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Volume 198, Issue 5, Pages 639-644 (November 2009)


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Seroma in ventral incisional herniorrhaphy: incidence, predictors and outcome

Haytham M.A. Kaafarani, M.D., M.P.H.abc, Kwan Hur, Ph.D.d, Angie Hirter, M.S., M.P.H.d, Lawrence T. Kim, M.D.ef, Anthony Thomas, M.D.gh, David H. Berger, M.D., M.H.C.M.ij, Domenic Reda, Ph.D.d, Kamal M.F. Itani, M.D.aklCorresponding Author Informationemail address

Received 4 May 2009; received in revised form 2 July 2009

Abstract 

Background

Factors leading to seroma following ventral incisional herniorrhaphy (VIH) are poorly understood.

Methods

Between 2004 and 2006, patients were prospectively randomized at 4 Veterans Affairs hospitals to undergo laparoscopic or open VIH. Patients who developed seromas within 8 weeks postoperatively were compared with those who did not. Multivariate analyses were performed to identify predictors of seroma.

Results

Of 145 patients who underwent VIH, 24 (16.6%) developed seromas. Patients who underwent open VIH had more seromas than those who underwent laparoscopic VIH (23.3% vs 6.8%, P = .011). Seroma patients had hernias that were never spontaneously reducible (0% vs 21%, P = .015), had more abdominal incisions preoperatively (mean, 2.4 vs 1.8; P = .037), and were less likely to have drain catheters placed than those without seromas (30.0% vs 63.1%, P = .011). In multivariate analyses, open VIH predicted seroma (odds ratio, 5.5; 95% confidence interval, 1.6–18.8), as well as the specific hospital at which the procedure was performed. Spontaneous resolution occurred in 71% of seromas; 29% required aspiration.

Conclusions

Procedural characteristics and hernia characteristics rather than patient comorbidities predicted seroma in VIH.

a VA Boston Healthcare System, West Roxbury, MA, USA

b University of South Florida, Tampa, FL, USA

c Harvard School of Public Health, Boston, MA, USA

d The VA Cooperative Studies Program Coordinating Center, Hines, IL, USA

e Central Arkansas Veterans Health Care System, Little Rock, AR, USA

f University of Arkansas for Medical Sciences, Little Rock, AR, USA

g The North Texas VA Health Care System, Dallas, TX, USA

h Southwestern University, Dallas, TX, USA

i The Michael E. DeBakey VA Medical Center, Houston, TX, USA

j Baylor College of Medicine, Houston, TX, USA

k Boston University School of Medicine, Boston, MA, USA

l Harvard Medical School, Boston, MA, USA

Corresponding Author InformationCorresponding author: Tel.: 857-203-6205; fax: 857-203-5549

PII: S0002-9610(09)00446-2

doi:10.1016/j.amjsurg.2009.07.019


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