Abstract
Over 90,000 legal claims for complications related to transvaginal mesh have been filed to date. Safety issues specifically related to the use of transvaginal mesh for pelvic organ prolapse have not been appropriately differentiated from the use of mesh for stress urinary incontinence by either attorneys or the media. This litigious environment and nebulous communication on the safety issues have led to patient and physician concern regarding mesh slings for the treatment of stress urinary incontinence. The ultimate result is likely to be a decrease in use of the gold standard of care for stress urinary incontinence—the mid-urethral synthetic sling.
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C. Perkins, K. Warrior, and L. McClelland declare that they have no conflict of interest.
K. Eilber and J. Anger declare that they are investigators for FDA 522 studies for Boston Scientific Corporation and American Medical Systems. J. Anger declares that she is an expert witness for Boston Scientific Corporation.
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This article does not contain any studies with human or animal subjects performed by any of the authors.
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This article is part of the Topical Collection on Stress Incontinence and Prolapse
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Perkins, C.E., Warrior, K., Eilber, K.S. et al. The Role of Mid-urethral Slings in 2014: Analysis of the Impact of Litigation on Practice. Curr Bladder Dysfunct Rep 10, 39–45 (2015). https://doi.org/10.1007/s11884-014-0278-z
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DOI: https://doi.org/10.1007/s11884-014-0278-z