Risk factors for mesh complications after trocar guided transvaginal mesh kit repair of anterior vaginal wall prolapse

Aims To identify risk factors for mesh exposures after anterior pelvic organ prolapse repair using a standardized trocar guided polypropylene mesh kit. Methods A secondary risk analysis combining patients from two prospective multicenter studies. Main outcome was clinical host‐vs‐implant reactions o...

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Published inNeurourology and urodynamics Vol. 31; no. 7; pp. 1165 - 1169
Main Authors Elmér, Caroline, Falconer, Christian, Hallin, Anders, Larsson, Gregor, Ek, Marion, Altman, Daniel
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.09.2012
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Summary:Aims To identify risk factors for mesh exposures after anterior pelvic organ prolapse repair using a standardized trocar guided polypropylene mesh kit. Methods A secondary risk analysis combining patients from two prospective multicenter studies. Main outcome was clinical host‐vs‐implant reactions one year after surgery using a macroscopic inflammatory scale. Results 353 patients were included in the study. Mean age at surgery was 65.3 (±9.6 SD) years and surgery was performed as a primary procedure in 224/353 (63.5%) patients. Mesh exposures, of which the majority were mild‐moderate, occurred in a total of 30/349 patients (8.6%). Multivariate logistic regression showed increased odds for mesh exposures for women who smoked before surgery (OR 3.48, 95% CI 1.18–10.28), who had given birth to more than two children (OR 2.64, 95% CI 1.07–6.51) and those with somatic inflammatory disease (OR 5.11, 95% CI 1.17–22.23). Age, body mass index, and menopausal status showed no significant association with clinical mesh exposures. Conclusions Smoking, multiple childbirth, and somatic inflammatory disease are possible risk factors for mesh exposure after trocar guided mesh kit surgery for anterior pelvic organ prolapse. Preoperative smoking cessation may decrease the risk for exposures. Neurourol. Urodynam. 31:1165–1169, 2012. © 2012 Wiley Periodicals, Inc.
Bibliography:ArticleID:NAU22231
The Regional Agreement on Medical Training and Clinical Research by the Stockholm County Council and Karolinska Institutet
ark:/67375/WNG-GLQG9GNM-Z
Conflict of interests: D.A. is an advisor to Gynecare Scandinavia and Ethicon US. C.F. is an advisor to Gynecare Scandinavia. None of the researchers in the Nordic transvaginal mesh group own stock or hold stock options in the mesh kit manufacturing company.
Dirk De Ridder led the peer-review process as the Associate Editor responsible for the paper.
Swedish Society of Medicine, Karolinska Institutet Research Foundations
Ethicon
Clinical trial registration: www.clinicaltrials.gov identifiers NCT00402844 and NCT00566917
Gynecare Scandinavia
istex:26C98ABCDB1CA94CB1843CC46E2E7E1503D4E6E0
identifiers NCT00402844 and NCT00566917
Clinical trial registration
Dirk De Ridder led the peer‐review process as the Associate Editor responsible for the paper.
www.clinicaltrials.gov
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0733-2467
1520-6777
1520-6777
DOI:10.1002/nau.22231