Transvaginal Mesh Lawsuits May Come After POP Surgery

Tue, 31 Jan 2012 19:52:57 +0100

When surgical mesh is used to correct pelvic organ prolapse (POP), it means an increased in the longevity of the repair. The surgery involves incision in the abdomen or by way of the vagina.

The correct a prolapse via abdominal procedure (aka transabdominal) through the uterus or top of the vagina was a highly successful procedure way back in the 80s. As such, the procedure is now considered an effective surgical approach in the treatment of POP.

In 2010 alone, there are about 300,000 women in the U.S. who underwent surgical treatment to remedy pelvic organ prolapse. With data supplied by the surgical mesh manufacturers, the FDA was able to report that one out of three of the 300,000 surgeries used the mesh. Three-fourths of these POP procedures were performed through the vagina.

However, between 2008 and 2010, pain became one of the most frequent complications brought by having a mesh POP surgery as reported to the FDA. The FDA stated that problem of pain correlated to mesh insertion through the vagina can be "life-altering." Despite the mesh’s removal, the problems still persist.

Additionally, a number of other problems in using vaginal mesh were received by the FDA between 2008 and 2010. Included are the following:

Vaginal mesh erosion, also called exposure, extrusion, or protrusion

Painful intercourse

Infection

Urinary problems

Bleeding

Organ perforation

Recurrent prolapse

Neuro-muscular problems

Vaginal scarring and shrinkage

Emotional problems

Several of the women who experienced the problems above necessitated further surgery, medical care, and hospitalization. In fact, there were seven women reported to have fatally succumbed to the dangers of surgical mesh POP procedure from 2008 to 2010. In further, it was shown that that three of these deaths were associated with POP repair with two bowel perforations and one hemorrhage. Furthermore, four of the deaths were associated by post-operative medical complications that were not necessarily having a direct relation to the procedure involved in placing the mesh.

You are not alone if you are undergoing pains in the aftermath of POP surgery with surgical mesh. A lot of women suffer the same problem. In cases such as this, legal help is necessary. More info about transvaginal mesh lawsuit here.

Transvaginal Mesh Lawyers Help Legal Assistance in Filing Tranvaginal Mesh Lawsuits

Wed, 18 Jan 2012 13:52:59 +0100

Vaginal mesh first came to be approved by the FDA as treatment symptoms correlated to pelvic organ prolapse (aka POP). The condition is characterized by the weakening of the pelvic floor muscles. Beginning 2008, the FDA came to receive complaints, of approximately 4,000, about the devices. From January 2008 through December 2010, the FDA listed more than 2800 Medical Device Reports involving urogynecologic surgery mesh devices that were fount to malfunctions, cause injury or even death.

The device is known by various names such as pelvic mesh, transvaginal mesh, surgical mesh and bladder slings.

The organization came up with a new warning in July 2011. It stated that vaginal mesh implants are potentially risky and of irrevocable side effects. In fact, the American College of Obstetricians and Gynecologists and the American Urogynecologic Society, around November 2011, came up with a joint statement recommending the limitation on the use of vaginal mesh for high-risk women who fail to respond with other available treatment.

As of date, an approximately 350 vaginal mesh lawsuits is pending in a New Jersey state court alone. The lawsuits, with Johnson & Johnson Company as defendant, claim that the Ethicon Gynecare vaginal mesh system brought serious injuries to the plaintiffs such as extensive bleeding, bowel and bladder perforation, infection, blood vessel damage, painful intercourse and scarring. The cases are set to go on trial in November 2012. Considering that there are 300,000 women receiving the device in 2010 alone, it is foreseen that lawsuits against the makers of the devices will increase.

For the last several years, the FDA has received the complaints of side effects involving the device:

Vaginal mesh erosion
Pain
Infection
Bleeding
Organ perforation
Recurrent prolapse
Neuro-muscular problems
Vaginal scarring/shrinkage
Emotional problems
Urinary problems

As of this writing, cases are individually filed and transvaginal mesh lawyers found that nationwide transvaginal mesh lawsuit has not yet been filed.

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Transvaginal Mesh Lawsuits May Come After POP Surgery

Transvaginal Mesh Lawyers Help Legal Assistance in Filing Tranvaginal Mesh Lawsuits