Where to for pelvic organ prolapse treatment after the FDA pronouncements?-Reference-Cited by-同舟云学术

Where to for pelvic organ prolapse treatment after the FDA pronouncements?

Published:2013-01-10 Issue:5 Volume:24 Page:707-718
ISSN:0937-3462
Container-title:International Urogynecology Journal
language:en
Short-container-title:Int Urogynecol J

Author:

van Geelen J. M.,Dwyer P. L.

Publisher

Springer Science and Business Media LLC

Subject

Urology,Obstetrics and Gynaecology

Link

http://link.springer.com/content/pdf/10.1007/s00192-012-2025-3.pdf

Reference92 articles.

1. Committee on Gynecologic Practice (2011) Committee opinion no. 513: vaginal placement of synthetic mesh for pelvic organ prolapse. Obstet Gynecol 118:1459–1464

2. Food and Drug Administration (2011) FDA Safety Communication: update on serious complications associated with transvaginal placement of surgical mesh for pelvic organ prolapse. http://www.fda.gov/MedicalDevices/Safety/AlertandNotices/umc262435.htm

3. Olsen AL, Smith VJ, Bergstrom JO, Colling JC, Clark AL (1997) Epidemiology of surgically managed pelvic organ prolapse and urinary incontinence. Obstet Gynecol 89:501–505

4. Hagen S, Stark D (2011) Conservative prevention and management of pelvic organ prolapse in women. Cochrane Database Syst Rev 12:CD003882

5. Kapoor DS, Thakar R, Sultan AH, Oliver R (2009) Conservative versus surgical management of prolapse: what dictates patient choice? Int Urogynecol J Pelvic Floor Dysfunct 20:1157–1161

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