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替卡西林治疗革兰氏阴性菌感染的临床及药理学研究。

Clinical and pharmacological studies of ticarcillin in gram-negative infections.

作者信息

Ervin F R, Bullock W E

出版信息

Antimicrob Agents Chemother. 1976 Jan;9(1):94-101. doi: 10.1128/AAC.9.1.94.

Abstract

Twenty-seven patients with serious gram-negative infections were treated with ticarcillin in an average daily dosage of 237 mg/kg (range, 174 to 307 mg/kg). Ticarcillin was bactericidal for all infecting organisms in concentrations ranging from 31.2 to 125 mug/ml. Five of 8 patients (62%) with overwhelming Pseudomonas pneumonia were cured or improved, and 9 of 12 (75%) were cured of pneumonia caused by other gram-negative organisms. Of six extrapulmonary infections caused by Pseudomonas, five (83%) were cured or improved. In seven cases, the infecting organism reisolated during therapy was more resistant to ticarcillin than the primary isolate. The serum half-life of ticarcillin in three patients with renal failure was 11.2 +/- 1.0 h, and during hemodialysis it decreased to 6.3 +/- 1.8 h. There were two episodes of superinfection with resistant organisms. Thirteen patients (48%) manifested eosinophilia, one of whom had severe urticaria. Prolongation of bleeding time was attributable to ticarcillin in two patients. Ticarcillin appears to be effective for therapy of serious gram-negative infections in dosages 30 to 50% less than those recommended for carbenicillin.

摘要

27例严重革兰阴性菌感染患者接受替卡西林治疗,平均日剂量为237mg/kg(范围为174至307mg/kg)。替卡西林对所有感染菌的杀菌浓度范围为31.2至125μg/ml。8例暴发性铜绿假单胞菌肺炎患者中有5例(62%)治愈或好转,12例由其他革兰阴性菌引起的肺炎患者中有9例(75%)治愈。6例由铜绿假单胞菌引起的肺外感染中,5例(83%)治愈或好转。7例患者在治疗期间重新分离出的感染菌对替卡西林的耐药性比原始分离株更强。3例肾衰竭患者中替卡西林的血清半衰期为11.2±1.0小时,血液透析期间降至6.3±1.8小时。有2例出现耐药菌二重感染。13例患者(48%)出现嗜酸性粒细胞增多,其中1例有严重荨麻疹。2例患者的出血时间延长归因于替卡西林。替卡西林似乎对严重革兰阴性菌感染有效,其剂量比羧苄西林推荐剂量低30%至50%。

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本文引用的文献

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Platelet function in renal failure.肾衰竭中的血小板功能。
N Engl J Med. 1969 Mar 27;280(13):677-81. doi: 10.1056/NEJM196903272801301.
6
Carbenicillin: a clinical and laboratory evaluation.羧苄青霉素:一项临床与实验室评估。
Ann Intern Med. 1970 Aug;73(2):179-87. doi: 10.7326/0003-4819-73-2-179.

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