Eltonsy Sherif, Kettani Fatima-Zohra, Blais Lucie
Faculty of Pharmacy, Université de Montréal, Montreal, Quebec, Canada; Hôpital du Sacré-Cœur de Montréal, Montreal, Quebec, Canada.
Faculty of Pharmacy, Université de Montréal, Montreal, Quebec, Canada; Hôpital du Sacré-Cœur de Montréal, Montreal, Quebec, Canada.
Respir Med. 2014 Jan;108(1):9-33. doi: 10.1016/j.rmed.2013.07.009. Epub 2013 Dec 17.
Short and long-acting beta2-agonists (SABA and LABA) have a crucial role in asthma management during pregnancy, as stated in the current guidelines.
To systematically review the evidence on beta2-agonists use during pregnancy and adverse perinatal outcomes.
Six databases were searched before January 1, 2013 for beta2-agonists use during pregnancy and congenital malformations, small for gestational age, mean and low birth weight, gestational age and preterm delivery. Original English language articles were included with no cut-off date. Quality assessment and post-hoc power calculations were performed.
Twenty-one original studies were identified. Four studies reported a significant increased risk of congenital malformations with SABA, while one study reported a significant decreased risk with high doses of SABA. One study reported a significant increased risk of congenital malformations with LABA and four studies reported a significant increased risk of congenital malformations with beta2-agonists (SABA and/or LABA). One study reported a decrease in birth weight centiles among LABA users.
All studies reporting significant results, except two, used non-asthmatic women as reference group, making it difficult to differentiate between the effect of the disease from the one of the beta2-agonists. Non-significant results should be interpreted with caution due to the low statistical power of several studies.
Methodological limitations and lack of power of several studies prevent us to conclude on the perinatal safety of beta2-agonists. Until further evidence is available, physicians should continue prescribing them as recommended in the guidelines whenever needed to attain asthma control.
如当前指南所述,短效和长效β2受体激动剂(SABA和LABA)在孕期哮喘管理中发挥着关键作用。
系统评价孕期使用β2受体激动剂与围产期不良结局的相关证据。
2013年1月1日前检索了六个数据库,以获取孕期使用β2受体激动剂与先天性畸形、小于胎龄儿、平均出生体重和低出生体重、孕周和早产相关的信息。纳入无截止日期的英文原文。进行了质量评估和事后效能计算。
共识别出21项原始研究。四项研究报告SABA会显著增加先天性畸形的风险,而一项研究报告高剂量SABA会显著降低风险。一项研究报告LABA会显著增加先天性畸形的风险,四项研究报告β2受体激动剂(SABA和/或LABA)会显著增加先天性畸形的风险。一项研究报告LABA使用者的出生体重百分位数降低。
除两项研究外,所有报告有显著结果的研究均将非哮喘女性作为参照组,因此难以区分疾病影响与β2受体激动剂的影响。由于多项研究的统计效能较低,对无显著结果的解读应谨慎。
多项研究存在方法学局限性且效能不足,这使我们无法就β2受体激动剂的围产期安全性得出结论。在获得进一步证据之前,医生应继续按照指南建议,在需要控制哮喘时按需开具此类药物。