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作 者:陈陵海 吴悦[1] 王丽霞[1] 刘艳彬[1] 郑权[1] 张思智[2]
机构地区:[1]四川省成都市温江区人民医院,四川成都611130 [2]四川省人民医院,四川成都610072
出 处:《儿科药学杂志》2013年第11期31-33,共3页Journal of Pediatric Pharmacy
摘 要:目的:观察喜炎平治疗小儿细菌性肺炎的疗效及其对血清细胞因子IL-1B、IL-6、IL-8、TNF-a的影响,探讨其免疫作用机制。方法:将94例小儿细菌性肺炎患儿随机分为对照组和治疗组各47例,均给予头孢噻肟50—100mg/(kg·d)加入5%GS100~250mL中静脉滴注,3次/日;治疗组在此基础上加用喜炎平注射液5~10mg/(kg·d)加入5%GS或生理盐水100~150mL中缓慢静脉滴注;两组均以5d为1疗程,治疗2~3疗程之后停3d再治疗3d,并酌情给予止咳、祛痰等对症治疗,观察疗效;检测两组患儿治疗前后血清IL-1β、IL-6、IL-8、TNF-a水平,进行对比分析。结果:与治疗前比较,治疗后两组患儿血清IL-1β、IL-6、IL-8、TNF—a水平均降低(P〈0.05),治疗组比对照组降低更明显(P〈0.05);治疗组痊愈率、总有效率分别为68.09%、93.62%,对照组分别为48.94%、80.85%,两组比较差异有统计学意义(P〈0.05)。结论:喜炎平注射液治疗小儿细菌性肺炎的机制可能与改变细胞因子水平、调节免疫功能有关。Objective: To observe the efficacy of Xiyanping injection in the treatment of bacterial pneumonia in children and its influence on serum cytokines IL-1β, IL-6, IL-8, and TNF-ct. Methods: Ninety-four eases of children with bacterial pneumonia were randomly divided into a control group and a treatment group equally. Both groups were given cefotaxime 50 - 100 mg/(kg·d) with 5% GS 100 -250 mL 3 times per day by intravenous infusion. On this basis, the treatment group received Xiyanping injection 5 - 10 rag/( kg·d) intravenously. The treatment course of the two groups was five days. After treatment for two to three courses, the therapy was stopped for three days, and then the patients L were retreated for three days. According to the patients' condition, antitussive and expectorant agents were given. The effects were observed. The level of serum IL-1β, IL-6, IL-8 and TNF-α in both groups before and after treatment were detected: Results: The level of serum IL-β, IL-6, IL-8 and TNF-α in the two groups after treatment were significantly lower than those before treattnent (P〈0.05). The cure rate and the total effective rate in the treatment group were 68.09% and 93.62% ; in the control group were 48.94% and 80. 85% ; the difference was statistically significant (P〈0. 05). Conclusions: The mechanism of drug action of Xiyanping in treating infantile pneumonia may change eytokines levels and regulate immune functions.
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