Evaluation of Sexual Function After Artificial Urinary Sphincter Implantation

The primary objective of the study is to evaluate sexual function in women 6 months after implantation of an artificial urinary sphincter. Patients will be informed during the preoperative consultation, with an information sheet provided. Consent to non-opposition will be collected either during the preoperative consultation or on the day of the procedure, if additional time for reflection is needed. Questionnaires will be completed during follow-up visits at 6 and 12 months postoperatively. The patients concerned are women who have undergone implantation of an artificial urinary sphincter. Patients will be informed during the preoperative consultation, with an information sheet provided. Consent to non-opposition will be collected either during the preoperative consultation or on the day of the procedure, if additional time for reflection is needed. Questionnaires will be completed during follow-up visits at 6 and 12 months postoperatively.