Four years of real-world sexual function outcomes after Rezum therapy in men with and without baseline erectile dysfunction.

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Noah Hawks-Ladds, Ryan Cook, Mustufa Babar, Michael Zhu, Alison Schulz, Justin Loloi, Zaki Masoud, Jaskirat Singh, Hasan Jamil, Rahman Sayed, Matthew Ines, Michael Ciatto
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Abstract

Background: Rezum alleviates lower urinary tract symptoms secondary to benign prostatic hyperplasia (BPH) while preserving sexual function, but long-term sexual function outcomes are lacking in patients with baseline erectile dysfunction (ED).

Aim: The study sought to analyze 4 years of real-world sexual function outcomes of Rezum using the International Index of Erectile Function (IIEF) questionnaire, stratified by baseline ED status.

Methods: Participants included multiethnic Rezum-treated patients from a single outpatient office. IIEF domains and BPH medication usage were compared at baseline and 6, 12, and 48 months using t tests, Mann-Whitney U tests, chi-square tests, and Wilcoxon signed rank tests.

Outcomes: Primary outcomes over 4 years included the IIEF functional domains (erectile function [EF], orgasmic function [OF], sexual desire [SD], intercourse satisfaction [IS], overall satisfaction [OS]) and BPH medication usage.

Results: A total of 91 patients were included: 40 (44%) in the ED cohort and 51 (56%) in the no ED cohort. History of diabetes was more prevalent in the ED cohort (35% vs 15.7%; P = .048). Baseline scores in the EF, OF, IS, and OS domains were lower in the ED cohort. Compared with baseline, there were no significant changes in any IIEF domains in either cohort at 6 months. At 12 months, the ED cohort had significant percent decreases in OF (-25%; P = .02), SD (-22.2%; P = .04), and OS (-33.3%; P = .004); the no ED cohort had a significant percent increase in EF (5%; P = .04). At 48 months, the no ED cohort had no significant changes in any IIEF domains, while the ED cohort had significant percent increases in EF (30%; P = .01), SD (22.5%; P = .02), IS (20%; P = .01), and OS (58.3%; P = .008). Both cohorts significantly discontinued BPH medications at all follow-ups. At 48 months, there were no cases of de novo ED in the no ED cohort.

Clinical implications: As modern BPH therapies continue to demonstrate efficacy in alleviating lower urinary tract symptoms, the preservation or improvement of sexual function emerges as an increasingly important consideration for patients, with our study suggesting Rezum as a compelling option.

Strengths and limitations: Our study has the strength of long-term Rezum outcomes in an ethnically diverse patient population, stratified by the presence of baseline ED, but is limited by retrospective design, single-center nature, and small sample sizes at long-term follow-ups.

Conclusion: Rezum preserved long-term sexual function in patients without baseline ED and improved sexual function in those with baseline ED; however, individuals with ED may experience temporary decreases in sexual function at 12 months.

对有和没有勃起功能障碍基线的男性进行 Rezum 治疗后四年的实际性功能结果。
背景:Rezum 可减轻继发于良性前列腺增生症(BPH)的下尿路症状,同时保留性功能,但缺乏对基线勃起功能障碍(ED)患者的长期性功能结果。目的:该研究旨在使用国际勃起功能指数(IIEF)问卷分析 Rezum 4 年的实际性功能结果,并根据基线 ED 状态进行分层:方法:参与者包括来自一家门诊部的多种族锐速治疗患者。采用t检验、曼-惠特尼U检验、卡方检验和Wilcoxon符号秩检验对基线、6、12和48个月的IIEF域和良性前列腺增生症药物使用情况进行比较:4年的主要结果包括IIEF功能域(勃起功能[EF]、性高潮功能[OF]、性欲[SD]、性交满意度[IS]、总体满意度[OS])和良性前列腺增生症药物使用情况:共纳入 91 名患者:结果:共纳入 91 名患者:40 人(44%)患有前列腺增生,51 人(56%)未患有前列腺增生。有糖尿病史的患者在急诊科队列中更为普遍(35% vs 15.7%; P = .048)。急诊室队列中 EF、OF、IS 和 OS 领域的基线分数较低。与基线相比,两个队列中任何一个 IIEF 领域在 6 个月时都没有显著变化。12 个月时,ED 队列的 OF(-25%;P = .02)、SD(-22.2%;P = .04)和 OS(-33.3%;P = .004)显著下降;无 ED 队列的 EF 显著增加(5%;P = .04)。48 个月时,无 ED 队列在任何 IIEF 领域均无显著变化,而有 ED 队列的 EF(30%;P = .01)、SD(22.5%;P = .02)、IS(20%;P = .01)和 OS(58.3%;P = .008)均显著增加。在所有随访中,两组患者均明显停用了良性前列腺增生症药物。在48个月时,无ED队列中没有新发ED病例:临床意义:随着现代良性前列腺增生症疗法在缓解下尿路症状方面的疗效不断显现,保持或改善性功能成为患者越来越重要的考虑因素,我们的研究表明 Rezum 是一种令人信服的选择:我们的研究在不同种族的患者群体中取得了长期的Rezum疗效,并根据是否存在基线ED进行了分层,这一点很有优势,但也受到了回顾性设计、单中心性质以及长期随访样本量较小的限制:结论:Rezum可保持无基线ED患者的长期性功能,改善基线ED患者的性功能;但ED患者在12个月后性功能可能会暂时下降。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
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