Women's Mood and Anxiety Clinic: Reproductive Transitions, Department of Psychiatry, FG 29, Sunnybrook Health Sciences Centre, 2075 Bayview Ave, Toronto, ON M4N 3M5, Canada.
J Clin Psychiatry. 2013 Apr;74(4):e293-308. doi: 10.4088/JCP.12r07966.
Depression is often not optimally treated during pregnancy, partially because of conflicting data regarding antidepressant medication risk. This meta-analysis was conducted to determine whether antenatal antidepressant exposure is associated with congenital malformations and to assess the effect of known methodological limitations.
EMBASE, CINAHL, PsycINFO, and MEDLINE were searched from their start dates to June 2010. Keywords of various combinations were used, including, but not limited to depressive/mood disorder, pregnancy, antidepressant drug/agent, congenital malformation, and cardiac malformation.
English language studies reporting congenital malformations associated with antidepressants were included. Of 3,074 abstracts reviewed, 735 studies were retrieved and 27 studies were included.
Two reviewers working independently assessed article quality. Data on use of any antidepressant, including fluoxetine and paroxetine specifically, were extracted. Outcomes included congenital malformations, major congenital malformations, cardiovascular defects, septal heart defects (ventral septal defects and atrial septal defects), and ventral septal defects only.
Nineteen studies were above quality threshold and make up the primary meta-analyses. Pooled relative risks (RRs) were derived by using random-effects methods. Antidepressant exposure was not associated with congenital malformations (RR = 0.93; 95% CI, 0.85-1.02; P = .113) or major malformations (RR = 1.07; 95% CI, 0.99-1.17; P = .095). However, increased risk for cardiovascular malformations (RR = 1.36; 95% CI, 1.08-1.71; P = .008) and septal heart defects (RR = 1.40; 95% CI, 1.10-1.77; P = .005) were found; the RR for ventral septal defects was similar to septal defects, although not significant (RR = 1.54; 95% CI, 0.71-3.33; P = .274). Pooled effects were significant for paroxetine and cardiovascular malformations (RR = 1.43; 95% CI, 1.08-1.88; P = .012). These results are contrasted with those addressing methodological limitations but are typically consistent.
Overall, antidepressants do not appear to be associated with an increased risk of congenital malformations, but statistical significance was found for cardiovascular malformations. Results were robust in several sensitivity analyses. Given that the RRs are marginal, they may be the result of uncontrolled confounders. Although the RRs were statistically significant, none reached clinically significant levels.
怀孕期间抑郁症的治疗往往不尽人意,部分原因是抗抑郁药物风险的数据相互矛盾。本荟萃分析旨在确定产前抗抑郁药物暴露是否与先天畸形有关,并评估已知方法学局限性的影响。
从开始日期到 2010 年 6 月,检索了 EMBASE、CINAHL、PsycINFO 和 MEDLINE 数据库。使用了各种组合的关键词,包括但不限于抑郁/情绪障碍、妊娠、抗抑郁药物/药物、先天畸形和心脏畸形。
纳入了与抗抑郁药相关的先天畸形的英文研究报告。在审查了 3074 篇摘要后,检索到 735 篇研究,并纳入了 27 篇研究。
两名独立评估文章质量的研究人员提取了使用任何抗抑郁药的数据,包括氟西汀和帕罗西汀。结果包括先天畸形、重大先天畸形、心血管缺陷、间隔心脏缺陷(室间隔缺损和房间隔缺损)和室间隔缺损。
19 项研究质量超过了标准,构成了主要的荟萃分析。采用随机效应方法得出了合并相对风险(RR)。抗抑郁药暴露与先天畸形(RR=0.93;95%置信区间,0.85-1.02;P=0.113)或重大畸形(RR=1.07;95%置信区间,0.99-1.17;P=0.095)无关。然而,发现心血管畸形(RR=1.36;95%置信区间,1.08-1.71;P=0.008)和间隔心脏缺陷(RR=1.40;95%置信区间,1.10-1.77;P=0.005)的风险增加;尽管无统计学意义(RR=1.54;95%置信区间,0.71-3.33;P=0.274),但室间隔缺损的 RR 与间隔缺陷相似。帕罗西汀与心血管畸形的合并效应具有统计学意义(RR=1.43;95%置信区间,1.08-1.88;P=0.012)。这些结果与那些解决方法学局限性的结果形成对比,但通常是一致的。
总体而言,抗抑郁药似乎不会增加先天畸形的风险,但心血管畸形有统计学意义。在几项敏感性分析中,结果都是稳健的。鉴于 RR 是边缘的,它们可能是未被控制的混杂因素的结果。尽管 RR 具有统计学意义,但没有一个达到临床显著水平。