难治性勃起功能障碍患者富血小板血浆再生治疗:短期结果和平均血小板体积的预测价值

IF 2.5 Q3 ENDOCRINOLOGY & METABOLISM
Davide Francomano, Stefano Iuliano, Federico Dehò, Paolo Capogrosso, Piergiorgio Tuzzolo, Sandro LA Vignera, Gabriele Antonini, Antonio Aversa
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引用次数: 0

摘要

背景:目前绝大多数勃起功能障碍(ED)的治疗是有症状的,不影响疾病进展。再生医学可能通过恢复勃起能力来逆转或阻止复杂ED的进展。我们旨在评估富血小板血浆(PRP)注射对磷酸二酯酶-5抑制剂(PDE-5is)无反应的男性血管性ED患者的潜在安全性和有效性以及血小板功能的临床相关性。方法:150例血管性ED患者被纳入一项开放标签、单臂、多中心、前瞻性、介入性、非随机研究。pde -5药物洗脱1个月后,进行5项国际勃起功能指数(IIEF-5)问卷调查,并进行动态阴茎双相超声(d-PDU)检查。然后患者接受海绵内PRP注射。治疗1个月后,评估IIEF-5和d-PDU。本研究的主要目的是通过评估在IIEF-5问卷中达到最小临床重要差异(MCID)的患者比例来评估PRP治疗的有效性和安全性。次要终点是确定MPV是否与d-PDU参数的改善相关。结果:大多数患者(80%)的ED症状有显著改善(IIEF-5评分:12±2.6比19±3.0;结论:本研究首次证明,对于pde -5反应不良的患者,PRP可能是一种有效且安全的选择。MPV高于8.95 fL可以识别对治疗反应差的患者,可能受益于连续的PRP再挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Regenerative treatment with platelet-rich plasma in patients with refractory erectile dysfunction: short-term outcomes and predictive value of mean platelet volume.

Background: The vast majority of erectile dysfunction (ED) treatments are currently symptomatic and do not influence disease progression. Regenerative medicine may potentially reverse or stop the progression of complicated ED by restoring erectile capacity. We aimed to evaluate potential safety and effectiveness and the clinical correlates of platelet function before platelet-rich plasma (PRP) injection in men with vascular ED unresponsive to phosphodiesterase-5 inhibitors (PDE-5is).

Methods: A number of 150 patients with vascular ED were enrolled in an open-label, single arm, multicenter, prospective, interventional, non-randomized study. After 1-month pharmacological washout from PDE-5is, the 5-item International Index of Erectile Function (IIEF-5) questionnaire was administered and dynamic penile duplex ultrasound (d-PDU) was performed. Patients then underwent intracavernous PRP injection. One month after treatment, IIEF-5 and d-PDU were evaluated. Primary aim of the study was to assess efficacy and safety of PRP treatment by evaluating the proportion of patients achieving minimal clinically important differences (MCID) in the IIEF-5 questionnaire. Secondary endpoint was to determine whether MPV could correlate with improvement in d-PDU parameters.

Results: Most patients (80%) had a significant improvement in ED symptoms (IIEF-5 Score: 12±2.6 vs. 19±3.0; P<0.0001) and in PSV (32±3.5 cm/s vs. 42±7.6 cm/s; P<0.0001) after d-PDU evaluation. The ROC curve analysis showed a significant accuracy (72.1%, CI: 64.0-80.2, P≤0.0001) for MPV in identifying men clinically responding to PRP with favorable MCID≥5 at 1 month follow-up. The MPV<8.95 fL was identified as the best predictor of success rate with a sensitivity of 90% and a specificity of 54.1%.

Conclusions: This study provides the first evidence that PRP could represent an effective and safe option for patients poorly responding to PDE-5is. MPV higher than 8.95 fL may identify patients with poor response to treatment that might benefit of successive re-challenge with PRP.

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CiteScore
4.60
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