Robotic female artificial urinary sphincter implantation vs male artificial urinary sphincter implantation for non-neurogenic stress urinary incontinence

Peyronnet B1, Lethuillier V1, Dubois A1, Richard C1, Haudebert C1, El-Akri M1, Freton L1, Manunta A1, Hascoet J1

Research Type

Clinical

Abstract Category

Male Stress Urinary Incontinence (Post Prostatectomy Incontinence)

Abstract 169
Open Discussion ePosters
Scientific Open Discussion Session 11
Thursday 8th September 2022
16:10 - 16:15 (ePoster Station 1)
Exhibition Hall
Robotic-assisted genitourinary reconstruction Incontinence Stress Urinary Incontinence
1. university of rennes
In-Person
Presenter
B

Benoit Peyronnet

Links

Abstract

Hypothesis / aims of study
In 2006, Ananias Diokno and is team reported what remains to date the only series comparing male vs female artificial urinary sphincter (AUS) implantation suggesting better functional outcomes and longer device survival for female implantations (Petero VG, J Urol 2006). We hypothesize that the rapidly spreading robotic approach for female implantation may have changed this comparison. The aim of this study was to compare the outcomes of robotic female AUS vs male AUS implantation for non-neurogenic SUI.
Study design, materials and methods
The charts of all male patients who had an AUS implantation and of all female patients who underwent robotic AUS implantation between 2008 and 2020 for non-neurogenic SUI at a single center were reviewed retrospectively. All the implantations were performed by three surgeons in their learning curves over the study period. All the female implantations were performed using a robotic “anterior” transperitoneal approach. The primary endpoint was the continence status at 3 months categorized as: complete resolution of SUI (0 pad), improved SUI or unchanged SUI.
Results
After exclusion of 19 neurogenic patients, 149 patients were included: 58 women and 91 men. The operative time was significantly shorter in the male group (137.4 vs. 179.4 min; p<0.0001). The postoperative complications rate was similar in both groups (20.8% vs. 27.6%; p=0.34) as was the median length of hospital stay (3 vs. 2 days; p=0.89). The continence status at 3 months and at last follow-up favored the female group with 76.4% vs. 42.3% and 70.4% vs. 34.1% of complete continence in the female and male groups respectively (p<0.001; see table). The median number of pads per day was lower in the female group at 3 month post-operatively (0 vs. 1;p<0.001). The ICIQ-SF decrease at 3 months was significantly greater in the female group (-8.8 vs. -15.2; p=0.001). The 5-year estimated explantation-free survival was similar in both groups (78.2% vs. 74.6%; p=0.69) as well as the 5-year estimated revision-free survival (78.7% vs. 69.3%; p=0.30)
Interpretation of results
Robotic female AUS implantation and male AUS implantation have similar morbidity and similar device survivals but female AUS implantation may be associated with better functional outcomes which would confirm findings previously published (Petero VG, J Urol 2006). This may be explained by the bladder neck vs bulbar urethra location of the cuff.
Concluding message
In the robotic era, AUS implantation may have similar morbidities for both male and female patients but may yield better functional outcomes in female patients. This data does not support the FDA decision to label AUS use only in male patients.
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Disclosures
Funding None Clinical Trial No Subjects Human Ethics Committee CNIL Helsinki Yes Informed Consent Yes
27/04/2024 17:06:36