routine drainage after thyroid surgery—a meta-analysis
TRANSCRIPT
![Page 1: Routine drainage after thyroid surgery—A meta-analysis](https://reader030.vdocuments.net/reader030/viewer/2022020311/575005741a28ab1148a47676/html5/thumbnails/1.jpg)
Journal of Surgical Oncology 2007;96:273–280
REVIEW
Routine Drainage After Thyroid Surgery—AMeta-Analysis
ALVARO SANABRIA, MD, MSc,1,2 ANDRE L. CARVALHO, MD, PhD,2 CARL E. SILVER, MD, FACS,3
ALESSANDRA RINALDO, MD, FACS,4 ASHOK R. SHAHA, MD, FACS,5 LUIZ P. KOWALSKI, MD, PhD,2
AND ALFIO FERLITO, MD, DLO, DPath, FRCS, FRCSEd, FRCSGlasg, FRCSI, FACS, FHKCORL, FDSRCS, FRCPath, FASCP, MCAP4*
1Department of Surgery, Universidad de La Sabana, Bogota, Colombia2Department of Head and Neck Surgery and Otorhinolaryngology, Hospital do Cancer AC Camargo, Sao Paulo,
Brazil3Department of Surgery, Albert Einstein College of Medicine, Montefiore Medical Center, Bronx, New York
4Department of Surgical Sciences, ENT Clinic, University of Udine, Udine, Italy5Head and Neck Service, Memorial Sloan-Kettering Cancer Center, New York, New York
Thyroidectomy is a common surgical procedure. The results of some clinical trialssuggest that routine drainage does not offer advantages, but the evidence is not strongeither in favor of or against this intervention. The effect of routine drainage comparedto no drainage in patients subject to thyroidectomy was measured using a meta-analysis. After an extensive literature review, suitable randomized clinical trials wereselected for analysis. Outcome measures included the comparative incidence of neckhematoma or seroma and length of hospital stay. Eleven randomized clinical trialswere included. There were no statistically significant differences in the incidence ofneck hematoma/seroma (OR 1.03, 95% CI 0.59-1.81) between the groups. The meanlength of hospital stay was 1.53 days longer for the drainage group (95% CI 1.39–1.68). There was no difference found between routine drainage and no drainage withregard to the frequency of postoperative hematoma/seroma in patients followingthyroidectomy. In addition, the mean length of hospital stay was longer in the routinedrainage group.J. Surg. Oncol. 2007;96:273–280. � 2007 Wiley-Liss, Inc.
KEY WORDS: drainage; thyroidectomy; thyroid; complications; hematoma;seroma; meta-analysis
INTRODUCTION
Operations on the thyroid are the most commonsurgical procedures performed in the neck. In the pastmost surgeons employed wound drains routinely with thehope of decreasing the risk of acute airway obstruction byhematoma as well as postoperative hematoma or seroma[1–5]. Several authors, however, have suggested that useof drains could increase the risk of infection, the length ofhospital stay, treatment costs, and discomfort for thepatient. Moreover, the routine use of drains is not asubstitute for meticulous surgical technique with carefulhemostasis [6–11]. Therefore, the use of routine drainagein thyroid surgery has become controversial.
To solve this controversy, some randomized controlledtrials have been performed [12–24]. These trials couldnot identify a statistical difference in the rates of neckhematoma/seroma between groups using drains and those
*Correspondence to: Alfio Ferlito, MD, DLO, DPath, FRCS, FRCSEd,FRCSGlasg, FRCSI, FACS, FHKCORL, FDSRCS, FRCPath, FASCP,MCAP, Director of the Department of Surgical Sciences, Professor andChairman of the ENT Clinic, University of Udine, Policlinico Universitario,Piazzale S. Maria della Misericordia, I-33100 Udine, Italy. Fax: þ39 0432559339. E-mail: [email protected]
Received 2 November 2006; Accepted 5 March 2007
DOI 10.1002/jso.20821
Published online 27 April 2007 in Wiley InterScience(www.interscience.wiley.com).
� 2007 Wiley-Liss, Inc.
