
additional decade of age (Skoretz et al., 2014).
Prolonged intubation and thereby prolonged use of mechanical ventilation is precipitated
by numerous factors following CV surgery (Reddy et al., 2007; Trouillet et al., 2009; Widyastuti
et al., 2012; Yende & Wunderink, 2002). For example, those patients experiencing prolonged
mechanical ventilation following CV surgery tend to be older (Cislaghi et al., 2009; Ji et al.,
2010; Légaré et al., 2001; Reddy et al., 2007; Suematsu et al., 2000) and more medically
complex (Cislaghi et al., 2009; Cohen et al., 2000; Combes et al., 2003; Pappalardo et al., 2004).
Barriers to early extubation often include impaired preoperative respiratory function (Ingersoll &
Grippi, 1991), multi-system inflammatory response (Ji et al., 2010; Widyastuti et al., 2012),
hemodynamic instability, bleeding, inadequate oxygenation (Doering, 1997), and acute
respiratory distress syndrome (Widyastuti et al., 2012). As a result, the duration for which
patients require mechanical ventilation is not typically dictated by a single variable therefore
intubation duration cannot truly be considered in isolation when exploring potential causative
factors for dysphagia. Rather intubation duration could be considered a measurable marker by
which clinicians may gauge dysphagia risk following extubation.
As already noted above and similar to previous research (Barker et al., 2009; Ferraris et
al., 2001; Hogue et al., 1995), our second study showed age as an independent predictor of
dysphagia in post-operative cardiovascular patients. Other work has shown that advanced age
results in more protracted recovery of swallowing following extubation when compared to

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younger patients (El Solh et al., 2003). Unfortunately, no previous study has investigated
underlying physiological reasons for dysphagia and its poor recovery in elderly post-operative
CV patients.
In keeping with our goal to address gaps in the literature, our aim for our final study was
to design and trial a small-scale study using prospective design and consecutive enrollment. In
turn, this design may be utilized as a future large-scale study to then determine dysphagia
incidence and swallowing physiology of patients following CV surgery after prolonged
intubation. Therefore, our primary objective was to determine the feasibility and patient
tolerance of the instrumental procedures used to assess swallowing physiology in this population.
We assessed study impact on patient comfort, nursing workflow and each participant’s ability to
accommodate study procedures as well as other feasibility parameters including recruitment rate,
task completion durations and measurement reliability. The findings of our earlier studies
informed the design of this final study in the following areas: assessor blinding,
videofluoroscopy swallowing study (VFS) interpretation methods, and eligibility criteria the
intubation time point of > 48 hours for our study eligibility criteria. All enrolled patients were
able to participate in the VFS procedure making this work the first of its kind to describe
swallowing physiology on consecutively enrolled, recently extubated patients following CV
surgery using psychometrically validated and objective measures. In addition, all nursing staff
reported that our study had minimal impact on their workload.
In the end, however, our study as proposed proved not feasible. Specifically, our
recruitment was slow with no patients agreeing to all study assessments. We had poor patient
response rates to our study impact questionnaire and poor reliability of some VFS measures.
Even with these challenges, our study was successful as it provided the feasibility parameter

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estimates we sought. These estimates will eventually inform future study designs and in doing
so, improve enrollment and minimize patient burden. In addition, this study enabled us to reflect
on the challenges of obtaining reliable VFS interpretations in this acutely ill patient population.
From this final study, several suggestions were derived for the future research with this
population. Specifically, to increase enrollment we suggested the inclusion of: 1) multiple
recruitment sites; 2) patients intubated for over 24 hours; and 3) access to instrumental
swallowing assessments throughout the week. In addition, we suggested using only one rather
than two instrumental procedures in order to minimize patient burden. However, which method
to use depends on study objectives. If, for example, the primary objective is to report on
physiology (Logemann, 1997; Logemann et al., 1998), swallowing kinematics along with timing
measures of all oral, pharyngeal and upper airway structures (Kendall, McKenzie, Leonard,
Goncalves, & Walker, 2000; Leonard & McKenzie, 2006; Leonard et al., 2009; Leonard et al.,
2000; Steele et al., 2011), then the VFS would be the tool of choice. However, if the goal is to
assess swallowing physiology by obtaining a direct view of the upper airway and therefore any
structural problems, then FEES may be more appropriate (Hiss & Postma, 2003; Langmore,
2003; Langmore et al., 1988; Langmore et al., 1991).
FEES may in fact be the most ideal instrumentation for this patient population
considering the likelihood that intubation poses high risk for upper aerodigestive tract
pathologies (Langmore, 2003; Langmore et al., 1988). FEES ensures direct assessments of
laryngopharyngeal pathologies (Hiss & Postma, 2003; Langmore, 2003; Langmore et al., 1988)
while allowing for sensory testing (Aviv, 2000a; Aviv et al., 2000; Aviv, Kim, Sacco, et al.,
1998; Aviv, Kim, Thomson, et al., 1998) and serial examinations over time without excessive
risks to patients (Hiss & Postma, 2003; Langmore, 2003; Langmore et al., 1988). Patients

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undergoing CV surgery comprise a diagnostic group at increased risk of vocal fold immobility
(VFI) and its negative sequelae including airway penetration and aspiration (Bhattacharyya et al.,
2003; Itagaki et al., 2007; Joo et al., 2009).
Clinical Implications
Our collective findings have provided evidence to support clinical practice. From
dysphagia risk factors to the timing of oral intake following extubation, our contributions can be
utilized in the identification of patients at risk for dysphagia. Our findings have underscored the
need for focused clinical observation and speech-language pathology service provision
particularly for those patients who are elderly, medically complex or intubated for periods of
greater than 24 hours.
Across our studies we have shown that dysphagia is indeed prevalent in the days
following extubation particularly following prolonged intubation (Skoretz, Flowers, et al., 2010;
Skoretz et al., 2014). In our systematic review, the studies reporting the highest dysphagia
frequencies conducted assessments within 48 hours of extubation regardless of patient diagnosis
(Skoretz, Flowers, et al., 2010). In our second study, we ensured our identification of dysphagia
was in close time proximity to extubation proving that following extubation, particularly
following intubation periods of greater than 24 hours, dysphagia occurs in nearly one of every
two patients (Skoretz et al., 2014). Furthermore, in our final prospective feasibility study, we
observed that pharyngeal swallowing impairments persist for at least 48 hours following
extubation. As a result, patients who were intubated for greater than 24 hours should be closely
monitored when oral feeding is initiated following extubation.
Not only has our research highlighted the need for attending medical staff to monitor the
swallow function of those at-risk patients following extubation, but our collective findings may

DISCUSSION
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also be used to inform clinical guidelines and advocate for qualified dysphagia personnel. From
our work we have determined a dysphagia risk profile for this patient population. Those patients
at greatest risk of dysphagia following CV surgery have been intubated for greater than 24 hours,
are 70 years of age or older and have post-operative sepsis. Early dysphagia diagnosis and
intervention minimizes morbidities and shortens the duration of hospitalizations (Altman et al.,
2010). At the time of this writing, stroke is the only diagnoses for which published guidelines
have been established for dysphagia assessment and management (Jauch et al., 2013; Lindsay et
al., 2008). Recommended practice suggests that swallowing screenings, and upon screening
failure, swallowing evaluations be conducted on stroke patients early upon admission and prior
to the initiation of oral intake of food or fluids (Casaubon, Suddes, & Acute Stroke Best
Practices Working Group 2013, 2013). Our findings have provided evidence enabling the
construction of a risk profile for recently extubated post-operative CV patients. As a result, we
suggest that similar guidelines be developed with the inclusion of our risk factors in order to
ensure high-quality provision of care and positive patient outcomes.
Collectively, the findings from our three studies confirm high dysphagia risk for patients
following extubation, and with the risk factors of prolonged intubation, advance age and medical
complexity identified in our first and second studies, we have provided the items needed for a
cardiac dysphagia risk index. This tool, when used in conjunction with a validated bedside
swallowing screening assessment, would help attending medical staff in the identification of “at-
risk” patients soon after extubation following CV surgery. Ultimately, these collective steps
would enable early dysphagia diagnosis and management, reduce possible complications
secondary to dysphagia and as a result, improve patient outcomes and minimize healthcare costs.

DISCUSSION
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Research Implications
At present, there are no validated tools by which to identify patients who are at risk for
dysphagia following CV surgery. With the findings of our current work providing the
information needed for a cardiac dysphagia risk index and, along with the lessons learned from
our feasibility study, we have the foundation necessary to inform aspects of a validation study for
this risk index. Moving forward, this future work would be done in two stages. First, we would
determine if other factors, particularly operative variables, should be considered for inclusion in
our risk index. Second, using the findings of this first stage and the outcomes of our feasibility
study, we would propose a validation study, which would determine if our index could identify
cardiac patients at risk for dysphagia.
Along with the independent predictors identified in our current work, which include age
and intubation duration, special consideration should be given to other factors significantly
associated with dysphagia, particularly operative variables, in the development of this cardiac
dysphagia risk index. While not independent predictors, we reported in our second study that
more patients with dysphagia underwent valve surgery, required peri-operative TEE and had
longer cardiopulmonary bypass times (Skoretz et al., 2014). Those with dysphagia also required
inotropic support and intra-aortic balloon pump placement more frequently (Skoretz et al., 2014).
These dysphagia risk factors, specifically surgery type (Barker et al., 2009; Ferraris et al., 2001),
peri-operative TEE (Hogue et al., 1995; Rousou et al., 2000) and intra-aortic balloon pump
placement (Hogue et al., 1995) corroborate the findings of previous studies. Furthermore,
although debatable (Sellke et al., 2005), particular cardiac interventions have been associated
with other adverse short-, mid- and/or long-term outcomes as well (Ivanov et al., 2008; Moller,
Penninga, Wetterslev, Steinbruchel, & Gluud, 2008; van Dijk et al., 2000; Wijeysundera et al.,

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2005). For example, patients undergoing valve surgery, particularly when involving multiple
cardiac interventions, are at increased risk of post-operative morbidities including stroke (Ricotta
et al., 1995; Vasques, Lucenteforte, et al., 2012) and gastrointestinal complications (Bolcal et al.,
2005; D'Ancona et al., 2003). Additionally, prolonged cardiopulmonary bypass, aortic
cannulation and cross clamping durations have been implicated in the precipitation of adverse
outcomes (Nissinen et al., 2009).
When considered together, both in our research and others, variables including surgery
type (Barker et al., 2009; Ferraris et al., 2001; Skoretz, Flowers, et al., 2010), peri-operative TEE
(Hogue et al., 1995; Rousou et al., 2000; Skoretz, Flowers, et al., 2010; Skoretz et al., 2014) and
intra-aortic balloon pump placement (Hogue et al., 1995; Skoretz, Flowers, et al., 2010; Skoretz
et al., 2014) may indicate more severe disease and/or greater surgical complexity therefore
increasing the patient’s risk for complications including dysphagia. However, without an
objective measure for surgical complexity or studies comparing specific cardiac interventions or
operative variables and their subsequent swallowing outcomes, the usefulness of surgery type or
operative variables in the risk index is only speculative. Future work should compare
swallowing outcomes across surgery types, including isolated, multiple or combination surgeries
for valve and/or bypass along with the inclusion of minimally invasive approaches using a
consecutive patient sample large enough to allow for detailed comparisons.
Once the complete index is derived, the next step would be to conduct a validation study
in order to determine if our index is able to identify patients at risk of dysphagia. The validation
of our cardiac dysphagia risk index would ultimately involve a consecutive sample of post-
surgical CV patients from multiple institutions following intubation periods of 24 hours or longer
using prospective enrollment. In order to reliably identify the presence of post-extubation

