Faculty of Pharmacy, Université de Montréal, Succursale Centre-ville, Montreal, Quebec, Canada.
J Allergy Clin Immunol. 2010 Oct;126(4):772-777.e2. doi: 10.1016/j.jaci.2010.08.018.
Four studies investigating the association between inhaled corticosteroid (ICS) use during pregnancy and perinatal mortality reported no significantly increased risk. These studies must be interpreted with caution because they have insufficient statistical power and a lack of adjustment for potential confounders.
We sought to evaluate whether asthmatic women exposed to ICSs during pregnancy are more at risk of perinatal mortality than asthmatic women not exposed. We also sought to estimate the risk of perinatal mortality as a function of the daily ICS dose taken during pregnancy.
From the linkage of 3 administrative databases from Quebec, a cohort including 13,004 single pregnancies from asthmatic women was constructed. We used a 2-stage sampling cohort design to obtain information on cigarette smoking from the medical charts of 487 mothers. The final estimates of the odds ratios (ORs) of perinatal mortality were estimated with a logistic regression model.
The cohort was formed of 4,140 women who used greater than 0 to 250 μg/d ICS, 1,140 women who used greater than 250 μg/d ICS, and 7,724 nonusers of ICSs during pregnancy. Women exposed to ICSs (any dose) had a nonsignificant increased risk of perinatal mortality (OR, 1.07; 95% CI, 0.70-1.61). The use of greater than 250 μg/d ICS was associated with a nonsignificant 52% increased risk of perinatal mortality (OR, 1.52; 95% CI, 0.62-3.76).
The risk of perinatal mortality was not found to be significantly associated with ICS use during pregnancy. The result associated with higher doses of ICSs is limited due to a lack of statistical power and a possibility of residual confounding by asthma severity and control.
四项研究调查了孕期吸入皮质类固醇(ICS)使用与围产儿死亡率之间的关联,均未报告风险显著增加。这些研究必须谨慎解释,因为它们的统计效力不足,且缺乏对潜在混杂因素的调整。
我们旨在评估孕期暴露于 ICS 的哮喘女性是否比未暴露于 ICS 的哮喘女性面临更高的围产儿死亡风险。我们还试图根据孕期 ICS 日剂量评估围产儿死亡的风险。
通过魁北克三个行政数据库的链接,构建了一个包含 13004 例单胎妊娠哮喘女性的队列。我们使用两阶段抽样队列设计从 487 位母亲的病历中获取吸烟信息。使用逻辑回归模型估计围产儿死亡率的比值比(OR)的最终估计值。
队列由 4140 名使用大于 0 至 250μg/d ICS 的女性、1140 名使用大于 250μg/d ICS 的女性和 7724 名孕期未使用 ICS 的女性组成。暴露于 ICS(任何剂量)的女性围产儿死亡率风险无显著增加(OR,1.07;95%CI,0.70-1.61)。使用大于 250μg/d ICS 与围产儿死亡率风险无显著增加 52%相关(OR,1.52;95%CI,0.62-3.76)。
孕期 ICS 使用与围产儿死亡率风险无显著相关性。与更高剂量 ICS 相关的结果因统计效力不足且哮喘严重程度和控制的残余混杂因素的可能性而受到限制。