![Page 2: Routine drainage after thyroid surgery—A meta-analysis](https://reader030.vdocuments.net/reader030/viewer/2022020311/575005741a28ab1148a47676/html5/thumbnails/2.jpg)
without drains. However, these trials had small samplesizes, and thus did not offer a conclusive response. Onewayto solve this problem is to perform a systematic review ofthe literature and meta-analysis of reported results.Recently, Pothier [25] performed a meta-analysis andconcluded that there are no differences in complicationrates between patients who underwent drainage incomparison with those who did not. However, the authordid not report other important outcomes such as length ofstay, did not assess the quality of the studies reviewed, anddid not present the type of surgical procedures and dia-gnosis, as recommended by the QUORUM statement [26].The objective of the present study is to measure the
beneficial or harmful effects of routine drainage on thefrequency of neck hematoma/seroma and length of stayin patients who have undergone thyroidectomy.
MATERIALS AND METHODS
All randomized controlled trials comparing the use ofpostoperative drainage versus no drainage in patients whounderwent elective partial or total thyroidectomy due tobenign or malignant disease were evaluated, irrespectiveof the number of patients randomized, database registry,and language of the article. The studies included adultpatients (older than 18 years) with a preoperative clinicaldiagnosis of benign (goiter, thyroiditis), indeterminate(follicular neoplasm) or malignant (papillary or follicularcarcinoma) disease of the thyroid, scheduled for partial ortotal thyroidectomy. Studies that included patients whoneeded radical or modified radical neck dissection as apart of surgical treatment and cases with giant goiters,were excluded.Interventions assessed were ‘‘active’’ (closed wound
suction) postoperative drainage versus no drainage andoutcomes measured were neck hematoma/seroma,detected clinically or by an imaging exam, recorded asyes or no (primary outcome) and length of hospital stay(secondary outcome). All outcome measures wereconfined to the period of hospitalization and the 30 daysafter discharge.
Search Strategy
We searched The Cochrane Central Register of Cont-rolled Trials (CENTRAL) on The Cochrane Library(Issue 4, 2005), The National Library of Medicine(PubMed) (1966 to February 2006), The IntelligentGateway to Biomedical and Pharmacological Informa-tion (EMBASE) (1980 to February 2006), The LatinA-merican and Caribbean Health Sciences Library(LILACS) (1980 to February 2006), and Science CitationIndex Expanded (SCI-EXPANDED) (1980 to February2006). The search strategy identified studies in all langu-ages. When necessary, non-English language papers were
translated for a full assessment. The search strategy forthe review was constructed by using a combination ofMESH subject headings and text words (thyroid diseases,thyroid neoplasms, parathyroid, thyroidectomy, surgery,drainage), relating to the use of drains in partial or totalthyroidectomy. Authors of included trials were contactedto seek further information on any published, unpub-lished, and ongoing trials. We also checked the referencelists of all the identified trials for more relevant reports.If inclusion criteria were not fulfilled, trials were
excluded and reasons for exclusion were listed. Metho-dological quality assessment was performed includingevaluation of randomization, allocation concealment,blinding, lost to follow-up and intention to treat analysis,and each criterion was classified as adequate, inadequateor unclear, as stated by the Cochrane Reviewers’Handbook [27].Inclusion and exclusion criteria were recorded for each
trial. Details regarding the use of drains in the post-operative period, disease that indicated surgery (benignor malignant), type of surgical resection, length ofhospital stay, presence or absence of neck hematoma/seroma and necessity for procedures to manage theselocal complications were recorded. Data regarding themethodological quality as number of randomized patients,number of patients not randomized, and reasons for non-randomization, ‘‘drop-outs,’’ blinding of patient and ob-server and intention-to-treat analysis were also recorded.Parathyroid surgery was included in the search
strategy, and some of the studies reviewed reportedsome parathyroidectomies, Kristoffersson et al. [12]included 26 patients who underwent parathyroidectomy,representing 26% of the study population and Ayyashet al. [15] included 7 patients, representing 7% of thatpopulation. Only these 33 patients, constituting 2.6% ofthe total population analyzed, had been submitted toparathyroidectomy. Consequently, these individuals wereeliminated from the study, and conclusions of this studycannot be applied to this subgroup of patients.
