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氟西汀与其他选择性 5-羟色胺再摄取抑制剂治疗早泄的比较:系统评价和荟萃分析。

Comparison of fluoxetine with other selective serotonin reuptake inhibitors in the treatment of premature ejaculation: A systematic review and meta-analysis.

机构信息

The Department of Urology, The First Affiliated Hospital of Anhui Medical University, Hefei, China.

The Department of Urology, Peking University Third Hospital, Beijing, China.

出版信息

Andrologia. 2022 Sep;54(8):e14500. doi: 10.1111/and.14500. Epub 2022 Jun 27.

Abstract

The primary goal of this systematic review and meta-analysis was to compare the efficacy and safety of fluoxetine with other oral pharmaceuticals in the treatment of premature ejaculation (PE). We searched through databases including CNKI, PubMed, EMBASE and Cochrane to find research published up to 31 March 2022. PROSPERO was used to pre-register this meta-analysis (registration number CRD42022315459). Two separate writers extracted relevant details from all of the papers included in the study. To analyse the quality of literature publishing, we used the Cochrane risk of bias tool. The severity of premature ejaculation was determined using intravaginal ejaculatory latency time (IELT), and the effectiveness and safety of pharmacological interventions were determined using standardized mean difference (SMD) and risk ratio (RR) values with matching 95% confidence level intervals (95% CIs). Our meta-analysis includes a total of ten trials to investigate into the differences in treatment efficacy and safety between fluoxetine and other medicines. The findings revealed that fluoxetine was more effective than placebo in treating PE, whereas sertraline and paroxetine were more effective than fluoxetine (p < 0.05). The side effects of the medications were not significantly different, and they were all acceptable. The results of the sensitivity analysis were unaffected by the removal of any of the articles. There was no evidence of bias in the media. This meta-analysis examined the differences in efficacy and safety between fluoxetine and other oral medications and can be used by clinicians in the treatment of PE.

摘要

本系统评价和荟萃分析的主要目的是比较氟西汀与其他口服药物治疗早泄(PE)的疗效和安全性。我们检索了中国知网、PubMed、EMBASE 和 Cochrane 等数据库,以查找截至 2022 年 3 月 31 日发表的研究。PROSPERO 用于对本次荟萃分析进行预注册(注册号 CRD42022315459)。两位独立的作者从研究中包含的所有论文中提取相关细节。为了分析文献出版的质量,我们使用了 Cochrane 偏倚风险工具。使用阴道内射精潜伏期时间(IELT)来确定早泄的严重程度,使用标准化均数差(SMD)和风险比(RR)值及其匹配的 95%置信区间(95%CI)来确定药物干预的有效性和安全性。我们的荟萃分析共纳入了十项试验,以研究氟西汀与其他药物治疗效果和安全性的差异。研究结果表明,氟西汀治疗 PE 的效果优于安慰剂,而舍曲林和帕罗西汀的效果优于氟西汀(p<0.05)。药物的副作用无明显差异,且均可以接受。敏感性分析的结果不受任何文章剔除的影响。荟萃分析并未发现存在偏倚。本研究考察了氟西汀与其他口服药物在疗效和安全性方面的差异,可供临床医生在治疗 PE 时参考。

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