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dysphagia, all patients would undergo and instrumental swallowing assessment within 48 hours
following extubation.
Future Studies
While our line of research provided novel contributions to the literature and clinically
applicable findings, many questions remain unanswered regarding post-extubation dysphagia.
Ultimately, future research goals should enable clinicians to identify patients who are at greater
risk of dysphagia enabling them to target appropriate interventions. In order to do so, future
research endeavours should include homogeneous patient populations or larger sample sizes and
rigorous methodology. Answering the question of “who is at risk for post-operative dysphagia”
whole or in part, requires further investigation of swallowing physiology including upper airway,
anesthesia and respiratory variables in order to systematically target measurable dysphagia risk
factors in recently extubated patients.
The ultimate goal of our line of research was to design a future large-scale protocol that
would provide the most objective and comprehensive measurement of post-extubation
swallowing physiology. Moving forward from this work, our goal is to conduct a study using
comprehensive swallowing measures on patients following prolonged intubation after CV
surgery in order to document the swallowing physiology of this population. If using
videofluoroscopy, we would include structural displacement, timing and latency measurements
across all swallowing stages along with measures of structural movement, airway penetration,
aspiration and residue using psychometrically validated scales. Future assessment protocols
should also incorporate previously published barium concentrations, bolus size and textures,
swallowing paradigms and bolus administration techniques in order to allow for comparisons to
other work.

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Our motivation to include nasendoscopy in our third study was to provide the foundation
for determining the impact of laryngopharyngeal morbidity and upper airway sensitivity on
swallowing physiology, particularly airway protection capabilities, in recently extubated patients
following CV surgery. The inclusion of FEESST into future work would not only provide
objective information regarding swallowing physiology (Aviv, 2000a; Aviv et al., 2000; Aviv,
Kim, Sacco, et al., 1998; Aviv, Kim, Thomson, et al., 1998), it would also provide further
diagnostic information regarding those at risk for post-extubation dysphagia and whether the
inclusion of upper airway related information, such as endotracheal tube size or induction
medications, should be included in a cardiac dysphagia risk index.
Intubation has been deemed a potential antagonist of swallowing physiology and airway
protection (Postma et al., 2007; Tolep et al., 1996). In addition, those patients with cardiac
pathologies (Adkins et al., 1986; Cappell, 1991, 1995; Dines & Anderson, 1966) or those
undergoing CV surgery (Itagaki et al., 2007; Joo et al., 2009; Rosenthal et al., 2007) comprise
diagnostic groups at increased risk of vocal fold immobility. While many studies have reported
on upper airway pathologies following extubation (Colice et al., 1989; Colton House et al., 2011;
Mencke et al., 2003; Owall et al., 1992; Santos et al., 1994; Stauffer et al., 1981; Tadié et al.,
2010; Thomas et al., 1995; Wittekamp, van Mook, Tjan, Zwaveling, & Bergmans, 2009) or
alternatively, have suggested a link between swallowing impairment and these pathologies
(Postma et al., 2007; Tolep et al., 1996), no study has systematically investigated this dynamic
specifically following recent extubation. Presently, no study has determined airway sensory
thresholds, and thereby glottal competence, and its relationship to swallowing physiology of
recently extubated patients of varying intubation durations. As a result, incorporating the use of
FEESST would begin the process of cataloguing upper airway sensory thresholds (Aviv, 2000a;

DISCUSSION
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Aviv et al., 2000; Aviv, Kim, Sacco, et al., 1998; Aviv, Kim, Thomson, et al., 1998) while
linking these thresholds to airway protection mechanisms in this population.
Post-extubation respiratory variables, including respiration rate and lung volumes, may
prove to be informative in the determination of dysphagia risk following extubation. The
respiration of patients with medical diagnoses such as stroke (Leslie, Drinnan, Ford, & Wilson,
2002) or chronic obstructive pulmonary disease (Gross et al., 2009; Mokhlesi, Logemann,
Rademaker, Stangl, & Corbridge, 2002) or of those following recent extubation (Hasegawa &
Nishino, 1999; Jian, Sheng, Min, & Zhongxiang, 2013; Nishino, 2012; Nishino et al., 1998;
Nishino & Hiraga, 1991), often differs from that of healthy individuals (Krieger et al., 1988).
Alterations in respiratory cycling (Gross et al., 2009; Hasegawa & Nishino, 1999; Nishino, 2012;
Nishino et al., 1998; Nishino & Hiraga, 1991), lung volumes (Gross et al., 2003; Mokhlesi et al.,
2002), swallow apneic periodicity (Hasegawa & Nishino, 1999; Nishino, 2012; Nishino et al.,
1998; Nishino et al., 1989) and respiratory rate (Hasegawa & Nishino, 1999; Leslie et al., 2002;
Nishino, 2012; Nishino et al., 1998; Nishino et al., 1989) can induce changes in swallowing
physiology increasing the individual’s risk of prandial aspiration. While these respiratory
variations and their impact on swallowing have been documented for numerous diagnostic
groups (Gross et al., 2009; Leslie et al., 2002; Mokhlesi et al., 2002; Nishino & Hiraga, 1991)
along with healthy subjects (Gross et al., 2003; Isono et al., 1991; Nishino et al., 1998; Nishino
et al., 1989; Nishino, Takizawa, Yokokawa, & Hiraga, 1987), these details are lacking in those
who have been recently extubated. Future studies should compare pre- and post-intubation
swallowing and respiratory measurements thereby determining whether the risk or severity of
dysphagia increases as a result of respiratory factors.

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Limitation of the Thesis
Throughout our systematic review, we espoused stringent selection criteria, blinding and
excluded known causes of dysphagia. Despite this rigor, we were limited by the existing
literature given the heterogeneity and bias risk across included studies. Few studies have been
published on post-extubation dysphagia and those that met our inclusion criteria, had
heterogeneous patient samples and when compared to each other, varied in regards to their
identification of dysphagia. Given this heterogeneity across numerous design aspects, a meta-
analysis was impossible. As a result, we were unable to: 1) determine effect of intubation
duration on the frequency of dysphagia across all studies and 2) calculate the relative risk of
dysphagia following a range of intubation durations. Instead, we were able to report dysphagia
frequencies according to diagnostic group, provide a comprehensive review of dysphagia-
associated risk factors and evaluate the quality of the existing literature.
Our second study was limited by virtue of its retrospective design. While we utilized
blinding throughout our chart reviews and were conservative in our identification of dysphagia,
identifying dysphagia retrospectively presents limitations. Since very few patients had received
instrumental swallowing assessments, we had to rely upon clinical speech-language pathology
assessments as well as surrogate nutrition variables such as modified texture diets or tube
feeding. In addition, we were unable to investigate variables that may potentially affect post-
operative swallowing physiology such as baseline swallowing status, medical conditions that
may predispose a patient to dysphagia as well as post-operative delirium. Finally, our data was
collected at a single large, quaternary care cardiac center serving a multi-cultural urban center.
While our results may potentially be applicable to similar institutions, the generalizability of our
findings is yet unknown.

DISCUSSION
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Our final study was designed and executed as a feasibility study. By definition, it was
descriptive and exploratory in nature. Despite this, we ensured methodological rigor throughout
the process including a study protocol determined a priori, consecutive prospective enrollment
and assessor blinding. Due to the limited number of patients enrolled, we were unable to
conduct statistical comparisons of our swallowing outcomes and as a result, the swallowing
physiology we described is unlikely to be representative of the population as a whole. The
acuity of our patients also restricted VFS duration, conduct and interpretation. For example, we
were able to administer only a limited number of oral trials and due to patient mobility
restrictions, we conducted lateral fluoroscopic views only. Additionally, all of our patients had a
nasogastric tube and/or central line present during the VFS and in our field of view. While we
attempted to adjust the lines to the best of our ability, these were likely factors in the poor
reliability of some VFS measures. We included nasendoscopy in our protocol due to the
likelihood of upper airway pathologies in a population such as this. Unfortunately, no patient
agreed to the procedure thereby limiting our ability to assess the possible impact of upper airway
pathologies on swallow physiology. Regardless of the limitations throughout each of our
studies, we were able to ensure that our study definitions and protocols were determined a priori,
our studies utilized consecutive enrollment, and that our reviewers and/or assessors were blinded
to each other and clinical data as applicable.
Conclusions
We have made novel contributions to the post-extubation dysphagia literature, which
have implications for clinical practice and research. With the completion of our studies, we were
the first to: evaluate the post-extubation dysphagia literature, confirm the high frequency of

DISCUSSION
153
dysphagia following extubation regardless of diagnosis, and report on the association between
intubation duration and dysphagia following CV surgery.
Throughout our systematic review, we were the first to confirm that prolonged intubation
durations are associated with higher dysphagia risk regardless of diagnosis. We also determined
that identified studies were inherently limited by their design and as a result, are of very low
quality with high risk of bias. There are relatively few studies with specific outcomes focusing
on dysphagia following intubation and even fewer focusing on swallowing physiology following
CV surgery.
Given the need for further research on post-extubation dysphagia while using
homogeneous patient populations and rigorous methodology, our second study included only
consecutive patients following CV surgery. We were the first to stratify dysphagia frequencies
according to clinically meaningful intubation durations and subsequently demonstrated that those
with the highest risk of dysphagia following CV surgery experience intubation periods greater
than 48 hours. We identified numerous risk factors associated with dysphagia as well as
independent predictors including age, sepsis and prolonged intubation. Collectively, these
findings may assist clinicians in gauging a patient’s dysphagia risk through the use of these
measurable surrogate variables.
While our final study proved not feasible as designed, it was an important first step in
determining the most suitable instrumental and interpretation methods for assessing swallowing
physiology following prolonged intubation after CV surgery. This study afforded us the
opportunity to evaluate the study design, execution and patient tolerance of diagnostic tests used
to evaluate post-operative swallow function. We were the first to conduct displacement and

DISCUSSION
154
physiological measurements using psychometrically validated tools on these patients.
Furthermore, we determined that the impact of our research was minimal on study participants.
Future prospective studies are needed to elucidate both risk factors and swallowing
physiology of recently extubated patients. In order to develop tools to identify at-risk patients,
we need to determine the impact of other perioperative or comorbid factors on the swallow as
well as those that affect dysphagia severity and/or recovery. While the prospective incidence of
dysphagia as well as the swallowing physiology of CV surgical patients remains elusive, our line
of research has provided the foundation for the successful conduct of future studies focusing on
the mechanisms underlying dysphagia in these recently extubated patients. We have confirmed
that this diagnostic sub-group is one at greater risk of dysphagia and provided risk factors that
may be used to identify these patients. Ultimately, our findings will inform clinical practice and
as a result, improve patient outcomes.