Statistics
The statistical package STATA 8.0 was used. Fordichotomous outcomes, the impact of the interventionwas expressed as an odds ratio (OR) with 95% confidenceinterval; and for continuous outcomes, a mean differencewith 95% confidence interval was used. A random effectsmodel was used. The Chi-square test for heterogeneitywas used to provide an indication of between-studyheterogeneity, and the degree of heterogeneity observedwas quantified using the I-squared statistic. Sensitivityanalysis was performed using trials with high methodo-logical quality. Causes of heterogeneity, where hetero-geneity was found, (Chi-squared test P< 0.10) were
Journal of Surgical Oncology DOI 10.1002/jso
274 Sanabria et al.
![Page 3: Routine drainage after thyroid surgery—A meta-analysis](https://reader030.vdocuments.net/reader030/viewer/2022020311/575005741a28ab1148a47676/html5/thumbnails/3.jpg)
explained subjectively. Funnel plot [28] and Begg test[29] were used to assess publication bias.
RESULTS
Sixteen studies were identified by the primary search[12–24,30–32]. One was excluded because it hadduplicated data [17], three because they compared twotypes of drains [19,20,30] and one more because it used asoft drain [14]. Fifteen studies were identified in MED-LINE and one in LILACS. Those from MEDLINE werein English and German and those from LILACS inSpanish. Inclusion criteria were similar for selected trials:adult patients admitted for elective thyroidectomy, withpreoperative diagnosis of benign or malignant condition.Peix et al. [16] admitted only patients with a diagnosis ofcold nodule and Tubergen et al. [31] admitted onlypatients with euthyroid goiter. Exclusion criteria alsowere similar for included studies: (a) associated neckdissection, (b) extension to thoracic cavity, (c) previousneck surgery, (d) hematologic disorders, and (e) para-thyroid surgery. Nonetheless, the Khanna et al. [24] studyreported 102 procedures corresponding to 94 patients,including eight partial thyroidectomies performed in asecond operative time on the same patients.
With the exception of one study, primary trials did notreport differences in age, gender, type of surgery, anddiagnosis between groups. The Ayyash et al. [15] andDebry et al. [21] studies reported no differences indiagnosis, but did not report the actual numbers. Pezzulloet al. [23] reported statistically significant differences inage and weight of the surgical specimen, which suggeststhe introduction of bias in the randomization andassigning process.
The Hurtado-Lopez et al. [22] study randomizedpatients to three groups: a control group, a soft draingroup, and a suction drain group. We decided to excludepatients from the soft drain group, because there was aclear clinical difference between it and the suction group.
All the included procedures reported by Peix et al. [16]and Kristoffersson et al. [12] were unilateral lobectomy.Schoretsanitis et al. [18] and Tubergen et al. [31] includedonly near total and unilateral thyroidectomy. The otherstudies included all types of thyroid operations. Debryet al. [21] included four patients with central compartmentdissection, without complications in any of them. Hurtado-Lopez et al. [22], Debry et al. [21], Wihlborg et al. [13],Pezzullo et al. [23], Kristoffersson et al. [12], and Susluet al. [32] studies did not report criteria for drain removal.Peix et al. [16] removed drains after ‘‘24–48 hr’’ andTubergen et al. [31] at the second postoperative day.Ayyash et al. [15] and Khanna et al. [24] removed thedrain when drainage was less than 30 ml/24 hr and
Schoretsanitis et al. [18] when drainage was less than25 ml/24 hr.
Hematoma/seroma was defined clinically by physi-cians, but criteria used were not stated. Debry et al. [21]used ultrasonography in case of doubt and Khannaet al. [24] and Tubergen et al. [31] used postoperativelyultrasonography in all cases.
Methodological Quality
Studies included were parallel randomized controlledtrials. Randomization was considered adequate in theDebry et al. [21], Schoretsanitis et al. [18], and Khannaet al. [24] studies, and unclear in the others because theydidn’t specify the method used. Allocation concealmentwas adequate in the Peix et al. [16], Ayyash et al. [15], andKristoffersson et al. [12] studies, which used sealedenvelopes, inadequate in Debry et al. [21] and unclear inthe others because they didn’t specify the method used.The Pezzullo et al. [23] study describes a procedure ofrandomization and allocation concealment, but their datareveal statistical differences in patient age and specimenweight that could be related to some bias in these qualitycharacteristics. Double blinding was not performed in thestudies, for the obvious reason of the impossibility ofblinding the intervention. However, only the Peixet al. [16] study used a mechanism to decrease thepossibility of bias, using an independent evaluator ofoutcome. Follow-up was adequate in all studies and noneof them reported dropouts. Intention to treat analysis forprimary outcomes was made in all studies.
