Abstract
Purpose of Review
Pelvic organ prolapse (POP) is a common condition and there is a plethora of surgical techniques available to address this problem. We present a review of biologic grafts, including the latest literature to help guide a surgeon’s choice on the type of biologic materials to augment repairs.
Recent Findings
Since the 2019 Food and Drug Administration (FDA) ban on mesh, including xenograft, there is a sparsity of biologic graft products available for POP repairs. This has led to a significant decrease in surgical application. Surgeons must be familiar with the biochemical properties, processing, and clinical application of biologic grafts prior to use. They should also be familiar with alternative operative techniques that utilize autografts, although there is limited outcome data on these techniques.
Summary
With heightened awareness of mesh and its complications, biologic grafts have made a resurgence. Surgeons must be well versed on their available options. Current literature is limited, and studies have not demonstrated superiority of biologic graft over native tissue repairs for prolapse. Nevertheless, there is a role for these types of biologic graft material in specific patient populations. Future studies are warranted.
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Amanda Merriman declares no potential conflicts of interest. Michael Kennelly receives grant/research support from Allergan, Amphora, Axonics, Boston Scientific, Cook Myosite, Coloplast, Dignify Therapeutics, Ipsen, Taris, Uro1, FemPulse, and EBT Medical and is a consultant for Laborie, Avadel, and Urovant.
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Merriman, A.L., Kennelly, M.J. Biologic Grafts for Use in Pelvic Organ Prolapse Surgery: a Contemporary Review. Curr Urol Rep 21, 52 (2020). https://doi.org/10.1007/s11934-020-01013-x
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DOI: https://doi.org/10.1007/s11934-020-01013-x