Centre for Asthma and Respiratory Diseases, University of Newcastle and Hunter Medical Research Institute, Newcastle, NSW, Australia.
Lancet. 2011 Sep 10;378(9795):983-90. doi: 10.1016/S0140-6736(11)60971-9.
Asthma exacerbations during pregnancy are common and can be associated with substantial maternal and fetal morbidity. Treatment decisions based on sputum eosinophil counts reduce exacerbations in non-pregnant women with asthma, but results with the fraction of exhaled nitric oxide (F(E)NO) to guide management are equivocal. We tested the hypothesis that a management algorithm for asthma in pregnancy based on F(E)NO and symptoms would reduce asthma exacerbations.
We undertook a double-blind, parallel-group, controlled trial in two antenatal clinics in Australia. 220 pregnant, non-smoking women with asthma were randomly assigned, by a computer-generated random number list, before 22 weeks' gestation to treatment adjustment at monthly visits by an algorithm using clinical symptoms (control group) or F(E)NO concentrations (active intervention group) used to uptitrate (F(E)NO >29 ppb) or downtitrate (F(E)NO <16 ppb) inhaled corticosteroid dose. Participants, caregivers, and outcome assessors were masked to group assignment. Longacting β2 agonist and minimum dose inhaled corticosteroid were used to treat symptoms when F(E)NO was not increased. The primary outcome was total asthma exacerbations (moderate and severe). Analysis was by intention to treat. This study is registered with the Australian and New Zealand Clinical Trials Registry, number 12607000561482.
111 women were randomly assigned to the F(E)NO group (100 completed) and 109 to the control group (103 completed). The exacerbation rate was lower in the F(E)NO group than in the control group (0·288 vs 0·615 exacerbations per pregnancy; incidence rate ratio 0·496, 95% CI 0·325-0·755; p=0·001). The number needed to treat was 6. In the F(E)NO group, quality of life was improved (score on short form 12 mental summary was 56·9 [95% CI 50·2-59·3] in F(E)NO group vs 54·2 [46·1-57·6] in control group; p=0·037) and neonatal hospitalisations were reduced (eight [8%] vs 18 [17%]; p=0·046).
Asthma exacerbations during pregnancy can be significantly reduced with a validated F(E)NO-based treatment algorithm.
National Health and Medical Research Council of Australia.
怀孕期间哮喘加重很常见,可能会对母亲和胎儿造成严重的不良后果。基于痰中嗜酸性粒细胞计数的治疗决策可以减少非孕期哮喘患者的加重,但使用呼气一氧化氮分数(F(E)NO)来指导管理的结果则存在争议。我们测试了一种基于 F(E)NO 和症状的妊娠哮喘管理算法可以减少哮喘加重的假设。
我们在澳大利亚的两个产前诊所进行了一项双盲、平行组、对照试验。220 名患有哮喘的非吸烟孕妇在妊娠 22 周前被随机分配,通过计算机生成的随机数列表,根据每月就诊时的临床症状(对照组)或 F(E)NO 浓度(主动干预组)使用算法进行治疗调整,以增加(F(E)NO > 29 ppb)或减少(F(E)NO < 16 ppb)吸入皮质类固醇剂量。参与者、护理人员和结果评估人员对分组情况不知情。当 F(E)NO 没有增加时,长效β2 激动剂和最低剂量的吸入皮质类固醇用于治疗症状。主要结局是总哮喘加重(中度和重度)。分析采用意向治疗。这项研究在澳大利亚和新西兰临床试验注册中心注册,编号为 12607000561482。
111 名妇女被随机分配到 F(E)NO 组(100 名完成),109 名妇女被分配到对照组(103 名完成)。F(E)NO 组的哮喘加重率低于对照组(每妊娠 0.288 次 vs 0.615 次;发病率比 0.496,95%CI 0.325-0.755;p=0.001)。需要治疗的人数为 6 人。在 F(E)NO 组,生活质量得到改善(短表单 12 精神总结评分在 F(E)NO 组为 56.9 [95%CI 50.2-59.3],在对照组为 54.2 [46.1-57.6];p=0.037),新生儿住院治疗减少(8 [8%] vs 18 [17%];p=0.046)。
使用经过验证的基于 F(E)NO 的治疗算法可以显著减少妊娠期间的哮喘加重。
澳大利亚国家卫生和医学研究委员会。