AI Article Synopsis

  • * A study reviewed 16 high-risk female patients who underwent AFPVS between 2019 and 2021, reporting a 56.3% success rate in resolving SUI after three months, while 25% showed improvement without complete resolution.
  • * The study concluded that AFPVS is a viable treatment option for women at high risk for complications associated with synthetic slings, despite noting some patients experienced significant post-operative challenges.

Article Abstract

Introduction: Very popular in many parts of the world, autologous fascial pubovaginal sling (AFPVS) remains marginally used in France. However, it may be of particular interest in patients carrying a high risk of mesh-related or device-related related complications. The aim of the present series was to report the outcomes of AFPVS in this high-risk population.

Material And Methods: The charts of all female patients who underwent a fascial sling for SUI at a single academic center between April 2019 and May 2021 were reviewed retrospectively. Only patients deemed at high-risk of device/mesh related complications were included in the present analysis: female with a neurological condition who were doing clean intermittent catheterization (CIC), female with SUI after radical cystectomy and ileal neobladder, female with urethral/bladder extrusion of any synthetic material placed for SUI. Success was defined as complete resolution of SUI at 3 months.

Results: Sixteen patients were included in this study: 13 rectus fascia slings and 3 fascia lata slings. The success rate was 56.3% (9/16 patients). Four patients were improved but not completely dry (25%). Two patients had major postoperative complications (i.e. Clavien grade 3 or higher, 11.2%). Two patients had a persisting significant post-void residual (PVR) postoperatively, managed by self-catheterization (transition to self-catheterization at 3 months: 2/8, 25%).

Conclusion: The use of autologous fascia pubovaginal sling is an interesting option in female SUI patients with high risk of device/mesh related complications with satisfactory functional outcomes.

Level Of Proof: 4.

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Source
http://dx.doi.org/10.1016/j.purol.2022.02.007DOI Listing

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