REFERENCES
155
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Appendix A – CHEST Licenses

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Appendix B - Systematic Review Proposal The Question
Is duration of intubation associated with the outcome of dysphagia in adults? Operational Definitions Intubation – the presence of an endotracheal tube in the oropharynx Duration – time length: may be specified in minutes, hours or days Dysphagia – is defined as any impairment or abnormality of the oral, pharyngeal or upper esophageal stage of deglutition. Dysphagia, or deglutition disorders, may be identified by clinical swallow evaluations (CSE) or instrumental assessment techniques which include, but are not limited to, videofluoroscopic swallow study (VFSS) or fiberoptic endoscopic evaluation of the swallow (FEES) Inclusion and Exclusion Criteria Inclusion: Participants – Adults (>18 years) who have undergone endotracheal intubation during their hospitalization Assessment Methods/Outcomes – Studies reporting the presence or absence of dysphagia as assessed/reported through clinical swallow evaluations or instrumental assessment techniques (including but not limited to VFSS or FEES) Study designs - Case series (n>10), retrospective or prospective descriptive studies with consecutive enrollment, and case control studies Exclusion: Participants- Studies with samples including pediatric enrollees will be excluded unless they comprise <25% of the study’s total sample. Those studies including patients with tracheostomy tubes will be excluded unless: they comprise <25% of the study’s total sample, study authors included individual patient data or some statistical analyses excluded those with tracheostomy tubes. Assessment Methods/Outcomes – Studies using patient report to describe dysphagic symptoms will be excluded. Studies focusing on dysphagia secondary to distal esophageal or gastric etiologies will also be excluded. Studies that fail to compare patients without dysphagia to those with dysphagia on the variables of interest will also be excluded. Study designs – Case series (n<10)

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Data Sources A. Database search strategies.
1) Searches using “deglutition”, “deglutition disorders”, “dysphagia” and “intubation” (see reviewer’s terms attached) 2) Databases:
• MEDLINE (Ovid) 1950-current • EMBASE (Ovid) 1980-current • CINAHL (Ovid) 1982-current • PsycINFO (Ovid) 1960-current • AMED (Ovid) 1985-current • HealthSTAR (Ovid) • BIOSIS Previews 1980-current
B. Manual searching.
Manual searches of the following journals will be conducted using keywords of “swallowing”, “swallowing disorders”, “deglutition disorders”, “dysphagia” and “intubation” for the years 1988 to present. Manual searching will be conducted online for those years that are available.
1) Annals of Thoracic Surgery 2) The Journal of Thoracic and Cardiovascular Surgery 3) Critical Care Medicine 4) American Journal of Roentgeneology 5) Intensive Care Medicine 6) Chest 7) Journal of Anesthesia 8) The American Journal of Cardiology 9) Archives of Surgery 10) Heart and Lung Journal of Acute and Critical Care 11) Dysphagia 12) Canadian Journal of Surgery 13) Anaesthesia 14) Radiology 15) Radiographics 16) Circulation
C. Conference proceedings.
1) American Society of Anesthesiologists 2) UK Swallowing Research Group (2005-current) 3) European Study Group for Dysphagia and Globus
The following conference proceedings will be captured during manual searching of their respective journals (in brackets):
1) Dysphagia Research Society (Dysphagia) 2) American Heart Association scientific sessions (Circulation) 3) Radiological Society of North America scientific sessions (Radiology)

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D. Unpublished sources. 1) Doctoral dissertations as indexed on ProQuest Dissertations and Theses 2) Personal communication with known authors 3) Grey literature
• GrayLIT network accessed by http://www.science.gov • Grey Source accessed by http://www.greynet.org/greycourse.index.html • OpenSigle accessed by http://www.utoronto.ca
E. Cited references and reference lists from selected articles Study Selection Two observers, blinded to each other, will assess eligibility of each study. Disagreement will be resolved by consensus. Risk of Bias Assessment and Assessment of Study Quality Included studies will be assessed using the Risk of Bias Assessment tool and adapted GRADE approach as recommended by the Cochrane Collaboration (Higgins et al., 2008). Data Extraction Two independent observers will extract data from the selected studies. They will be blinded to each other’s results. Where available, the outcome of dysphagia, its operational definition, method of assessment, and specific dysphagia findings will be captured. Where available, variables pertaining to specific patient groups including duration of intubation and patient characteristics will be captured. Where available, consequences of dysphagia will also be extracted. Analyses and Presentation of Results The results will be summarized descriptively and using the tables and figures as recommended by the Cochrane Collaboration (Higgins et al., 2008). Summary of Findings tables with adapted headings will be used. Results will likely reveal high risk of bias along with poor study quality. Where possible meta-analyses will be conducted (e.g. relative risk calculations).

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Appendix C – Study Selection Form
Yes/Unknown No Appropriate study type?
[Reject case studies n<10, tutorial or educational
papers]
Adult patient group in study?
[Reject if adult patients<10]
Any oropharyngeal and upper esophageal dysphagia
outcomes reported?
[Reject if outcomes reported only during
intubation]
[Reject if only mid and lower esophageal outcomes]
Patients underwent endotracheal intubation?
[Reject if intubated patients <10]
[Reject if patients intubated via endoscopy for stent
placement (e.g., Atkinson/Celestin tubes), pulsion
technique, laser technique]
[Reject if noninvasive intubation techniques used]
Note: Some etiologies (e.g., diagnosis of stroke) or
operative procedures (e.g. general anesthetic & surgical
intervention for malignant dysphagia) may have required
patient to undergo endotracheal intubation during a
hospitalization
[Reject only if explicitly reported that the patients
were NOT intubated]
All inclusion criterion met (circle one):
YES NO

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Appendix D – Cochrane Collaboration’s Risk of Bias Assessment Tool
Domain Description Review authors’ judgment Sequence generation Was the allocation sequence adequately
generated? YES / NO / UNCLEAR
Allocation concealment Was allocation adequately concealed? YES / NO / UNCLEAR
Blinding of participants, personnel and outcome assessors Outcome:
Was knowledge of the allocated intervention adequately prevented during the study? YES / NO / UNCLEAR
Blinding of participants, personnel and outcome assessors Outcome:
Was knowledge of the allocated intervention adequately prevented during the study? YES / NO / UNCLEAR
Incomplete outcome data Outcome:
Were incomplete outcome data adequately addressed? YES / NO / UNCLEAR
Incomplete outcome data Outcome:
Were incomplete outcome data adequately addressed? YES / NO / UNCLEAR
Selective outcome reporting Are reports of the study free of suggestion of selective outcome reporting? YES / NO / UNCLEAR
Other sources of bias Was the study apparently free of other problems that could put it at a high risk of bias? YES / NO / UNCLEAR

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Appendix E – Data Extraction Form
Study Patient Sample Dysphagia Assessment Intubation Data Study Outcome
Author/Year Design Diagnoses (N)
Included for review (n)
Enrollment Criteria
Age (range/mean)
Incidence Method Timing Follow-up Duration (Mean)
Prolonged Definition
Findings/Risk Factors

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Appendix F – Exploratory Meta-Analyses
Methods
Post-hoc meta-analyses were conducted using studies that reported on the following
duration variables: intubation duration, hospital length of stay and intensive care unit (ICU)
length of stay. The weighted mean differences of each duration variable were compared
according to those with and without dysphagia using random effects statistical modeling.
Random effects model was employed in order to minimize the effect of within and between
study variance (Borenstein, 2009; Higgins, Whitehead, & Simmonds, 2011). Heterogeneity was
analyzed using the T2 and the I2 statistics. T2 reflects the dispersion or actual variance while the
I2 reports the proportion of variance between studies (Borenstein, 2009; Higgins & Thompson,
2002; Higgins et al., 2011). I2 cutpoints of 25%, 50% and 75% were considered low, moderate
and high heterogeneity respectively (Higgins et al., 2008). Meta-analyses were conducted using
the Cochrane Collaboration software program Review Manager (RevMan, version 5.0.20; The
Nordic Cochrane Centre; Copenhagen, Denmark). These exploratory findings were not included
in the published manuscript.
Results
Six studies reported on intubation duration (Barker et al., 2009; Barquist et al., 2001; El
Solh et al., 2003; Hogue et al., 1995; Leder, Cohn, et al., 1998; Rousou et al., 2000), four
reported on hospital length of stay (Barker et al., 2009; Ferraris et al., 2001; Hogue et al., 1995;
Rousou et al., 2000) and two reported ICU length of stay (El Solh et al., 2003; Hogue et al.,
1995). When comparing those with and without dysphagia, the summary estimates of intubation
duration (Figure F.1.), hospital length of stay (Figure F.2.) and ICU length of stay (Figure F.3.)

APPENDICES
244
were: 77.18h (95% CI 33.51-120.84), 17.15h (95% CI 11.19-23.0) and 6.33h (95% CI 1.37-
11.29) respectively. The heterogeneity statistics are summarized in Table F.1.
Table F.1.
Heterogeneity statistics
Variable Statistic
T2 I2 (%)
Intubation duration 2127.6 90.0
Hospital LOS 41.9 95.0
ICU LOS 17.4 94.0
Note. LOS = length of stay; ICU = intensive care unit.
Discussion
In our original publication of this systematic review, we reported that with increasing
intubation durations, we found an increase in the frequency of dysphagia; however, due to the
heterogeneity of patient diagnoses, study methodology and outcomes across accepted studies, we
summarized all results descriptively. This exploratory meta-analysis supported our descriptive
findings statistically in the following ways: 1) summary estimates revealed that longer weighted
mean durations of intubation, hospitalization and ICU stay favoured an increased frequency of
dysphagia and 2) high statistical heterogeneity was determined both within and across studies.
When comparing the forest plots across all duration variables, all studies reporting on
hospital length of stay (Barker et al., 2009; Ferraris et al., 2001; Hogue et al., 1995; Rousou et
al., 2000) favoured increased frequency of dysphagia with longer durations while reporting the
highest degrees of precision, as evidenced by the smallest confidence intervals. In contrast when

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comparing studies reporting on intubation duration, one study (Barquist et al., 2001) favoured
shorter intubation durations with higher frequencies of dysphagia while the remaining studies
reported the opposite (Barker et al., 2009; El Solh et al., 2003; Hogue et al., 1995; Leder, Cohn,
et al., 1998; Rousou et al., 2000). This comparison also revealed the largest confidence intervals
most notably in studies with the smallest sample sizes (Barquist et al., 2001; El Solh et al., 2003;
Leder, Cohn, et al., 1998).
When tested statistically, all included studies had high degrees of heterogeneity. Both the
T2 and I2 statistics reveal marked heterogeneity with high dispersion and variance proportions
across and between all studies (Barker et al., 2009; Barquist et al., 2001; El Solh et al., 2003;
Ferraris et al., 2001; Hogue et al., 1995; Leder, Cohn, et al., 1998; Rousou et al., 2000).
In conclusion, this meta-analysis, albeit exploratory, confirms our descriptive findings.
While the findings are not surprising considering the collinear nature of the duration variables,
longer durations of intubation, and thereby longer lengths of stay in the intensive care unit and
hospital, are associated with higher frequencies of dysphagia. These findings support our call for
large, high quality studies in this area using homogeneous patient samples.
Figure F.1. Weighted mean difference of intubation duration according to those with and without dysphagia.
Study or SubgroupBarker et al., 2009Barquist et al., 2001El Sohl et al. 2003El Sohl et al. 2003Hogue et al., 1995Leder et al., 1998Rousou et al., 2000
Total (95% CI)Heterogeneity: Tau² = 2127.57; Chi² = 62.02, df = 6 (P < 0.00001); I² = 90%Test for overall effect: Z = 3.46 (P = 0.0005)
Mean142.4254.4187.2223.2124.8
346.56200.9
SD63
175.2165.6
15640.8
298.5675
Total130
72215289
23
234
Mean87.1288
148.8184.850.4
283.6815.3
SD43.3
235.2127.2112.8
4.81921.6
Total124632027
81611
815
1876
Weight22.8%6.7%
11.9%11.8%22.7%3.2%
20.9%
100.0%
IV, Random, 95% CI55.30 [42.06, 68.54]
-33.60 [-175.79, 108.59]38.40 [-50.46, 127.26]38.40 [-51.28, 128.08]
74.40 [59.28, 89.52]62.88 [-162.78, 288.54]185.60 [154.95, 216.25]
77.18 [33.51, 120.84]
Dysphagia No dysphagia Mean Difference Mean DifferenceIV, Random, 95% CI
-200 -100 0 100 200Shorter durations Longer durations

