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发热性中性粒细胞减少患者中,一日一次异帕米星联合头孢曲松与阿米卡星联合头孢曲松的对比研究

Isepamicin once daily plus ceftriaxone versus amikacin plus ceftriaxone in febrile neutropenic patients.

作者信息

Herbrecht R, Blaise D, Espinouse D, Leblond V, Sadoun A, Sauvage C, Cordonnier C, Minozzi C

机构信息

Service d'Onco-Hématologie, Hôpital de Hautepierre, France.

出版信息

J Chemother. 1995 Jun;7 Suppl 2:103-10.

PMID:8622099
Abstract

Isepamicin is a new aminoglycoside with in-vitro activity superior to amikacin. It is a poor substrate for the 6'-aminoacetyltransferase-I enzyme which inactivates amikacin and therefore organisms possessing this enzyme are not resistant to isepamicin. The aim of this study was to compare the efficacy and safety of co-administration of isepamicin once daily plus ceftriaxone to amikacin twice daily plus ceftriaxone to amikacin twice daily plus ceftriaxone in febrile neutropenic cancer patients. Febrile episodes in 235 patients (156 in isepamicin group and 79 in amikacin group) were treated in this study. They occurred in 218 different patients. Fifteen patients were enrolled twice and one three times. Response rates to the two treatment regimens for microbiologically documented episodes, clinically documented episodes and further unexplained fever were similar. Tolerance of the treatment regimens, as measured by serum creatinine levels, hypoaccousia and cutaneous allergy was also similar in both treatment groups. In conclusion, isepamicin given once daily when combined with ceftriaxone in the treatment of febrile episodes in neutropenic cancer patients was as effective and no more toxic than amikacin.

摘要

异帕米星是一种新的氨基糖苷类抗生素,其体外活性优于阿米卡星。它是6'-氨基乙酰转移酶-I的不良底物,该酶可使阿米卡星失活,因此,具有这种酶的微生物对异帕米星不耐药。本研究的目的是比较在发热性中性粒细胞减少的癌症患者中,异帕米星每日一次联合头孢曲松与阿米卡星每日两次联合头孢曲松的疗效和安全性。本研究对235例患者(异帕米星组156例,阿米卡星组79例)的发热发作进行了治疗。这些发作发生在218名不同的患者身上。15名患者被纳入两次,1名患者被纳入三次。对于微生物学确诊的发作、临床确诊的发作和进一步原因不明的发热,两种治疗方案的有效率相似。通过血清肌酐水平、听力减退和皮肤过敏来衡量,两个治疗组对治疗方案的耐受性也相似。总之,在治疗中性粒细胞减少的癌症患者的发热发作时,异帕米星每日一次联合头孢曲松与阿米卡星疗效相当,且毒性不更大。

相似文献

1
Isepamicin once daily plus ceftriaxone versus amikacin plus ceftriaxone in febrile neutropenic patients.发热性中性粒细胞减少患者中,一日一次异帕米星联合头孢曲松与阿米卡星联合头孢曲松的对比研究
J Chemother. 1995 Jun;7 Suppl 2:103-10.
2
A prospective, controlled, randomized, non-blind, comparative study of the efficacy and safety of a once daily high dose of ceftriaxone plus ciprofloxacin versus thrice daily ceftazidime plus amikacin in empirical therapy for febrile neutropenic patients.一项前瞻性、对照、随机、非盲、比较性研究,旨在对比每日一次大剂量头孢曲松加环丙沙星与每日三次头孢他啶加阿米卡星在发热性中性粒细胞减少患者经验性治疗中的疗效和安全性。
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3
The efficacy and safety of isepamicin and ceftazidime compared with amikacin and ceftazidime in acute lower respiratory tract infection.异帕米星与头孢他啶联用对比阿米卡星与头孢他啶联用在急性下呼吸道感染中的疗效及安全性
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Comparison of the efficacy and safety of isepamicin and amikacin in the treatment of skin and skin structure infections.异帕米星与阿米卡星治疗皮肤及皮肤结构感染的疗效与安全性比较。
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Evaluation of the efficacy and safety of isepamicin compared with amikacin in the treatment of nosocomial pneumonia and septicaemia.异帕米星与阿米卡星治疗医院获得性肺炎和败血症的疗效及安全性评估。
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Empirical antibiotic therapy in febrile neutropenic patients with single-daily dose amikacin plus ceftriaxone.发热性中性粒细胞减少患者每日单次剂量阿米卡星加头孢曲松的经验性抗生素治疗。
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引用本文的文献

1
Extended-interval aminoglycoside therapy for adult patients with febrile neutropenia: a systematic review.成人发热性中性粒细胞减少症患者的延长疗程氨基糖苷类治疗:一项系统评价
Can J Hosp Pharm. 2011 May;64(3):182-91. doi: 10.4212/cjhp.v64i3.1020.
2
Ceftriaxone/Amikacin vs Ceftazidime/Amikacin as Empirical Therapy for Fever in Patients with Haematological Malignancy and Severe Granulocytopenia: Clinical and Economic Outcomes.头孢曲松/阿米卡星与头孢他啶/阿米卡星治疗血液恶性肿瘤伴严重粒细胞减少发热患者的经验性治疗:临床和经济结局。
Clin Drug Investig. 1998;15(5):425-33. doi: 10.2165/00044011-199815050-00007.
3
Clinical pharmacokinetics and pharmacodynamics of isepamicin.
异帕米星的临床药代动力学与药效学
Clin Pharmacokinet. 2000 Mar;38(3):205-23. doi: 10.2165/00003088-200038030-00002.
4
Cost-effectiveness of ceftazidime or imipenem/cilastatin versus ceftriaxone + aminoglycoside in the treatment of febrile episodes in neutropenic cancer patients in Germany.德国头孢他啶或亚胺培南/西司他丁与头孢曲松+氨基糖苷类药物治疗中性粒细胞减少癌症患者发热性发作的成本效益
Infection. 1999 Jan-Feb;27(1):23-7. doi: 10.1007/BF02565166.