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富血小板血浆(PRP)改善勃起功能:一项双盲、随机、安慰剂对照的临床试验。

Platelet-Rich Plasma (PRP) Improves Erectile Function: A Double-Blind, Randomized, Placebo-Controlled Clinical Trial.

机构信息

First Department of Urology, G. Gennimatas Hospital, Aristotle University of Thessaloniki, Thessaloniki, Greece.

First Department of Urology, G. Gennimatas Hospital, Aristotle University of Thessaloniki, Thessaloniki, Greece; Institute for the Study of Urological Diseases, Thessaloniki, Greece.

出版信息

J Sex Med. 2021 May;18(5):926-935. doi: 10.1016/j.jsxm.2021.03.008. Epub 2021 Apr 24.

Abstract

BACKGROUND

Animal studies postulate that platelet-rich plasma (PRP) injections improve key elements of the pathophysiologic mechanisms leading to erectile dysfunction (ED).

AIM

To conduct the first double-blind, randomized, placebo-controlled trial assessing the efficacy and safety of PRP injections in patients with mild and moderate ED.

METHODS

Sixty sexually active patients with mild and moderate ED were randomly assigned to two sessions, with a one-month difference, of 10 mL PRP (n = 30) or placebo (n = 30) intracavernosal injections. An FDA-approved separation system was used. Patients were evaluated at 1, 3 and 6 months after completion of the treatment protocol. A per-protocol analysis was applied. All participants withheld any ED treatment during the trial.

OUTCOMES

The achievement of minimal clinically important difference (MCID) in the International Index of Erectile Function - Erectile Domain (IIEF-EF) from baseline to 6 months after final treatment. Erectile function at all time points, as well as safety of PRP injections, were also evaluated.

RESULTS

At 6 months, a MCID was achieved by 20/29 (69%) patients in the PRP group compared to 7/26 (27%) in the placebo group. The risk difference between the two groups was 42% (95%CI: 18-66), P < 0.001 and the baseline-adjusted mean between-group-difference in the IIEF-EF score was 3.9 points (95%CI: 1.8-5.9). Similarly, a statistically significant difference of both the number of participants attaining a MCID and the IIEF-EF score was also observed at the 1- and 3-month evaluation between the two groups. Accordingly, patients receiving PRP were more satisfied with the treatment. No adverse events were observed during the study period.

CLINICAL IMPLICATIONS

Intracavernosal PRP injection therapy used as outlined in this trial appears to be a safe and effective short-term treatment for the management of mild to moderate ED.

STRENGTHS & LIMITATIONS: We conducted the first clinical trial exploring the role of PRP in the management of ED. Conversely, our findings lack external validity due to single-center design. Furthermore, our results cannot be extrapolated to other PRP separation systems.

CONCLUSIONS

PRP intracavernosal injections may be a promising addition to the urologist's armamentarium for the management of ED. Still, further high-quality studies are warranted to corroborate our findings. Evangelos P, Mykoniatis I, Pyrgidis N, et al. Platelet-Rich Plasma (PRP) Improves Erectile Function: A Double-Blind, Randomized, Placebo-Controlled Clinical Trial. J Sex Med 2021;18:926-935.

摘要

背景

动物研究假设富含血小板的血浆(PRP)注射可以改善导致勃起功能障碍(ED)的病理生理机制的关键因素。

目的

进行首次双盲、随机、安慰剂对照试验,评估 PRP 注射治疗轻度和中度 ED 患者的疗效和安全性。

方法

60 名患有轻度和中度 ED 的活跃患者被随机分配到两个疗程,间隔一个月,分别接受 10 mL PRP(n=30)或安慰剂(n=30)阴茎海绵体内注射。使用 FDA 批准的分离系统。患者在治疗方案完成后 1、3 和 6 个月进行评估。应用符合方案分析。所有参与者在试验期间均未接受任何 ED 治疗。

结果

从基线到最后一次治疗后 6 个月,国际勃起功能指数 - 勃起功能域(IIEF-EF)达到最小临床重要差异(MCID)的患者在 PRP 组为 29/29(69%),而安慰剂组为 26/26(27%)。两组之间的风险差异为 42%(95%CI:18-66),P<0.001,IIEF-EF 评分的组间平均差异为 3.9 分(95%CI:1.8-5.9)。同样,在 1 个月和 3 个月的评估中,两组之间也观察到达到 MCID 的参与者数量和 IIEF-EF 评分的统计学显著差异。因此,接受 PRP 治疗的患者对治疗更满意。在研究期间未观察到不良反应。

临床意义

按照本试验方案使用阴茎海绵体内 PRP 注射治疗似乎是一种安全有效的短期治疗方法,可用于治疗轻度至中度 ED。

优势与局限性

我们进行了首次探索 PRP 在 ED 管理中的作用的临床试验。然而,由于单中心设计,我们的发现缺乏外部有效性。此外,我们的结果不能推广到其他 PRP 分离系统。

结论

PRP 阴茎海绵体内注射可能是泌尿科医生治疗 ED 的一种有前途的方法。然而,仍需要进一步的高质量研究来证实我们的发现。

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