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Efficacy of add-on montelukast in patients with non-controlled asthma: a Belgian open-label study.

机译:加入蒙特利亚斯特在非控制哮喘患者中的疗效:比利时开放标签研究。

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OBJECTIVE: To evaluate the efficacy of add-on montelukast on asthma control and allergic rhinitis symptoms in asthmatic patients still symptomatic with chronic treatment with inhaled corticosteroid and long-acting beta(2) agonist (ICS/LABA), irrespective of the dose. RESEARCH DESIGN AND METHODS: This 2-month, open-label, real-life, multicentre, observational study was undertaken by 499 general practitioners in Belgium. Patients (>or= 4 years old) with uncontrolled asthma despite fluticasone/salmeterol or budesonide/formoterol therapy had oral montelukast 4, 5, or 10 mg daily added to their therapy, depending on the registered dose for their age. Asthma control, assessed by the 6-item Juniper Asthma Control Questionnaire (ACQ) was recorded at baseline and after 2 months of treatment with montelukast and the patients' global evaluation of asthma was also recorded at the end of the study. Concomitant allergic rhinitis symptoms were evaluated according to the patients' perception. RESULTS: A total of 5769 patients were eligible for analysis. Addition of montelukast was associated with significant decrease in mean (SD) ACQ score (from 1.97 [0.77] at baseline to 1.05 [0.69] after add-on treatment, p < 0.001). There was also a significant improvement in all individual symptoms of the ACQ score (p < 0.001). After 2 months, 89% of the patients reported global improvement of their asthma, with a good correlation between patients' global evaluation and change in ACQ scores. Of the 2442 patients who reported allergic rhinitis symptoms at baseline, 91% showed a global improvement of their asthma symptoms and 82% in their rhinitis symptoms after adding montelukast. CONCLUSION: This open-label observational study showed an improvement, after 2 months of add-on therapy with montelukast, in both asthma and allergic rhinitis symptoms in patients not adequately controlled on a fixed association of ICS/LABA.
机译:目的:评价蒙特利亚斯特患者对哮喘患者哮喘控制和过敏性鼻炎症状的哮喘患者症状,与吸入的皮质类固醇和长效β(2)激动剂(ICS / LABA),无论剂量如何。研究设计和方法:今年,499名全科医生在比利时开展了2个月,开放标签,现实生活,多方形,观测研究。患者(>或= 4岁),尽管令人稳定的哮喘,尽管令人稳定的哮喘或萨米特洛尔或甲酚/福莫特醇治疗,每天服用口服蒙特洛特4,5,或10毫克,根据其年龄的注册剂量而添加到他们的治疗中。在基线中记录了6件juniper哮喘对照问卷(ACQ)的哮喘控制,并在蒙特洛斯特治疗2个月后,在研究结束时还记录了患者全球哮喘评估。伴随的过敏性鼻炎症状根据患者的感知评估。结果:共有5769名患者有资格进行分析。添加蒙特利亚斯特的添加与平均值(SD)ACQ评分的显着降低有关(在基线的1.97 [0.77]到1.05 [0.69],P <0.001)。 ACQ评分的所有个体症状也有显着改善(P <0.001)。 2个月后,89%的患者报告了其哮喘的全球改善,患者全球评估与ACQ分数变化之间的相关性良好。在2442名患者中,报告基线的过敏性鼻炎症状,91%在添加Montelukast后,91%的哮喘症状显示出对哮喘症状的全球性和82%。结论:这种开放标签观测研究表明,在2个月的蒙特洛斯特联系治疗后,在哮喘和过敏性鼻炎症状中,在固定的ICS / Laba的固定协会中没有充分控制的哮喘和过敏性鼻炎。

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