Outcomes
The eleven studies recruited a total of 1244 patients:617 in the drainage group and 627 in the no drainagegroup. Distribution of type of thyroidectomy, diagnosisand length of hospital stay are shown in Table I. For theDebry et al. [21] study, we found an inconsistency in thenumber and group with hematoma/seroma reported in thetext and in table IV. However the text clearly stated thatall hematoma/seroma occurred in the drainage group, sonumbers were registered in this way.
Thirty-three of 617 (5.35%) patients in the drainagegroup and 30 of 627 (4.78%) in the no drainage groupdeveloped a postoperative neck hematoma/seroma,respectively. The OR was 1.06 (95% CI 0.62–1.82). Nostatistically significant differences or heterogeneity wereobserved (P¼ 0.570) (Fig. 1).
Only Peix et al. [16], Schoretsanitis et al. [18],Hurtado-Lopez et al. [22], Pezzullo et al. [23], Tubergenet al. [31] and Suslu et al. [32] reported standard deviationfigures with respect to length of hospital stay. Debryet al. [21] and Ayyash et al. [15] reported length ofhospital stay but without a standard deviation and others
Journal of Surgical Oncology DOI 10.1002/jso
Routine Drainage After Thyroid Surgery 275
![Page 4: Routine drainage after thyroid surgery—A meta-analysis](https://reader030.vdocuments.net/reader030/viewer/2022020311/575005741a28ab1148a47676/html5/thumbnails/4.jpg)
didn’t reported length of hospital stay, so their data wereimpossible to use in the meta-analysis. Among the groupswith useable data, the mean difference was 1.48 days(95% CI 1.35–1.62), greater for the drain group, but theheterogeneity test was statistically significant (P< 0.01;I2 ¼ 88% (Fig. 2).In the Hurtado-Lopez et al. [22], Peix et al. [16]
Schoretsanitis et al. [18] Tubergen et al. [31] and Susluet al. [32] studies, lengths of stay had statisticallysignificant longer stays for the drainage group. In thePezzullo et al. [23], Debry et al. [21] and Ayyashet al. [15] studies, stays were longer for drainage groupbut the differences were not statistically significant.In the Hurtado-Lopez et al. [22] study, four patients
developed postoperative neck hematoma/seroma. Twopatients in the no drainage group were managed withaspiration. There was no report of management of the twopatients with hematoma/seroma in the drainage group. Inthe Ayyash et al. [15] study, two of the seven patients withhematoma/seroma in the no drainage group requiredintervention, but neither of the two patients withhematoma/seroma in the drainage group needed it. Inthe Kristoffersson et al. [12] study, the single patient withhematoma/seroma from the drainage group requiredevacuation. In the Wihlborg et al. [13] study, onepatient in each group needed reoperation, while in theSchoretsanitis et al. [18] study two patients from the nodrainage group and one from the drainage group werereoperated. In the Tubergen et al. [31] study two patientsfrom the drainage group needed intervention and in theSuslu et al. [32] study two patients from the drainagegroup needed reintervention and one patient in the non-drainage group was treated with multiple needle aspira-tions. None of the patients in the Peix et al. [16], Debryet al. [21], and Pezzullo et al. [23] studies neededintervention of the hematoma/seroma. In total, 10patients in the drainage group and 5 in the no drainagegroup needed an intervention.Although cosmetic results and discomfort were not
subjects of the meta-analysis, it is of interest that Ayyashet al. [15] stated that cosmetic results were equal at4 weeks follow-up, and Kristoffersson et al. [12] did notfind statistical differences in subjective or objective signsof discomfort at 1 and 3 months postoperatively.A funnel plot for selected studies is shown in Figure 3.
The adjusted rank correlation test and the regressionasymmetry test were not statistically significant (inter-cept P-value¼ 0.259) which does not support a publica-tion bias.We performed a sensitivity analysis by methodological
quality, excluding the Debry et al. [21] and Pezzulloet al. [23] studies, because of the inadequate randomiza-tion and allocation concealment. The OR for neckcollections (OR 0.98, IC 95% 0.55–1.72) and length of
Journal of Surgical Oncology DOI 10.1002/jso
TABLEI.
