首页> 外文期刊>Clinical Interventions in Aging >Efficacy and safety of short- and long-term, regular and on-demand regimens of phosphodiesterase type 5 inhibitors in treating erectile dysfunction after nerve-sparing radical prostatectomy: a systematic review and meta-analysis
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Efficacy and safety of short- and long-term, regular and on-demand regimens of phosphodiesterase type 5 inhibitors in treating erectile dysfunction after nerve-sparing radical prostatectomy: a systematic review and meta-analysis

机译:磷酸二酯酶5型抑制剂的短期和长期,定期和按需方案在保留神经性根治性前列腺切除术后勃起功能障碍的疗效和安全性:系统评价和荟萃分析

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Background: We performed a meta-analysis to evaluate the efficacy and safety of short-term (≤6?months) and long-term (>6?months), regular (OaD) and on-demand (PRN) regimens of phosphodiesterase type 5 inhibitors (PDE5-Is) in treating erectile dysfunction (ED) after nerve-sparing radical prostatectomy (NSRP). Methods: We conducted a literature search in August 2016. Sources included PubMed, EMBASE, and MEDLINE databases. The main outcome was International Index of Erectile Function-Erectile Function (IIEF-EF) domain score, and the secondary outcome was treatment-emergent adverse events (TEAEs). Results: Eight articles involving 13 randomized controlled trials (RCTs) were used in this analysis: they suggested that PDE5-Is can improve the IIEF-EF distinctly in comparison with placebo in short and long term (mean difference [MD]: 2.26, 95% confidence interval [CI]: 1.45–3.08, P 6?months) can improve the IIEF-EF distinctly in comparison with short-term use of PDE5-Is (≤6?months) (MD: 3.9, 95% CI: 3.01–4.8, P 6?months) (MD:??0.58, 95% CI: ?9.86 to 8.74, P =0.91). There were more TEAEs in PDE5-Is group in comparison with placebo (odds ratio [OR]: 1.55, 95% CI: 1.26–1.91, P <0.0001), and TEAEs in OaD group were not significantly different from those seen in PRN group (OR: 1.05, 95% CI: 0.78–1.4, P =0.77). Conclusion: Our meta-analysis suggests that PDE5-Is are efficient and safe for treatment of ED after NSRP, and we should choose the regular regimen for short term and regular or on-demand regimen for long term. Further high-quality RCTs are needed to validate this result.
机译:背景:我们进行了荟萃分析,以评估磷酸二酯酶类型的短期(≤6个月)和长期(> 6个月),常规(OaD)和按需(PRN)方案的疗效和安全性5种抑制剂(PDE5-Is)用于治疗保留神经的前列腺癌根治术(NSRP)后的勃起功能障碍(ED)。方法:我们于2016年8月进行了文献检索。来源包括PubMed,EMBASE和MEDLINE数据库。主要结局为国际勃起功能指数-勃起功能指数(IIEF-EF)域得分,次要结局为治疗紧急不良事件(TEAE)。结果:八篇涉及13个随机对照试验(RCT)的文章被用于此分析:他们认为PDE5-Is与安慰剂相比在短期和长期方面均可显着改善IIEF-EF(平均差异[MD]:2.26、95置信区间百分比[CI]:1.45–3.08,P 6?个月)与短期使用PDE5-Is(≤6?个月)相比,可以显着改善IIEF-EF(MD:3.9,95%CI:3.01 –4.8,P 6个月月)(MD:?? 0.58,95%CI:?9.86至8.74,P = 0.91)。与安慰剂相比,PDE5-Is组的TEAE更高(赔率[OR]:1.55,95%CI:1.26-1.91,P <0.0001),OaD组的TEAE与PRN组相比无显着差异(或:1.05,95%CI:0.78-1.4,P = 0.77)。结论:我们的荟萃分析表明,PDE5-Is治疗NSRP后的ED是安全有效的,我们应选择短期的常规治疗方案和长期的常规或按需治疗方案。需要进一步的高质量RCT来验证该结果。

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