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妊娠早期大剂量吸入皮质类固醇与先天畸形。

High doses of inhaled corticosteroids during the first trimester of pregnancy and congenital malformations.

机构信息

Faculty of Pharmacy, Université de Montréal, Montreal, Quebec, Canada.

出版信息

J Allergy Clin Immunol. 2009 Dec;124(6):1229-1234.e4. doi: 10.1016/j.jaci.2009.09.025.

DOI:10.1016/j.jaci.2009.09.025
PMID:19910032
Abstract

BACKGROUND

Although reassuring data exist on the use of low-to-moderate doses of inhaled corticosteroids (ICSs) during pregnancy, there are inadequate data for women receiving high doses.

OBJECTIVE

To investigate the association between doses of ICS during the first trimester of pregnancy and the risk of congenital malformations among women with asthma.

METHODS

We conducted a cohort study of 13,280 pregnancies of women with asthma (1990-2002) by linking 3 administrative databases from Quebec (Canada). By using generalized estimation equation models, we compared women taking >0 to 1000 microg/d ICS (beclomethasone dipropionate-chlorofluorocarbone equivalent) with women taking >1000 microg/d and those not taking ICSs. The main outcome measures were all and major congenital malformations.

RESULTS

We identified 1257 infants with a congenital malformation (9.5%) and 782 infants with a major malformation (5.9%). We found that women who used >1000 microg/d ICS (n = 154) were significantly more likely (63%) to have a baby with a malformation than the 4392 women who used >0 to 1000 microg/d (adjusted risk ratio, 1.63; 95% CI, 1.02-2.60). On the other hand, women who used >0 to 1000 microg/d were not found to be more at risk than women who did not use ICSs during the first trimester (n = 8734). Nonsignificant trends of similar magnitude were found for major malformations.

CONCLUSIONS

Our study adds evidence on the safety of low-to-moderate doses of ICS taken during the first trimester but raises concerns about high doses. However, we cannot rule out the possibility of residual confounding by severity in this association.

摘要

背景

尽管有关于孕妇使用低至中等剂量吸入性皮质类固醇(ICS)的令人安心的数据,但对于接受高剂量的孕妇来说,数据还不够充分。

目的

调查孕妇在妊娠早期使用 ICS 的剂量与哮喘女性先天性畸形风险之间的关系。

方法

我们通过链接来自魁北克(加拿大)的 3 个行政数据库,对 1990 年至 2002 年间 13280 例哮喘孕妇的队列进行了研究。我们使用广义估计方程模型,将使用>0 至 1000μg/d ICS(丙酸倍氯米松-氯氟烃等效物)的女性与使用>1000μg/d ICS 的女性和未使用 ICS 的女性进行了比较。主要结局指标为所有和主要先天性畸形。

结果

我们发现 1257 例婴儿患有先天性畸形(9.5%)和 782 例婴儿患有重大畸形(5.9%)。我们发现,使用>1000μg/d ICS 的女性(n=154)与使用>0 至 1000μg/d ICS 的女性(n=4392)相比,其婴儿发生畸形的可能性显著更高(63%)(校正风险比,1.63;95%CI,1.02-2.60)。另一方面,使用>0 至 1000μg/d ICS 的女性与妊娠早期未使用 ICS 的女性(n=8734)相比,风险没有增加。对于重大畸形,也发现了类似幅度的无显著趋势。

结论

我们的研究为妊娠早期使用低至中等剂量 ICS 的安全性提供了证据,但对高剂量提出了担忧。然而,我们不能排除这种关联中严重程度的残余混杂的可能性。

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