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舍曲林治疗早泄的疗效与安全性:系统评价与荟萃分析。

Efficacy and safety of sertraline for the treatment of premature ejaculation: Systematic review and meta-analysis.

作者信息

Yi Zhan-Miao, Chen Shi-Di, Tang Qi-Yu, Tang Hui-Lin, Zhai Suo-Di

机构信息

Department of Pharmacy, Peking University Third Hospital.

Department of Pharmacy Administration and Clinical Pharmacy, Peking University School of Pharmaceutical Science.

出版信息

Medicine (Baltimore). 2019 Jun;98(23):e15989. doi: 10.1097/MD.0000000000015989.

Abstract

BACKGROUD

Evidence on the efficacy and safety of sertraline in patients with premature ejaculation (PE) was inconsistent. The objective of this article is to evaluate the efficacy and safety of sertraline for the treatment of PE.

METHODS

We searched Medline (OVID), Embase, the Cochrane Library, and 2 Chinese databases for randomized controlled trials (RCTs) and randomized crossover trials (RTs) that evaluated the efficacy and safety of sertraline in patients with PE. A meta-analysis was performed to calculate their pooled estimates with 95% confidence interval.

RESULTS

Of the 645 records obtained, we included 12 RCTs and 2 RTs (n = 977). Meta-analysis showed that sertraline prolonged intravaginal ejaculation latency time (IELT) in PE patients ((standard mean difference (SMD) = 2.14, 95% CI 1.20 to 3.08). Subgroup analyses indicated a prolonged IELT for different treatment courses: 4 weeks (SMD = 2.66, 1.06 to 4.26), 6 weeks (SMD = 0.95, 0.31 to 1.58), and 8 weeks (SMD = 1.81, 0.78 to 2.85). The sexual satisfaction rates of patients (SMD = 2.20, 1.57 to 2.84) and spouses (SMD = 2.27, 1.44 to 3.09) were also improved. We observed a significant increased risk of gastrointestinal upset (risk ratio = 2.71, 1.39 to 5.28) in the sertraline group.

CONCLUSION

Sertraline can prolong IELT of PE patients, improve sexual satisfaction rates of patients and spouses, but increase risk of gastrointestinal upset.

摘要

背景

关于舍曲林治疗早泄(PE)患者的疗效和安全性的证据并不一致。本文的目的是评估舍曲林治疗PE的疗效和安全性。

方法

我们检索了医学文献数据库(OVID)、Embase、考克兰图书馆以及2个中文数据库,以查找评估舍曲林治疗PE患者疗效和安全性的随机对照试验(RCT)和随机交叉试验(RT)。进行荟萃分析以计算其合并估计值及95%置信区间。

结果

在获得的645条记录中,我们纳入了12项RCT和2项RT(n = 977)。荟萃分析表明,舍曲林可延长PE患者的阴道内射精潜伏期(IELT)(标准化均数差(SMD)= 2.14,95%置信区间为1.20至3.08)。亚组分析显示不同疗程的IELT均延长:4周(SMD = 2.66,1.06至4.26)、6周(SMD = 0.95,0.31至1.58)和8周(SMD = 1.81,0.78至2.85)。患者(SMD = 2.20,1.57至2.84)及其配偶(SMD = 2.27,1.44至3.09)的性满意度也有所提高。我们观察到舍曲林组胃肠道不适风险显著增加(风险比 = 2.71,1.39至5.28)。

结论

舍曲林可延长PE患者的IELT,提高患者及其配偶的性满意度,但会增加胃肠道不适风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dce/6571276/77b608ed1c74/medi-98-e15989-g001.jpg

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