Oberlander Tim F, Warburton William, Misri Shaila, Riggs Wayne, Aghajanian Jaafar, Hertzman Clyde
Department of Pediatrics, University of British Columbia, Vancouver, BC, Canada.
Birth Defects Res B Dev Reprod Toxicol. 2008 Feb;83(1):68-76. doi: 10.1002/bdrb.20144.
To determine a population-based incidence of congenital anomalies following prenatal exposure to serotonin reuptake inhibitor (SRI) antidepressants used alone and in combination with a benzodiazepines (BZ).
Population health data, maternal health, and prenatal prescription records were linked to neonatal records, representing all live births (British Columbia, Canada, N=119,547) during a 39-month period (1998-2001). The incidence and risk differences (RD) for major congenital anomalies (CA) and congenital heart disease (CHD), including ventricular and atrial septal defects (VSD, ASD), from infants of mothers treated with an SRI alone, a benzodiazepine (BZ) alone, or SRI+BZ in combinationcompared to outcomesno exposure.
Risk for a CA or CHD did increase following combined SRI+BZ exposure compared with no exposure. However, using a weighted regression model, controlling for maternal illness characteristics, combination therapy risk remained significantly associated only with CHD. The risk for an ASD was higher following SRI monotherapy compared with no exposure, after adjustment for maternal covariates. Dose/day was not associated with increased risk.
Infants exposed to prenatal SRIs in combination with BZs had a higher a incidence of CHD compared to no exposure, even after controlling for maternal illness characteristics. SRI monotherapy was not associated with an increased risk for major CA, but was associated with an increased incidence of ASD. Risk was not associated with first trimester medication dose/day.
确定产前单独使用血清素再摄取抑制剂(SRI)抗抑郁药以及与苯二氮䓬类药物(BZ)联合使用时先天性异常的基于人群的发病率。
将人群健康数据、孕产妇健康和产前处方记录与新生儿记录相关联,这些记录代表了39个月期间(1998 - 2001年)加拿大不列颠哥伦比亚省的所有活产婴儿(N = 119,547)。将单独接受SRI治疗、单独接受苯二氮䓬类药物(BZ)治疗或SRI + BZ联合治疗的母亲所生婴儿的主要先天性异常(CA)和先天性心脏病(CHD)(包括室间隔和房间隔缺损(VSD、ASD))的发病率和风险差异(RD)与未暴露的结果进行比较。
与未暴露相比,联合使用SRI + BZ暴露后CA或CHD的风险确实增加。然而,使用加权回归模型,在控制孕产妇疾病特征后,联合治疗风险仅与CHD仍有显著关联。在调整孕产妇协变量后,SRI单药治疗后ASD的风险高于未暴露。每日剂量与风险增加无关。
即使在控制孕产妇疾病特征后,产前暴露于SRI与BZ联合治疗的婴儿患CHD的发病率仍高于未暴露者。SRI单药治疗与主要CA风险增加无关,但与ASD发病率增加有关。风险与孕早期每日药物剂量无关。