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Study Says FDA Waited Too Long To Ban Pelvic Mesh For POP Repairs

Almost 20% of POP repair mesh patients with follow-ups face complications

 
• By Sue Darcey

Roughly 18.5% of patients who received reinterventions to fix mesh implants for pelvic organ prolapse (POP) repair experienced complications they will likely endure for the rest of their lives, and they also face a 2.5% higher rate of further surgeries than non-mesh patients, says a recent 54,194-woman study detailed in Obstetrics & Gynecology. The study authors lay out a case that the US FDA should have forced removal of mesh from the market sooner.

Synthetic Mesh for Inguinal Hernia Repair.

A recent population-based cohort study of more than 50,000 women in New York State who had pelvic mesh implanted for pelvic organ prolapse (POP) repair found that 18.5% of the women who had to go through re-intervention surgery are likely to face complications from the mesh implants for the rest of their lives.

That’s one of the big takeaways from the study, the results of which were recently detailed in Obstetrics & Gynecology. In it, the study authors criticized the US Food and...

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