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Empiric use of cefepime in the treatment of lower respiratory tract infections in children.

机译:头孢吡肟在儿童下呼吸道感染的治疗中的经验性使用。

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BACKGROUND: These studies were designed to assess the efficacy and safety of cefepime, a fourth generation cephalosporin, for the treatment of serious infections, including lower respiratory tract infections (LRTI) in children. METHODS: Four clinical trials of cefepime for the treatment of serious bacterial infections enrolled 259 children with LRTI. In 3 trials cefepime was compared with ceftazidime (n = 166), cefotaxime (n = 16) or cefuroxime (n = 12). One trial was noncomparative (n = 65). RESULTS: Treatment with cefepime 50 mg/kg/ dose administered every 8 to 12 h produced a satisfactory clinical response (clinical signs of infection resolved or improved with no evidence of recurrent infection at posttreatment follow-up) in 88 to 100% of patients, comparable with comparator therapy. In children from whom a causative pathogen was identified, bacteriologic eradication was comparable between cefepime and comparator therapy. Cefepime was as safe and well-tolerated as comparator therapy. Few treatment-related clinical or laboratory adverse events were noted and were equivalent to comparator in all studies. CONCLUSION: Cefepime is as effective, safe and well-tolerated for the empiric treatment of children with LRTI as comparator agents but offers the advantage of an enhanced spectrum of activity for Gram-positive and Gram-negative pathogens compared with second or third generation cephalosporins.
机译:背景:这些研究旨在评估第四代头孢菌素头孢吡肟治疗严重感染(包括儿童下呼吸道感染(LRTI))的有效性和安全性。方法:259例头孢吡肟治疗严重细菌感染的四项临床试验招募了259名LRTI儿童。在3个试验中,将头孢吡肟与头孢他啶(n = 166),头孢噻肟(n = 16)或头孢呋辛(n = 12)进行了比较。一项试验是非比较性的(n = 65)。结果:每8到12小时以50毫克/千克/头孢吡肟的剂量进行治疗,在88至100%的患者中产生了令人满意的临床反应(感染的临床症状已解决或改善,治疗后随访中无复发感染的迹象),与比较剂疗法相当。在鉴定出致病性病原体的儿童中,头孢吡肟与对照治疗之间的细菌学根除相当。头孢吡肟与比较剂治疗一样安全且耐受性良好。几乎没有注意到与治疗有关的临床或实验室不良事件,并且在所有研究中均与比较者相当。结论:头孢吡肟对LRTI患儿的经验性治疗与比较剂一样有效,安全且耐受性良好,但与第二代或第三代头孢菌素相比,头孢吡肟对革兰氏阳性和革兰氏阴性病原体的活性范围广。

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