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A randomized trial of symptom-based management in Japanese patients with COPD

机译:日本COPD患者基于症状的管理的随机试验

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Background: The Global initiative for chronic Obstructive Lung Disease strategy document for COPD recommends treatment changes according to the persistence of symptoms or exacerbations. This study assessed the feasibility and outcomes of a structured step-up/step-down treatment approach in a randomized controlled clinical trial setting. Methods: Japanese patients with moderate-to-severe COPD were randomized to blinded, double-dummy treatment with twice-daily fluticasone propionate/salmeterol (FP/SAL) 250/50 μg or once-daily tiotropium bromide (TIO) 18 μg for 24 weeks (dual bronchodilator was not available). At 4-weekly intervals, patients remaining symptomatic (COPD Assessment Test score 10) or experiencing an exacerbation were offered the option to use triple therapy. Primary endpoint was the proportion of patients remaining on randomized therapy. Results: In total, 406 patients participated (mean FEV1 59%±13% predicted; COPD Assessment Test 12±6). Of these, 204 and 201 patients were included in the FP/SAL and TIO groups, respectively, of whom 67% and 63% continued treatment throughout the study; this difference was not statistically significant. Time to first therapy switch was longer with FP/SAL, but not significantly ( P =0.21). More patients in Global initiative for chronic Obstructive Lung Disease (2011 criteria) groups C/D switched (FP/SAL 55%, TIO 63%) than in groups A/B (FP/SAL 27%, TIO 27%). Conclusion: Given the choice, patients with more symptoms or those experiencing an exacerbation will agree to step-up therapy. Effectiveness of disease management pathways can be tested using double-blind studies.
机译:背景:慢性阻塞性肺病的全球慢性阻塞性肺疾病倡议战略文件根据症状或恶化的持续性推荐治疗方案的改变。这项研究评估了在随机对照临床试验中采用结构化升压/降压治疗方法的可行性和结果。方法:将日本中度至重度COPD患者随机分为双盲,双盲治疗,每天两次丙酸氟替卡松/沙美特罗(FP / SAL)250/50μg或每天一次噻托溴铵(TIO)18μg,共24次周(没有双支气管扩张药)。每隔4周,仍保留症状(COPD评估测试分数> 10)或病情加重的患者可以选择使用三联疗法。主要终点是接受随机治疗的患者比例。结果:共有406例患者参加(FEV1平均预测值59%±13%; COPD评估测试12±6)。其中,FP / SAL和TIO组分别包括204和201位患者,其中67%和63%的患者在整个研究期间继续接受治疗;这种差异没有统计学意义。使用FP / SAL进行首次治疗切换的时间更长,但并不明显(P = 0.21)。在全球慢性阻塞性肺疾病倡议(2011年标准)组中,C / D切换(FP / SAL 55%,TIO 63%)组比A / B组(FP / SAL 27%,TIO 27%)更多。结论:如果有选择,症状更多或病情加重的患者将同意逐步治疗。可以使用双盲研究来检验疾病管理途径的有效性。

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