苍麻丸加味治疗支气管扩张急性加重期痰湿阻肺证患者的效果研究

刘新平, 王展儒, 原庆

刘新平, 王展儒, 原庆. 苍麻丸加味治疗支气管扩张急性加重期痰湿阻肺证患者的效果研究[J]. 实用临床医药杂志, 2021, 25(10): 33-36. DOI: 10.7619/jcmp.20210457
引用本文: 刘新平, 王展儒, 原庆. 苍麻丸加味治疗支气管扩张急性加重期痰湿阻肺证患者的效果研究[J]. 实用临床医药杂志, 2021, 25(10): 33-36. DOI: 10.7619/jcmp.20210457
LIU Xinping, WANG Zhanru, YUAN Qing. Efficacy of supplemented Cangma Pills in treatment of patients with acute exacerbation of bronchiectasis differentiated as syndrome of stagnation of phlegm-dampness in lung[J]. Journal of Clinical Medicine in Practice, 2021, 25(10): 33-36. DOI: 10.7619/jcmp.20210457
Citation: LIU Xinping, WANG Zhanru, YUAN Qing. Efficacy of supplemented Cangma Pills in treatment of patients with acute exacerbation of bronchiectasis differentiated as syndrome of stagnation of phlegm-dampness in lung[J]. Journal of Clinical Medicine in Practice, 2021, 25(10): 33-36. DOI: 10.7619/jcmp.20210457

苍麻丸加味治疗支气管扩张急性加重期痰湿阻肺证患者的效果研究

基金项目: 

北京市属医院科研培育项目 PZ2019026

详细信息
  • 中图分类号: R562.2;R242

Efficacy of supplemented Cangma Pills in treatment of patients with acute exacerbation of bronchiectasis differentiated as syndrome of stagnation of phlegm-dampness in lung

  • 摘要:
      目的  探讨苍麻丸加味治疗支气管扩张急性加重期痰湿阻肺证患者的临床疗效。
      方法  将68例支气管扩张急性加重期患者随机分为2组,对照组给予硫酸沙丁胺醇气雾剂和盐酸氨溴索片治疗,观察组在对照组基础上加用苍麻丸加味治疗。2组连续治疗2周。比较2组痰湿阻肺证症状评分、肺功能指标、临床疗效以及血清C反应蛋白(CRP)、白细胞计数(WBC)、中性粒细胞百分比(NEU%)水平。
      结果  治疗2周后,观察组痰湿阻肺证症状(咯痰色白、痰质稠、痞满、纳呆、周身沉重)评分以及血清CRP、WBC、NEU%水平低于对照组,第1秒用力呼气容积(FEV1)、用力肺活量(FVC)、第1秒用力呼气容积与用力肺活量比值(FEV1/FVC)、治疗总有效率高于对照组,差异均有统计学意义(P < 0.05或P < 0.01)。
      结论  在常规治疗基础上加用苍麻丸加味治疗支气管扩张急性加重期痰湿阻肺证患者的疗效显著,能改善患者肺功能,降低感染性相关指标水平。
    Abstract:
      Objective  To investigate the clinical efficacy of supplemented Cangma Pills in the treatment of patients with acute exacerbation of bronchiectasis differentiated as syndrome of stagnation of phlegm-dampness in lung.
      Methods  Totally 68 patients with acute exacerbation of bronchiectasis were randomly divided into two groups. The control group was treated with salbutamol sulfate aerosol and ambroxol hydrochloride tablets, and the observation group was treated with supplemented Cangma Pills on the basis of the control group. Both groups were treated for 2 weeks. The score of syndrome of stagnation of phlegm-dampness in lung, pulmonary functions, clinical efficacy and levels of serum C reactive protein (CRP), white blood cell count (WBC) and neutrophil percentage (NEU%) were compared between the two groups.
      Results  After 2 weeks of treatment, the scores of syndrome of stagnation of phlegm-dampness in lung (white expectoration, thick phlegm, fullness, poor appetite and digestion, heavy body) and the levels of serum CRP, WBC and NEU% in the observation group were significantly lower than those in the control group, while the forced expiratory volume in the first second (FEV1), forced vital capacity (FVC), the ratio of forced expiratory volume in the first second to forced vital capacity (FEV1/FVC) and the total effective rate in the observation group were significantly higher than those in the control group (P < 0.05 or P < 0.01).
      Conclusion  Application of supplemented Cangma Pills on the basis of conventional treatment is effective in the treatment of patients with acute exacerbation of bronchiectasis differentiated as syndrome of stagnation of phlegm-dampness in lung, which can improve the pulmonary functions of patients and reduce the levels of infectious related indicators.
  • 表  1   2组痰湿阻肺证症状评分比较(x±s

    组别 时点 咯痰色白 痰质稠 痞满 纳呆 周身沉重
    对照组(n=34) 治疗前 5.18±0.63 5.04±0.61 4.94±0.58 4.99±0.59 4.90±0.58
    治疗后 2.37±0.29** 2.31±0.31** 2.22±0.29** 2.18±0.30** 2.03±0.26**
    观察组(n=34) 治疗前 5.22±0.65 5.01±0.60 4.97±0.61 4.91±0.64 4.83±0.55
    治疗后 1.15±0.18**## 1.13±0.16**## 1.04±0.15**## 1.09±0.14**## 1.06±0.16**##
    与治疗前比较, **P<0.01; 与对照组比较, ##P<0.01。
    下载: 导出CSV

    表  2   2组肺功能指标水平比较(x±s)

    组别 时点 FEV1/L FVC/L FEV1/FVC
    对照组(n=34) 治疗前 1.73±0.31 2.41±0.34 65.64±8.74
    治疗后 2.47±0.37** 3.03±0.41** 75.11±9.91**
    观察组(n=34) 治疗前 1.81±0.33 2.49±0.37 66.03±8.91
    治疗后 3.14±0.43**## 3.37±0.47**## 82.03±9.94**##
    FEV1: 第1秒用力呼气容积; FVC: 用力肺活量; FEV1/FVC: 第1秒用力呼气容积与用力肺活量比值。与治疗前比较, * * P<0.01; 与对照组比较, ##P<0.01。
    下载: 导出CSV

    表  3   2组疗效比较[n(%)]

    组别 n 临床治愈 有效 未愈 总有效
    对照组 34 19(55.88) 5(17.41) 10(29.41) 24(70.59)
    观察组 34 27(79.41) 5(17.41) 2(5.88) 32(94.12)*
    与对照组比较, * P<0.05。
    下载: 导出CSV

    表  4   2组血清CRP、WBC、NEU%水平比较(x±s)

    组别 时点 CRP/(mg/L) WBC/(×109/L) NEU%/%
    对照组(n=34) 治疗前 68.44±8.30 12.38±1.81 87.09±10.03
    治疗后 20.04±3.63** 6.93±0.77** 66.04±8.21**
    观察组(n=34) 治疗前 68.63±8.44 12.22±1.75 87.63±10.15
    治疗后 14.34±2.95**## 4.99±0.57**## 63.51±7.94**##
    CRP: C反应蛋白; WBC: 白细胞计数; NEU%: 中性粒细胞百分比。与治疗前比较, * * P<0.01; 与对照组比较, ##P<0.01。
    下载: 导出CSV
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出版历程
  • 收稿日期:  2021-01-24
  • 网络出版日期:  2021-04-15
  • 发布日期:  2021-05-27

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