clinical writing for interventional cardiologists
DESCRIPTION
Clinical Writing for Interventional Cardiologists. What you will learn. Introduction General principles for clinical writing Specific techniques Practical session: critical review of a published article Writing the Title and the Abstract Bibliographic search and writing the Introduction - PowerPoint PPT PresentationTRANSCRIPT
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Clinical Writing for Interventional Cardiologists
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What you will learn• Introduction• General principles for clinical writing• Specific techniques• Practical session: critical review of a published article• Writing the Title and the Abstract• Bibliographic search and writing the Introduction• Principles of statistics and writing the Methods• Practical session: writing the Abstract• Writing the Results• Writing the Discussion• Writing Tables and preparing Figures• Principles of peer-review• Principles of grant writing/regulatory submission• Clinical writing at a glance• Conclusions and take home messages
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Materials and methods
How was the problem studied?
The answer is in the Methods
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Materials and methods
The Methods section is often the less read section, but it is the most important because allow us to understand how the study was conducted, thus giving us an idea of the value of its results
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Expanded IMRAD algorithmIntroduction Background
Limitations of current evidenceStudy hypothesis
Methods DesignPatientsProceduresFollow-upEnd-pointsAdditional analysesStatistical analysis
Results Baseline and procedural dataEarly outcomesMid-to-long term outcomesAdditional analyses
Discussion Summary of study findingsCurrent research contextImplications of the present studyAvenues for further researchLimitations of the present studyConclusions
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• Describe with full details what was done to answer the research question
• In the beginning include a clear statement of study design:“The study was a double-blind, randomized, parallel design … designed to compare the efficacy and safety of …”
• Include also a sentence about IRB approval, informed consent, or compliance with animal welfare regulations:“The protocol was approved by the institutional review board, and all patients gave informed consent …”
Materials and methods
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Materials and methods
RRISC JACC 2006
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• State the protocol/procedures. Repeat the question and the aims:“We tested the efficacy of drug XX administered orally in a dose of XX mg, given XX times daily for up to XX months.”“There were 2 primary endpoints. The first was event-free survival at XX days, with an event defined as…”
• Describe materials/methods or subjects adequately
• Write in a logical order (usually chronological) • Describe analytical methods
Materials and methods
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• Use subheadings (design, patients, procedures, follow-up, endpoints….)
• Do not include results in Methods
• Include appropriate figures and tables if useful to graphically explain concepts
• Write in past tense
• Use active voice whenever possible
• Cite references for published methods
• Describe new methods fully
Materials and methods
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• Briefly address questions you can anticipate from the reader, e.g. justify/clarify the design of your study:
“Intra-luminal recanalization of long coronary artery
occlusions cannot be obtained in all patients. …. We
thus tested the feasibility and safety of subintimal
angioplasty in patients in whom standard intra-luminal
approaches had failed and who were not candidate to
bypass surgery because of severe comorbidities…”
Materials and methods
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If you prevent major limitations in your study, treat them in a matter-of-fact way:
"This study was performed as part of a routine clinical assessment, so that no attempt was made to ensure either fasting of the patient or performance of the test at a particular time of day."
Materials and methods
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What you will learn
• Principles of statistics and writing the Methods
– study designs– intention-to-treat vs per-protocol analysis– type I and type II errors– p values and confidence intervals
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• State clearly the design of the study
• Was it retrospective or prospective?
• Was it a registry or controlled study?
• Did you randomly allocated patients?
• Did you follow a protocol (may add figure)?
You can also include here details of IRB approval
Design subsection
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Prospective non-RCT study
RESOLUTE EuroIntervention 2007
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Prospective non-RCT study
Cavallini et al. EHJ 2005
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Retrospective non-RCT study
Biondi-Zoccai et al. EHJ 2006
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Prospective RCT study
Tapas NEJM 2008
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TAPAS 1 year Lancet 2008
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Prospective RCT study • State clearly:
• If the trial was double-blind / single-blind / open-label
• If blinded, how blinding was granted
• how randomization was performed
ENDEAVOR II Circulation 2006
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Prospective RCT study
RRISC JACC 2006
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Patient subsection
• State clearly how you selected patients
• Specific inclusion criteria?
• Specific exclusion criteria?
You can include here details of written informed
consent Tapas NEJM 2008
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Patient subsection
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• State clearly how you performed the procedure
• Any novel approaches or devices?
