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Treatment with JianPiYiFei II granules for patients with moderate to very severe chronic obstructive pulmonary disease: A 52-week randomised, double-blinded, placebo-controlled, multicentre trial

医学 慢性阻塞性肺病 伯德指数 安慰剂 生活质量(医疗保健) 内科学 安慰剂对照研究 临床终点 随机对照试验 物理疗法 肺功能测试 肺康复 双盲 病理 护理部 替代医学
作者
Yuanbin Chen,Xiao Gong,Mingjuan Zhou,Yinji Xu,Feiting Fan,Jingmin Xiao,Liangji Liu,Kehua Shi,Suyun Li,Jinsheng Zhuo,Zhibin Chen,Xuhua Yu,Long Fan,Yaolong Chen,Lei Wu,Lin Lin
出处
期刊:Phytomedicine [Elsevier]
卷期号:100: 154057-154057 被引量:7
标识
DOI:10.1016/j.phymed.2022.154057
摘要

Complementary and alternative therapy is widely used to treat chronic obstructive pulmonary disease (COPD). A Chinese herbal medicine, JianPiYiFei (JPYF) II granules, have been shown to improve COPD patients' quality of life, however long-term effectiveness has not been examined.To investigate whether long-term treatment with JPYF II granules is effective and safe for patients with stable, moderate to very severe COPD.A multicentre, randomised, double-blinded, placebo-controlled trial was conducted. Eligible participants from six hospitals were randomly assigned 1:1 to receive either JPYF II granules or placebo for 52 weeks. The primary outcome was the change in St. George's Respiratory Questionnaire (SGRQ) score during treatment. Secondary outcomes included the frequency of acute exacerbations during treatment, COPD Assessment Test (CAT), 6-minute walking test (6MWT), lung function, body mass index, airflow obstruction, dyspnoea, exercise capacity (BODE) index, and peripheral capillary oxygen saturation (SpO2) at the end of treatment.A total of 276 patients (138 in each group) were included in the analysis. JPYF II granules led to a significantly greater reduction in SGRQ score (-7.33 points, 95% CI -10.59 to -4.07; p < 0.0001) which reflects improved quality of life. JPYF II granules improved CAT (-3.49 points, 95% CI -5.12 to -1.86; p < 0.0001) and 6MWT (45.61 metres, 95% CI 20.26 to 70.95; p = 0.0005), compared with placebo. Acute exacerbations were less frequent with JPYF II granules than with placebo (0.87 vs. 1.34 events per patient; p = 0.0043). There were no significant differences between the groups in lung function, BODE index and SpO2. JPYF II granules were well tolerated and no significant adverse effects were noted.Long-term treatment with JPYF II granules is effective in moderate to very severe COPD, improving quality of life and exercise capacity, decreasing the risk of acute exacerbation, and relieving symptoms.
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