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Long-term mesh exposure after minimally invasive total hysterectomy and sacrocolpopexy.
Matthews, Catherine A; Myers, Erinn M; Henley, Barbara R; Kenton, Kimberly; Weaver, Erica; Wu, Jennifer M; Geller, Elizabeth J.
  • Matthews CA; Department of Urology, Atrium Wake Forest Baptist Health, 1 Medical Center Boulevard, Winston Salem, NC, 27101, USA. camatthe@wakehealth.edu.
  • Myers EM; Atrium Health, Charlotte, NC, USA.
  • Henley BR; Augusta University, Augusta, GA, USA.
  • Kenton K; Northwestern Feinstein School of Medicine, Chicago, IL, USA.
  • Weaver E; Department of Urology, Atrium Wake Forest Baptist Health, 1 Medical Center Boulevard, Winston Salem, NC, 27101, USA.
  • Wu JM; Departments of Obstetrics and Gynecology, University of North Carolina, Chapel Hill, NC, USA.
  • Geller EJ; Departments of Obstetrics and Gynecology, University of North Carolina, Chapel Hill, NC, USA.
Int Urogynecol J ; 2022 Nov 02.
Article in English | MEDLINE | ID: covidwho-2243204
ABSTRACT
INTRODUCTION AND

HYPOTHESIS:

The objective was to evaluate total and incident mesh exposure rates at least 2 years after minimally invasive total hysterectomy and sacrocolpopexy. Secondary aims were to evaluate surgical success and late adverse events.

METHODS:

This extension study included women previously enrolled in the multicenter randomized trial of permanent vs delayed-absorbable suture with lightweight mesh for > stage II uterovaginal prolapse. Owing to COVID-19, women were given the option of an in-person (questionnaires and examination) or telephone visit (questionnaires only). The primary outcome was total and incident suture or mesh exposure, or symptoms suggestive of mesh exposure in women without an examination. Secondary outcomes were surgical success, which was defined as no subjective bulge, no prolapse beyond the hymen, and no pelvic organ prolapse retreatment, and adverse events.

RESULTS:

A total of 182 out of 200 previously randomized participants were eligible for inclusion, of whom 106 (58%) women (78 in-person and 28 via questionnaire only) agreed to the extension study. At a mean of 3.9 years post-surgery, the rate of mesh or suture exposure was 7.7% (14 out of 182) of whom only 2 were incident cases reported after 1-year follow-up. None reported vaginal bleeding or discharge, dyspareunia, or penile dyspareunia. Surgical success was 93 out of 106 (87.7%) 13 out of 94 (13.8%) failed by bulge symptoms, 2 out of 78 (2.6%) by prolapse beyond the hymen, 1 out of 85 (1.2%) by retreatment with pessary, and 0 by retreatment with surgery. There were no serious adverse events.

CONCLUSIONS:

The rate of incident mesh exposure between 1 and 3.9 years post-surgery was low, success rates remained high, and there were no delayed serious adverse events.
Keywords

Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Topics: Long Covid Language: English Journal subject: Gynecology / Urology Year: 2022 Document Type: Article Affiliation country: S00192-022-05388-y

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Topics: Long Covid Language: English Journal subject: Gynecology / Urology Year: 2022 Document Type: Article Affiliation country: S00192-022-05388-y