Abstract Short Summary
Abstract
Objective:
To assess the early safety profile and surgical outcomes of the Rigicon ContiReflex® artificial urinary sphincter in treating male stress incontinence.
Key Findings:
Among 50 patients, no infections or erosions occurred. One revision (2%) was required. A Kaplan–Meier analysis showed 98% device survival at 18 months.
Conclusion:
The Rigicon ContiReflex® AUS demonstrates a favorable early safety profile and is comparable to existing sphincter devices in treating male incontinence.
Clinical Relevance:
The ContiReflex® AUS offers a promising option for male incontinence treatment, with excellent early safety outcomes supporting broader clinical use.
Keywords
This publication is available through the external link above. See the abstract for a summary of the research.