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孕早期接触组胺H2受体阻滞剂的安全性。一项前瞻性队列研究。

Safety of first trimester exposure to histamine H2 blockers. A prospective cohort study.

作者信息

Magee L A, Inocencion G, Kamboj L, Rosetti F, Koren G

机构信息

Division of Clinical Pharmacology/Toxicology, Hospital for Sick Children, Toronto, Ontario, Canada.

出版信息

Dig Dis Sci. 1996 Jun;41(6):1145-9. doi: 10.1007/BF02088230.

Abstract

The objective of this study was to examine whether H2 blockers represent a major teratogenic risk. This prospective cohort study was done at the Motherisk Program, a Teratology Information Service, Toronto, Canada. The subjects included 178 women who contacted Motherisk about gestational H2-blocker use, and 178 controls matched for maternal age, smoking, and heavy alcohol consumption. The main outcome measures were primary--major malformations, and secondary--pregnancy outcome, method of delivery, gestational age, prematurity, birthweight, small for gestational age infants, neonatal health problems, and developmental milestones. No increase in major malformations was found following first trimester exposure to H2 blockers [2.1% vs 3.5% (controls), mean difference (95% CI) -1.4% (-5.2, +2.4)]. No other aspects of pregnancy outcome or neonatal health differed between groups. This study suggests that H2-blocker exposure during the first trimester does not represent a major teratogenic risk.

摘要

本研究的目的是检验H2受体阻滞剂是否存在重大致畸风险。这项前瞻性队列研究在加拿大多伦多的致畸信息服务机构Motherisk项目中进行。研究对象包括178名就孕期使用H2受体阻滞剂咨询Motherisk的女性,以及178名在母亲年龄、吸烟和大量饮酒方面与之匹配的对照者。主要结局指标为一级——严重畸形,以及二级——妊娠结局、分娩方式、孕周、早产、出生体重、小于胎龄儿、新生儿健康问题和发育里程碑。孕早期接触H2受体阻滞剂后,严重畸形并未增加[2.1% 对比3.5%(对照),平均差异(95%CI)-1.4%(-5.2,+2.4)]。两组之间妊娠结局或新生儿健康的其他方面没有差异。本研究表明,孕早期接触H2受体阻滞剂并不存在重大致畸风险。

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