• Complete with details on concomitant or post-intervention medications
• If evaluating bio-markers, state clearly which ones, which essay is used and how it works
You can include here pictures detailing what you did/use
Procedure subsection
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TAPAS NEJM 2008
Procedure subsection
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Lefevre et al. CCI 2000
Procedure subsection
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Lefevre et al. CCI 2000
Procedure subsection
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• State clearly outcomes and who adjudicated them (independent CEC?)
• Define each outcome thoroughly (death, MI, RR, TVF, TVR, TLR, ST, bleedings…)
• Define the timing of follow-up and specify info on follow-up means (how patients were contacted?)
• Make sure you use validated or consensus definitions / classifications (if available, otherwise you are in trouble!)
Outcome subsection
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Outcome subsection
ENDEAVOR II
Circulation 2006
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Outcome subsection
Spaulding et al.
NEJM 2007
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• Focus on additional analyses that may be pertinent to the study– QCA: late loss, binary restenosis…
– TIMI score, Myocardial Blush Grade
– IVUS: neointimal hyperplasia volume, minimal lumen area…
– CT: coronary stenosis > 50%...
– MRI: myocardial infarction mass…
– Echocardiography: LV ejection fraction…
• Quote thoroughly for established methods
• Define explicitly terms and ways to compute secondary variables
Additional analysis subsection
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Additional analysis subsection
TAPAS NEJM 2008
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What you will learn
• Principles of statistics and writing the Methods
– study designs– intention-to-treat vs per-protocol analysis– type I and type II errors– p values and confidence intervals
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• Explain how you handled and reported categorical and continuous variables
• Explain how you tested for significance at both univariate and multivariate analysis
• Define tails and threshold p value
• State width of confidence intervals
• Provide sample size computation
• Spell out which software package was used
Quote extensively and be ready to defend
yourself if you use sophisticated analytic tools
Statistics subsection
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Variables
nominal ordinal discrete continuous
orderedcategories
ranks counting measuring
Death: yes/noTLR: yes/no
TIMIflow
BMIBlood pressure
QCA data (MLD, late loss)
Stent diameterStent length
Types of variables
Radial/brachial/femoral
QUANTITYCATEGORY
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• Categorical variables are probably the most
important ones provided by a clinical study, as
hard clinical end-points are always expressed so
• Specifically, focus on:
• Choose few statistics, and use them consistently• Provide confidence intervals (usually 95%)• May also provide number needed to treat/harm
Categorical variables
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a b
c d
TVFNo TVF
Endeavor
Driver
Absolute Risk = [ d / ( c + d ) ]
Absolute Risk Reduction = [ d / ( c + d ) ] - [ b / ( a + b ) ]
Relative Risk = [ d / ( c + d ) ] / [ a / ( a + b ) ]
Relative Risk Reduction = 1 - RR
Odds Ratio = (d/c)/(b/a) = ( a * d ) / ( b * c )
Compare event rates
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Absolute Risk (AR) 7.9% (47/592) & 15.1% (89/591)
Absolute Risk Reduction (ARR) 7.9% (47/592) – 15.1% (89/591) = -7.2%
Relative Risk (RR)7.9% (47/592) / 15.1% (89/591) = 0.52(given an equivalence value of 1)
Relative Risk Reduction (RRR)1 – 0.52 = 0.48 or 48%
Odds Ratio (OR) 8.6% (47/545) / 17.7% (89/502) = 0.49(given an equivalence value of 1)
Odds Ratio Reduction (ORR)1 – 0.49 = 0.51 or 51%
STENT * TVF Crosstabulation
Count
502 89 591545 47 592
1047 136 1183
DriverEndeavor
STENT
Total
no yesTVF
Total
Compare event rates
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Continuous variables • Continuous variables are important for the
appraisal of baseline/procedural characteristics (eg stent length per lesion), or additional analyses (eg QCA)
• Focus on these points:
• Provide mean and standard deviation
• Or median (interquartile range) if non-Gaussian
• May check for normality assumptions
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Cardiology
xxN
Characteristics:-summarises information well-discards a lot of information
(dispersion??)
