评估富血小板血浆注射治疗勃起功能障碍的疗效和安全性:随机对照试验的系统回顾和荟萃分析。

IF 3.6 2区 医学 Q1 UROLOGY & NEPHROLOGY Sexual medicine reviews Pub Date : 2024-04-08 DOI:10.1093/sxmrev/qeae018
Mostafa Deabes, Mohammad Ghassab Deameh, Baha' Aldeen Bani Irshid, Ali Hasan Al Darraji, Ibrahim Serag, Nereen A Almosilhy, Ahmed Dwidar, Mohamed A Aldemerdash, Hatim Nasruldin Shahin
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引用次数: 0

摘要

简介富血小板血浆(PRP)含有丰富的因子,可在干细胞招募、炎症调节和血管生成方面发挥作用。许多临床前和临床研究都在探索将PRP作为治疗勃起功能障碍(ED)的潜在方法,本研究的重点是根据随机对照试验(RCT)评估体腔内注射PRP对ED患者的疗效。方法本研究遵循PRISMA(系统综述和荟萃分析首选报告项目)指南。在在线数据库(PubMed、Scopus 和 ScienceDirect)中进行了全面搜索,以确定将 PRP 与安慰剂用于 ED 治疗进行比较的 RCT。评估的主要结果是在国际勃起功能指数(IIEF)领域达到最小临床重要差异的患者比例,以及 IIEF 领域与基线相比的变化。研究结果以 PRP 组和安慰剂组之间的标准化平均差进行合并。总体效果 PRP 优于安慰剂:在 IIEF 领域达到最小临床重要差异的患者总数(几率比 [OR],5.64;95% 置信区间 [CI],2.05 至 15.55;P = .0008)、IIEF 与基线相比的变化(平均差 [MD],2.99;95% 置信区间 [CI],1.74 至 4.24;P = .00001)、PSV(MD,9.34;95% 置信区间 [CI],0.84 至 17.84;P = .结论PRP似乎是治疗轻度至中度ED的一种安全有效的方法。然而,还需要更多高质量 RCT 的支持来加强这些研究结果。
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Evaluating the efficacy and safety of platelet-rich plasma injection for erectile dysfunction: a systematic review and meta-analysis of randomized controlled trials.
INTRODUCTION Platelet-rich plasma (PRP) is rich in factors that play a role in stem cell recruitment, inflammation modulation, and angiogenesis. With numerous preclinical and clinical studies exploring PRP as a potential treatment for erectile dysfunction (ED), this study focused on assessing the effectiveness of intracorporeal PRP injection for ED patients based on randomized controlled trials (RCTs). OBJECTIVES The study sought to evaluate the efficacy and safety of intracorporeal injection of PRP in treating ED through a systematic review and meta-analysis of RCTs. METHODS This study adhered to PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) guidelines. A comprehensive search was conducted on online databases (PubMed, Scopus, and ScienceDirect) to identify RCTs comparing PRP with a placebo for ED treatment. The primary outcomes assessed were the proportion of patients achieving the minimal clinically important difference in the International Index of Erectile Function (IIEF) domain and the change in the IIEF domain from baseline. The results were combined as a standardized mean difference between the PRP and placebo groups. RESULTS Three RCTs comprising 230 patients were included. The overall effect favored PRP over placebo: total patients attaining minimal clinically important difference in the IIEF domain (odds ratio [OR], 5.64; 95% confidence interval [CI], 2.05 to 15.55; P = .0008), IIEF change from baseline (mean difference [MD], 2.99; 95% CI, 1.74 to 4.24; P = .00001), PSV (MD, 9.34; 95% CI, 0.84 to 17.84; P = .03), end-diastolic volume (standardized MD, 0.50; 95% CI, 0.17 to 0.83; P = .003), Sexual Encounter Profile question 3 (standardized MD, 0.78; 95% CI, 0.45 to 1.12; P = .00001), and visual analog scale score (MD, -0.30; 95% CI, -0.53 to -0.08; P = .008). CONCLUSION PRP appears to be a safe and effective treatment for mild-to-moderate ED. However, further support from high-quality RCTs is needed to strengthen these findings.
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来源期刊
Sexual medicine reviews
Sexual medicine reviews UROLOGY & NEPHROLOGY-
CiteScore
7.60
自引率
8.30%
发文量
5
期刊最新文献
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