摘要
目的评价苏黄止咳胶囊治疗感冒后咳嗽的临床疗效与安全性。方法检索中国知网、万方、维普、中国生物医学文献数据库、Pubmed数据库和The Cochrane Library中关于苏黄止咳胶囊治疗感冒后咳嗽的临床随机对照试验,按照Cochrane系统评价手册推荐的方法评估纳入研究的偏倚风险,采用Review Manager 5.3软件进行Meta分析。结果共纳入9个符合标准的RCT研究,共741例患者。纳入研究多数存在较高的方法学偏倚风险。Meta结果显示,1咳嗽总疗效治疗组优于对照组,差异有统计学意义[OR=3.43,95%CI(2.23,5.29),P<0.000 01];2在咳嗽积分[SMD=?0.53,95%CI(?0.92,?0.15),P=0.007]、中医证候疗效[OR=2.64,95%CI为(1.32,5.31),P=0.006]上,苏黄止咳胶囊也均优于对照组,其差异均有统计学意义。3在咳嗽消失时间上,两组间差异有统计学意义[MD=?3.04,95%CI(?5.86,?0.22),P=0.03],但在咳嗽起效时间上,2组间差异无统计学意义[SMD=?1.2,95%CI(?2.65,0.26),P=0.11]。4不良反应发生率治疗组和对照组差异无统计学意义[OR=0.91,95%CI(0.31,2.65),P=0.86]。结论苏黄止咳胶囊治疗感冒后咳嗽疗效肯定,安全可靠。临床上具有一定的可替代性,但尚需更多大样本、高质量随机对照试验来证实。
OBJECTIVE To evaluate the clinical efficacy and safety of suhuang zhike capsule in the treatment of postinfectious cough. METHODS Retrieval of CNKI, Wanfang, VIP,CBM, Pubmed and The Cochrane Library on suhuang zhike capsule in the treatment of PIC clinical randomized controlled trials. Evaluate the risk of bias in the study of the method recommended by the Cochrane system. Used Review Manager 5.3 software to analysis. RESULTS A total of 9 studies were included in 741 patients. There was a higher risk of bias included in the study methodology majority. The result showed that: 1The treatment group was better than the control group, the difference was statistically significant(OR=3.43, 95%CI(2.23, 5.29), P〈0.000 01); 2On cough integration(SMD=-0.53, 95%CI(-0.92, -0.15), P=0.007), TCM syndrome(OR=2.64, 95%CI(1.32, 5.31), P=0.006), Suhuang Zhike capsules were also better than the control group, the differences were statistically significant. 3There was significant difference between the two groups on cough disappearance time(MD=-3.04, 95%CI(-5.86, -0.22), P=0.03); But there was no significant difference between the two groups on cough onset time(SMD=-1.2, 95%CI(-2.65, 0.26), P=0.11). 4 The incidence of adverse reactions in the treatment group and the control group were not statistically significant(OR=0.91, 95%CI(0.31, 2.65), P=0.86). CONCLUSION Suhuang Zhike capsule treatment of PIC is effective, safe and reliable. The clinical practice has an alternative. But still need more large samples, high quality randomized controlled trials to be confirmed.
作者
韩佳颖
王真
徐凯丽
HAN Jiaying WANG Zhen XU Kaili(The First Clinical Medical College of Zhejiang Chinese Medical University, Hangzhou 310053, China The First Affiliated Hospital of Zhejiang Chinese Medical University, Hangzhou 310006, China)
出处
《中国现代应用药学》
CAS
CSCD
2016年第10期1328-1333,共6页
Chinese Journal of Modern Applied Pharmacy