Abstract Short Summary
Abstract
Objective:
To report the first safety outcomes of the Rigicon ContiClassic® artificial urinary sphincter in the treatment of male stress urinary incontinence.
Key Findings:
The study found a low revision rate of 6.9% with no infections among 116 patients implanted with the ContiClassic® AUS. The 12-month Kaplan-Meier survival rate was 93.2%. Most revisions were due to iatrogenic errors like incorrect cuff sizing or connector misplacement.
Conclusion:
The early clinical experience with the Rigicon ContiClassic® AUS shows a favorable safety profile with low complication and revision rates. The device appears comparable in safety to other sphincters on the market.
Clinical Relevance:
The results support the Rigicon ContiClassic® AUS as a viable alternative to existing artificial urinary sphincters, potentially expanding treatment options for male stress urinary incontinence.
Keywords
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