芩香清解口服液联合利巴韦林治疗儿童上呼吸道感染的临床研究
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  • 英文篇名:Clinical study on Qinxiang Qingjie Oral Liquid combined with ribavirin in treatment of upper respiratory tract infection in children
  • 作者:王金彩 ; 石太新
  • 英文作者:WANG Jin-cai;SHI Tai-xin;Department of Pharmacy, the First Affiliated Hospital of Xinxiang Medical University;Department of Pediatrics, the First Affiliated Hospital of Xinxiang Medical University;
  • 关键词:芩香清解口服液 ; 利巴韦林注射液 ; 儿童上呼吸道感染 ; 炎症因子
  • 英文关键词:Qinxiang Qingjie Oral Liquid;;Ribavirin Injection;;children upper respiratory tract infection;;inflammatory factor
  • 中文刊名:GWZW
  • 英文刊名:Drugs & Clinic
  • 机构:新乡医学院第一附属医院药学部;新乡医学院第一附属医院小儿内科;
  • 出版日期:2019-02-26
  • 出版单位:现代药物与临床
  • 年:2019
  • 期:v.34
  • 语种:中文;
  • 页:GWZW201902021
  • 页数:4
  • CN:02
  • ISSN:12-1407/R
  • 分类号:105-108
摘要
目的探讨芩香清解口服液联合利巴韦林注射液治疗儿童上呼吸道感染的临床疗效。方法选取2017年7月—2018年9月新乡医学院第一附属医院收治的上呼吸道感染患儿114例作为研究对象,将患儿根据随机数字表法分为对照组和治疗组,每组各57例。对照组静脉滴注利巴韦林注射液,10mg/kg加入到100m L葡萄糖注射液中充分稀释,1次/d。治疗组在对照组的基础上口服芩香清解口服液,10 mL/次,3次/d。两组患儿均治疗3 d。观察两组患儿的临床疗效,同时比较两组治疗前后的临床症状改善时间和炎症因子水平。结果治疗后,治疗组的总有效率为92.98%,显著高于对照组的78.95%,两组比较差异具有统计学意义(P<0.05)。治疗后,治疗组的退热时间、止咳时间、咽痛消失时间、止涕时间均显著短于对照组,两组比较差异具有统计学意义(P<0.05)。治疗后,两组超敏C反应蛋白(hs-CRP)、肿瘤坏死因子α(TNF-α)、白细胞介素-6(IL-6)、白细胞介素-4(IL-4)水平均显著降低,同组治疗前后比较差异具有统计学意义(P<0.05);治疗后,治疗组炎症因子水平明显低于对照组,两组比较差异具有统计学意义(P<0.05)。结论芩香清解口服液联合利巴韦林注射液能提高儿童上呼吸道感染的疗效,降低血清炎症因子水平,具有一定的临床推广应用价值。
        Objective To investigate the clinical efficacy of Qinxiang Qingjie Oral Liquid combined with Ribavirin Injection in treatment of children upper respiratory tract infection. Methods Children(114 cases) with upper respiratory tract infection in the First Affiliated Hospital of Xinxiang Medical University from July 2017 to September 2018 were randomly divided into control and treatment groups, and each group had 57 cases. Children in the control group were iv administered with Ribavirin Injection, 10 mg/kg added into glucose injection 100 mL, once daily. Children in the treatment group were po administered with Qinxiang Qingjie Oral Liquid 10 mL/time, three times daily. Children in two groups were treated for 3 d. After treatment, the clinical efficacy was evaluated, the improvement time of clinical symptoms and inflammatory factor levels in two groups before and after treatment were compared. Results After treatment, the clinical efficacy in the treatment group was 92.98%, which was significantly higher than 78.95% in the control group, there were differences between two groups(P < 0.05). After treatment, times of defervescence, cough relief, pharyngalgia disappearance, and runny nose relief in the treatment group were significantly shorter than those in the control group, and there were differences between two groups(P < 0.05). After treatment, hs-CRP, TNF-α, IL-6, and IL-4 levels in two groups were significantly decreased, and the difference was statistically significant in the same group(P < 0.05). After treatment, inflammatory factors levels in the treatment group were significantly lower than those in the control group, with significant difference between two groups(P < 0.05). Conclusion Qinxiang Qingjie Oral Liquid combined with Ribavirin Injection can improve the efficacy of children upper respiratory tract infection, and reduce the level of serum inflammatory factors, which has a certain clinical application value.
引文
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