Transvaginal Mesh (TVM) Lawyer Reports on Recent AJOG Publication on Failure Rates

FREE CASE EVALUATION: 1-800-632-1404

Tens of thousands of women receive a transvaginal mesh (TVM) device each and every year from numerous suppliers: American Medical Systems, Bard, Boston Scientific, Ethicon,Gynecare, and Johnson & Johnson.  Thousands of women have been injured through no fault of their own, including vaginal erosion, pain, urinary problems, bleeding, infection and more. Our attorneys are representing women in all fifty states and Canada who have been injured.  For a free case evaluation, call 1-800-632-1404.

New Article Published:

Many women who have suffered from bladder prolapse, pelvic prolapse and other related complications have had transvaginal mesh implanted to treat the problem. Atransvaginal mesh is a surgical mesh made from polyester or polypropylene and feels like a woven fabric and is implanted in the vagina. It reinforces the vaginal wall and creates what is at times referred to as a pelvic sling or baldder sling.

Dr. Andrew Sokol, among with others, recently published an article in the American Journal of Obstetrics & Gynecology, on the failure rates of transvaginal mesh (TVM) devices implanted for correction of pelvic organ prolapse (POP). You can read a copy of the Abstract for this article by clicking HERE. The article, entitled “One-year objective and functional outcomes of a randomized clinical trial of vaginal mesh for prolapse” was presented orally at the 31st annual meeting of the American Urogynecologic Society, Long Beach, CA, Sept. 30-Oct. 2, 2010. It was received at the Journal on 21 April 2011; received in revised form 6 July 2011; accepted 4 August 2011 and published online 12 August 2011. The authors are Andrew I. Sokol, MD, Cheryl B. Iglesia, MD, Bela I. Kudish, MD, Robert E. Gutman, MD, David Shveiky, MD, Richard Bercik, MD, Eric R. Sokol, MD.

The study found that women who are fitted with a transvaginal mesh device to treat pelvic organ prolapse typically require additional surgery more often than women who are treated using other methods. Pelvic organ prolapse (POP) is a condition that causes a weakening of the pelvic floor muscles in certain women. Depending on its severity, POP can cause the internal organs to bulge or sag outward through the vagina.

The study looked at post-treatment outcomes for 32 women who received a mesh implant and 33 women who underwent traditional prolapse repair methods. Researchers found that 15.6 percent of the women who received a transvaginal mesh device required additional surgery within one year of the initial treatment. They also concluded that women who were treated using other methods saw a comparable reduction in prolapse symptoms compared with mesh recipients.

Our team of attorneys is reviewing case evaluations for women across the country who have received TVM and TVT products from manufactures such as C.R. Bard, Avaulta, Boston Scientific, and Johnson & Johnson’s Ethicon.

If you need help from a transvaginal mesh device injury, call us today for help.

The Problem

In 2008, the FDA first released concerns about the safety of transvaginal placement of mesh. From 2008 to 2010, the FDA received three to five times as many adverse reports associated with mesh used for pelvic organ prolapse repair than what agency received from 2005 to 2007 (nearly 1,000 reports of adverse events were received from 2005-2007).

Many of these patients complain because of erosion or contraction of the mesh material (which has been described as being of a similar material as Rubbermaid storage containers).  The erosion leads to bleeding, severe pelvic pain, painful (or impossible) sexual performance and a recurrence of urinary problems.

In July 2011, the Food and Drug Administration (FDA) issued an update related to what it called ‘serious complications’ related to the use of vaginal mesh for treatment of pelvic organ prolapse (POP) and stress urinary incontinence (SUI).  It is now known that complications linked to transvaginal placement of surgical mesh in SUI and POP patients are not rare and can require multiple surgeries to correct problems related to the use of surgical mesh. In fact, the FDA now says that additional surgeries may actually not be able to repair damage caused by implantation of the mesh.

In other words, the side effects of the mesh placement may be permanent.  These complications from transvaginal placement of surgical mesh include:

  • -Erosion of the implanted mesh
  • -Infection and/or bleeding
  • -Pain, including pain during sexual intercourse
  • -Problems with organs near the implantation site

Helping You

You may have experienced mesh erosion, bleeding, urinary infections, vaginal scarring, pain during sexual intercourse, failure to conduct sexual intercourse and more. A physician may have tried to remove the mesh and been unable to do so. You may be in excruciating pain, and need help. We are offering free case evaluations to the general public across the United States and Canada. Manufacturers we consider include American Medical Systems, Bard, Boston Scientific, Ethicon,Gynecare, and Johnson & Johnson.

If you received a transvaginal mesh / sling and have been injured, you may be entitled to monetary compensation. Problems include pain, inability to have intercourse,bleeding, mesh growth into the body, mesh erosion, and more. Problems could be irreversible. Please fill out the form to the right or call us so that we can provide you with forms to evaluate your potential case immediately.

We are accepting case evaluations nationwide and in Canada, as well.  Please do not hesitate or delay in contacating TVM / TVT Sling and transvaginal mesh attorneys :

CALL: 1-800-632-1404

EMAIL: clicking here

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    NOTE: Our team of attorneys will review potential cases for all fifty states, including Alabama Alaska Arizona Arkansas California Colorado Connecticut Delaware Florida Georgia Hawaii Idaho Illinois Indiana Iowa Kansas Kentucky Louisiana Maine Maryland Massachusetts Michigan Minnesota Mississippi Missouri Montana Nebraska Nevada New Hampshire New Jersey New Mexico New York North Carolina North Dakota Ohio Oklahoma Oregon Pennsylvania Rhode Island South Carolina South Dakota Tennessee Texas Utah Vermont Virginia Washington West Virginia Wisconsin and Wyoming.

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