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A randomised comparison of single-incision versus traditional transobturator midurethral sling in women with stress urinary incontinence: results of a 24-month follow-up
Authors:René P Schellart  Katrien Oude Rengerink  Frank Van der Aa  Jean-Philippe Lucot  Bart Kimpe  Marcel G W Dijkgraaf  Jan-Paul W R Roovers
Institution:1.Department of Obstetrics and Gynecology,Spaarne Gasthuis,Haarlem,The Netherlands;2.Department of Obstetrics and Gynecology,Academic Medical Center Amsterdam,Amsterdam,The Netherlands;3.Department of Urology,University Hospitals Leuven,Leuven,Belgium;4.Department of Obstetrics and Gynecology,Jeanne de Flandre H?pital,Lille Cedex,France;5.Department of Urology,General Hospital Sint Lucas,Bruges,Belgium;6.Clinical Research Unit,Academic Medical Center Amsterdam,Amsterdam,The Netherlands
Abstract:

Introduction and hypothesis

Midurethral sling procedures have become the principal surgical treatment for women with stress urinary incontinence (SUI). The 1-year results of this international trial comparing the efficacy and morbidity of a single-incision midurethral sling (SIMS; MiniArc) and a transobturator standard midurethral sling (SMUS; Monarc) showed that MiniArc is non-inferior regarding subjective cure and superior with regard to postoperative pain and recovery. The objective was to compare subjective and objective cure, morbidity and surgery-related discomfort following SIMS and transobturator SMUS up to a 24-month follow-up.

Methods

We carried out a non-blinded, randomised, controlled trial. Women with symptomatic SUI were eligible. Primary outcome was subjective cure, defined as an improvement on the Patient Global Impression of Improvement (PGI-I), at 12, 24 and 36 months. Secondary outcomes were objective cure based on the cough stress test, disease-specific quality of life questionnaires, surgical parameters and physical performance during recovery. Analysis was by intent to treat. Differences between the two groups regarding dichotomous variables were Chi-squared tested and presented as relative risks (RR) with corresponding 95 % confidence intervals.

Results

We randomised 97 women to MiniArc and 96 to Monarc. At the 24-month follow-up, subjective cure was 84 % following MiniArc and 89 % following Monarc (RR ?5; 95% CI ?0.17 to 0.06). Objective cure was 93 % following MiniArc and 94 % following Monarc (RR ?1; 95% CI ?0.10 to 0.07). Both procedures have low complication rates.

Conclusions

At the 2-year follow-up, the non-prespecified analysis of this randomised trial showed that the MiniArc, a single-incision sling, had similar subjective and similar objective cure rates, although non-inferiority to Monarc for subjective cure could not be demonstrated.
Keywords:
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