首页> 外文期刊>International Journal of Basic & Clinical Pharmacology >A comparative study of the efficacy and tolerability of parenteral ceftriaxone and cefotaxime in pediatric population for acute bacillary dysentery in a tertiary care hospital
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A comparative study of the efficacy and tolerability of parenteral ceftriaxone and cefotaxime in pediatric population for acute bacillary dysentery in a tertiary care hospital

机译:三级医院急诊肠外头孢曲松钠和头孢噻肟在小儿急性细菌性痢疾的疗效和耐受性比较研究

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Background: Diarrheal disorders in childhood account for a large proportion (18%) of childhood mortality. Among diarrheal diseases, dysentery is a major cause of childhood morbidity and mortality, especially in developing countries. Methods: This is an open labelled, prospective, randomised, comparative study carried out at Dr. B. R. Ambedkar Medical College Hospital, Bangalore from November 2014 to November 2015 after Institutional Ethics Committee approval. A total of 80 Paediatric patients who met the inclusion criteria were included in the study after taking written informed consent from parents and assigned into two groups, Group A- Inj. Ceftriaxone (50-100mg/kg/day) and Group B- Inj. Cefotaxime (100 mg/kg/day) in divided doses for a period of 3-5 days based on requirement. Results: In this study, Cefotaxime was non inferior to Ceftriaxone as the Mean Duration of Hospitalisation was 3.30±0.72 days in Group A and 3.30± 0.72 days in Group B with p value of 1.000, showing no statistically significant difference. Both were well tolerated without any reports of ADR (Adverse Drug Reaction). Conclusions: In this study shows that Inj. Cefotaxime is equally efficacious and well tolerated as Inj. Ceftriaxone in the treatment of Acute Bacillary Dysentery in paediatric patients.
机译:背景:儿童期腹泻病占儿童死亡率的很大一部分(18%)。在腹泻疾病中,痢疾是儿童发病率和死亡率的主要原因,尤其是在发展中国家。方法:这是经机构伦理委员会批准,于2014年11月至2015年11月在班加罗尔的B. R. Ambedkar医学院附属医院进行的开放标签,前瞻性,随机对照研究。在征得父母的书面知情同意后,共有80名符合纳入标准的儿科患者被纳入研究,并分为两组,即A组。头孢曲松钠(50-100mg / kg /天)和B组注射剂。头孢噻肟(100 mg / kg /天),根据需要分三到五天服用。结果:在这项研究中,头孢噻肟不亚于头孢曲松,因为A组的平均住院时间为3.30±0.72天,B组的平均住院时间为3.30±0.72天,p值为1.000,差异无统计学意义。两者均耐受良好,无任何ADR(药物不良反应)的报道。结论:本研究表明Inj。头孢噻肟与注射剂一样有效且耐受性良好。头孢曲松钠治疗小儿急性细菌性痢疾。

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