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Exposure to trimethoprim/sulfamethoxazole but not other {FDA} category C and D anti-infectives is associated with increased risks of preterm birth and low birth weight

机译:暴露于甲氧苄啶/磺胺甲恶唑而不是其他 {FDA } C类和D类抗感染药会增加早产和低出生体重的风险

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SummaryObjective To examine the association between trimethoprim/sulfamethoxazole, other {US} Food and Drug Administration (FDA) C and D anti-infectives, and non anti-infective {FDA} C, D, and X drugs used during pregnancy with preterm birth and low birth weight. Methods We carried out a retrospective cohort study based on a 50% random sample of women who gave birth in the Canadian province of Saskatchewan from 1997 to 2000. The association between trimethoprim/sulfamethoxazole, other {FDA} C and D anti-infectives (fluconazole, clarithromycin, doxycycline, and tetracycline), and non anti-infective {FDA} C, D, and X drugs used during pregnancy with preterm birth and low birth weight was evaluated using multiple logistic regression, with adjusted odds ratios (aORs) and 95% confidence intervals (CIs) as association measures. Results A total of 17?939 women were included in the final analysis. Trimethoprim/sulfamethoxazole was associated with significantly increased risks for preterm birth (aOR 1.51, 95% {CI} 1.10, 2.08) and low birth weight (aOR 1.67, 95% {CI} 1.14, 2.46). Exposure to non anti-infective {FDA} category C, D and X drugs was also associated with increased risks for preterm birth (aOR 1.17, 95% {CI} 1.09, 1.31) and low birth weight (aOR 1.14, 95% {CI} 0.92, 1.42), but to a lesser degree. Other {FDA} C and D anti-infectives were not (statistically) significantly associated with increased risks for preterm birth (aOR 0.93, 95% {CI} 0.49, 1.77) or low birth weight (aOR 0.65, 95% {CI} 0.27, 1.60). Conclusions Among {FDA} C, D and X drugs, trimethoprim/sulfamethoxazole, a folic acid antagonist, has the strongest association with preterm birth and low birth weight.
机译:摘要目的探讨三甲氧苄啶/磺胺甲恶唑与其他 {US }食品和药物管理局(FDA)C和D抗感染药以及非抗感染 {FDA } C,D和X药物之间的关联早产和低出生体重。方法我们对1997年至2000年在加拿大萨斯喀彻温省分娩的妇女随机抽取50%的样本进行了回顾性队列研究。甲氧苄啶/磺胺甲恶唑与其他 {FDA } C和D抗感染药之间的关联(氟康唑,克拉霉素,强力霉素和四环素),以及早产,低出生体重的孕妇在妊娠期间使用的非抗感染药物{FDA } C,D和X,均采用多元logistic回归法和调整后的优势比进行了评估( aOR和95%置信区间(CI)作为关联度量。结果最终分析共纳入17?939名女性。甲氧苄氨嘧啶/磺胺甲基异恶唑与早产风险显着增加(aOR 1.51,95% {CI } 1.10,2.08)和低出生体重(aOR 1.67,95% CI 1.14,2.46)。暴露于非抗感染 {FDA } C,D和X类药物也与早产风险(aOR 1.17,95% {CI } 1.09,1.31)和低出生体重(aOR 1.14, 95% {CI } 0.92,1.42),但程度较低。其他 {FDA } C和D抗感染剂与早产风险(aOR 0.93,95% {CI } 0.49,1.77)或低出生体重(aOR 0.65,95%)的增加无统计学意义 {CI } 0.27,1.60)。结论在 {FDA } C,D和X药物中,叶酸拮抗剂甲氧苄氨嘧啶/磺胺甲恶唑与早产和低出生体重之间的关联最强。

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