Assumptions:-data are not skewed
– distorts the mean– outliers make the mean very different
-Measured on measurement scale– cannot find mean of a categorical measure
‘average’ stent diameter may be meaningless
Mean (arithmetic)
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Cardiology
What is it?– The one in the middle– Place values in order– Median is central
Definition:– Equally distant from all other values
Used for:– Ordinal data– Skewed data / outliers
Median
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Cardiology
Mean is usually best– If it works– Useful properties (with standard deviation [SD])– But…
Driver Endeavor17 21 19 2119 2117 2118 6
Mean 18 18Median 18 21
Lesion length
Comparing Measures of central tendency
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Cardiology
It also depends on the underlying distribution…
Symmetric? mean = median = mode
Comparing Measures of central tendency
Value
Freq
uenc
y
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Cardiology
It also depends on the underlying distribution…
Asymmetric? mean ≠ median ≠ mode
0
5
10
15
20
25
30
0 1 2 3 4 5 6 7 8 9
Number of Endeavor implanted per patient
Freq
uenc
y
Mode Mode Median Median Mean Mean
Comparing Measures of central tendency
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Cardiology
0 0.30 0.60 0.90 1.20 1.50
Late loss
Freq
uenc
y
DriverEndeavor
Measures of dispersion: examples
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Cardiology
0 0.30 0.60 0.90 1.20 1.50
Late loss
Freq
uenc
y
DriverEndeavor
Measures of dispersion: examples
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Cardiology
0 0.30 0.60 0.90 1.20 1.50
Late loss
Freq
uenc
y
DriverEndeavor
Measures of dispersion: examples
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Cardiology
• Standard deviation (SD)– Used with mean– Parametric tests
• Interquartile range– Used with median– 25% (1/4) to 75% (3/4) percentile– Non-parametric tests
• Range– First to last value– Not commonly used
Measures of dispersion: types
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Cardiology
Standard deviation (SD):– approximates population σ as N increases
Advantages:– with mean enables powerful synthesis
mean±1*SD 68% of datamean±2*SD 95% of data (1.96)mean±3*SD 99% of data (2.86)
Disadvantages:– is based on normal assumptions
1)( 2
--
Nxx
SDSD
Standard deviation
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Cardiology
Rules of thumb
1. Refer to previous data or analyses (eg landmark articles, large databases)
2. Inspect tables and graphs (eg outliers, histograms)
3. Check rough equality of mean, median, mode
4. Perform ad hoc statistical tests• Levene’s test for equality of means• Kolmogodorov-Smirnov tests• …
Testing normality assumptions
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Inferential statistics
P values tell you whether there is a DIFFERENCE and its DIRECTION
Confidence intervals tell you what is the MAGNITUDE (or SIZE) of such difference
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2.1 vs 2.4%
Difference and direction
0.3 vs 2.8%
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Size of the difference
7.2 vs 2.4%
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Sample size calculation
To compute the sample size for a study we need:1. Preferred alpha value2. Preferred beta value (remember: power is (1-beta)x100)3. Control event rate or average value
(with measure of dispersion if appliable)4. Expected relative reduction in experimental group
ENDEAVOR II Circulation 2006
Whenever designing Whenever designing a study or analyzing a study or analyzing
a dataset, it is a dataset, it is important to important to
estimate the sample estimate the sample size or the power of size or the power of
the comparisonthe comparison
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Intention-to-treat analysis
• Intention-to-treat (ITT) analysis is an analysis based on the initial treatment intent, irrespectively of the treatment eventually administered
• ITT analysis is intended to avoid various types of bias that can arise in intervention research, especially procedural, compliance and survivor bias
• However, ITT dilutes the power to achieve statistically and clinically significant differences, especially as drop-in and drop-out rates rise
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Per-protocol analysis
• In contrast to the ITT analysis, the per-protocol (PP) analysis includes only those patients who complete the entire clinical trial or other particular procedure(s), or have complete data
• In PP analysis each patient is categorized according to the actual treatment received, and not according to the originally intended treatment assignment
• PP analysis is largely prone to bias, and is useful almost only in equivalence or non-inferiority studies
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ITT vs PP
100 pts enrolled RANDOMIZATION
50 pts to group A (more toxic)
50 pts to group B (conventional Rx, less toxic)
45 pts treated with A, 5 shifted to B because of poor
global health (all 5 died)
50 patients treated with B (none died)
ACTUAL THERAPY
• ITT: 10% mortality in group A vs 0% in group B, p=0.021 in favor of B
• PP: 0% (0/45) mortality in group A vs 9.1% (5/55) in group B, p=0.038 in favor of A
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Questions?
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Take home messages
The most important points to remember when writing the Methods section are:
1. State exactly what you did, no more than that
2. Concentrate on the primary aim of the study, not on the ancillary goals
3. Ensure reproducibility
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Take home messages
When writing the Methods always ask yourself in every step:
1. What has been done
2. How it has been done
3. When it has been done
4. Who did it
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For further slides on these topics please feel free to visit the
metcardio.org website:
http://www.metcardio.org/slides.html