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Figure F.2. Weighted mean difference of hospital LOS according to those with and without dysphagia.
Figure F.3. Weighted mean difference of ICU LOS according to those with and without dysphagia.
Study or SubgroupBarker et al., 2009Ferraris et al., 2001Hogue et al., 1995Rousou et al., 2000Rousou et al., 2000
Total (95% CI)Heterogeneity: Tau² = 41.88; Chi² = 82.48, df = 4 (P < 0.00001); I² = 95%Test for overall effect: Z = 5.74 (P < 0.00001)
Mean26.116.133.434.528.1
SD15.611.7
4.45
6.2
Total130
31281310
212
Mean16.2
5.712.3
7.911
SD113.10.40.4
1
Total124
1011816699116
2766
Weight19.9%19.3%20.9%20.4%19.5%
100.0%
IV, Random, 95% CI9.90 [6.59, 13.21]
10.40 [6.28, 14.52]21.10 [19.47, 22.73]26.60 [23.88, 29.32]17.10 [13.25, 20.95]
17.15 [11.29, 23.00]
Dysphagia No dysphagia Mean Difference Mean DifferenceIV, Random, 95% CI
-100 -50 0 50 100Shorter LOS duration Longer LOS duration
Study or SubgroupEl Sohl et al. 2003El Sohl et al. 2003Hogue et al., 1995
Total (95% CI)Heterogeneity: Tau² = 17.39; Chi² = 32.99, df = 2 (P < 0.00001); I² = 94%Test for overall effect: Z = 2.50 (P = 0.01)
Mean14.413.415.1
SD3.37.33.1
Total221528
65
Mean9.4
10.94.4
SD3.35.30.2
Total2027
816
863
Weight34.8%29.1%36.1%
100.0%
IV, Random, 95% CI5.00 [3.00, 7.00]
2.50 [-1.70, 6.70]10.70 [9.55, 11.85]
6.33 [1.37, 11.29]
Dysphagia No dysphagia Mean Difference Mean DifferenceIV, Random, 95% CI
-100 -50 0 50 100Shorter LOS duration Longer LOS duration

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247
Appendix G - Search Strategies Across Databases.
Databases Search strategya Yieldb AMED [(SH “Deglutition Disorders” exp) OR (“dysphagia.mp” OR “deglutition disorder*.mp” OR “swallow*.mp”) OR (swallow: adj2
dysfunction:).mp OR (swallow: adj2 deficit:).mp OR (impair: adj3 swallow:).mp OR (swallow: adj2 disturb:).mp OR (swallow: adj2 disorder:).mp OR (swallow: adj2 difficult:).mp] OR (swallow: adj2 abnormal:).mp OR (swallow: adj2 problem:).mp] AND [(SH “Intubation” exp) OR (“intubat*.mp”)]
15 ref
BIOSIS Previews (TS “dysphagia”, OR TS “deglutition disorder*”, OR TS “swallow*”, OR TS “intubat*”) AND (TN = Humans) 265 ref CINAHLc [(SH “Deglutition Disorders” exp) OR (“dysphagia.mp” OR “deglutition disorder*.mp” OR “swallow*.mp”) OR (swallow: adj2
dysfunction:).mp OR (swallow: adj2 deficit:).mp OR (impair: adj3 swallow:).mp OR (swallow: adj2 disturb:).mp OR (swallow: adj2 disorder:).mp OR (swallow: adj2 difficult:).mp] OR (swallow: adj2 abnormal:).mp OR (swallow: adj2 problem:).mp] AND [(SH “Intubation” OR SH “Intratracheal intubation” OR SH “Laryngeal masks”) OR (“intubation.mp” OR “intubat*.mp”)]
71 ref
CINAHLd [(MH “Deglutition Disorders” exp) OR (TX “dysphagia” OR TX “deglutition disorder*” OR TX “swallow*”) OR (TX swallow* N2 dysfunction*) OR (TX swallow* N2 deficit*) OR (TX impair* N3 swallow*) OR (TX swallow* N2 disturb*) OR (TX swallow* N2 disorder*) OR (TX swallow* N2 difficult*) OR (TX swallow* N2 dysfunction*) OR (TX swallow* N2 problem*) OR (TX swallow* N2 abnormal*)] AND [(MH “Intubation” OR MH “Intratracheal intubation” OR MH “Laryngeal masks”) OR (TX “intubat*”)]
90 ref
EBM Reviewse (“deglutition disorder*.mp” OR “dysphagia.mp” OR “swallow*.mp” OR “swallowing disorder*.mp”) AND (“intubat*.mp”) 113 ref EMBASE [(SH “Dysphagia” exp) OR (“dysphagia.mp” OR “deglutition disorder*.mp” OR “swallow*.mp” OR (swallow: adj2 dysfunction:).mp OR
(swallow: adj2 deficit:).mp OR (impair: adj3 swallow:).mp OR (swallow: adj2 disturb:).mp OR (swallow: adj2 disorder:).mp OR (swallow: adj2 difficult:).mp] OR (swallow: adj2 abnormal:).mp OR (swallow: adj2 problem:).mp] AND [(SH “Endotracheal intubation” OR SH “Nasotracheal intubation” OR SH “Intubation” OR SH “Respiratory tract intubation”) OR (“intubation.mp” OR “intubat*.mp”)]
606 ref
Healthstar [(SH “Deglutition Disorders” exp) OR (“dysphagia.mp” OR “deglutition disorder*.mp” OR “swallow*.mp”) OR (swallow: adj2 dysfunction:).mp OR (swallow: adj2 deficit:).mp OR (impair: adj3 swallow:).mp OR (swallow: adj2 disturb:).mp OR (swallow: adj2 disorder:).mp OR (swallow: adj2 difficult:).mp] OR (swallow: adj2 abnormal:).mp OR (swallow: adj2 problem:).mp] AND [(SH “Intubation” OR SH “Intratracheal intubation” OR SH “Laryngeal masks”) OR (“intubation.mp” OR “intubat*.mp”)]
588 ref
Medline [(SH “Deglutition Disorders” exp) OR (“dysphagia.mp” OR “deglutition disorder*.mp” OR “swallow*.mp”) OR (swallow: adj2 dysfunction:).mp OR (swallow: adj2 deficit:).mp OR (impair: adj3 swallow:).mp OR (swallow: adj2 disturb:).mp OR (swallow: adj2 disorder:).mp OR (swallow: adj2 difficult:).mp] OR (swallow: adj2 abnormal:).mp OR (swallow: adj2 problem:).mp] AND [(SH “Intubation” OR SH “Intratracheal intubation” OR SH “Laryngeal masks”) OR (“intubation.mp” OR “intubat*.mp”)]
767 ref
PsycInfo [(DE “dysphagia” OR DE “deglutition disorder*”) OR “swallow*”, OR “dysphagia” OR “pharyngeal disorder”] AND (“intubat*”) 29 ref
Note. AMED = Allied and Complementary Medicine; SH = subject heading (MeSH in Medline and Healthstar); exp = explode heading term; .mp = multi-purpose field location; adjn = defined adjacency (Ovid platform); TS = subject terms; TN = taxa notes; ref = references; CINAHL = Cumulative Index of Nursing and Allied Health; MH = major heading; Nn = defined adjacency (EbscoHost platform); TX = free text; EBM = Evidence Based Medicine; EMBASE = Excerpta Medica database; DE = subject heading; DSR = Database of Systematic Reviews; ACP = American College of Physicians; DARE = Database of Abstracts of Reviews of Effects; CCTR = Cochrane Controlled Trials Register; CMR = Cochrane Methodology Register; HTA = Health Technology Assessment; NHSEED = National Health Service Economic Evaluation Database. alimits applied to all searches: human and abstracts. b duplicate references not removed. c search strategy for Ovid platform. d updated search strategy for EbscoHost platform. e includes Cochrane DSR, ACP Journal Club, DARE, CCTR, CMR, HTA, and NHSEED.

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Appendix H – Non-English Articles
Language Yield
Bulgarian 1 ref
Chinese 1 ref
Croatian 1 ref
Czechoslovakian 1 ref
French 3 ref
German 9 ref
Hebrew 1 ref
Japanese 4 ref
Korean 1 ref
Russian 1 ref
Spanish 4 ref
Turkish 2 ref
Ukrainian 1 ref
Note. Ref = references

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Appendix I - Handsearched Journals and Reference Yield
Journal Yield
Acta Anaesthesia 3 ref
America Journal of Respiratory and Critical Care 1 ref
American Journal of Roentgeneology 6 ref
Anaesthesia 0 ref
Anaesthesia and Analgesia 3 ref
Annals of Thoracic Surgery 5 ref
Archives of Surgery 1 ref
Canadian Journal of Surgery 1 ref
Chest 6 ref
Circulation 0 ref
Critical Care Medicine 0 ref
Dysphagia 9 ref
Heart and Lung Journal of Acute and Critical Care 4 ref
Intensive Care Medicine 0 ref
Journal of Anesthesia 0 ref
Journal of Trauma 7 ref
Radiographics 0 ref
Radiology 1 ref
The American Journal of Cardiology 1 ref
The Journal of Thoracic and Cardiovascular Surgery 0 ref
Note. Search strategy included the following terms: deglutition, deglutition disorder*, dysphagia, intubat*, swallow*; * denotes truncated term ; ref = references

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Appendix J – Dysphagia Licenses

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Appendix K – Data Abstraction Manual
RA’s Guide to Review of TWH Medical Records Dysphagia Frequency Following Extubation
Order of Chart Review-Sections Start 1. Confirm patient’s age and date of admission with spreadsheet 2. View Scanned Documents
a. ICU Flow Sheet – Cardiac (CV Flow) from date of OR date/time of extubation(s) and tracheostomy found here (if date and time of tracheostomy earlier than in DO (below), change to this time), feeding method post-extubation also captured here
b. Doctor’s Orders (DO/MD Scan) Diet and tube feeding orders may be found here (record date of referral/orders, if earlier than in CV Flow above, change to this date)
c. Doctor’s Orders SLP referral or diet orders may be found here (record date of referral/orders)
d. Doctor’s Orders SLP suggestions (if SLP suggestions found to be earlier here change date)
e. Doctor’s Orders Tracheostomy order found here (record date/time if available) f. Clinical Notes (CN) SLP suggestions if not recorded in the DO
3. Chart Review a. Nutrition Record diet order and date/time for 96 hours following each extubation
Finish
1. Airway Data 1A. When was the patient extubated?
- This info will be found in the ICU Flow Sheet – Cardiac. You must find the note that corresponds with the OR date listed on the database sheet.
a. Find the first CVICU flow sheet following OR date. The ventilation data is captured on the third sheet for that date. It contains the vent settings as well as extubation time at the top. If the extubation time is not captured, the patient was either: 1) not extubated on that day or 2) extubation time is captured on the grid below. The second row of the flow grid contains the mode of ventilation. Mechanical ventilation modes include: AC, PS, PV, PC, CPAP. The patient will be extubated if modes include: FM, NP, SP. When modes change as previously listed, patient will have been extubated and time will be recorded along the top of the grid. Review 96 hours following each extubation. b. If the patient was intubated/extubated multiple times, record the date and time of each using the methods listed above.

