Effect of antidepressants on ejaculation dysfunction in patients with depression and anxiety: A systematic review and network meta‐analysis

医学 依西酞普兰 内科学 性功能障碍 荟萃分析 不利影响 帕罗西汀 度洛西汀 焦虑 重性抑郁障碍 萧条(经济学) 安慰剂 氯丙咪嗪 优势比 随机对照试验 精神科 心情 抗抑郁药 宏观经济学 经济 替代医学 病理
作者
Qihua Wang,Zhunan Xu,Xiangyu Chen,Lei Zhu,Xiaoqiang Liu
出处
期刊:International Journal of Andrology [Wiley]
标识
DOI:10.1111/andr.13770
摘要

Abstract Introduction Antidepressants may lead to a series of sexual adverse effects (SAEs), among which ejaculation dysfunction (EjD) is often overlooked by clinicians. The purpose of the present network meta‐analysis was to assist drug adjustment by comparing and ranking the incidence of EjD among various antidepressants. Methods Relevant studies were retrieved from PubMed, Embase, Scopus, Web of Science, ClinicalTrials.gov, and other additional records. Eligible randomized controlled trials (RCTs) assessed the rate of EjD in patients with major depressive disorder (MDD) and anxiety disorder after taking anti‐depressants. The incidences of EjD, erectile dysfunction (ED), decreased libido (DL), adverse events (AE), withdrawal due to adverse events (WDAE) and withdrawal due to lack of efficacy (WDLE) were pooled using odds ratio (OR) with their 95% confidence intervals (CI). The values of surface under the cumulative ranking curve (SUCRA) helped to rank the risk of each outcome in different antidepressants. Results Thirty RCTs comprising 18,157 patients were included. Results of all node‐splitting analysis demonstrated no statistical inconsistency (all P > 0.05). Clomipramine (OR 42.11, 95% CI [9.90, 179.08]), WS5570 (OR 28.99, 95% CI [1.48, 568.97]) and paroxetine (OR 18.63, 95% CI [9.33, 37.23]) had significant risk of EjD comparing to placebo. Additionally, duloxetine (OR 7.37, 95% CI [2.61, 20.78]), clomipramine (OR 5.29, 95% CI [1.72, 16.25]), paroxetine (OR 3.75, 95% CI [1.37, 10.26]) and escitalopram (OR 3.04, 95% CI [1.20, 7.71]) presented higher risk of ED comparing to placebo. Agomelatine, levomilnacipran, vortioxetine, trazodone, vilazodone, fluvoxamine and imipramine exhibited similar incidence of EjD with placebo (all P > 0.05). Besides, trazodone, vilazodone and vortioxetine had the top‐five SUCRA values in each of SAEs (EjD, ED and DL), and agomelatine might be alternative in EjD and DL. Considering about AE, WDAE and WDLE, vilazodone appeared to offer more satisfactory performance across all these aspects. Conclusions For patients undergoing SAEs following the administration of antidepressants, trazodone, vortioxetine, vilazodone and agomelatine are alternative antidepressants.
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