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Article ; Online: Bu-Fei Yi-Shen Granules Reduce Acute Exacerbations in Patients with GOLD 3-4 COPD: A Randomized Controlled Trial.

Yu, Xue-Qing / Di, Jia-Qi / Zhang, Wei / Wei, Geng-Shu / Ma, Zhan-Ping / Wu, Lei / Yu, Xue-Feng / Zhu, Hui-Zhi / Zhou, Miao / Feng, Cui-Ling / Feng, Ji-Hong / Fan, Ping / Li, Jian-Sheng / Yang, Jian-Ya

International journal of chronic obstructive pulmonary disease

2023  Volume 18, Page(s) 2439–2456

Abstract: Purpose: Chronic obstructive pulmonary disease (COPD) is a disease characterized by frequent acute exacerbations (AEs), especially in severe and very severe cases. We aimed to evaluate the efficacy and safety of Bu-fei Yi-shen granules (BYGs) for COPD.!# ...

Abstract Purpose: Chronic obstructive pulmonary disease (COPD) is a disease characterized by frequent acute exacerbations (AEs), especially in severe and very severe cases. We aimed to evaluate the efficacy and safety of Bu-fei Yi-shen granules (BYGs) for COPD.
Patients and methods: We conducted a multicenter, randomized, double-blinded, placebo-controlled trial of 348 COPD patients with GOLD 3-4 COPD. The patients were randomly assigned into experimental or control groups in a 1:1 ratio. Patients in the experimental group were prescribed BYG, while those in the control group were administered a placebo, orally, twice daily, with 5 days on and 2 days off per week for 52 weeks. The outcomes included AEs, pulmonary function, clinical signs and symptoms, dyspnea scores (mMRC), quality of life scores, and a 6-minute walk test (6MWT).
Results: A total of 280 patients completed the trial, including 135 patients in the experimental group and 145 in the control group. Compared to the control group, significant differences were observed in frequencies of AEs (mean difference: -0.35; 95% CI: -0.61, -0.10;
Conclusion: BYG, as compared to a placebo, could significantly reduce the frequencies of AEs and AE-related hospitalizations for GOLD 3-4 COPD patients. Clinical symptoms, treatment satisfaction, quality of life, and exercise capacity improved. There was no significant improvement in mortality and pulmonary function.
MeSH term(s) Humans ; Pulmonary Disease, Chronic Obstructive/diagnosis ; Pulmonary Disease, Chronic Obstructive/drug therapy ; Quality of Life ; Lung ; Dyspnea ; Walking
Language English
Publishing date 2023-11-06
Publishing country New Zealand
Document type Randomized Controlled Trial ; Multicenter Study ; Case Reports ; Clinical Trial
ZDB-ID 2212419-6
ISSN 1178-2005 ; 1176-9106
ISSN (online) 1178-2005
ISSN 1176-9106
DOI 10.2147/COPD.S413754
Database MEDical Literature Analysis and Retrieval System OnLINE

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