APPENDICES
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1B. When did the patient receive a tracheostomy? - This info will be found in the ICU Flow Sheet – Cardiac and in the Doctor’s Orders.
a. During the review of extubation(s), if the patient received a trach, it will be documented at the top of the flow sheet, rather than ETT circled, trach will be circled. Vent modes will also be adjusted and may be listed at TP, TM. Also, find the first order for trach in the scanned Doctor’s Orders. Record the earliest date/time listed in either the ICU Flow notes or DOs.
2. Dysphagia Data
- This info will be primarily found in the “View Scanned Documents” - Doctor’s Orders, ICU Flow Sheet – Cardiac, or Clinical Notes. Be sure to review orders 96 hours following each extubation.
2A. Was there a new or continuing order for alternative to oral feeding following extubation? Doctor’s notes could be documented in:
i. Doctor’s Orders ii. Clinical Notes iii. Consultation Form iv. Chart Review – Radiology
a. Doctor ordered a feeding tube:
First, look in the doctor’s orders. This type of intervention should be in the orders and may have been initially ordered previous to the extubation. The patient has tube feeding as some orders throughout admission may be written as “hold feeds prior to extubation”. Restart/resume feeds will then be written following extubation. Second, look in the ICU Flow – Cardiac nursing notes. On the first page of that particular day of hospitalization, there is a section entitled “gastrointestinal”. The nurse will document in that section the feeding method or the diet that was administered to the patient if any. If it is not in the orders or CV Flow, look in the patient’s electronic record (chart review section) under radiology (#7), to find surgical reports (PEG or PEG-J) or chest x-rays (used to confirm placement of NG or OG tube) shortly after extubation. Feeding Tube Terms: i. orogastric feeding tube, orogastric tube, OG tube, OGT, or OG ii. nasogastric feeding tube, nasogastric tube, NG Tube, NGT, or NG iii. percutaneous endoscopic gastrostomy, or PEG tube or PEG iv. jejunostomy tube or JG tube or J tube or PEG-J or J-PEG

APPENDICES
256
b. Feeding tube was inserted:
NGT or OGT: Look for nursing notes (in Clinical Notes) to find a report that a tube was inserted. If you do not find a nursing note, then look in the electronic record under radiology (#7) if not done in step a. Find a chest x-ray that confirms tube placement.
PEG or PEG-J: Look first in the electronic record under radiology (#7) if not done
in step a. Find a surgical report that describes tube placement. This will tell you for sure if a PEG or PEG-J was inserted. The word ‘jejunostomy’ or ‘jejunum’ will mean it is a PEG-J.
It is possible that a nurse may have not entered the information that an NG or OG tube was inserted. Also, chest x-rays don’t always happen or they are not clear. Last Check: You can also look in the Nutrition section to confirm alternative to oral feeding, because the dietician orders the feeds and the formula. Formulae could be listed as Isosource, Resource, Novasource. 2B. Was there an NPO and swallowing assessment/SLP to see/special swallow study order?
AND 2C. Was there an order for SLP to see/speech to see/special swallow study?
- This info will be primarily found in the “View Scanned Documents” - Doctor’s Orders. Be sure to review orders 96 hours following each extubation.
a. This will likely be found in the doctor’s orders or a doctor’s note in the Clinical Notes (interdisciplinary section) of scanned documents. Doctor’s orders may say “SLP to see”, “SLP to assess”, “swallowing assessment”, “swallow study/SS”, “speech to see/assess”, “Cookie Swallow”, “VFSS”, “MBS”, “VFS” – any one of these would indicate that a referral to Speech Language Pathology has been made.
b. When recording SLP suggest orders, only document the diet or tube feeding order. c. If an “SLP to see” order was written, however, no further orders were written by the SLP,
confirm lack of SLP involvement by scanning Clinical Notes for SLP/Swallowing entry. 2D. Did SLP or medical staff recommend modified textures?
-This info will be primarily found in the “View Scanned Documents” - Doctor’s Orders. Be sure to review orders 96 hours following each extubation.
a. This will likely be found in the doctor’s orders or a doctor’s note in the Clinical Notes
(interdisciplinary section) of scanned documents. Modified textures may be listed as: i. dysphagia diet ii. honey thick liquid iii. nectar thick liquid iv. pudding thick liquid v. pureed diet vi. thickened liquid

APPENDICES
257
vii. minced solids or minced texture viii. dental soft solids or soft solids ix. no mixed textures x. no particulate matter
AND/OR SLP may also recommend or order:
i. Nil per os (NPO) ii. Nothing by mouth iii. No food or liquid by mouth iv. Clear Fluids v. Full Fluids
2E. Was the first diet order following extubation for an oral diet?
a. This info will be primarily found in the “View Scanned Documents” - Doctor’s Orders.
Be sure to review orders 96 hours following each extubation. The diet orders may also only be captured in the nutrition section below. If this is the case, draw an arrow from this section to the nutrition section on the data abstraction form.
Nutrition Notes Confirmation List diet orders, date and time (brk, lun, sup) during the first 96 hours following each extubation. Itemize the corresponding diet orders with extubation number (i.e, for the first extubation list diet orders under #1). Diets listed may be recorded with the following abbreviation on the data abstraction form if applicable:
Clear Fluids: CF Full Fluids: FF Therapeutic no added sugar 1800Kcal, Heart Healthy etc.: DAT
Chart Location Shorthand Notation If the note was found in: Scanned Doctor’s Orders then write MD Scan ICU Flow Sheet – Cardiac then write CV Flow

APPENDICES
258 Appendix L – Medical Record Review Form
Date of Chart Review:_________________ Name of Reviewer: _________________ PATIENT CODE: ____________________ Admission Date: ___________________
1. Airway data
1a. When was the patient extubated?
1st
Give date and time of FIRST order:
____________________
(dd/mm/yy;hr:min)
give chart location of first note ____________________
2nd
Date and time of reintubation: ____________________
(dd/mm/yy;hr:min)
Date and time of 2nd extubation: ____________________
(dd/mm/yy;hr:min)
give chart location of note ____________________
3rd
Date and time of reintubation: ____________________
(dd/mm/yy;hr:min)
Date and time of 3rd extubation: ____________________
(dd/mm/yy;hr:min)
give chart location of note ____________________
1b. Was there a physician order for tracheotomy? Yes No if ‘no’ skip to 2a
if ‘yes’ give date and time of FIRST order: ______________________________________________ (dd/mm/yy;hr:min) if ‘yes’, give chart location of first note ______________________________________________
2. Dysphagia data – within first 96 hours post-extubation 2a. Was there a new or continuing order for alternative to oral feeding (i.e. tube feeding [NG, NJ, PEG], TPN, PPN) following extubation? 1st
Yes No if ‘no’ skip to 2c
if ‘yes’ give date and time of first note _________________
(dd/mm/yy;hr:min) if ‘yes’, give chart location of first note ________________________
2nd
Yes No
if ‘yes’ give date and time of first note______________________
(dd/mm/yy;hr:min) if ‘yes’, give chart location of first note _________________________
3rd
Yes No
if ‘yes’ give date and time of first note _________________
(dd/mm/yy;hr:min) if ‘yes’, give chart location of first note _________________________
2b. Was there was an NPO and swallowing assessment/SLP to see/special swallow study order? 1st
Yes No if ‘no’ skip to 2c
if ‘yes’ give date and time of first note _________________
(dd/mm/yy;hr:min) if ‘yes’, give chart location of first note ________________________
2nd
Yes No
if ‘yes’ give date and time of first note________________
(dd/mm/yy;hr:min) if ‘yes’, give chart location of first note
3rd
Yes No
if ‘yes’ give date and time of first note ______________________
(dd/mm/yy;hr:min) if ‘yes’, give chart location of first note ______________________

APPENDICES
259
2c. Was there an order for SLP to see/speech to see/special swallow study?
1st
Yes No if ‘no’ skip to 2c
if ‘yes’ give date and time of first note _________________
(dd/mm/yy;hr:min) if ‘yes’, give chart location of first note ________________________ if ‘yes’, what did SLP suggest ____________________
2nd
Yes No
if ‘yes’ give date and time of first note__________________
(dd/mm/yy;hr:min) if ‘yes’, give chart location of first note _________________________ if ‘yes’, what did SLP suggest _____________________
3rd
Yes No
if ‘yes’ give date and time of first note ______________________
(dd/mm/yy;hr:min) if ‘yes’, give chart location of first note ______________________ if ‘yes’, what did SLP suggest ______________________
2d. Did SLP or medical staff recommended modified texture(s)?
1st
Yes No if ‘no’ skip to 2c
if ‘yes’ give date and time of first note _________________
(dd/mm/yy;hr:min) if ‘yes’, give chart location of first note ________________________
2nd
Yes No
if ‘yes’ give date and time of first note__________________
(dd/mm/yy;hr:min) if ‘yes’, give chart location of first note __________________________
3rd
Yes No
if ‘yes’ give date and time of first note _________________
(dd/mm/yy;hr:min) if ‘yes’, give chart location of first note __________________
2e. Was the first diet order following extubation for an oral diet?
1st
Yes No if ‘no’ skip to 2c
if ‘yes’ give date and time of first note _________________
(dd/mm/yy;hr:min) if ‘yes’, give chart location of first note _________________________
2nd
Yes No
if ‘yes’ give date and time of first note___________________
(dd/mm/yy;hr:min) if ‘yes’, give chart location of first note _________________________
3rd
Yes No
if ‘yes’ give date and time of first note _________________
(dd/mm/yy;hr:min) if ‘yes’, give chart location of first note __________________
NUTRITION NOTES (list diet orders, date and time during first 96 hours following corresponding extubation): #1 #2 #3

APPENDICES
260
Appendix M – Retrospective Study Sample Size Estimation
In order to determine the sample size required to capture sufficient event rates in the
intubation groups, our sample size estimation for our retrospective study was conducted using
information from the study conducted by Barker and colleagues (2009). This study was
conducted at the same institution using similar inclusion and exclusion criteria. They reported
that 2033 cardiovascular surgeries were completed per annum and of those, 85 patients annually
required intubation for longer than 48 hours. Of those, 51% had dysphagia. Of the 85 patients,
61 met our study’s inclusion criterion, which thereby comprises 3% of the total population. Base
on this estimate of dysphagia and using the formula below (Aday & Cornelius, 2006; Lemeshow,
et al., 1990), we calculated a minimum sample size of 26 patients for the >48h stratum which
would require a total sample population of 900 patients (α = .05, β = .20).
n = z2 1-α/2 P(1-P) _____________
d2

