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Surgical and Functional Outcomes of Penile Prosthesis Implantation in Men with Neurological Conditions

The Journal of Sexual Medicine(2023)

Molinette Mauriziano Hosp | ASST Sette Laghi | Citta Salute Sci Torino Molinette Hosp | IRCCS Osped San Raffaele | Univ Sapienza | Univ Bari | Santa Chiara Reg Hosp | AORN Cardarelli | Osped Cardinal Massaia | Hesperia Hosp | StOrsola Univ Hosp | Area Vasta 3 Asur Marche | Osped Circolo & Fondazione Macchi Varese | Univ Naples Federico II

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Abstract
Abstract Objectives Pharmacological treatment for erectile dysfunction (ED) is not always effective in patients with neurological disease; as such, penile prosthesis implant (PPI) can be a valid treatment option. We investigated outcomes of PPI in neurological patients using the Italian multi-institutional national registry of penile prostheses (INSIST-ED) Methods INSIST-ED registry, relating to patients implanted from 2014 to 2021, was analyzed. All data were prospectively recorded by 45 surgeons on a dedicated website (www.registro.andrologiaitaliana.it) and revised by a data-manager. We selected patients with neurological disease undergoing PPI for ED. Follow-up was scheduled at 3,6 and 12 months, then annually. We evaluated postoperative complications and functional outcomes through validated questionnaires (IIEF and EDITS). A non-validated questionnaire was administered to evaluate patient’satisfaction. Results 33 patients were included with a median age of 52 (IQR: 44.75-55.25). Peno-scrotal approach for PPI was performed in most cases (90.9%) while infra-pubic was used in 3 cases (9.1%). An inflatable and a malleabel device was implanted in 30 (90.9 %) and 3 cases (9.1 %), respectively. Median follow-up was 83 months (IQR: 67-99.5). Intraoperative complications occurred in one case (3%). Early postoperative complications (<90 days) were observed in 4 cases (12.1%): 3 peno-scrotal hematoma (Clavien-Dindo G1), 1 device infection requiring prosthesis explant (Clavien-Dindo G3a). At the last follow-up, 29 prostheses (87.9%) were still in place and well-functioning. Mechanical failure of inflatable PP occurred in 3 cases (9.1%). Median IIEF before surgery was 32 (IQR 30.25-36). At the last follow-up, IIEF was 61.5 (IQR 60.25-64.25), and median EDITS was 45.5 (IQR 39-46.75). Overall, 29 patients (87.9%) affirmed to be fully satisfied with the PPI. Conclusions Although PPI in the neurological population has been historically limited by the evidence of common complications and infections, our study showed that PPI represents a safe and effective procedure to treat ED in neurological patients. Conflicts of Interest The Authors have no conflict of interest.
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要点】:本研究通过意大利多机构国家阴茎假体注册数据(INSIST-ED),探讨了阴茎假体植入(PPI)在神经疾病患者中的手术和功能结果,证实了该疗法的安全性和有效性。

方法】:研究分析了2014至2021年间在45位医师协作下记录于特定网站(www.registro.andrologiaitaliana.it)的INSIST-ED注册数据,选取了患有神经疾病并进行PPI手术的病人,通过IIEF和EDITS问卷评估术后并发症和功能结果。

实验】:共纳入33名患者,中位年龄52岁,大部分采用阴茎阴囊途径进行PPI手术,术后中位随访时间为83个月。研究中一例发生术中并发症,早期术后并发症发生率为12.1%,最后随访时87.9%的假体仍在正常工作。通过问卷评估,患者术后性功能显著改善,满意度高。