The international discussion and the new regulations concerning transvaginal mesh implants in pelvic organ prolapse surgery
- PMID: 32696186
- PMCID: PMC7497328
- DOI: 10.1007/s00192-020-04407-0
The international discussion and the new regulations concerning transvaginal mesh implants in pelvic organ prolapse surgery
Abstract
The use of transvaginal mesh implants for POP and urinary incontinence is currently being extensively debated among experts as well as the general public. Regulations surrounding the use of these implants differ depending on the country. Although in the USA, the UK, in Canada, Australia, New Zealand, and France, transvaginal mesh implants have been removed from the market, in most mainland European countries, Asia, and South America, they are still available as a surgical option for POP correction. The aim of this review is to provide an overview of the historical timeline and the current situation worldwide, as well as to critically discuss the implications of the latest developments in urogynecological patient care and the training of doctors.
Keywords: Alloplastic meshes; Pelvic organ prolapse; Regulations; Transvaginal mesh implants; Urinary incontinence.
Conflict of interest statement
Nathalie Ng-Stollmann: none; Christian Fünfgeld: consultant for Serag-Wiessner, A.M.I, PFM (acceptance of paid travel expenses and honoraria); Boris Gabriel: Serag-Wiessner (acceptance of paid travel expenses and honoraria); Achim Niesel: consultant for Serag-Wiessner, A.M.I (acceptance of paid travel expenses and honoraria).
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