APPENDICES
261
Appendix N – Characteristics of Intubation Stratum I
A. Pre-operative demographics and presenting clinical characteristics for patients intubated <12h
Variable
All patients (n = 699)
Without Dysphagia (n = 692)
With Dysphagia
(n = 7)
Age [mean (SD)] (yrs)
64.89 (12.08)
64.79 (12.08)
75.14 (7.18)
[median (IQR)] (yrs) 66.0 (17.0) 65.5 (17) 76.0 (15) Male, [n (%)] 509 (72.8) 503 (72.7) 6 (58.7)
Family history of heart diseasea, [n (%)]
373 (53.4) 369 (53.3) 4 (57.1)
Diabetes Risksb
Insulin-controlled diabetes mellitus, [n (%)]
47 (6.7) 45 (6.5) 2 (28.6)
Oral hypoglycemics, [n (%)]
156 (22.3) 154 (22.2) 2 (28.6)
Cardiovascular Surgical Risks
Circulatory shock, [n (%)]
5 (0.7) 5 (0.7) 0 (0.0)
Non-Q-wave infarction, [n (%)]
93 (13.3) 92 (13.3) 1 (14.3)
Q-wave infarction, [n (%)] 9 (1.3) 9 (1.3) 0 (0.0)
LV gradec 1, [n (%)] 476 (68.1) 474 (68.5) 2 (28.6) 2, [n (%)] 144 (20.6) 140 (20.2) 4 (57.1) 3, [n (%)] 73 (10.4) 73 (10.5) 0 (0.0) 4, [n (%)] 3 (0.4) 2 (0.3) 1 (14.3)
NYHA classificationd I, [n (%)] 117 (16.7) 116 (16.8) 1 (14.3) II, [n (%)] 156 (22.3) 156 (22.5) 0 (0.0) III, [n (%)] 226 (32.3) 223 (32.2) 3 (42.9) IV, [n (%)] 194 (27.8) 191 (27.6) 3 (42.9)
Congestive heart failure, [n (%)]
106 (15.2) 104 (15.0) 2 (28.6)
Hypertensive, [n (%)] 493 (70.5) 487 (70.4) 6 (85.7)

APPENDICES
262
Variable
All patients (n = 699)
Without Dysphagia (n = 692)
With Dysphagia
(n = 7)
Diet or medically-treated hyperlipidemiae, [n (%)]
502 (71.8)
495 (71.5)
7 (100.0)
Previous stroke or TIA, [n (%)]
58 (8.3) 56 (8.1) 2 (28.6)
Normal sinus rhythm, [n (%)]
651 (93.1) 644 (93.1) 7 (100.0)
Heart block / pacemaker, [n (%)]
9 (1.3) 9 (1.3) 0 (0.0)
Atrial fibrillation or flutter, [n (%)]
39 (5.6) 39 (5.6)
0 (0.0)
Left main artery stenosis, [n (%)]
152 (21.7) 151 (21.8) 1 (14.3)
Respiratory Risksf
Smoker, [n (%)] 83 (11.9) 83 (12.0) 0 (0.0)
Ex-Smoker, [n (%)] 318 (45.5) 313 (45.2) 5 (71.4)
Severe COPD, [n (%)]
21 (3.0) 21 (3.0) 0 (0.0)
Renal Risks
Serum creatinine [mean (SD)] (µmol/L)
87.71 (56.94)
87.71 (57.18)
88.29 (26.27)
[median (IQR)](µmol/L) 78.0 (24.0) 78.0 (24.0) 95.0 (38.0)
Estimated creatinine clearance [mean (SD)]
88.78 (32.63) 88.88 (32.58) 78.73 (38.37)
[median (IQR)] 86.80 (43.64) 86.82 (43.49) 62.56 (77.54)
Note. SD = standard deviation; yrs = years; IQR = interquartile range; LV = left ventricular; NYHA = New York Heart Association; TIA = transient ischemic attack; COPD = chronic obstructive pulmonary disease; µmol/L = micromol per liter. a missing data: 7 patients without dysphagia, 1 patient with dysphagia. b missing data: 1 patient without dysphagia. c missing data: 3 patients without dysphagia. d missing data: 6 patients without dysphagia. e missing data: 1 patient without dysphagia f missing smoking history data: 1 patient with dysphagia.

APPENDICES
263
B. Peri-operative characteristics for patients intubated <12h
Variable
All patients (n=699)
Without Dysphagia
(n=692)
With Dysphagia (n=7)
Procedure CABG, [n (%)] 444 (63.5) 438 (63.3) 6 (85.7) Valve, [n (%)] 255 (36.5) 254 (36.7) 1 (14.3)
Urgency Elective, [n (%)] 457 (65.4) 453 (65.5) 4 (57.1) Inpatient, [n (%)] 197 (28.2) 194 (28.0) 3 (42.9) Urgent, [n (%)] 37 (5.3) 37 (5.3) 0 (0.0) Emergent, [n (%)] 8 (1.1) 8 (1.2) 0 (0.0)
CPB 635(90.8) 629 (90.9) 6 (85.7)
CPB duration [mean (SD)] (min)
80.55(38.15)
80.64 (38.18)
71.57 (35.95)
[median (IQR)] (min) 82.0 (41.0) 82.0 (41.0) 77.0 (33.0)
TEE, [n (%)] 304 (44.9) 303 (43.7) 1 (64.7)
Perioperative Complications
Stroke, [n (%)] 3 (0.4) 3 (0.4) 0 (0.0)
Sepsis, [n (%)] 5 (0.7) 4 (0.6) 1 (14.3)
Use of dopamine in ICU, [n (%)]
233 (33.3) 232(33.5) 1 (14.3)
MI, [n (%)] 7 (1.0) 7 (1.0) 0 (0.0)
Low-output syndrome, [n (%)]
2 (0.3) 2 (0.3) 0 (0.0)
IABP usage
Pre-operative, [n (%)] 6 (0.9) 6 (0.9) 0 (0.0) Peri-operative, [n (%)] 1 (0.1) 1 (0.1) 0 (0.0) Post-operative, [n (%)] 0 (0.0) 0 (0.0) 0 (0.0)
Note. CABG = coronary artery bypass graft; CPB = cardiopulmonary bypass; SD = standard deviation; IQR = interquartile range; min = minutes; TEE = transeophageal echocardiogram; ICU = intensive care unit; MI = myocardial infarction; IABP = intraaortic balloon pump.

APPENDICES
264
C. Post-operative patient outcomes for patients intubated <12h
Variable
All patients (n=699)
Without Dysphagia
(n=692)
With Dysphagia
(n=7)
Post-operative atrial fibrillation
238 (34.0) 233 (33.7) 5 (71.4)
Intubation duration [mean (SD)] (h)
6.37 (2.17)
6.38 (2.18)
6.31 (1.46)
[median (IQR)] (h) 6.08 (3.0) 6.04 (3.04) 6.42 (1.92)
Reintubation, [n (%)] 5 (0.7) 4 (0.6) 1 (14.3) Number of intubations
1, [n (%)] 694 (99.3) 688 (99.4) 6 (85.7) 2, [n (%)] 5 (0.7) 4 (0.6) 1 (14.3) 3, [n (%)] 0 (0.1) 0 (0.0) 0 (0.0) 4, [n (%)] 0 (0.1) 0 (0.0) 0 (0.0)
Re-operation, [n (%)] 7 (1.0) 7 (1.0) 0 (0.0)
Post-extubation repeat ICU Admission, [n (%)]
8 (1.1)
8 (1.2)
0 (0.0)
ICU stay [mean (SD)] (h)
44.40 (38.06)
44.27 (37.78)
57.22 (62.63)
[median (IQR)](h) 25.50 (29.08) 25.5 (28.8) 25.33 (56.72)
Preoperative hospital stay [mean (SD)] (d)
1.26 (3.22)
1.25 (3.22)
2.14 (3.02)
[median (IQR)] (d) 1.0 (1.0) 1.0 (1.0) 1.0 (6.0)
Postoperative hospital stay [mean (SD)] (d)
7.33 (3.44)
7.27(3.35)
13.43 (6.35) [median (IQR)] (d) 6.0 (3.0) 6.0 (3.0) 11.0 (13.0)
Total inpatient stay [mean (SD)] (d)
8.92(5.70)
8.87 (5.7)
14.0 (4.24)
[median (IQR)] (d) 7.0 (4.0) 7.0 (4.0) 14.0 (7.0)
Note. SD = standard deviation; h = hours; IQR = interquartile range; ICU = intensive care unit; d = days.

APPENDICES
265
Appendix O – Characteristics of Intubation Stratum II A. Pre-operative demographics and presenting clinical characteristics for patients intubated >12h and ≤ 24h
Variable
All patients (n = 134)
Without Dysphagia (n = 123)
With Dysphagia
(n = 11)
Age [mean (SD)] (yrs)
68.22 (11.84)
67.22 (11.67)
79.36 (7.47)
[median (IQR)] (yrs) 68.5 (15.25) 68.00 (16.0) 81.0 (12.0) Male, [n (%)] 92 (68.6) 84 (68.3) 8 (72.7)
Family history of heart diseasea, [n (%)]
63 (47.0) 59 (48.0) 4 (36.4)
Diabetes Risks
Insulin-controlled diabetes mellitus, [n (%)]
13 (9.7) 10 (8.1) 3 (27.3)
Oral hypoglycemics, [n (%)]
35 (26.1) 33 (26.8) 2 (18.2)
Cardiovascular Surgical Risks
Circulatory shock, [n (%)]
2 (1.5) 1 (0.8) 1 (9.1)
Non-Q-wave infarction, [n (%)]
22 (16.4) 21 (17.1) 1 (9.1)
Q-wave infarction, [n (%)]
4 (3.0) 3 (2.4) 1 (9.1)
LV gradeb 1, [n (%)] 70 (52.2) 63 (51.2) 7 (63.6) 2, [n (%)] 37 (27.6) 36 (29.3) 1 (9.1) 3, [n (%)] 22 (16.4) 19 (15.4) 3 (27.3) 4, [n (%)] 4 (3.0) 4 (3.3) 0 (0.0)
NYHA classificationc I, [n (%)] 12 (9.0) 12 (9.8) 0 (0.0) II, [n (%)] 21 (15.7) 20 (16.3) 1 (9.1) III, [n (%)] 45 (33.6) 42 (34.1) 3 (27.3) IV, [n (%)] 52 (38.8) 45 (36.6) 7 (63.6)
Congestive heart failure, [n (%)]
31 (23.1) 28 (22.8) 3 (27.3)
Hypertensive, [n (%)] 105 (78.4) 95 (77.2) 10 (90.9)

APPENDICES
266
Variable
All patients (n = 134)
Without Dysphagia (n = 123)
With Dysphagia
(n = 11)
Diet or medically-treated hyperlipidemiad, [n (%)]
97 (72.4)
90 (73.2)
7 (63.6)
Previous stroke or TIA, [n (%)]
18 (13.4) 15 (12.2) 3 (27.3)
Normal sinus rhythm, [n (%)] 123 (91.8) 114 (92.7) 9 (81.8)
Heart block / pacemaker, [n (%)]
2 (1.5) 2 (1.6) 0 (0.0)
Atrial fibrillation or flutter, [n (%)] 9 (6.7) 7 (5.7)
2 (18.2)
Left main artery stenosis, [n (%)] 37 (27.6) 32 (26.0) 5 (45.5)
Respiratory Risks
Smoker, [n (%)] 23 (17.2) 23 (18.7) 0 (0.0)
Ex-Smoker, [n (%)] 58 (43.3) 54 (43.9) 4 (36.4)
Severe COPD, [n (%)] 13 (9.7) 13 (10.6) 0 (0.0)
Renal Risks
Serum creatinine [mean (SD)] (µmol/L)
92.79 (41.23)
91.25 (40.35)
110.0 (48.9)
[median (IQR) (µmol/L) 83.0 (27.0) 83.0 (26.0) 87.0 (55.0)
Estimated creatinine clearance [mean (SD)]
79.11 (33.54)
81.24 (33.46)
55.22 (24.88)
[median (IQR)] 71.89 (39.6) 74.36 (40.02) 48.98 (48.19)
Note. SD = standard deviation; yrs = years; IQR = interquartile range; LV = left ventricular; NYHA = New York Heart Association; TIA = transient ischemic attack; COPD = chronic obstructive pulmonary disease; µmol/L = micromol per liter. a missing data: 1 patient without dysphagia. b missing data: 1 patients without dysphagia. c missing data: 4 patients without dysphagia. d missing data: 1 patient without dysphagia.