ClinicalCharacteristics
ofIncluded
Studies
Study
Year
Typeofthyroidectomy
Diagnosis
Total
Partial
Benign
Malignanta
Length
ofstay
(days)
(mean�SD)
Drain
Nodrain
Total
Drain
Nodrain
Total
Drain
Nodrain
Total
Drain
Nodrain
Total
Drain
Nodrain
Total
Kristofferssonet
al.[12]
1986
050
50
100
40
31
71
10
19
29
100
Wihlborg
etal.[13]
1988
10
11
21
65
64
129
51
50
101
25
24
49
150
Ayyashet
al.[15]
1991
63
944
47
91
00
4.4
4.15
100
Peixet
al.[16]
1992
048
49
97
36
39
75
12
10
22
3.81�1.06
3.26�1.33
97
Schoretsanitiset
al.[18]
1998
0100
100
200
85
88
173
15
12
27
3.4�0.65
1.6�0.58
200
Debry
etal.[21]
1999
21
19
40
22
38
60
00
2.09
1.72
100
Hurtado-Lopez
etal.[22]
2001
59
14
45
41
86
41
37
78
913
22
3.11�2.7
2�0.94
100
Pezzulloet
al.[23]
2001
76
13
23
24
47
22
24
46
86
14
5.9�2.4
4.7�1.9
60
Tubergen
etal.[31]
2001
52
48
100
52
48
100
4.56�1.09
3.88�1.3
100
Khannaet
al.[24]
2005
3.71
3.07
102
Susluet
al.[32]
2006
31
29
60
37
38
75
68
67
135
2.6�1.0
1.3�0.7
135
Total
80
77
157
486
499
985
395
384
779
79
84
163
1,244
aIncludingundetermined
nodules.
276 Sanabria et al.
![Page 5: Routine drainage after thyroid surgery—A meta-analysis](https://reader030.vdocuments.net/reader030/viewer/2022020311/575005741a28ab1148a47676/html5/thumbnails/5.jpg)
hospital stay (mean difference 1.49, IC 95% 1.36–1.62)was not different from those globally reported.
DISCUSSION
Basis of the Analysis
Routine drainage for thyroid surgery is a controversialsubject. The use of passive drains, which was ineffectivefor its purpose of prevention of tracheal compression byhematoma has been supplanted by the availability and useof ‘‘active’’ simple portable closed wound suction drains,which serve mainly to prevent hematoma and seromabeneath the skin flaps. Thus the study was confined to use
of active suction drains and the outcomes included onlythe factors stated above.
While some authors have recommended the routineuse of drainage after thyroidectomy for the above statedreasons [1–5], this recommendation has been debatedextensively in the literature [6–11]. Ruark and Abdel-Misih [6] reviewed retrospectively 110 thyroid operationswithout drainage, without encountering a single instanceof acute hematoma, nor did Ariyanayagam et al. [7] in aretrospective review of 260 thyroid procedures performedwithout drainage. The latter series included toxic goitersand reoperations. Daou [9] studied prospectively 150thyroid procedures without drainage, and found only two
Journal of Surgical Oncology DOI 10.1002/jso
Fig. 1. Forrest plot for the frequency of neck hematoma/seroma.
Fig. 2. Forrest plot for the length of stay in thyroidectomy. Fig. 3. Funnel plot of included studies.
Routine Drainage After Thyroid Surgery 277
![Page 6: Routine drainage after thyroid surgery—A meta-analysis](https://reader030.vdocuments.net/reader030/viewer/2022020311/575005741a28ab1148a47676/html5/thumbnails/6.jpg)
late hematomas. Defechereux et al. [10] with 1,789 andTabaqchali et al. [11] reviewed 606 thyroidectomies inretrospective comparative studies, and found no statisti-cally significant differences between drainage and nodrainage groups. These studies, however, are prone tobias because of their retrospective or non-randomizedcomparative design.Some randomized controlled trials were performed to
solve this difficulty [12–24]. None of them were able todemonstrate statistically significant differences in thefrequency of acute or late neck hematoma/seroma.However, some studies included groups with soft drains,which have a drainage mechanism different fromnegative pressure suction drains, or compared differenttypes of drains, variables that could introduce significantheterogeneity. Each individual study was unable toaccrue a large enough sample size and had insufficientpower to definitively answer the question of the utility ofthyroid surgery drainage. As the complication of seroma/hematoma occurs in only about 5% of cases, a cohort ofapproximately 1,000 patients would be necessary in orderto find a 50% reduction in incidence attributable to anyintervention. Thus, systematic review with meta-analysiscould help to overcome this difficulty because it canincrease the power of individual studies if they areclinically and statistically homogeneous.
