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奈替米星每日一次与每日三次给药联合β-内酰胺类抗生素作为发热性中性粒细胞减少患者的经验性治疗

Once-daily versus thrice-daily dosing of netilmicin in combination with beta-lactam antibiotics as empirical therapy for febrile neutropenic patients.

作者信息

Rozdzinski E, Kern W V, Reichle A, Moritz T, Schmeiser T, Gaus W, Kurrle E

机构信息

Section of Infectious Diseases, Ulm University Hospital and Medical Center, Germany.

出版信息

J Antimicrob Chemother. 1993 Apr;31(4):585-98. doi: 10.1093/jac/31.4.585.

Abstract

In a prospective, randomized trial, netilmicin given once daily (OD) was compared in terms of efficacy and safety with the conventional 8-hourly dosing regimen (TD), both in combination with a broad spectrum beta-lactam, as initial empirical therapy for febrile neutropenic patients; the total daily dosage of netilmicin in each group was 6 mg/kg body weight. Twenty-nine of the 116 (25%) evaluable patients had microbiologically documented septicaemia, most of which were caused by Gram-positive bacteria, 41 (35%) had microbiologically documented infection without bacteraemia and 46 (40%) had possible infection. Highest peak serum concentrations of netilmicin in the OD group were significantly higher and trough serum concentrations significantly lower than in the TD group. A multivariate analysis revealed that neither the dosage regimen nor the peak serum concentration of netilmicin were determinants of a favourable outcome. The response rates of both groups to the initial treatment regimens were comparable and increased similarly following modification of the initial therapy. Response rates were particularly poor in patients with lower respiratory tract infection and in those who remained neutropenic throughout the course of treatment. The incidence of nephrotoxicity was low and did not differ significantly between groups. Once-daily dosing of netilmicin appears to be as effective and as safe as thrice-daily dosing, but is unlikely to further improve the response of febrile neutropenic patients to empirical therapy.

摘要

在一项前瞻性随机试验中,将每日一次(OD)给予奈替米星与传统的每8小时给药方案(TD)在疗效和安全性方面进行了比较,二者均与一种广谱β-内酰胺类药物联合使用,作为发热性中性粒细胞减少患者的初始经验性治疗;每组中奈替米星的每日总剂量为6mg/kg体重。116例可评估患者中有29例(25%)有微生物学证实的败血症,其中大多数由革兰氏阳性菌引起,41例(35%)有微生物学证实的无菌血症感染,46例(40%)有可能的感染。OD组中奈替米星的最高血清峰浓度显著高于TD组,而血清谷浓度显著低于TD组。多变量分析显示,给药方案和奈替米星的血清峰浓度均不是良好预后的决定因素。两组对初始治疗方案的反应率相当,在初始治疗调整后反应率的升高情况相似。下呼吸道感染患者和在整个治疗过程中仍为中性粒细胞减少的患者的反应率特别低。肾毒性的发生率较低,两组之间无显著差异。每日一次给予奈替米星似乎与每日三次给药一样有效和安全,但不太可能进一步改善发热性中性粒细胞减少患者对经验性治疗的反应。

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