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子宫内暴露于甾体避孕药与妊娠结局

In utero exposure to steroid contraceptives and outcome of pregnancy.

作者信息

Pardthaisong T, Gray R H

机构信息

Department of Community Medicine, University of Chiang Mai, Thailand.

出版信息

Am J Epidemiol. 1991 Oct 15;134(8):795-803. doi: 10.1093/oxfordjournals.aje.a116152.

Abstract

A cohort study of women who used steroid contraceptives during pregnancy was conducted in Chiang Mai, northern Thailand, between 1984 and 1987. There were 1,573 pregnancies in which the fetus was exposed to the injectable contraceptive Depo-Provera (The Upjohn Company, Kalamazoo, Michigan) (830 accidental pregnancies and 743 infants conceived before the mother started use of Depo-Provera), 601 accidental pregnancies in women who were using oral contraceptives, and 2,578 planned pregnancies with no steroid exposures (controls). Subjects were followed up for interview, and medical records were traced for birth weight. Women using Depo-Provera had more risk factors for adverse pregnancy outcomes than did the other groups. The adjusted odds ratios for low birth weight were increased for accidental pregnancies with fetal exposure to Depo-Provera (odds ratio (OR) = 1.5, 95% confidence interval (Cl) 1.2-1.9) or oral contraceptives (OR = 1.5, 95% Cl 1.2-2.0). The higher risk of low birth weight among infants exposed in utero to Depo-Provera or oral contraceptives is due in part to self-selection for adverse outcomes among women with unplanned pregnancies. However, among accidental pregnancies with Depo-Provera, the risk of low birth weight was significantly increased when conception was estimated to have occurred within 4 weeks of injection. The odds ratios were 1.9 (95% Cl 1.4-3.2) for injection-to-conception intervals of less than or equal to 4 weeks, 1.5 (95% Cl 0.9-2.3) for intervals of 5-8 weeks, and 1.2 (95% Cl 0.7-1.9) for intervals of greater than or equal to 9 weeks. This trend was highly significant. Thus, the authors conclude that early, high-dose in utero exposures to Depo-Provera may affect fetal growth.

摘要

1984年至1987年期间,在泰国北部清迈对孕期使用甾体避孕药的女性进行了一项队列研究。共有1573例妊娠,其中胎儿接触了注射用避孕药醋酸甲羟孕酮(美国密歇根州卡拉马祖的普强公司生产)(830例意外妊娠,743例婴儿在母亲开始使用醋酸甲羟孕酮之前受孕),601例使用口服避孕药的女性意外妊娠,以及2578例未接触甾体药物的计划妊娠(对照组)。对受试者进行随访访谈,并追查医疗记录以获取出生体重信息。使用醋酸甲羟孕酮的女性比其他组有更多不良妊娠结局的风险因素。胎儿接触醋酸甲羟孕酮(比值比(OR)=1.5,95%置信区间(Cl)1.2 - 1.9)或口服避孕药(OR = 1.5,95% Cl 1.2 - 2.0)的意外妊娠中,低出生体重的调整后比值比升高。子宫内接触醋酸甲羟孕酮或口服避孕药的婴儿出生体重较低的较高风险部分归因于意外妊娠女性中不良结局的自我选择。然而,在接触醋酸甲羟孕酮的意外妊娠中,当估计受孕发生在注射后4周内时,低出生体重的风险显著增加。注射至受孕间隔小于或等于4周时,比值比为1.9(95% Cl 1.4 - 3.2),5 - 8周时为1.5(95% Cl 0.9 - 2.3),大于或等于9周时为1.2("95% Cl 0.7 - 1.9)。这种趋势非常显著。因此,作者得出结论,子宫内早期、高剂量接触醋酸甲羟孕酮可能会影响胎儿生长。

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