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

Authors :
Yu XQ
Di JQ
Zhang W
Wei GS
Ma ZP
Wu L
Yu XF
Zhu HZ
Zhou M
Feng CL
Feng JH
Fan P
Li JS
Yang JY
Source :
International journal of chronic obstructive pulmonary disease [Int J Chron Obstruct Pulmon Dis] 2023 Nov 06; Vol. 18, pp. 2439-2456. Date of Electronic Publication: 2023 Nov 06 (Print Publication: 2023).
Publication Year :
2023

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.<br />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).<br />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; P = 0.006) and AE-related hospitalizations (-0.18; 95% CI: -0.36, -0.01; P = 0.04), 6MWD (40.93 m; 95% CI: 32.03, 49.83; P < 0.001), mMRC (-0.57; 95% CI: -0.76, -0.37; P < 0.001), total symptoms (-2.18; 95% CI: -2.84, -1.53; P < 0.001), SF-36 (11.60; 95% CI: 8.23, 14.97; P < 0.001), and mCOPD-PRO (-0.45; 95% CI: -0.57, -0.33; P < 0.001) after treatment. However, there were no significant differences in mortality, pulmonary function, and mESQ-PRO scores ( P > 0.05). No obvious adverse events were observed.<br />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.<br />Competing Interests: The authors report no conflicts of interest in this work.<br /> (© 2023 Yu et al.)

Details

Language :
English
ISSN :
1178-2005
Volume :
18
Database :
MEDLINE
Journal :
International journal of chronic obstructive pulmonary disease
Publication Type :
Report
Accession number :
37955027
Full Text :
https://doi.org/10.2147/COPD.S413754