益气活血化痰方治疗气虚血瘀痰阻型慢性阻塞性肺疾病稳定期临床研究
DOI:
CSTR:
作者:
作者单位:

作者简介:

通讯作者:

中图分类号:

R256.14;R563

基金项目:

河南省医学科技攻关计划联合共建项目(2018020324)


Clinical Study on Yiqi Huoxue Huatan Prescription in the Treatment of Stable-Stage Chronic Obstructive Pulmonary Disease of Qi Deficiency, Blood Stasis, and Phlegm Obstruction Type
Author:
Affiliation:

Fund Project:

  • 摘要
  • |
  • 图/表
  • |
  • 访问统计
  • |
  • 参考文献
  • |
  • 相似文献
  • |
  • 引证文献
  • |
  • 资源附件
  • |
  • 文章评论
    摘要:

    目的:观察益气活血化痰方治疗气虚血瘀痰阻型慢性阻塞性肺疾病(COPD) 稳定期的效果。方 法:选取河南大学第一附属医院2023年1月—2025年1月收治的92例气虚血瘀痰阻型COPD稳定期患者,采用 抽签法随机分为西药组和汤方组各46例。西药组予常规治疗,汤方组在西药组的基础上加用益气活血化痰方 治疗。治疗12周后,比较2组临床疗效和不良反应发生率,以及治疗前后中医证候评分、肺功能状态与症状严 重程度[6 min 步行试验(6MWT)、改良英国医学研究学会呼吸困难指数(mMRC)、COPD 评估测试评 分(CAT)]、肺功能[用力肺活量(FVC)、第1秒用力呼气容积(FEV1)、FEV1/FVC]、炎症因子[白细胞介 素-6 (IL-6)、肿瘤坏死因子-α (TNF-α)] 水平的变化。结果:治疗后,汤方组总有效率为91.30% (42/ 46),西药组为73.91%(34/46),组间比较,差异有统计学意义(P<0.05)。治疗后,2组中医证候评分均较治 疗前降低(P<0.05),且汤方组评分低于西药组(P<0.05)。治疗后,2组6MWT均较治疗前增加(P<0.05), 且汤方组6MWT高于西药组(P<0.05);2组CAT、mMRC评分均较治疗前降低(P<0.05),且汤方组2项评分 均低于西药组(P<0.05)。治疗后,2组FEV1、FVC、FEV1/FVC水平均较治疗前升高(P<0.05),且汤方组 3项指标水平均高于西药组(P<0.05)。治疗后,2组TNF-α、IL-6水平均较治疗前降低(P<0.05),且汤方 组2项指标水平均低于西药组(P<0.05)。汤方组不良反应发生率为8.70% (4/46),西药组为4.35% (2/46), 2组比较,差异无统计学意义(P>0.05)。结论:益气活血化痰方可调节气虚血瘀痰阻型COPD稳定期患者肺 功能及炎症因子水平,改善中医证候、运动耐力与症状严重程度,提高临床疗效。

    Abstract:

    Abstract:Objective:To observe the efficacy of Yiqi Huoxue Huatan Prescription in the treatment of stable-stage chronic obstructive pulmonary disease (COPD) of qi deficiency, blood stasis, and phlegm obstruction type. Methods:A total of 92 patients with stable-stage COPD of qi deficiency,blood stasis,and phlegm obstruction type, admitted to The First Affiliated Hospital of Henan University from January 2023 to January 2025,were selected.They were randomly divided into the western medicine group and the decoction group using the lottery method,with 46 cases in each group.The western medicine group received conventional treatment,while the decoction group received Yiqi Huoxue Huatan Prescription in addition to the conventional treatment. After 12 weeks of treatment, the clinical efficacy and incidence of adverse reactions were compared between the two groups. Changes in traditional Chinese medicine syndrome scores,pulmonary functional status and symptom severity [6-minute walk test (6MWT),modified Medical Research Council Dyspnea Scale (mMRC),COPD Assessment Test (CAT) score],lung function [forced vital capacity( FVC),forced expiratory volume in one second( FEV1),FEV1/FVC ratio],and levels of inflammatory factors [interleukin-6 (IL-6),tumor necrosis factor-α (TNF-α)] before and after treatment were also compared.Results: After treatment,the total effective rate was 91.30% (42/46) in the decoction group and 73.91% (34/46) in the western medicine group, with a statistically significant difference between the two groups (P<0.05). After 12 weeks of treatment, the traditional Chinese medicine syndrome scores in both groups decreased compared with those before treatment( P<0.05),and the score in the decoction group was lower than that in the western medicine group( P<0.05). After treatment,the 6MWT distance increased in both groups compared with that before treatment (P<0.05),and the distance in the decoction group was longer than that in the western medicine group (P<0.05).The CAT and mMRC scores decreased in both groups compared with those before treatment (P<0.05), and both scores in the decoction group were lower than those in the western medicine group (P<0.05). After treatment, the levels of FEV1, FVC, and FEV1/FVC increased in both groups compared with those before treatment (P<0.05),and the levels of all three indicators in the decoction group were higher than those in the western medicine group (P<0.05). After treatment, the levels of TNF-α and IL-6 decreased in both groups compared with those before treatment (P<0.05),and the levels of both indicators in the decoction group were lower than those in the western medicine group (P<0.05).The incidence of adverse reactions was 8.70% (4/46) in the decoction group and 4.35% (2/46) in the western medicine group, showing no statistically significant difference between the two groups (P>0.05).Conclusion:Yiqi Huoxue Huatan Prescription can regulate lung function and inflammatory factor levels in patients with stable-stage COPD of qi deficiency, blood stasis, and phlegm obstruction type. It can improve traditional Chinese medicine syndromes, exercise tolerance,symptom severity,and enhance clinical efficacy.

    参考文献
    相似文献
    引证文献
引用本文

单远莹,齐红松,杨贝贝.益气活血化痰方治疗气虚血瘀痰阻型慢性阻塞性肺疾病稳定期临床研究[J].新中医,2026,58(6):73-78

复制
分享
相关视频

文章指标
  • 点击次数:
  • 下载次数:
  • HTML阅读次数:
  • 引用次数:
历史
  • 收稿日期:
  • 最后修改日期:
  • 录用日期:
  • 在线发布日期: 2026-03-31
  • 出版日期:
文章二维码