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在一项为期 6 个月的开放性研究中,对于控制不佳的哮喘患者加用孟鲁司特:慢性哮喘中的孟鲁司特研究(MONICA)。

Add-on montelukast in inadequately controlled asthma patients in a 6-month open-label study: the MONtelukast In Chronic Asthma (MONICA) study.

机构信息

Department of Pneumology, University of Rostock, Rostock, Germany.

出版信息

Respir Med. 2010 May;104(5):644-51. doi: 10.1016/j.rmed.2009.11.022. Epub 2009 Dec 23.

Abstract

Bronchial asthma often remains uncontrolled despite treatment with inhaled corticosteroids (ICS), long-acting beta(2)-agonists (LABA) or both, necessitating additional treatment. Patients >or=18 years (n=1681) with mild-to-moderate asthma received oral montelukast 10mg added to ICS or ICS+LABAs, and were followed for 6 months in a prospective, open-label observational study. The primary endpoint was change in Asthma Control Test (ACT) score. Secondary endpoints included mini-Asthma Quality-of-Life Questionnaire (mini-AQLQ) and FEV(1)/PEF. Mean ACT scores improved from 14.6+/-4.6 (baseline) to 19.4+/-4.4 (month 6; p<0.0001). Using ACT score categories, the percentage of patients with uncontrolled (57.5%) or poorly controlled (25.0%) asthma at baseline decreased at month 6 (17.6 and 21.7%, respectively); the percentage of patients with well controlled (13.9%) or completely controlled (1.2%) asthma at baseline increased at month 6 (47.5 and 11.4%, respectively). The mini-AQLQ score (mean+/-SD) improved from 4.0+/-1.1 to 5.3+/-1.1 (p<0.0001); FEV(1) increased from 2.46+/-0.89 to 2.60+/-0.92L (p<0.0001). Treatment with montelukast was generally well tolerated. In patients insufficiently controlled with ICS or ICS+LABAs, daily add-on montelukast improved both asthma control and asthma-related quality of life. Clinicaltrials.gov registry number NCT00802789.

摘要

尽管使用吸入性皮质类固醇(ICS)、长效β2-激动剂(LABA)或两者联合治疗,支气管哮喘仍经常得不到控制,需要额外的治疗。在一项前瞻性、开放性观察研究中,将 1681 名年龄>18 岁、轻度至中度哮喘患者接受口服孟鲁司特 10mg 联合 ICS 或 ICS+LABA 治疗,并随访 6 个月。主要终点是哮喘控制测试(ACT)评分的变化。次要终点包括迷你哮喘生活质量问卷(mini-AQLQ)和 FEV1/PEF。平均 ACT 评分从基线时的 14.6+/-4.6 分提高到 6 个月时的 19.4+/-4.4 分(p<0.0001)。根据 ACT 评分类别,基线时控制不佳(57.5%)或控制极差(25.0%)的患者百分比在 6 个月时下降(分别为 17.6%和 21.7%);基线时控制良好(13.9%)或完全控制(1.2%)的患者百分比在 6 个月时增加(分别为 47.5%和 11.4%)。迷你 AQLQ 评分(平均值+/-标准差)从 4.0+/-1.1 提高到 5.3+/-1.1(p<0.0001);FEV1 从 2.46+/-0.89 增加到 2.60+/-0.92L(p<0.0001)。孟鲁司特治疗通常耐受性良好。对于 ICS 或 ICS+LABA 控制不佳的患者,每日加用孟鲁司特可改善哮喘控制和哮喘相关生活质量。Clinicaltrials.gov 注册号 NCT00802789。

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