Ennis Zandra Nymand, Damkier Per
Department of Clinical Chemistry and Pharmacology, Odense University Hospital, Odense, Denmark.
Basic Clin Pharmacol Toxicol. 2015 Apr;116(4):315-20. doi: 10.1111/bcpt.12372. Epub 2015 Jan 28.
To review available data on first-trimester exposure to olanzapine, quetiapine, risperidone and aripiprazole and risk of congenital malformations. We performed a systematic literature search in accordance with PRISMA guidelines identifying studies containing original data on first-trimester exposure and pregnancy outcome with respect to congenital malformations. Cumulated data for olanzapine were 1090 first-trimester-exposed pregnancies with 38 malformations resulting in a malformation rate of 3.5%. The corresponding numbers for quetiapine, risperidone and aripiprazole were 443/16 (3.6%), 432/22 (5.1%) and 100/5 (5.0%), respectively. Relative risk estimates and 95% confidence intervals were 1.0 (0.7-1.4) (olanzapine), 1.0 (0.6-1.7) (quetiapine), 1.5 (0.9-2.2) (risperidone) and 1.4 (0.5-3.1) (aripiprazole). First-trimester exposure to olanzapine is not associated with an increased risk of congenital malformation. Data for quetiapine and risperidone do not suggest a substantially increased risk, while the risk estimate for aripiprazole remains imprecise owing to a low amount of data.
回顾关于孕早期暴露于奥氮平、喹硫平、利培酮和阿立哌唑与先天性畸形风险的现有数据。我们按照PRISMA指南进行了系统的文献检索,以确定包含关于孕早期暴露与先天性畸形妊娠结局原始数据的研究。奥氮平的累积数据为1090例孕早期暴露妊娠,其中38例畸形,畸形率为3.5%。喹硫平、利培酮和阿立哌唑的相应数字分别为443/16(3.6%)、432/22(5.1%)和100/5(5.0%)。相对风险估计值和95%置信区间分别为1.0(0.7 - 1.4)(奥氮平)、1.0(0.6 - 1.7)(喹硫平)、1.5(0.9 - 2.2)(利培酮)和1.4(0.5 - 3.1)(阿立哌唑)。孕早期暴露于奥氮平与先天性畸形风险增加无关。喹硫平和利培酮的数据未表明风险大幅增加,而由于数据量少,阿立哌唑的风险估计值仍不精确。