De Vries Courtney, Gadzhanova Svetla, Sykes Matthew J, Ward Michael, Roughead Elizabeth
Clinical and Health Sciences, University of South Australia, North Terrace adjacent Morphett St Bridge, Adelaide, 5000, SA, Australia.
Quality Use of Medicines and Pharmacy Research Centre, University of South Australia, Adelaide, SA, Australia.
Drug Saf. 2021 Mar;44(3):291-312. doi: 10.1007/s40264-020-01027-x. Epub 2020 Dec 22.
Antidepressant use during the first trimester is reported in 4-8% of pregnancies. The use of some selective serotonin reuptake inhibitors during the first trimester has been identified as increasing the odds for congenital heart defects; however, little is known about the safety of non-selective serotonin reuptake inhibitor antidepressants.
The objective of this study was to assess the odds of congenital heart defects associated with the use of antidepressants during the first trimester of pregnancy, and to update the literature as newer studies have been published since the latest systematic literature review and meta-analysis.
PubMed and Embase were searched till 3 June, 2020. Study quality was assessed, and study details were extracted. Meta-analyses were performed using RevMan 5.4, which assessed: (1) any antidepressant usage; (2) classes of antidepressants; and (3) individual antidepressants.
Twenty studies were identified, encompassing 5,337,223 pregnancies. The odds ratio for maternal use of any antidepressant during the first trimester of pregnancy and the presence of congenital heart defects from the random effects meta-analysis was 1.28 (95% confidence interval [CI] 1.17-1.41). Significant odds ratios of 1.69 (95% CI 1.37-2.10) and 1.25 (95% CI 1.15-1.37) were reported for serotonin norepinephrine reuptake inhibitors and selective serotonin reuptake inhibitors, respectively. A non-statistically significant odds ratio of 1.02 (95% CI 0.82-1.25) was reported for the tricyclic antidepressants. Analyses of individual SSRIs produced significant odds ratios of 1.57 (95% CI 1.25-1.97), 1.36 (95% CI 1.08-1.72), and 1.29 (95% CI 1.14-1.45) for paroxetine, fluoxetine, and sertraline, respectively. The norepinephrine-dopamine-reuptake inhibitor bupropion also produced a significant odds ratio of 1.23 (95% CI 1.01-1.49).
The selective serotonin reuptake inhibitor and serotonin norepinephrine reuptake inhibitor classes of antidepressants pose a greater risk for causing congenital heart defects than the tricyclic antidepressants. However, this risk for individual antidepressants within each class varies, and information regarding some antidepressants is still lacking.
据报道,4%-8%的孕妇在孕早期使用过抗抑郁药。已确定在孕早期使用某些选择性5-羟色胺再摄取抑制剂会增加先天性心脏缺陷的几率;然而,对于非选择性5-羟色胺再摄取抑制剂类抗抑郁药的安全性知之甚少。
本研究的目的是评估孕早期使用抗抑郁药与先天性心脏缺陷相关的几率,并随着自最新系统文献综述和荟萃分析以来发表的更新研究对文献进行更新。
检索截至2020年6月3日的PubMed和Embase数据库。评估研究质量并提取研究细节。使用RevMan 5.4进行荟萃分析,评估内容包括:(1)任何抗抑郁药的使用情况;(2)抗抑郁药类别;(3)个别抗抑郁药。
共纳入20项研究,涵盖5337223例妊娠。随机效应荟萃分析显示,孕早期母亲使用任何抗抑郁药与先天性心脏缺陷存在之间的比值比为1.28(95%置信区间[CI]1.17-1.41)。血清素去甲肾上腺素再摄取抑制剂和选择性血清素再摄取抑制剂的显著比值比分别为1.69(95%CI 1.37-2.10)和1.25(95%CI 1.15-1.37)。三环类抗抑郁药的比值比为1.02(95%CI 0.82-1.25),无统计学意义。对个别选择性5-羟色胺再摄取抑制剂的分析显示,帕罗西汀、氟西汀和舍曲林的显著比值比分别为1.57(95%CI 1.25-1.97)、1.36(95%CI 1.08-1.72)和1.29(95%CI 1.14-1.45)。去甲肾上腺素-多巴胺再摄取抑制剂安非他酮的显著比值比也为1.23(95%CI 1.01-1.49)。
选择性血清素再摄取抑制剂和血清素去甲肾上腺素再摄取抑制剂类抗抑郁药比三环类抗抑郁药导致先天性心脏缺陷的风险更大。然而,每类中个别抗抑郁药的这种风险各不相同,并且关于某些抗抑郁药的信息仍然缺乏。