Quality of Studies Evaluated
In this study, it was possible to find 11 randomizedcontrolled trials [12,13,15,16,18,21–24,31,32], clinicallyand statistically homogeneous that were appropriate for ameta-analysis. In general terms, the quality of studiesincluded was acceptable. Unfortunately, most studies donot report broadly each step in the trial design, assuggested by the CONSORT statement [33], whichclassifies many quality criteria as unclear. This makes itdifficult to assess methodological quality. Only the Debryet al. [21] study had a clear violation of assignationconcealment and the Pezzullo et al. [23] study had astatistically significant difference in the groups at thebeginning, which suggests a bias in randomization andassignation process. A subgroup analysis excluding thesestudies did not show any difference compared withthe global summary OR, which support the results of themeta-analysis adjusted by methodological quality. Inaddition, study conclusions are not at risk because ofpublication bias, which makes the results stronger.
Conclusions of the Analysis
Results of this systematic review confirm that routinedrainage in thyroid surgery does not offer any advantagein decreasing the frequency of acute or late neckhematoma/seroma compared with no drainage. With the
number of patients included, this study has a posterioripower calculation of 80% to find an absolute 3%difference between groups. Moreover, when neck hema-toma/seroma was analyzed, there had been no differencein management between the two groups.As a secondary outcome, this study evaluated length of
hospital stay, because randomized studies, as well ascommon logic suggests a delay in hospital discharge forthe drainage group. Meta-analysis showed an increase oflength of hospital stay in drainage group of 1.49 days, butthis result should be analyzed carefully, because the testfor heterogeneity was statistically significant. With theexception of the Ayyash et al. [15] study, all the studiesfound an increase in length of hospital stay in drainagegroups; statistically significant in three. Therefore, thesummary result probably represents a real difference. Onthe other hand, a bias against the no drainage group inlength of hospital stay measures must be recognized,because trials included did not report an early dischargestrategy for patients without drainage, and length ofhospital stay found for the no drainage groups couldrepresent the clinical routine that was applied to drainedpatients. Thus, it is expected that no drainage couldproduce a more significant decrease in length of stay if anearly hospital discharge policy is considered. Moreover,as only randomized controlled trials were included,influence of other variables that could modify the lengthof stay such as particular health care reimbursements andlocal practices, was counterbalanced in each individualtrial. The results of this systematic review indicate thatlength of hospital stay could be unnecessarily prolongedwhen routine drainage is used.It is important to realize that conclusions of this study
can only be applied to patients who undergo total orsubtotal thyroidectomy for benign or malignant diseasebut without previous neck surgery, hemostasis disorders,extension to the thoracic cavity or those who require neckdissection. It is possible that this concept can beextended. A recent report by Lee et al. [34] concludedthat thyroidectomy without drains is safe and effectiveeven in combination with central neck dissection withseveral advantages to the patients compared to routinedrainage and with significant reduction of hospital stay.Nevertheless, central neck dissection as defined by thisgroup consisted only of dissection of level VI lymphnodes and did not include dissection of the lateral neck(levels III and IV) which is considered ‘‘central neckdissection’’ by many other surgeons.
Practical Considerations
Despite many prospective randomized studies andmeta-analyses, the issue of routine use of drains inthyroid surgery remains controversial. The reasons
Journal of Surgical Oncology DOI 10.1002/jso
278 Sanabria et al.
![Page 7: Routine drainage after thyroid surgery—A meta-analysis](https://reader030.vdocuments.net/reader030/viewer/2022020311/575005741a28ab1148a47676/html5/thumbnails/7.jpg)
include attitudes of individual surgeons, the size andextent of the operative field, and fear of trachealcompression from major postoperative bleeding. Manysenior surgeons, who have used drains successfullythroughout their careers will continue to use drains inthyroid surgery. Surgeons generally will use drains ifthere is a large dead space, a concern for bleeding, an‘‘oozing’’ thyroid bed, or if any other unusual concernabout postoperative accumulation of blood or fluidbeneath the skin flaps. Though the drains do not preventhematoma, observation of blood issuing from the drainsin the immediate postoperative period may expedite earlydiagnosis of significant hemorrhage. Such hemorrhage,confined to a closed space around the trachea maycompromise the airway. Drains alone cannot decompressan expanding hematoma from major arterial bleeding,and the complication must be treated by immediatelyreopening the wound. Fortunately, this occurrence isquite rare, but may be encountered once or twice duringthe career of an experienced surgeon, and its possibilityshould always be considered.
