Coughlin Catherine G, Blackwell Katherine A, Bartley Christine, Hay Madeleine, Yonkers Kimberly A, Bloch Michael H
Connecticut Mental Health Center, Yale Child Study Center, Yale University, and the Departments of Psychiatry and Obstetrics, Gynecology, and Reproductive Sciences, Yale School of Medicine, New Haven, Connecticut.
Obstet Gynecol. 2015 May;125(5):1224-1235. doi: 10.1097/AOG.0000000000000759.
Antipsychotic medications are used by increasing numbers of women of reproductive age. The safety of these medications during pregnancy has not been well described. We undertook a systematic review and meta-analysis of the adverse obstetric and neonatal outcomes associated with exposure to antipsychotics during pregnancy.
PubMed, Reprotox, and ClinicalTrials.gov were searched to identify potential studies for inclusion.
Case-control or cohort studies estimating adverse birth outcomes associated with antipsychotic exposure during pregnancy were included. Pooled odds ratios (ORs) were used for dichotomous outcomes and weighted mean differences were used for neonatal birth weight and gestational age. Thirteen cohort studies, including 6,289 antipsychotic-exposed and 1,618,039 unexposed pregnancies, were included.
TABULATION, INTEGRATION, AND RESULTS: Antipsychotic exposure was associated with an increased risk of major malformations (absolute risk difference [ARD] 0.03, 95% confidence interval [CI] 0.00-0.05, P=.04, Z=2.06), heart defects (ARD 0.01, 95% CI 0.00-0.01, P<.001, Z=3.44), preterm delivery (ARD 0.05, 95% CI 0.03-0.08, P<.001, Z=4.10), small-for-gestational-age births (ARD 0.05, 95% CI 0.02-0.09, P=.006, Z=2.74), elective termination (ARD 0.09, 95% CI 0.05-0.13, P<.001, Z=4.69), and decreased birth weight (weighted mean difference -57.89 g, 95% CI -103.69 to -12.10 g, P=.01). There was no significant difference in the risk of major malformations (test for subgroup differences: χ²=0.07, degrees of freedom=1, P=.79) between typical (OR 1.55, 95% CI 1.21-1.99, P=.006) and atypical (OR 1.39, 95% CI 0.66-2.93, P=.38) antipsychotic medications. Antipsychotic exposure was not associated with risk of large-for-gestational-age births, stillbirth, and spontaneous abortion. Although antipsychotic exposure during pregnancy was associated with increased risk of adverse obstetric and neonatal outcomes, this association does not necessarily imply causation. This analysis was limited by the small number of included studies and limited adjustment in studies for possible confounders.
Women requiring antipsychotic treatment during pregnancy appear at higher risk of adverse birth outcomes, regardless of causation, and may benefit from close monitoring and minimization of other potential risk factors during pregnancy.
育龄期女性使用抗精神病药物的人数日益增加。这些药物在孕期的安全性尚未得到充分描述。我们对孕期接触抗精神病药物相关的不良产科和新生儿结局进行了系统评价和荟萃分析。
检索了PubMed、Reprotox和ClinicalTrials.gov以确定可能纳入的研究。
纳入估计孕期接触抗精神病药物与不良出生结局相关的病例对照研究或队列研究。二分类结局采用合并比值比(OR),新生儿出生体重和孕周采用加权均数差。纳入了13项队列研究,包括6289例接触抗精神病药物的妊娠和1618039例未接触抗精神病药物的妊娠。
制表、整合与结果:接触抗精神病药物与 major畸形风险增加相关(绝对风险差[ARD] 0.03,95%置信区间[CI] 0.00 - 0.05,P = 0.04,Z = 2.06)、心脏缺陷(ARD 0.01,95% CI 0.00 - 0.01,P < 0.001,Z = 3.44)、早产(ARD 0.05,95% CI 0.03 - 0.08,P < 0.001,Z = 4.10)、小于胎龄儿出生(ARD 0.05,95% CI 0.02 - 0.09,P = 0.006,Z = 2.74)、选择性终止妊娠(ARD 0.09,95% CI 0.05 - 0.13,P < 0.001,Z = 4.69)及出生体重降低(加权均数差 - 57.89 g,95% CI - 103.69至 - 12.10 g,P = 0.01)。典型抗精神病药物(OR 1.55,95% CI 1.21 - 1.99,P = 0.006)和非典型抗精神病药物(OR 1.39,95% CI 0.66 - 2.93,P = 0.38)之间major畸形风险无显著差异(亚组差异检验:χ² = 0.07,自由度 = 1,P = 0.79)。接触抗精神病药物与大于胎龄儿出生、死产和自然流产风险无关。尽管孕期接触抗精神病药物与不良产科及新生儿结局风险增加相关,但这种关联不一定意味着因果关系。该分析受纳入研究数量少及研究中对可能混杂因素调整有限的限制。
孕期需要抗精神病治疗的女性出现不良出生结局的风险似乎更高,无论因果关系如何,且孕期密切监测及尽量减少其他潜在风险因素可能对其有益。