Transactions from the Thirty-Second Annual Scientific Meeting of the Society of Gynecologic Surgeons
Obesity and retropubic surgery for stress incontinence: Is there really an increased risk of intraoperative complications?

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Objective

The objective of the study was to evaluate the impact of obesity on length of surgery, blood loss, and intra- and postoperative complications in women who underwent retropubic surgery for stress urinary incontinence.

Study design

Of 449 women participating in a multicenter, randomized trial evaluating antibiotic prophylaxis in women with suprapubic catheters, 250 women underwent retropubic anti-incontinence procedures. This is a prospective nested cohort study of these women, 79 (32%) of whom were obese (body mass index 30 or greater) and 171 (68%) overweight or normal weight (body mass index less than 30). Data collected included demographic variables, past medical history, physical examination, and intraoperative and postoperative complications. Data were analyzed with Fisher's exact for dichotomous variables, Student t tests for continuous variables, and analysis of variance for multivariate analysis. Significance was set at P < .05.

Results

Obese women undergoing stress urinary incontinence surgery were younger than nonobese women (48.7 versus 51.9 years, respectively, P < .019). The number and type of additional surgeries performed were similar between groups with the exception that obese women were less likely to undergo abdominal apical suspensions (P = .006) or abdominal paravaginal repairs (P = .001); therefore, estimated blood loss, change in hematocrit, length of stay, surgery, and suprapubic catheterization comparisons are adjusted for the performance of these procedures. Estimated surgical blood loss was greater for obese women (344 versus 284 P = .03); however, change in hematocrit was lower for obese than nonobese women (6.6 versus 7.3, P = .048). Mean length of surgery was 15 minutes longer in obese women (P = .02). Length of hospital stay did not vary between groups (P = NS). Major intraoperative complications were uncommon (14 [5.6%]), with no difference between weight groups. Incidence of postoperative urinary tract infection, wound infections, or postoperative major complications were likewise similar between groups (all P > .05).

Conclusion

Surgery takes longer for obese patients, but blood loss as recorded by change in hematocrit is lower. Major complications were rare and similar between weight groups, as were infectious complications.

Section snippets

Material and methods

Women participating in a multicenter, randomized trial to evaluate the use of prophylactic antibiotics in women who had suprapubic catheters placed after surgery for SUI were eligible to participate. All 6 sites obtained institutional review board approval. Two hundred fifty of the 449 women (56%) recruited for the main study underwent retropubic urethropexy as well as other reparative procedures, gave BMI data, and were included in the present analysis. Results of the main study have been

Results

Two hundred fifty women underwent retropubic urethropexy and gave BMI data, of whom 79 (32%) were obese, 92 (36%) overweight, and 79 (32%) normal weight. No differences in demographic or outcome variables between overweight and normal-weight women were observed (all P = NS); therefore, all comparisons are between obese and nonobese women. Retropubic procedures performed included 168 open Burch (67%), 12 laparoscopic Burch (5%), 44 Marshall-Marchetti-Krantz (18%), and 25 Ball-Burch procedures

Comment

Results of the National Health and Nutrition Examination Survey 1999 to 2000 indicate that an estimated 64% of U.S. adults are either overweight or obese.5 Obese women are at increased risk for SUI with each 5-unit increase in BMI, resulting in a 60% to 100% increase in the risk of daily incontinence.6, 7 Weight loss as small as 5% to 10% of body weight results in significant reduction of incontinence symptoms and should be part of the first line therapy for SUI for obese women.6, 7 Weight

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Supported in part by Department of Health and Human Services/National Institutes of Health/National Center Research Resources/General Clinical Research Center Grant 5M01 RR00997.

Presented at the 32nd Annual Meeting of the Society of Gynecologic Surgeons, April 3-5, 2006, Tucson, AZ.

Reprints not available from the authors.

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