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首页> 外文期刊>Expert opinion on pharmacotherapy >Comparative evaluation of efficacy and safety of cefotaxime-sulbactam with amoxicillin-clavulanic acid in children with lower respiratory tract infections.
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Comparative evaluation of efficacy and safety of cefotaxime-sulbactam with amoxicillin-clavulanic acid in children with lower respiratory tract infections.

机译:头孢噻肟舒巴坦与阿莫西林-克拉维酸治疗儿童下呼吸道感染的疗效和安全性比较评估。

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OBJECTIVE: Beta-lactamase producing bacteria present a major problem in treating lower respiratory tract infections. The objective of this study was to evaluate efficacy and safety of cefotaxime-sulbactam combination versus amoxicillin-clavulanic acid injection as an alternative therapeutic option for treatment of lower respiratory tract infections in pediatric patients. METHODS: This randomized, multicentric, comparative study enrolled 102 inpatients with lower respiratory tract infections, in the age range of 3 months - 12 years. Patients received cefotaxime-sulbactam or amoxicillin-clavulanic acid injection intravenously for up to 7 days. RESULTS: There was no difference between the two groups in demography or disease characteristics (p > 0.05) at baseline. Efficacy was evaluated in a total of 96 patients. Both the treatment groups were comparable in response rate at the end of the therapy (p > 0.05). Clinical success rate was 93.6% and 89.8%, respectively for cefotaxime-sulbactam and co-amoxiclav. One patient from the cefotaxime-sulbactam group reported convulsions, which were probably not related to the study medication in the opinion of the investigator. Except for this serious adverse event, both the study medications were safe and well tolerated in the study population. CONCLUSION: In conclusion, cefotaxime-sulbactam administered 3 times a day for up to 7 days was found to be as effective as co-amoxiclav therapy. However, further studies with a large number of patients are required to confirm these findings with more robust microbiological evaluation.
机译:目的:产生β-内酰胺酶的细菌是治疗下呼吸道感染的主要问题。这项研究的目的是评估头孢噻肟-舒巴坦组合与阿莫西林-克拉维酸注射液作为儿科患者下呼吸道感染的替代治疗选择的疗效和安全性。方法:这项随机,多中心,比较研究纳入了102名年龄在3个月至12岁之间的下呼吸道感染患者。患者接受静脉注射头孢噻肟舒巴坦或阿莫西林克拉维酸注射长达7天。结果:两组在基线时的人口统计学或疾病特征方面无差异(p> 0.05)。评估了总共96例患者的疗效。在治疗结束时,两个治疗组的缓解率均相当(p> 0.05)。头孢噻肟舒巴坦和coamoxiclav的临床成功率分别为93.6%和89.8%。研究人员认为,头孢噻肟舒巴坦组的一名患者报告有惊厥,这可能与研究药物无关。除此严重不良事件外,两种研究药物在研究人群中都是安全且耐受性良好的。结论:总的来说,发现头孢噻肟舒巴坦每天3次,共7天,与阿莫西非治疗有效。但是,需要对大量患者进行进一步研究,以通过更可靠的微生物学评估来证实这些发现。

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