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Transvaginal Mesh Lawsuit Update: New Study Concerning Use of Vaginal Mesh in Prolapse Procedures, Bernstein Liebhard LLP Reports
Date:12/8/2012

New York, New York (PRWEB) December 08, 2012

As transvaginal mesh lawsuits continue to move forward in state and federal courts, a newly-published study has found that prolapse procedures that utilize vaginal mesh products rose significantly between 2005 and 2010, Bernstein Liebhard LLP reports. The study, published online November 19, 2012, in the American Journal of Obstetrics & Gynecology, drew on claims data to examine trends in vaginal mesh prolapse procedures (VMs), abdominal sacrocolpopexy (ASC), and minimally invasive sacrocolpopexy (MISC) from 2005 to 2010. Overall, 74.9% of the procedures performed during that time period were vaginal mesh surgeries, for an overall rate of 56.9 per 100,000 person-years.*

“The increase in the use of vaginal mesh products during the period covered by the study is consistent with the introduction to the market of various transvaginal mesh kits for the treatment of pelvic organ prolapse. In light of the recent regulatory advisories regarding transvaginal mesh devices, we do not believe this study reflects current trends,” says Bernstein Liebhard LLP, a nationwide law firm representing victims of defective drugs and medical devices. The firm is currently evaluating potential lawsuits on behalf of women who suffered mesh erosion, pain, scarring, infection and other serious injuries, allegedly due to vaginal mesh.

Transvaginal Mesh Lawsuits
In July 2011, the U.S. Food & Drug Administration (FDA) warned that there had been a five-fold increase in reports of serious complications associated with the use of transvaginal mesh. The FDA also modified its previous position on the frequency of such complications, stating in the alert that vaginal mesh injuries associated with POP repair were not rare.**

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