Ciółkowski J, Mazurek H, Stasiowska B
The Regional Public Hospital in Lesko, Poland.
Department of Pneumonology and Cystic Fibrosis, National Institute of Tuberculosis and Lung Disorders, Rabka Branch, Poland.
Allergol Immunopathol (Madr). 2014 Jul-Aug;42(4):282-8. doi: 10.1016/j.aller.2013.01.005. Epub 2013 May 16.
Asthma guidelines allow antileukotriene medications to be used as an alternative to inhaled corticosteroids (ICSs) in second-step intensity therapy. The aim of this study was to determine whether asthma control can be maintained after reducing treatment from low-dose ICS to montelukast.
In this prospective, real-life 12-week trial, 84 young patients with asthma (7-18 years) controlled by low-dose ICS, had treatment switched to montelukast. Symptoms and PEF were monitored daily; exhaled nitric oxide (eNO) and spirometry every four weeks; sputum eosinophil (sEo) and bronchial hyperreactivity (BHR) assessed at the beginning and at the end of the study. The primary endpoint was number of patients discontinued from the study due to asthma exacerbations.
Eleven patients (13.1%) were discontinued due to asthma exacerbations. At the beginning, patients with elevated percentage of sEo had increased risk of exacerbations (relative risk RR, 6.6; 95% CI, 1.2-35.6), as well as those with augmented BHR (RR, 4.24; 95% CI, 1.1-16.2) as compared to patients who completed the study. An intensification of symptoms and increased use of beta-adrenergics were observed during the last visit before exclusion from the study, but not changes in spirometry, PEF, and eNO. No change in clinical parameters, inflammatory markers or BHR was observed in patients remaining in the study.
After treatment switch from low-dose ICS to montelukast, asthma control was maintained in the majority of patients during the 12-week observation period. Sputum eosinophilia or BHR before the treatment switch was exacerbation risk factor.
哮喘指南允许在第二步强化治疗中使用抗白三烯药物作为吸入性糖皮质激素(ICS)的替代药物。本研究的目的是确定在将治疗从低剂量ICS减至孟鲁司特后,哮喘控制是否能够维持。
在这项前瞻性、真实生活的12周试验中,84例由低剂量ICS控制的哮喘青年患者(7至18岁),其治疗改为孟鲁司特。每天监测症状和呼气峰流速(PEF);每四周监测呼出一氧化氮(eNO)和肺功能;在研究开始和结束时评估痰液嗜酸性粒细胞(sEo)和支气管高反应性(BHR)。主要终点是因哮喘加重而退出研究的患者数量。
11例患者(13.1%)因哮喘加重而退出。开始时,与完成研究的患者相比,sEo百分比升高的患者加重风险增加(相对风险RR,6.6;95%置信区间,1.2 - 35.6),BHR增强的患者也是如此(RR,4.24;95%置信区间,1.1 - 16.2)。在被排除出研究前的最后一次访视期间,观察到症状加重和β-肾上腺素能药物使用增加,但肺功能、PEF和eNO没有变化。继续留在研究中的患者,其临床参数、炎症标志物或BHR没有变化。
在从低剂量ICS改为孟鲁司特治疗后,大多数患者在12周观察期内维持了哮喘控制。治疗转换前的痰液嗜酸性粒细胞增多或BHR是加重的危险因素。