苏黄止咳胶囊联合三联雾化吸入治疗慢性阻塞性肺疾病急性加重期临床研究OA
Clinical Study on Suhuang Zhike Capsules Combined with Triple Nebulization Inhalation for Acute Exacerbation of Chronic Obstructive Pulmonary Disease
目的:观察苏黄止咳胶囊联合三联雾化吸入治疗慢性阻塞性肺疾病急性加重期(AECOPD)的疗效.方法:选取2021年5月—2024年5月德清县人民医院收治的121例AECOPD患者,按治疗方案差异分为观察组61例及对照组60例.2组均给予常规基础治疗,对照组在常规基础治疗上给予三联雾化吸入,观察组在对照组基础上联合苏黄止咳胶囊治疗.2组均治疗14天.比较2组临床疗效及不良反应发生率,比较2组治疗前后6 min步行距离、肺功能[每分钟最大通气量(MMV)、用力肺活量、第1秒用力呼气容积]指标值、炎症指标值[C-反应蛋白(CRP)、降钙素原(PCT)、白细胞介素-17A(IL-17A)、白细胞介素-8(IL-8)]及免疫功能(CD3+、CD4+、CD4+/CD8+)的变化.结果:治疗14天,观察组临床疗效总有效率为95.08%(59/61),对照组为83.33%(50/60),2组临床疗效比较,差异有统计学意义(P<0.05).治疗后,2组6 min步行距离、MMV、用力肺活量、1秒用力呼气容积均较治疗前提高(P<0.05),观察组6 min步行距离、MMV、用力肺活量、1秒用力呼气容积均高于对照组(P<0.05).治疗后,2组CRP、PCT、IL-17A、IL-8指标值均较治疗前下降(P<0.05),观察组上述4项指标值均低于对照组(P<0.05).治疗后,2组CD3+、CD4+、CD4+/CD8+指标值均较治疗前升高(P<0.05),观察组上述3项指标值均高于对照组(P<0.05).观察组不良反应发生率为3.28%(2/61),对照组不良反应发生率为5.00%(3/60),2组不良反应发生率比较,差异无统计学意义(P>0.05).结论:苏黄止咳胶囊联合三联雾化吸入治疗AECOPD的疗效较好,能有效恢复患者肺功能,改善免疫功能,安全性高.
Objective:To observe the efficacy of Suhuang Zhike Capsules combined with triple nebulization inhalation in treating acute exacerbation of chronic obstructive pulmonary disease(AECOPD).Methods:A total of 121 AECOPD patients treated at Deqing County People's Hospital from May 2021 to May 2024 were selected and divided into the observation group(n=61)and the control group(n=60)according to the treatment schemes.Both groups were treated with conventional basic treatment,the control group was treated with triple atomization inhalation on the basis of conventional treatment,and the observation group was treated with Suhuang Zhike Capsules on the basis of the control group.Both groups were treated for 14 days.The clinical efficacy and incidence of adverse reactions in the two groups were compared,and the changes in 6-minute walking distance,lung function indexes[maximum ventilation volume per minute(MMV),forced vital capacity,forced expiratory volume in one second],inflammatory indexes[C-reactive protein(CRP),procalcitonin(PCT),interleukin-17A(IL-17A),interleukin-8(IL-8)]and immune function(CD3+,CD4+,CD4+/CD8+)in the two groups were compared before and after treatment.Results:After 14 days of treatment,the total efficiency of clinical efficacy in the observation group was 95.08%(59/61),and that in the control group was 83.33%(50/60),the difference being significant(P<0.05).After treatment,the 6-minute walking distance,MMV,forced vital capacity,and forced expiratory volume in one second in the two groups were improved compared with those before treatment,and the above indexes in the observation group were greater than those in the control group(P<0.05).After treatment,the CRP,PCT,IL-17A,and IL-8 values of the two groups were decreased compared with those before treatment(P<0.05),and the above four index values of the observation group were lower than those of the control group(P<0.05).After treatment,the values of CD3+,CD4+,and CD4+/CD8+in the two groups were increased compared with those before treatment(P<0.05),and the above three index values in the observation group were higher than those in the control group(P<0.05).The incidence of adverse reactions in the observation group was 3.28%(2/61),and that in the control group was 5.00%(3/60).There was no significant difference in the incidence of adverse reactions between the two groups(P>0.05).Conclusion:Suhuang Zhike Capsules combined with triple nebulization inhalation shows good efficacy in the treatment of AECOPD,significantly improves lung function,enhances immune function,and has high safety.
徐丹丹;章晶晶
德清县人民医院呼吸与危重症医学科,浙江 德清 313200德清县人民医院呼吸与危重症医学科,浙江 德清 313200
医药卫生
慢性阻塞性肺疾病急性加重期苏黄止咳胶囊三联雾化吸入肺功能
Chronic obstructive pulmonary diseaseAcute exacerbationSuhuang Zhike CapsulesTriple nebulization inhalationLung function
《新中医》 2026 (17)
7-12,6
浙江省医药卫生科技计划项目(2023KY327)
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