Long-term follow-up of persistent vaginal polypropylene mesh exposure for transvaginally placed mesh procedures |
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Authors: | Xavier Deffieux Thibault Thubert Renaud de Tayrac Hervé Fernandez Vincent Letouzey |
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Affiliation: | Paris-Sud University, Obstetrics-Gynecology and Reproductive Medicine Department, Antoine Beclere Hospital, Public Assistance - Paris Hospitals (AP-HP), Clamart, 92141, France, x.deffieux@free.fr. |
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Abstract: | Introduction and hypothesis The surgical treatment of a cystocele via the vaginal route may require the placement of a synthetic mesh below the bladder. However, the placement of a synthetic mesh via the vaginal route can be associated with specific complications, such as vaginal mesh exposure. There is a lack of data concerning the long-term follow-up of asymptomatic persistent vaginal polypropylene mesh exposure. Methods This was a retrospective case series of nine patients presenting with persistent vaginal mesh exposure following the placement of a macroporous monofilament polypropylene mesh for cystocele treatment. Expectant management has been proposed since the patients were asymptomatic. Results The median follow-up duration was 121?months interquartile range (IQR) 119–132]. The median surface area of vaginal mesh exposure (1?cm2; IQR 1–1) did not change significantly during the follow-up. No pelvic or perineal abscess occurred during the follow-up. Only one of them was sexually active; she complained of dyspareunia at the last follow-up, but refused renewed surgery since she had sexual intercourse on only a small number of occasions per year. Clinical examination using the International Continence Society Pelvic Organ Prolapse Quantification system: Ba ?3 to ?2 (n?=?7; 88?%), Ba ?1 (n?=?1; 12?%), Ba 0 or greater (n?=?0). Conclusions Persistent asymptomatic vaginal polypropylene mesh exposure is associated with few complications at long-term follow-up. |
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