Raheel Muhammad, Rai Jaskarn, Ahmad Bilal, Gashaan Malek, Odedra Roocha, Bochinski Antoni J
Urology, Leicester General Hospital, University Hospitals of Leicester NHS Trust, Leicester, GBR.
Urology, Leicester Royal Infirmary, University Hospitals of Leicester NHS Trust, Leicester, GBR.
Cureus. 2025 Aug 15;17(8):e90179. doi: 10.7759/cureus.90179. eCollection 2025 Aug.
This study aimed to analyze and evaluate the effectiveness and safety of Rezum (water vaporization of the prostate), a minimally invasive treatment for managing lower urinary tract symptoms (LUTS) due to benign prostatic hyperplasia (BPH), with a focus on postoperative outcomes. Methodology: Seventy-three patients meeting the inclusion criteria were enrolled in the study at Leicester General Hospital (University Hospitals of Leicester NHS (UHL), NHS trust), Leicester, England, from 1 August 2023 to 31 August 2024. In this prospective cohort study, the following variables were recorded: name, date of birth, date of admission, pre-/postoperative International Prostate Symptom Score (IPSS), pre-/postoperative Quality of Life Score (QOLS), pre-/postoperative International Index of Erectile Function (IIEF-5), prostate size, urodynamics, prostate-specific antigen (PSA) level, Rezum injections, anesthesia, post-procedure side effects and symptoms on follow-up, recommendations to family and friends, and status on discharge. To assess the procedure outcomes, these variables were analyzed using IBM SPSS Statistics, version 23 (IBM Corp., Armonk, NY), and the results were depicted in the form of graphs, charts, and tables. Results: In our study, the mean preoperative IPSS was 22.6 ± 7.5, reduced to 12.8 ± 9.4, showing a 27% improvement. The highest pre-procedure QOLS was five (n=19, 26.4%), compared to three (n=21, 29.2%) after Rezum, representing a 33.3% improvement. Preoperative assessment of erectile function, as measured by the IIEF-5 with a maximum possible score of 25, revealed a mean score of 15.1 ± 1.1. Post-operative evaluation indicated a slight decline, with the mean score decreasing to 14.7 ± 4.03, reflecting a 1.5% reduction in erectile function. The reduction in symptomatic LUTS showed a statistically significant improvement with injections targeting the left side and the median lobe (p = 0.002). Furthermore, a statistically significant correlation was observed between Rezum injections targeting the median lobe and post-procedure quality of life (p = 0.003).
Through this single-center retrospective cohort, we concluded that Rezum is a minimally invasive outpatient procedure that offers safe and effective treatment for LUTS. It has a low side-effect profile and preserves sexual function. Further long-term studies are recommended.
本研究旨在分析和评估Rezum(前列腺水蒸气消融术)治疗良性前列腺增生(BPH)所致下尿路症状(LUTS)的有效性和安全性,重点关注术后结果。方法:2023年8月1日至2024年8月31日,73名符合纳入标准的患者在英国莱斯特的莱斯特综合医院(莱斯特大学医院国民保健服务信托基金,NHS信托)入组该研究。在这项前瞻性队列研究中,记录了以下变量:姓名、出生日期、入院日期、术前/术后国际前列腺症状评分(IPSS)、术前/术后生活质量评分(QOLS)、术前/术后国际勃起功能指数(IIEF-5)、前列腺大小、尿动力学、前列腺特异性抗原(PSA)水平、Rezum注射情况、麻醉、术后副作用及随访症状、对家人和朋友的建议以及出院状态。为评估手术结果,使用IBM SPSS Statistics 23版(IBM公司,纽约州阿蒙克)对这些变量进行分析,并以图表和表格形式呈现结果。结果:在我们的研究中,术前IPSS平均为22.6±7.5,术后降至12.8±9.4,改善了27%。术前QOLS最高为5分(n = 19,26.4%),Rezum术后为3分(n = 21,29.2%),改善了33.3%。通过IIEF-5对勃起功能进行术前评估,最高可能得分为25分,平均得分为15.1±1.1。术后评估显示略有下降,平均得分降至14.7±4.03,反映勃起功能下降了1.5%。针对左侧和中叶注射时,有症状的LUTS减轻显示出统计学上的显著改善(p = 0.002)。此外,针对中叶的Rezum注射与术后生活质量之间存在统计学上的显著相关性(p = 0.003)。结论:通过这项单中心回顾性队列研究,我们得出结论,Rezum是一种微创门诊手术,为LUTS提供安全有效的治疗。它副作用小且能保留性功能。建议进一步开展长期研究。