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Six-Month Prospective Multi-Center Study Reports Efficacy Rates for AMS' Elevate Anterior and Apical Prolapse Repair System
Date:3/10/2011

MINNEAPOLIS, March 10, 2011 /PRNewswire/ -- American Medical Systems® (AMS) (Nasdaq: AMMD), a leading provider of world-class devices and therapies for male and female pelvic health, today announced the results of a six-month prospective multi-center study of the Elevate® Anterior and Apical Prolapse Repair System. The pelvic organ prolapse quantification exam (POP-Q), used to quantify, describe and stage pelvic support, was implemented in the study and concluded efficacy rates of Stage One or less to be 86.3% for Anterior and 98.8% for Apical.  

The study was conducted with 142 women who were enrolled at 16 centers located in the United States and Europe. When questioned about quality of life benefits after receiving the procedure, 94.7 percent of patients reported feeling some or a lot of improvement.

"The Elevate Anterior and Apical system, completed with a single vaginal incision and no external needle passes, has shown at six months to be effective at treating both anterior and apical prolapse," said Dr. Edward J. Stanford, principal investigator of the study. "The results of this study were especially significant given that many of the patients had severe Stage Three or Four prolapse."

Elevate is a minimally invasive, comprehensive solution to treat anterior and apical defects. The total transvaginal approach is designed to minimize tissue trauma. Elevate offers safe, simple and precise apical mesh placement in the sacrospinous ligament through a single vaginal incision.

"We are very pleased to see these positive efficacy rates coupled with significant patient satisfaction," stated John Nealon, senior vice president and general manager of Women's Health at AMS. "This data continues to validate our technology and helps confirm why Elevate is the top-selling prolapse repair system in the market place."

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SOURCE American Medical Systems
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