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1.
China Pharmacy ; (12): 1702-1706, 2018.
Article in Chinese | WPRIM | ID: wpr-704874

ABSTRACT

OBJECTIVE:To evaluate the efficacy and safety of Bacterial lysates(hereinafter referred to as"Broncho-Vaxom") for recurrent respiratory tract infections (RRTIs) of children,and to provide evidence-based reference for clinic. METHODS:Retrieved from PubMed,EMBase,Cochrane Library,CBM,CNKI,Wanfang database and VIP database,domestic and foreign published randomized controlled trials (RCTs) about Broncho-Vaxom (trail group) vs. placebo (control group) for RRTIs of children were collected during database establishment to Jan. 2018. After literature scanning and data extraction,the risk of bias of included trials were evaluated by using Cochrane 5.1.0 risk bias evaluation tool. Meta-analysis was performed by using Rev Man 5.3 software. RESULTS:A total of 13 RCTs involving 1 228 children were included. The results showed that the trial group was superior to control group in frequency of respiratory infection [MD=-1.14,95%CI(-1.29,-0.99),P<0.001],total response rate [RR=9.47,95%CI(2.33,38.54),P=0.002],the time of antibiotics use [MD=-4.36,95%CI(-6.52,-2.21),P<0.001], infection duration [MD=-3.89,95%CI(-4.47,-3.04),P<0.001],febrile time [MD=-1.81,95%CI(-3.40,-0.22),P=0.03],serum immunoglobulin (Ig)G level [MD=1.25,95%CI(0.13,2.37)),P=0.03],IgA level [MD=0.77,95%CI(0.07, 1.46),P=0.03] and the level of T cell subgroup CD4+[MD=1.33,95%CI(0.90,1.76),P<0.001] and CD8+[MD=0.64,95%CI (0.24,1.04),P=0.002],there was statistical significance. Trail group was similar to control group in respect of cough time [MD=-6.00,95%CI(-13.86,1.86),P=0.13] and IgM level [MD=-0.10,95%CI(-0.32,0.12),P=0.39] and the incidence of ADR [RR=0.76,95%CI(0.43,1.35),P=0.35]. CONCLUSIONS:The current evidence shows that Broncho-Vaxom could effectively prevent the RRTIs of children with good safety.

2.
China Pharmacy ; (12): 337-340, 2016.
Article in Chinese | WPRIM | ID: wpr-501491

ABSTRACT

OBJECTIVE:To systematically review the efficacy and safety of Xiyanping injection versus Ribavirin injection in the treatment of herpangina in children,and provide evidence-based reference for clinical treatment. METHODS:Retrieved from PubMed,Cochrane Library,EMBase,VIP Database,CJFD,Wanfang Database and CBM,randomized controlled trials (RCT) about efficacy and safety of Xiyanping injection versus Ribavirin injection in the treatment of herpangina in children were collected. Meta-analysis was performed by using Rev Man 5.3 software after data extracting and quality evaluating by modified Jadad. RE-SULTS:Totally 14 RCTs were enrolled,involving 1 939 patients. Results of Meta-analysis showed total effective rate [OR=4.69, 95%CI(3.36,6.55),P<0.001],fever clearance time [MD=-1.36,95% CI(-1.60,-1.12),P<0.001],herpes regression time [MD=-1.34,95%CI(-1.61,-1.06),P<0.001],hospitalization time [MD=-1.88,95% CI(-3.68,-0.07),P=0.04] and sali-vation disappearance time [MD=-1.07,95% CI(-1.30,-0.84),P<0.001] of Xiyanping injection were significantly better than Ribavirin injection,there were statistically significant differences. And there was no significant difference in the incidence of ad-verse reactions [OR=0.56,95% CI(0.31,1.03),P=0.06]. CONCLUSIONS:The efficacy of Xiyanping injection is better than Rib-avirin injection in the treatment of herpangina in children,with similar safety.

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