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首页> 外文期刊>Respiratory medicine >Add-on montelukast in inadequately controlled asthma patients in a 6-month open-label study: the MONtelukast In Chronic Asthma (MONICA) study.
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Add-on montelukast in inadequately controlled asthma patients in a 6-month open-label study: the MONtelukast In Chronic Asthma (MONICA) study.

机译:在一项为期6个月的开放标签研究中,在控制不佳的哮喘患者中添加了孟鲁司特:MONTELUKAST在慢性哮喘(MONICA)研究中。

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摘要

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.
机译:尽管使用吸入性糖皮质激素(ICS),长效β(2)激动剂(LABA)或同时使用这两种药物进行治疗,但支气管哮喘常常仍无法控制,因此需要进一步治疗。年龄≥18岁(n = 1681)的轻度至中度哮喘患者接受口服孟鲁司特10mg口服补给品ICS或ICS + LABAs,并在一项前瞻性,开放性观察研究中随访6个月。主要终点是哮喘控制测试(ACT)得分的变化。次要终点包括小型哮喘生活质量问卷(mini-AQLQ)和FEV(1)/ PEF。平均ACT评分从14.6 +/- 4.6(基线)提高到19.4 +/- 4.4(第6个月; p <0.0001)。使用ACT评分类别,在基线的第6个月,哮喘未控制(57.5%)或控制不佳(25.0%)的患者百分比下降(分别为17.6和21.7%);在第6个月,处于基线状态的哮喘完全控制(13.9%)或完全控制(1.2%)的患者百分比有所增加(分别为47.5和11.4%)。 mini-AQLQ得分(平均值+/- SD)从4.0 +/- 1.1提高到5.3 +/- 1.1(p <0.0001); FEV(1)从2.46 +/- 0.89升至2.60 +/- 0.92L(p <0.0001)。孟鲁司特的治疗一般耐受良好。对于用ICS或ICS + LABA不能充分控制的患者,每日补充孟鲁司特可改善哮喘控制和与哮喘相关的生活质量。 Clinicaltrials.gov注册表号NCT00802789。

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