Ciółkowski Janusz, Mazurek Henryk, Hydzik Paweł, Stasiowska Barbara
The Regional Public Hospital, 38-600 Lesko, ul.Kochanowskiego 2, Poland.
Department of Pneumonology and Cystic Fibrosis, Institute of Tuberculosis and Lung Disorders, ul.Prof.Rudnika 3b, 34-700 Rabka - Zdrój, Poland.
Pulm Pharmacol Ther. 2016 Aug;39:7-13. doi: 10.1016/j.pupt.2016.05.002. Epub 2016 May 24.
Asthma guidelines allow anti-leukotriene medications to be used as an alternative to inhaled corticosteroids (ICS) in second-step intensity therapy. The aim of the study was to analyze the risk factors of exacerbations, particularly inflammatory markers, during the 12-month period following therapy reduction from an ICS to montelukast in young patients with mild asthma.
A total of 84 patients (aged 7-18 years old) with mild asthma controlled by low-dose ICS, had their treatment switched to montelukast. Exhaled nitric oxide (eNO), sputum eosinophils (sEos), and bronchial hyperreactivity (BHR) were assessed at the beginning and then every three months throughout the one-year period. The patients with asthma exacerbations (first severe or third mild) were discontinued from the study.
Over the study period, 22 patients (26%) discontinued montelukast due to asthma exacerbations. An increased risk of exacerbations was noted among patients with initial sEos above 2.5% (relative risk, RR 36.6; 95% CI: 7.1-189.3; p < 0.001), as well as those with augmented BHR (RR 9.5; 2.8-31.6; p < 0.001), or eNO greater than 20 ppb (RR 3.7; 95% CI: 1.3-10.7; p = 0.013). An increase in BHR and eNO was observed during the last visit before exclusion.
After switching treatment from a low-dose ICS, montelukast maintained control of asthma symptoms in 75% of patients. High sEos before the treatment change was the strongest exacerbation risk factor. In patients with asthma controlled by low-dose ICS and low inflammatory markers, treatment could be safely switched to montelukast.
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。本研究的目的是分析轻度哮喘年轻患者从ICS减量至孟鲁司特治疗后的12个月内哮喘加重的危险因素,尤其是炎症标志物。
共有84例(年龄7 - 18岁)通过低剂量ICS控制的轻度哮喘患者,其治疗改为孟鲁司特。在开始时以及整个一年期间每三个月评估一次呼出一氧化氮(eNO)、痰嗜酸性粒细胞(sEos)和支气管高反应性(BHR)。哮喘加重(首次重度或第三次轻度)的患者退出研究。
在研究期间,22例(26%)患者因哮喘加重停用孟鲁司特。初始sEos高于2.5%的患者(相对风险,RR 36.6;95%置信区间:7.1 - 189.3;p < 0.001)、BHR增加的患者(RR 9.5;2.8 - 31.6;p < 0.001)或eNO大于20 ppb的患者(RR 3.7;95%置信区间:1.3 - 10.7;p = 0.013)中,哮喘加重风险增加。在排除前的最后一次访视中观察到BHR和eNO增加。
从低剂量ICS转换治疗后,孟鲁司特使75%的患者维持了哮喘症状的控制。治疗改变前高sEos是最强的加重危险因素。在由低剂量ICS和低炎症标志物控制的哮喘患者中,治疗可安全地转换为孟鲁司特。