Clinical effect of Qingfei Decoction for patients with acute exacerbation of chronic obstructive pulmonary disease differentiated as phlegm-heat accumulation in lung
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摘要:目的 观察清肺汤对慢性阻塞性肺病急性加重期(AECOPD)痰热蕴肺型患者的临床疗效。方法 将72例AECOPD痰热蕴肺型患者随机分为治疗组和对照组,各36例。对照组给予抗炎、解痉、化痰等西医常规治疗,治疗组在对照组基础上加服清肺汤, 1剂/d。2组疗程均为14 d。观察2组治疗前后临床症状、体征、肺功能的改善情况及安全性评估。结果 治疗组症状总积分显著优于对照组; 2组患者治疗后临床症状均有显著改善,但治疗组改善情况优于对照组(P < 0.05); 治疗组综合治疗疗效优于对照组,差异有统计学意义(P < 0.01); 2组患者治疗前后组间和组内肺功能变化比较差异无统计学意义(P>0.05)。结论 清肺汤对AECOPD痰热蕴肺型患者临床疗效确切,能改善患者健康状态,提高活动耐力。Abstract:Objective To observe the clinical effect of Qingfei Decoction for patients with acute exacerbation of chronic obstructive pulmonary disease (AECOPD)differentiated as phlegm-heat accumulation in lung.Methods A total of 72 AECOPD patients with phlegm-heat accumulation were randomly divided into treatment group and control group, with 36 cases per group. The control group was given routine treatment, such as anti-inflammation, spasmolysis, and phlegm relieving, and the treatment group was additionally given Qingfei Decoction on the basis of the control group for 1 dose per day. The course of treatment of both groups was 14 days. The clinical symptoms, signs, improvement of lung function and safety evaluation of the two groups before and after treatment were observed.Results The total scores of symptoms in the treatment group were significantly better than of the control group; the clinical symptoms of the two groups were significantly improved after treatment, but the improvement of the treatment group was better than that of the control group (P < 0.05); the treatment group had better comprehensive treatment efficacy than the control group(P < 0.01); there were no between-group and intra-group significant differences in lung function before and after treatment (P>0.05).Conclusion Qingfei Decoction has a definite clinical effect for AECOPD patients differentiated as phlegm-heat accumulating, which can improve their health status and activity endurance.
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表 1 2组临床症状及体征量化评分比较(x±s)
分 临床症状 时点 n 治疗组 对照组 咳嗽 治疗前 36 2.43±0.48 2.67±0.32 治疗后 36 0.67±0.40**# 0.9±0.35** 咳痰 治疗前 36 2.54±0.40 2.56±0.35 治疗后 36 0.58±0.54**# 1.86±0.56* 喘息 治疗前 36 2.53±0.41 2.64±0.47 治疗后 36 1.12±0.53**# 1.28±0.45** 啰音 治疗前 36 2.15±0.45 2.25±0.64 治疗后 36 0.46±0.45** 1.26±0.36** 发热 治疗前 36 2.56±0.22 2.69±0.18 治疗后 36 0.23±0.22** 0.28±0.20** 与治疗前比较, *P < 0.05, **P < 0.01; 与对照组比较, #P < 0.05。 表 2 2组治疗前后肺功能变化情况比较(x±s)
% 组别 时点 n FEV1% FEV1/FVC 治疗组 治疗前 36 60.26±9.08 57.86±9.08 治疗后 36 61.28±10.56 58.23±10.45 对照组 治疗前 36 59.45±10.56 58.68±9.63 治疗后 36 60.56±9.56 59.45±10.52 FEV1%: 1秒钟用力呼气量占预计值的百分比; FEV1/FVC: 1秒钟用力呼气量与用力肺活量占预计值的百分比。 -
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