APPENDICES
267
B. Peri-operative characteristics for patients intubated >12h and ≤ 24h
Variable
All patients (n = 134)
Without Dysphagia (n = 123)
With Dysphagia (n = 11)
Procedure CABG, [n (%)] 88 (65.7) 83 (67.5) 5 (45.5) Valve, [n (%)] 46 (34.3) 40 (32.5) 6 (54.5)
Urgency Elective, [n (%)] 74 (55.2) 68 (55.3) 6 (54.5) Inpatient, [n (%)] 42 (31.3) 38 (30.9) 4 (36.4) Urgent, [n (%)] 15 (11.2) 14 (11.4) 1 (9.1) Emergent, [n (%)] 3 (2.2) 3 (2.4) 0 (0.0)
CPB 118 (88.1) 112 (91.1) 6 (54.5)
CPB duration [mean (SD)] (min)
88.94 (48.51)
90.75 (45.67)
68.73 (73.28)
[median (IQR)] (min) 92.0 (51.25) 92.0 (47.0) 69.0 (123.0)
TEE, [n (%)] 59 (44.0) 51 (41.5) 8 (72.7)
Perioperative Complications
Stroke, [n (%)] 1 (0.7) 0 (0.0) 1 (9.1)
Sepsis, [n (%)] 1 (0.7) 1 (0.8) 2 (18.2)
Use of dopamine in ICU, [n (%)]
78 (58.2) 73 (59.3) 5 (45.5)
MI, [n (%)] 1 (0.7) 1 (0.8) 0 (0.0)
Low-output syndrome, [n (%)] 2 (1.5) 2 (1.6) 0 (0.0)
IABP usage
Pre-operative, [n (%)] 4 (3.0) 3 (2.4) 1 (9.1) Peri-operative, [n (%)] 1 (.07) 1 (0.8) 0 (0.0) Post-operative, [n (%)] 0 (0.0) 0 (0.0) 0 (0.0)
Note. CABG = coronary artery bypass graft; CPB = cardiopulmonary bypass; SD = standard deviation; IQR = interquartile range; min = minutes; TEE = transeophageal echocardiogram; ICU = intensive care unit; MI = myocardial infarction; IABP = intraaortic balloon pump.

APPENDICES
268
C. Post-operative patient outcomes for patients intubated >12h and ≤ 24h
Variable
All patients (n = 134)
Without Dysphagia (n = 123)
With Dysphagia (n = 11)
Post-operative atrial fibrillation
58 (47.2) 52 (42.3) 6 (54.5)
Intubation duration [mean (SD)] (h)
16.86 (3.13)
16.80 (3.07)
17.66 (3.81)
[median (IQR)] (h) 16.5 (4.7) 16.50 (4.6) 17.83 (6.82) Reintubation, [n (%)] 4 (3.0) 4 (3.3) 0 (0.0)
Number of intubations 1, [n (%)] 130 (97.0) 119 (96.7) 11 (100.0) 2, [n (%)] 4 (3.0) 4 (3.3) 0 (0.0) 3, [n (%)] 0 (0.0) 0 (0.0) 0 (0.0)
4, [n (%)] 0 (0.0) 0 (0.0) 0 (0.0)
Re-operation, [n (%)] 14 (10.4) 14 (11.4) 0 (0.0)
Post-extubation repeat ICU admission, [n (%)]
10 (7.5)
8 (6.5)
2 (18.2)
ICU stay [mean (SD)] (h)
81.52 (70.49)
77.60 (66.14)
125.34 (102.02)
[median (IQR)] (h) 67.49(54.0) 66.17 (52.42) 116.50 (93.25) Preoperative hospital stay [mean (SD)] (d)
1.13 (1.85)
1.04 (1.69)
2.18 (3.06)
[median (IQR)] (d) 1.0 (1.0) 1.0 (1.0) 1.0 (3.0) Postoperative hospital stay [mean (SD)] (d)
10.74 (7.60)
9.61(5.10)
23.36 (16.10)
[median (IQR)] (d) 8.0 (5.0) 8.0 (4.0) 17.0 (19.0) Total inpatient stay [mean (SD)] (d)
11.43 (7.49)
10.8 (7.09)
18.36 (8.58)
[median (IQR)] (d) 9.0 (6.0) 9.0 (5.0) 15.0 (9.0)
Note. SD = standard deviation; h = hours; IQR = interquartile range; ICU = intensive care unit; d = days.

APPENDICES
269
Appendix P – Characteristics of Intubation Stratum III A. Pre-operative demographics and presenting clinical characteristics for patients intubated >24h and ≤48h
Variable
All patients (n = 36)
Without Dysphagia
(n = 30)
With Dysphagia
(n = 6)
Age [mean (SD)] (yrs)
70.81 (11.72)
70.53 (11.81)
72.17 (12.22)
[median (IQR)] (yrs) 75.0 (16.25) 74.5 (15.0) 76.5 (22.0) Male, [n (%)] 23 (63.9) 17 (56.7) 6 (100.0)
Family history of heart disease, [n (%)]
19 (52.8) 14 (46.7) 5 (83.3)
Diabetes Risks
Insulin-controlled diabetes mellitus, [n (%)]
5 (13.9) 5 (16.7) 0 (0.0)
Oral hypoglycemics, [n (%)]
10 (27.8) 9 (30.0) 1 (16.7)
Cardiovascular Surgical Risks
Circulatory shock, [n (%)] 2 (5.6) 2 (6.7) 0 (0.0)
Non-Q-wave infarction, [n (%)]
7 (19.4) 6 (20.0) 1 (16.7)
Q-wave infarction, [n (%)]
1 (2.8) 1 (3.3) 0 (0.0)
LV grade 1, [n (%)] 14 (38.9) 12 (40.0) 2 (33.3) 2, [n (%)] 16 (44.4) 13 (43.3) 3 (50.0) 3, [n (%)] 5 (13.9) 4 (13.3) 1 (16.7) 4, [n (%)] 1 (2.8) 1 (3.3) 0 (0.0)
NYHA classification I, [n (%)] 1 (2.8) 1 (3.3) 0 (0.0) II, [n (%)] 6 (16.7) 6 (20.0) 0 (0.0) III, [n (%)] 8 (22.2) 4 (13.3) 4 (66.7) IV, [n (%)] 21 (58.3) 19 (63.3) 2 (33.3)
Congestive heart failure, [n (%)]
12 (33.3) 8 (26.7) 4 (66.7)
Hypertensive, [n (%)] 25 (69.4) 22 (73.3) 3 (50.0)

APPENDICES
270
Variable
All patients (n = 36)
Without Dysphagia
(n = 30)
With Dysphagia
(n = 6)
Diet or medically-treated hyperlipidemia, [n (%)]
29 (80.6)
26 (86.7)
3 (50.0)
Previous stroke or TIA,
[n (%)]
3 (8.3)
3 (10.0)
0 (0.0) Normal sinus rhythm, [n (%)]
27 (75.0) 22 (73.3) 5 (83.3)
Heart block / pacemaker, [n (%)]
6 (16.7) 6 (20.0) 0 (0.0)
Atrial fibrillation or flutter, [n (%)]
3 (8.3) 2 (6.7)
1 (16.7)
Left main artery stenosis, [n (%)]
11 (30.6) 10 (33.3) 1 (16.7)
Respiratory Risksa
Smoker, [n (%)] 2 (5.6) 0 (0.0) 2 (33.3)
Ex-smoker, [n (%)] 19 (52.8) 17 (56.7) 2 (33.3)
Severe COPD, n (%)
1 (2.8) 1 (3.3) 0 (0.0)
Renal Risks
Serum creatinine [mean (SD)] (µmol/L)
90.06 (23.14)
87.0 (21.94)
105.33 (24.91)
[median (IQR)] (µmol/L) 89.5 (28.25) 87.0 (30.0) 115.50 (51.0)
Estimated creatinine clearance [mean (SD)]
74.6 (30.79)
75.14 (29.52)
71.90 (39.65) [median (IQR)] 70.29 (37.47) 72.97 (37.72) 53.52 (60.55)
Note. SD = standard deviation; yrs = years; IQR = interquartile range; LV = left ventricular; NYHA = New York Heart Association; TIA = transient ischemic attack; COPD = chronic obstructive pulmonary disease; µmol/L = micromol per liter. a missing data: 2 patients with dysphagia.

APPENDICES
271
B. Peri-operative characteristics for patients intubated >24h and ≤48h
Variable
All patients (n = 36)
Without Dysphagia
(n = 30)
With Dysphagia
(n = 6)
Procedure CABG, [n (%)] 16 (62.4) 15 (63.8) 1 (39.2) Valve, [n (%)] 20 (37.6) 15 (36.2) 5 (60.8)
Urgency Elective, [n (%)] 20 (55.6) 17 (56.7) 3 (50.0) Inpatient, [n (%)] 12 (33.3) 9 (30.0) 3 (50.0) Urgent, [n (%)] 3 (8.3) 3 (10.0) 0 (0.0) Emergent, [n (%)] 1 (2.8) 1 (3.3) 0 (0.0)
CPB 35 (97.2) 29 (96.7) 6 (100.0)
CPB duration [mean (SD)] (min)
111.31 (37.75)
108.47 (39.07)
125.50 (28.82)
[median (IQR)] (min) 110.5 (43.75) 101.50 (42.0) 130.0 (49.0)
TEE, [n (%)] 24 (66.7) 18 (60.0) 6 (100.0)
Perioperative Complications
Stroke, [n (%)] 1 (2.8) 0 (0.0) 1 (16.7)
Sepsis, [n (%)] 0 (0.0) 0 (0.0) 0 (0.0)
Use of dopamine in ICU, [n (%)]
367 (40.4) 339 (39.5) 28 (54.9)
MI, [n (%)] 28 (77.8) 23 (76.7) 5 (83.3)
Low-output syndrome, [n (%)] 7 (2.2) 7 (1.5) 0 (13.7)
IABP usage
Pre-operative, [n (%)] 4 (11.1) 4 (13.3) 0 (0.0) Peri-operative, [n (%)] 6 (16.7) 6 (20.0) 0 (0.0) Post-operative, [n (%)] 1 (2.8) 1 (3.3) 0 (0.0)
Note. CABG = coronary artery bypass graft; CPB = cardiopulmonary bypass; SD = standard deviation; IQR = interquartile range; min = minutes; TEE = transeophageal echocardiogram; ICU = intensive care unit; MI = myocardial infarction; IABP = intraaortic balloon pump.

