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Transvaginal Mesh Lawsuit News: Bernstein Liebhard LLP Comments on New Study Finding that Vaginal Mesh Does Not Improve Pelvic Organ Prolapse Cure Rate
Date:9/13/2013

New York, NY (PRWEB) September 13, 2013

As transvaginal mesh lawsuits (http://www.meshrecall.com/) continue to move forward in courts around the country, Bernstein Liebhard LLP notes that a new study has found that the use of vaginal mesh in pelvic prolapse repair does not appear to be associated with improved cure rates compared to traditional non-mesh procedures. The study, which was published on September 9th in the journal, Obstetrics & Gynecology, found no difference in the three-year cure rates between the two groups. However, the research was halted early due to a mesh exposure rate of more than 15%. Three women in the mesh group also required revision surgery for recurrent prolapse, while none in the non-mesh group experienced this complication. The study followed 65 women, 33 of whom received vaginal mesh, with the remainder undergoing a non-mesh procedure.*

“The issues that brought this study to a halt echo the types of vaginal mesh complications many of our own clients have allegedly suffered. Its results also confirm that the use of vaginal mesh in pelvic organ prolapse repair may carry substantial risks compared to alternate procedures, without offering patients any additional benefits,” says Bernstein Liebhard LLP, a nationwide law firm representing victims of defective drugs and medical devices. The Firm is currently representing hundreds of women in vaginal mesh lawsuits who suffered mesh erosion, pain, scarring, infection and other serious injuries, allegedly due to transvaginal mesh products marketed by American Medical Systems, Inc., Boston Scientific, Inc., C.R. Bard and Ethicon, Inc.

Vaginal Mesh Lawsuits
Transvaginal mesh has been the subject of growing safety concerns since October 2008, when the

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