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首页> 外文期刊>Allergy, Asthma & Immunology Research >Addition of Montelukast to Low-Dose Inhaled Corticosteroid Leads to Fewer Exacerbations in Older Patients Than Medium-Dose Inhaled Corticosteroid Monotherapy
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Addition of Montelukast to Low-Dose Inhaled Corticosteroid Leads to Fewer Exacerbations in Older Patients Than Medium-Dose Inhaled Corticosteroid Monotherapy

机译:与中等剂量吸入皮质类固醇单一疗法相比,将孟鲁司特添加至低剂量吸入类固醇激素可使老年患者加重的次数减少

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Purpose There have been few reports regarding the efficacy of antiasthmatics in older patients. To compare the efficacy of the addition of montelukast to low-dose inhaled budesonide (MON-400BUD) versus increasing the dose of inhaled steroid (800BUD) on asthma control in older asthmatics. Methods A randomized, open-label, parallel-designed trial was conducted for 12 weeks. The primary endpoint was the rate of patients who reached "well-controlled asthma status" after the 12-week treatment period. Additionally, asthma exacerbations, sputum inflammatory cells, asthma control test (ACT) and physical functioning scale (PFS), and adverse reactions were monitored. Results Twenty-four (36.9%) and 22 (34.9%) subjects in the MON-400BUD (n=65) and 800BUD (n=63) groups had well-controlled asthma at the end of the study, respectively. The numbers of asthma exacerbations requiring oral corticosteroid treatment (20 vs 9, respectively, P =0.036) and the development of sore throat (22 vs 11, respectively, P =0.045) were significantly higher in the 800BUD group than in the MON-400BUD group. Body mass index and changes in ACT, FEV1%, 6-min walk distance and PFS from baseline were all significant determinants for distinguishing subjects with well-controlled and partly controlled asthma from those with uncontrolled asthma ( P Conclusions The efficacy of 12-week treatment with MON-400BUD in older asthmatics was comparable to that of 800BUD on asthma control but associated with reduced frequency of asthma exacerbations requiring oral steroids and sore throat events. Changes in ACT and PFS can be useful predictors of asthma control status in older patients.
机译:目的很少有关于抗哮喘药在老年患者中疗效的报道。为了比较在低剂量吸入布地奈德(MON-400BUD)中添加孟鲁司特与增加吸入类固醇剂量(800BUD)在控制老年哮喘中的疗效。方法一项随机,开放标签,平行设计的试验进行了12周。主要终点是治疗12周后达到“哮喘控制良好”状态的患者比率。此外,还监测哮喘发作,痰液炎症细胞,哮喘控制测试(ACT)和身体功能量表(PFS)以及不良反应。结果MON-400BUD(n = 65)和800BUD(n = 63)组中的24名(36.9%)和22(34.9%)受试者在研究结束时分别得到了良好的哮喘控制。 800BUD组中需要口服皮质类固醇治疗的哮喘加重次数(分别为20比9,P = 0.036)和喉咙痛的发生情况(分别为22 vs 11,P = 0.045)明显高于MON-400BUD组。体重指数以及ACT,FEV1%,6分钟步行距离和距基线的PFS的变化都是区分哮喘控制良好和部分控制与未控制哮喘的重要决定因素(P结论12周治疗的疗效MON-400BUD在老年哮喘患者中的控制效果与800BUD在控制哮喘方面相当,但与需要口服类固醇和喉咙痛的哮喘发作频率降低有关,ACT和PFS的变化可有效预测老年患者的哮喘控制状况。

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