APPENDICES
272
C. Post-operative patient outcomes for patients intubated >24h and ≤48h
Variable
All patients
(n = 36)
Without Dysphagia
(n = 30)
With Dysphagia
(n = 6)
Post-operative atrial fibrillation
24 (66.7) \
21 (70.0)
3 (50.0)
Intubation duration [mean (SD)] (h)
33.94 (7.77)
32.32 (7.4)
42.08 (3.17)
[median (IQR)] (h) 33.04 (13.6) 30.25 (13.17) 41.46 (5.89) Reintubation, [n (%)] 2 (5.6) 2 (6.7) 0 (0.0)
Number of intubations 1, [n (%)] 34 (94.4) 28 (93.3) 6 (100.0) 2, [n (%)] 2 (5.6) 2 (6.7) 0 (0.0) 3, [n (%)] 0 (0.0) 0 (0.0) 0 (0.0)
4, [n (%)] 0 (0.0) 0 (0.0) 0 (0.0)
Re-operation, [n (%)] 4 (11.1) 4 (13.3) 0 (0.0)
Post-Extubation Repeat ICU Admission, [n (%)]
2 (5.6)
2 (6.7)
0 (0.0)
ICU stay [mean (SD)] (h)
93.67 (32.38)
90.60 (30.02)
109.02 (29.98)
[median (IQR)] (h) 93.33 (44.23) 90.96 (43.52) 105.21 (53.31) Preoperative hospital stay [mean (SD)] (d)
1.53 (2.32)
1.20 (1.8)
3.17 (3.97)
[median (IQR)] (d) 1.0 (1.0) 1.0 (1.0) 1.0 (6.0) Postoperative hospital stay [mean (SD)] (d)
11.28 (8.68)
11.03 (9.38)
12.50 (3.94)
[median (IQR)] (d) 9.0 (2.75) 9.0 (3.0) 12.50 (8.0) Total inpatient stay [mean (SD)] (d)
11.78 (7.25)
10.4 (4.2)
18.67 (14.05)
[median (IQR)] (d) 9.5 (7.75) 9.0 (7.0) 15.0 (21.0)
Note. SD = standard deviation; h = hours; IQR = interquartile range; ICU = intensive care unit; d = days.

APPENDICES
273
Appendix Q – Characteristics of Intubation Stratum IV A. Pre-operative demographics and presenting clinical characteristics for patients intubated >48h
Variable
All patients (n = 40)
Without Dysphagia
(n = 13)
With Dysphagia
(n = 27)
Age [mean (SD)] (yrs)
72.2 (7.9)
71.4 (7.4)
72.6 (8.3)
[median (IQR)] (yrs) 73.0 (10.8) 71.0 (13.0) 74.0 (11.0) Male, [n (%)] 25 (62.5) 8 (61.5) 17 (63.0)
Family history of heart disease, [n (%)]
21 (52.5) 7 (53.8) 14 (51.9)
Diabetes Risks
Insulin-controlled diabetes mellitus, [n (%)]
3 (7.5) 2 (15.4) 1 (3.7)
Oral hypoglycemics, [n (%)] 7 (17.5) 3 (23.1) 4 (14.8)
Cardiovascular Surgical Risks
Circulatory Shock, [n (%)] 1 (2.5) 1 (7.7) 0 (0.0)
Non-Q-wave infarction, [n (%)]
5 (12.5) 5 (38.5) 0 (0.0)
Q-wave infarction, [n (%)] 1 (2.5) 1 (7.7) 0 (0.0)
LV grade 1, [n (%)] 22 (55.0) 7 (53.8) 15 (55.6) 2, [n (%)] 10 (25.0) 4 (30.8) 6 (22.2) 3, [n (%)] 7 (17.5) 2 (15.4) 5 (18.5) 4, [n (%)] 1 (2.5) 0 (0.0) 1 (3.7)
NYHA classificationa I, [n (%)] 1 (2.5) 1 (7.7) 0 (0.0) II, [n (%)] 6 (15.0) 1 (7.7) 5 (18.5) III, [n (%)] 16 (40.0) 4 (30.8) 12 (44.4) IV, [n (%)] 16 (40.0) 7 (53.8) 9 (33.3)
Congestive heart failure [n (%)]
17 (42.5) 5 (38.5) 12 (44.4)
Hypertensive, [n (%)] 32 (80.0) 12 (92.3) 20 (74.1)
Diet or medically-treated hyperlipidemia, [n (%)]
30 (75.0) 9 (69.2) 21 (77.8)
Previous stroke or TIA, [n (%)]
9 (22.5) 1 (7.7) 8 (29.6)

APPENDICES
274
Variable
All patients (n = 40)
Without Dysphagia
(n = 13)
With Dysphagia
(n = 27) Normal sinus rhythm, [n (%)]
33 (82.5)
13 (100.0)
20 (74.1)
Heart block / pacemaker, [n (%)]
1 (2.5) 0 (0.0) 1 (3.7)
Atrial fibrillation or flutter, [n (%)]
6 (15.0) 0 (0.0)
6 (22.2)
Left main artery stenosis, [n (%)]
9 (22.5) 4 (30.8) 5 (18.5)
Respiratory Risksb
Smoker, [n (%)] 7 (17.5) 3 (23.1) 4 (14.8)
Ex-smoker, [n (%)] 19 (47.5) 5 (38.5) 14 (51.9)
Severe COPD, [n (%)] 3 (7.5) 2 (15.4) 1 (3.7)
Renal Risks
Serum creatinine [mean (SD)] (µmol/L)
107.63 (40.08)
91.54 (26.13)
115.37 (43.61)
[median (IQR)] (µmol/L) 96.0 (49.25) 90.0 (47.0) 107.0 (54.0)
Estimated creatinine clearance [mean (SD)]
61.56(21.79) 75.23 (24.76) 54.98 (17.06)
[median (IQR)] 56.58 (25.31) 71.21 (38.3) 51.72 (26.98)
Note. SD = standard deviation; yrs = years; IQR = interquartile range; LV = left ventricular; NYHA = New York Heart Association; TIA = transient ischemic attack; COPD = chronic obstructive pulmonary disease; µmol/L = micromol per liter. a missing data: 1 patient with dysphagia. b missing data: 1 patients with dysphagia.

APPENDICES
275
B. Peri-operative characteristics for patients intubated >48h
Variable
All patients (n = 40)
Without Dysphagia
(n = 13)
With Dysphagia
(n = 27)
Procedure CABG, [n (%)] 19 (62.4) 11 (63.8) 8 (39.2) Valve, [n (%)] 21 (37.6) 2 (36.2) 19 (60.8)
Urgency Elective, [n (%)] 23 (57.5) 5 (38.5) 18 (66.7) Inpatient, [n (%)] 12 (30.0) 4 (30.8) 8 (32.1) Urgent, [n (%)] 4 (10.0) 3 (23.1) 1 (3.7) Emergent, [n (%)] 1 (2.5) 1 (7.7) 0 (0.0)
CPB 38 (95.0) 13 (100.0) 25 (92.6)
CPB duration [mean (SD)] (min)
109.03 (53.21)
93.85 (22.51)
116.33 (61.98)
[median (IQR)] (min) 94.0 (60.25) 92.0 (22.0) 94.0 (76.0)
TEE, [n (%)] 31 (44.9) 8 (43.7) 23 (64.7)
Perioperative Complications
Stroke, [n (%)] 5 (12.5) 1 (7.7) 4 (14.8)
Sepsis, [n (%)] 1 (0.9) 0 (0.6) 1 (5.9)
Use of dopamine in ICU, [n (%)]
28 (70.0) 11 (84.6) 17 (63.0)
MI, [n (%)] 4 (10.0) 1 (7.7) 3 (11.1)
Low-output syndrome, [n (%)] 9 (22.5) 2 (15.4) 7 (25.9)
IABP usage
Pre-operative, [n (%)] 3 (7.5) 2 (15.4) 1 (3.7) Peri-operative, [n (%)] 5 (12.5) 1 (7.7) 4 (14.8) Post-operative, [n (%)] 2 (5.0) 0 (0.0) 2 (7.4)
Note. CABG = coronary artery bypass graft; CPB = cardiopulmonary bypass; SD = standard deviation; IQR = interquartile range; min = minutes; TEE = transeophageal echocardiogram; ICU = intensive care unit; MI = myocardial infarction; IABP = intraaortic balloon pump.

REFERENCES
276
C. Post-operative patient outcomes for patients intubated >48h
Variable
All patients (n = 40)
Without Dysphagia
(n = 13)
With Dysphagia
(n = 27)
Post-operative atrial fibrillation
22 ( 55.0) 6 (46.2) 16 (59.3)
Intubation duration [mean (SD)] (h)
104.1 (43.05)
83.13 (36.34)
114.20 (42.95)
[median (IQR] (h) 89.33 (46.89) 70.5 (34.25) 103.50 (58.25) Reintubation, [n (%)] 14 (35.0) 3 (23.1) 11 (40.7)
Number of intubations 1, [n (%)] 26 (65.0) 10 (76.9) 16 (59.3) 2, [n (%)] 12 (30.0) 3(23.1) 9 (33.3) 3, [n (%)] 1 (2.5) 0 (0.0) 1 (3.7)
4, [n (%)] 1 (2.5) 0 (0.0) 1 (3.7)
Re-operation, [n (%)] 10 (25.0) 2 (15.4) 8 (29.6)
Post-Extubation Repeat ICU Admission, [n (%)]
1 (2.5)
0 (0.0)
1 (3.7)
ICU stay [mean (SD)] (h)
201.57 (129.36)
142.99 (45.10)
229.77 (147.04)
[median (IQR)] (h) 166.0 (82.66) 119.75 (57.67) 170.67 (133.50) Preoperative hospital stay [mean (SD)] (d)
1.65 (2.76)
0.54 (0.66)
2.19 (3.21)
[median (IQR)] (d) 1.0 (1.0) 0.0 (1.0) 1.0 (0.0) Postoperative hospital stay [mean (SD)] (d)
18.7 (11.75)
13.69 (6.20)
21.11 (13.08)
[median (IQR)] (d) 15.0 (9.5) 12.0 (5.0) 15.0 (2.12) Total inpatient stay [mean (SD)] (d)
17.08 (12.15)
13.31 (13.83)
18.90 (11.07)
[median (IQR)] (d) 12.0 (11.25) 10.0 (4.0) 16.0 (11.0)
Note. SD = standard deviation; h = hours; IQR = interquartile range; ICU = intensive care unit; d = days.