The First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450052, Henan, People's Republic of China.
College of Physical Education (Based School), Zhengzhou University, Zhengzhou, 450001, Henan, People's Republic of China.
Sci Rep. 2022 Feb 28;12(1):3304. doi: 10.1038/s41598-022-05560-w.
Depression is very common after stroke, causing multiple sequelae. We aimed to explore the efficacy of escitalopram for poststroke depression (PSD). PubMed, Embase, Scopus, Cochrane Central Register of Controlled Trials, Clinical trials. gov, Wan fang Data (Chinese), VIP (Chinese) and CNKI (Chinese) were retrieved from inception to May 2021. We recruited Randomized Controlled Trials (RCTs) which met the inclusion criteria in our study. The depression rating scores, the incidence of PSD, adverse events as well as functional outcomes were analyzed. 11 studies and 1374 participants were recruited in our work. The results were depicted: the reduction of depression rating scores was significant in the escitalopram groups and the standard mean difference (SMD) was - 1.25 (P < 0.001), 95% confidence interval (95% CI), - 1.82 to - 0.68; the risk ratio (RR) of the incidence of PSD was 0.52 (95% CI, 0.29 to 0.91; P = 0.007 < 0.05), which was significantly lower in the escitalopram groups; Escitalopram is safe for stroke patients; there was improvement of the motor function. However, in sensitivity analyses, the conclusions of the motor function and the incidence of drowsiness were altered. The study suggests that escitalopram has a potentially effective role compared with control groups and demonstrates escitalopram is safe. However, the results of the motor function and the incidence of drowsiness should be considered carefully and remain to be discussed in the future.
抑郁症在中风后很常见,会导致多种后遗症。我们旨在探索依西酞普兰治疗中风后抑郁症(PSD)的疗效。我们从建库到 2021 年 5 月检索了 PubMed、Embase、Scopus、Cochrane 中央对照试验注册库、Clinicaltrials.gov、万方数据(中文)、维普(中文)和中国知网(中文)。我们招募了符合纳入标准的随机对照试验(RCT)。分析抑郁评分、PSD 发生率、不良反应和功能结局。我们的研究纳入了 11 项研究和 1374 名参与者。结果显示:依西酞普兰组的抑郁评分降低更显著,标准化均数差(SMD)为-1.25(P<0.001),95%置信区间(95%CI)为-1.82 至-0.68;PSD 发生率的风险比(RR)为 0.52(95%CI,0.29 至 0.91;P=0.007<0.05),依西酞普兰组显著更低;依西酞普兰对中风患者是安全的;运动功能有所改善。然而,在敏感性分析中,运动功能和嗜睡发生率的结论发生了改变。该研究表明,与对照组相比,依西酞普兰具有潜在的治疗效果,且证明了依西酞普兰是安全的。然而,运动功能和嗜睡发生率的结果应谨慎考虑,并在未来进一步讨论。