Skip to Content

Get the facts about transvaginal mesh complications

If you're a woman who has a pelvic floor disorder, you've likely heard of treatments involving transvaginal mesh. However, reports about complications might have you confused or hesitant to seek treatment. Understand the concerns about transvaginal mesh and what they might mean for you.

Medically reviewed by Drugs.com. Last updated on Jul 22, 2017.

What is surgical mesh?

Surgical mesh is a medical device that is used to provide extra support when repairing weakened or damaged tissue. Most surgical mesh devices are made from synthetic materials or animal tissue.

How is surgical mesh used to treat pelvic floor disorders?

Surgical mesh can be used to treat:

  • Pelvic organ prolapse (POP). When the muscles and ligaments supporting a woman's pelvic organs weaken, the pelvic organs can slip out of place (prolapse). To treat POP, surgical mesh can be implanted to reinforce the weakened vaginal wall. Surgery can be done through the abdomen (transabdominal). Surgery through the vagina (transvaginal) has also been an option in the past. However, in 2019 the FDA ordered manufacturers of surgical mesh for the transvaginal repair of POP to stop selling and distributing their products in the U.S.
  • Stress urinary incontinence (SUI). This is the unintentional loss of urine due to a physical movement or activity — such as coughing, sneezing, running or heavy lifting — that puts pressure (stress) on your bladder. Surgical mesh can be implanted through the vagina to support the urethra or bladder neck. This is known as a midurethral sling or a mesh sling procedure.

What are the safety concerns about use of surgical mesh to treat pelvic floor disorders?

Each type of mesh procedure carries its own risks and benefits.

Treating SUI with a mesh sling can cause complications, including mesh erosion, infection and pain.

Before the FDA ordered manufacturers of surgical mesh for the transvaginal repair of POP to stop selling and distributing their products in the U.S., there were growing safety concerns. Due to reports of complications during or after surgery for POP, in 2016 the FDA changed the classification of surgical mesh to repair POP transvaginally from a moderate-risk device to a high-risk device. The FDA orders applied only to transvaginal use of surgical mesh to treat POP, not the use of transvaginal mesh for SUI.

Research has shown that surgical mesh for transvaginal repair of POP can cause complications such as mesh erosion, pain, infection, bleeding, pain during sex, organ perforation and urinary problems. Many of these complications require additional treatment, including surgery.

If you've had transvaginal mesh placed for the surgical repair of POP, continue with your checkups and follow-up care. If you have complications or symptoms, talk to your doctor.

What questions should I ask before seeking a mesh treatment for a pelvic floor disorder?

If you're considering treatment for a pelvic floor disorder that involves surgical mesh, be sure to have your doctor explain all of your options, as well as their possible risks and benefits.

© 1998-2019 Mayo Foundation for Medical Education and Research (MFMER). All rights reserved. Terms of use

Hide