Sexual outcomes following the surgical treatment of traumatic rupture of the corpora cavernosa.

Introduction: Penile fracture is a post-traumatic condition affecting the tunica albuginea of the corpora cavernosa when erect. Clinical diagnosis and urgent surgical intervention are crucial to avoid severe functional complications, particularly erectile dysfunction. We aimed to evaluate male sexual function after surgical treatment in patients with penile fracture and to identify predictive factors of postoperative erectile dysfunction.
Methods: We underwent a hospital-based retrospective study on patients who underwent surgical repair for fractures of the corpora cavernosa between 2012 and 2023. Included in this study were all patients who have a postoperative follow-up of at least 12 months. Patients were clinically evaluated for the presence of erectile dysfunction and the presence of postoperative penile curvature. The patients were asked to answer the structured questionnaire of the International Index of Erectile Function (IIEF-15).
Results: We included 87 patients. The mean age was 38 ± 12 years. Fourteen patients (16%) developed a fibrous plaque, with a median onset time of 30 days postoperatively. Erectile dysfunction was noted in forty-four patients (51%). Active smoking (p < 0.002), the surgical approach (p = 0.02), a consultation time > 7.5 h (p = 0.01), a length of the discontinuity of the corpora cavernosa > 2.5 cm (p = 0.01) and the use of an erection inhibitor postoperatively (p = 0.021) were independent predictive factors of erectile dysfunction at 1 year postoperatively.
Conclusion: Considering the results of our study, we propose rapid and urgent surgical management for penile fractures, and an elective surgical approach may be considered. We emphasize the fundamental role of sexual education, especially for young people, in preventing this sexual accident that could negatively impact their sexual life.
Competing Interests: Declarations Conflict of interest The authors declare no competing interests. Ethical approval and consent to participate The study was approved by the ethics committee of THE RABTA UNIVERSITY HOPITAL, TUNIS. Approval was granted by THE RABTA UNIVERSITY HOPITAL LOCAL ETHICS COMMITTEE (ID: 19011989) (Approval date: 20/03/2023). All methods were performed in accordance with the relevant guidelines and regulations set out by the Declaration of Helsinki. An informed consent was obtained from all participants. Proof of consent to participate can be requested at any time.
(© 2024. The Author(s).)