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Comparison of two trocar-guided trans-vaginal mesh systems for repair of pelvic organ prolapse: a retrospective cohort study

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Abstract

Introduction and hypothesis

The aim of this study was to compare failure and complication rates in patients who underwent a trocar-guided vaginal mesh repair with either a non-absorbable or a partially absorbable mesh.

Methods

Retrospective analysis of prospectively collected data from consecutive women undergoing either non-absorbable or partially absorbable mesh for symptomatic stage 2 prolapse or higher were evaluated at 12 months. Outcome measures included objective and subjective failure rates, patient’s satisfaction, complications and perioperative outcomes.

Results

Five hundred and sixty-nine women (347 with non-absorbable mesh, 222 with partially absorbable mesh) were included. Failure rates were similar in the two groups; the re-operation rate in the untreated compartments was higher in the non-absorbable mesh group compared with the partially absorbable mesh group (5 % vs 1 %). Mesh exposure rate in the non-absorbable mesh group was 12 % and in the partially absorbable mesh group it was 5 %. Other complication and patient satisfaction rates were similar.

Conclusions

Non-absorbable and partially absorbable mesh demonstrated similar outcome rates at 12 months. The risk of reoperation was lower for partially absorbable mesh. The mesh exposure rate was significantly lower for the partially absorbable mesh group compared with the non-absorbable mesh group.

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Abbreviations

POP:

Pelvic organ prolapse

POP-Q:

Pelvic organ prolapse quantification

SUI:

Stress urinary incontinence

UUI:

Urgency urinary incontinence

NIH:

National Institutes of Health

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Acknowledgements

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Conflict of interest/disclaimers

Dr. Milani had a consultancy agreement with Ethicon Women’s Health and Urology. Drs. Withagen and Milani were on the speaker’s bureau of Ethicon Women’s Health and Urology in 2006–2010. Drs. Withagen and Vierhout received an unrestricted educational grant from Ethicon Women’s Health and Urology in 2005. The other authors did not report any potential conflicts of interest. Ethicon Women’s Health and Urology (the manufacturer of the Prolift and Prolift+M) had no influence over the design or the execution of the study. Also, no funding was obtained for this study.

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Correspondence to E. J. M. Lensen.

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Lensen, E.J.M., Withagen, M.I.J., Kluivers, K.B. et al. Comparison of two trocar-guided trans-vaginal mesh systems for repair of pelvic organ prolapse: a retrospective cohort study. Int Urogynecol J 24, 1723–1731 (2013). https://doi.org/10.1007/s00192-013-2098-7

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  • DOI: https://doi.org/10.1007/s00192-013-2098-7

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