In a series by Shaha and Jaffe [1], the majority of thehematomas occurred in patients with drains in place, butthis may represent preselection of cases at greater risk.The meta-analysis presented here did confirm that theincidence of hematoma and seroma remain unchangedwith or without drains.
This meta-analysis also offers important clinicalinformation related to the length of hospitalization withthe drains. The presence of drains will usually commit thepatient to, at least, an overnight stay. Although patientscould be discharged with drains in place, most are quitereluctant to go home under such circumstances.
Another issue is the type of drain. The majority ofsurgeons today use a portable closed suction drainagesystem. The fear of retrograde contamination has beenexpressed, but is generally not accepted as a significantcause of postoperative infection. In general, the overalluse of drains in thyroid surgery appears to be veryselective and almost 80% of the thyroid surgeries, at thepresent time, are performed without the use of drains.
CONCLUSIONS
While drains have been employed routinely for manyyears in order to prevent postoperative hematoma orseroma formation after thyroid or parathyroid surgery, ameta-analysis of 11 prospective randomized studiestotaling 1,244 patients revealed no significant differencein the incidence of postoperative hematoma or seroma inpatients in whom postoperative drains were or were notplaced. In addition, there was an increase in length ofhospital stay for the patients with drains, found to be
statistically significant in three of 11 studies. Patientswith giant goiters, mediastinal dissection or neckdissection were not included in the analysis, nor werepatients in whom soft ‘‘passive’’ drains had been used.The meta-analysis demonstrates no advantage withregard to prevention of hematoma or seroma by theroutine placement of postoperative closed wound suctiondrains beneath the skin flaps after uncomplicated thyroidsurgery.
REFERENCES
1. Shaha AR, Jaffe BM: Selective use of drains in thyroid surgery.J Surg Oncol 1993;52:241–243.
2. Jeng LB, Chen MF: The use of a small feeding tube for suctiondrainage after thyroidectomy. Changgeng Yi Xue Za Zhi 1994;17:235–238.
3. Karayacin K, Besim H, Ercan F, Hamamci O, Korkmaz A:Thyroidectomy with and without drains. East Afr Med J 1997;74:431–432.
4. Ardito G, Revelli L, Guidi ML, et al.: Drainage in thyroid surgery.Ann Ital Chir 1999;70:511–516. (in Italian)
5. Williams J, Toews D, Prince M: Survey of the use of suctiondrains in head and neck surgery and analysis of theirbiomechanical properties. J Otolaryngol 2003;32:16–22.
6. Ruark DS, Abdel-Misih RZ: Thyroid and parathyroid surgerywithout drains. Head Neck 1992;14:285–287.
7. Ariyanayagam DC, Naraynsingh V, Busby D, Sieunarine K, RajuG, Jankey N: Thyroid surgery without drainage: 15 years ofclinical experience. J R Coll Surg Edinb 1993;38:69–70.
8. Wax MK, Valiulis AP, Hurst MK: Drains in thyroid andparathyroid surgery. Are they necessary? Arch Otolaryngol HeadNeck Surg 1995;121:981–983.
9. Daou R: Thyroidectomy without drainage. Chirurgie 1997;122:408–410. (in French)
10. Defechereux T, Hamoir E, Nguyen DD, Meurisse M: Drainage inthyroid surgery. Is it always a must? Ann Chir 1997;51:647–652. (in French)
11. Tabaqchali MA, Hanson JM, Proud G: Drains for thyroidectomy/parathyroidectomy: Fact or fiction? Ann R Coll Surg Engl1999;81:302–305.
12. Kristoffersson A, Sandzen B, Jarhult J: Drainage in uncompli-cated thyroid and parathyroid surgery. Br J Surg 1986;73:121–122.
13. Wihlborg O, Bergljung L, Martensson H: To drain or not to drainin thyroid surgery. A controlled clinical study. Arch Surg1988;123:40–41.
14. Perez M, Rubiano J, Mendez M, Garcia A: Inutilidad de drenajesen cirugia tioridea. Estudio clinico controlado. Colombia Medica1989;20:148–150.
