首页 | 本学科首页   官方微博 | 高级检索  
     

Randomized controlled trial on treatment of bronchial asthma of qi-deficiency cold syndrome type by Pingchuan Yiqi Granule (平喘益气颗粒)
引用本文:张颖,常静,迟焕海,毛兵,唐文富,王蕾,黄素珍,李廷谦,张瑞明. Randomized controlled trial on treatment of bronchial asthma of qi-deficiency cold syndrome type by Pingchuan Yiqi Granule (平喘益气颗粒)[J]. 中国结合医学杂志, 2007, 13(1): 27-32. DOI: 10.1007/s11655-007-0027-7
作者姓名:张颖  常静  迟焕海  毛兵  唐文富  王蕾  黄素珍  李廷谦  张瑞明
作者单位:Department of Integrative Chinese and Western Medicine, Huaxi Hospital of Sichuan University, Chengdu 610041
摘    要:
Objective: To evaluate the effect and safety of Pingchuan Yiqi Granule (平喘益气颗粒, PYG) in treating bronchial asthma of qi-deficiency cold syndrome type (BS-QDC). Methods: With the randomized, positive agent parallel controlled design adopted, the 80 subjects enrolled were assigned in the ratio of 3:1 to two groups, the 60 patients in the trial group were treated with PYG and the 20 in the control group treated with Ruyi Dingchuan Pill (如意定喘丸,RDP), with the therapeutic course consisting of 7 days for both groups. The clinical effects, effects on TCM syndrome and the changes of lung function after treatment were observed. Results: The effect of the treatment on asthma in the trial group: clinically controlled rate was 6.67%, markedly effective rate 51.67%, improved rate 33.33% and ineffective rate 8.33%; and the corresponding rates in the control group were 5.00%, 50.00%, 30.00%, and 15.00% respectively. Comparison between the two groups showed insignificant difference (P〉0.05). The effect on TCM syndrome in the treated group: clinically controlled rate was 11.67%, markedly effective rate 58.33%, effective rate 21.67% and ineffective rate 8.33%; and those in the control group were 10.00%, 50.00%, 30.00% and 10.00% respectively, also showing insignificant difference between the two groups (P〉0.05). Lung function test showed that the change on forced expiratory volume in 1 second (FEV1) after treatment in the trial group was of statistical significance (P〈0.05), but no significant difference was shown in the change of peak expiratory flow (PEE P〉0.05); while the changes in the control group were just the opposite, showing insignificance in FEV1 (P〉0.05) but significance in PEF (P〈0.05). Comparison of the therapeutic effect on lung function between the two groups showed no significant difference (P〉0.05). No adverse reaction was found in either group in the course of treatment. Conclusion: PYG used to treat BS-QDC is effective and safe, it's effect is similar to that of RDP.

关 键 词:控制实验 支气管哮喘 平喘益气颗粒 中医
收稿时间:2006-12-02

Randomized controlled trial on treatment of bronchial asthma of qi-deficiency cold syndrome type by pingchuan yiqi granule
Dr. Ying Zhang,Jing Chang,Huan-hai Chi,Bing Mao,Wen-fu Tang,Lei Wang,Su-zhen Huang,Ting-qian Li and Rui-ming Zhang. Randomized controlled trial on treatment of bronchial asthma of qi-deficiency cold syndrome type by pingchuan yiqi granule[J]. Chinese journal of integrative medicine, 2007, 13(1): 27-32. DOI: 10.1007/s11655-007-0027-7
Authors:Dr. Ying Zhang  Jing Chang  Huan-hai Chi  Bing Mao  Wen-fu Tang  Lei Wang  Su-zhen Huang  Ting-qian Li  Rui-ming Zhang
Affiliation:(1) Department of Integrative Chinese and Western Medicine, Huaxi Hospital of Sichuan University, Chengdu, 610041, China
Abstract:
Objective To evaluate the effect and safety of Pingchuan Yiqi Granule (平喘益气颗粒, PYG) in treating bronchial asthma of qi-deficiency cold syndrome type (BS-QDC). Methods With the randomized, positive agent parallel controlled design adopted, the 80 subjects enrolled were assigned in the ratio of 3:1 to two groups, the 60 patients in the trial group were treated with PYG and the 20 in the control group treated with Ruyi Dingchuan Pill (如意定喘丸, RDP), with the therapeutic course consisting of 7 days for both groups. The clinical effects, effects on TCM syndrome and the changes of lung function after treatment were observed. Results The effect of the treatment on asthma in the trial group: clinically controlled rate was 6.67%, markedly effective rate 51.67%, improved rate 33.33% and ineffective rate 8.33%; and the corresponding rates in the control group were 5.00%, 50.00%, 30.00%, and 15.00% respectively. Comparison between the two groups showed insignificant difference (P>0.05). The effect on TCM syndrome in the treated group: clinically controlled rate was 11.67%, markedly effective rate 58.33%, effective rate 21.67% and ineffective rate 8.33%; and those in the control group were 10.00%, 50.00%, 30.00% and 10.00% respectively, also showing insignificant difference between the two groups (P>0.05). Lung function test showed that the change on forced expiratory volume in 1 second (FEV1) after treatment in the trial group was of statistical significance (P<0.05), but no significant difference was shown in the change of peak expiratory flow (PEF, P>0.05); while the changes in the control group were just the opposite, showing insignificance in FEV1 (P>0.05) but significance in PEF (P<0.05). Comparison of the therapeutic effect on lung function between the two groups showed no significant difference (P>0.05). No adverse reaction was found in either group in the course of treatment. Conclusion PYG used to treat BS-QDC is effective and safe, it’s effect is similar to that of RDP.
Keywords:Pingchuan Yiqi Granule  randomized controlled trial  bronchial asthma  qi-deficiency cold syndrome type
本文献已被 维普 万方数据 PubMed SpringerLink 等数据库收录!
点击此处可从《中国结合医学杂志》浏览原始摘要信息
点击此处可从《中国结合医学杂志》下载全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号