15. Ayyash K, Khammash M, Tibblin S: Drain vs. no drain inprimary thyroid and parathyroid surgery. Eur J Surg 1991;157:113–114.
16. Peix JL, Teboul F, Feldman H, Massard JL: Drainage afterthyroidectomy: A randomized clinical trial. Int Surg 1992;77:122–124.
17. Teboul F, Peix JL, Guibaud L, Massard JL, Ecochard R:Prophylactic drainage after thyroidectomy: A randomized trial.Ann Chir 1992;46:902–904. (in French)
18. Schoretsanitis G, Melissas J, Sanidas E, Christodoulakis M,Vlachonikolis JG, Tsiftsis DD: Does draining the neck affectmorbidity following thyroid surgery? Am Surg 1998;64:778–780.
19. Schwarz W, Willy C, Ndjee C: Gravity or suction drainage inthyroid surgery? Control of efficacy with ultrasound determina-tion of residual hematoma. Langenbecks Arch Chir 1996;381:337–342. (in German)
Journal of Surgical Oncology DOI 10.1002/jso
Routine Drainage After Thyroid Surgery 279
![Page 8: Routine drainage after thyroid surgery—A meta-analysis](https://reader030.vdocuments.net/reader030/viewer/2022020311/575005741a28ab1148a47676/html5/thumbnails/8.jpg)
20. Willy C, Steinbronn S, Sterk J, Gerngross H, Schwarz W:Drainage systems in thyroid surgery: A randomised trialof passive and suction drainage. Eur J Surg 1998;164:935–940.
21. Debry C, Renou G, Fingerhut A: Drainage after thyroid surgery: Aprospective randomized study. J Laryngol Otol 1999;113:49–51.
22. Hurtado-Lopez LM, Lopez-Romero S, Rizzo-Fuentes C,Zaldivar-Ramirez FR, Cervantes-Sanchez C: Selective use ofdrains in thyroid surgery. Head Neck 2001;23:189–193.
23. Pezzullo L, Chiofalo MG, Caraco C, Marone U, Celentano E,Mozzillo N: Drainage in thyroid surgery: A prospectiverandomised clinical study. Chir Ital 2001;53:345–347. (in Italian)
24. Khanna J, Mohil RS, Chintamani, et al.: Is the routine drainage aftersurgery for thyroid necessary? A prospective randomized clinicalstudy [ISRCTN63623153]. BMC Surg 2005; 5:11.
25. Pothier M: The use of drains following thyroid and parathy-roid surgery: A meta-analysis. J Laryngol Otol 2005;119:669–671.
26. Moher D, Cook D, Eastwood S, Olkin I, Rennie D, Stroup D:Improving the quality of reports of meta-analyses of randomisedcontrolled trials: The QUOROM statement. Lancet 1999;354:1896–1900.
27. Alderson P, Green S, Higgins JPT (eds): CochraneReviewers’ Handbook 4. 2. 2 [updated December 2003]. The
Cochrane Library. Chichester, UK: John Wiley & Sons, Ltd,2004.
28. Egger M, Davey Smith G, Schneider M, Minder C: Bias in meta-analysis detected by a simple, graphical test. BMJ 1997;315:629–634.
29. Begg CB, Mazumdar M: Operating characteristics of a rankcorrelation test for publication bias. Biometrics 1994;50:1088–1101.
30. De Salvo L, Arezzo A, Razzetta F, Tassone U, Mattioli FP:Connection between the type of drainage and sepsis in thyroidsurgery. Ann Ital Chir 1998;69:165–167. (in Italian)
31. Tubergen D, Moning E, Richter A, Lorenz D: Assessment of draininsertion in thyroid surgery? Zentralbl Chir 2001;126:960–963.(in German)
32. Suslu N, Vural S, Oncel M, et al.: Is the insertion of drains afteruncomplicated thyroid surgery always necessary? Surg Today2006;36:215–218.
33. Altman DG, Schulz KF, Moher D, et al.: The revised CONSORTstatement for reporting randomized trials: explanation andelaboration. Ann Intern Med 2001;134:663–694.
34. Lee SW, Choi EC, Lee YM, Lee JY, Kim SC, Koh YW. Is lack ofplacement of drains after thyroidectomy with central neckdissection safe? A prospective, randomized study. Laryngoscope2006;116:1632–1635.
Journal of Surgical Oncology DOI 10.1002/jso
280 Sanabria et al.