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头孢他啶在肝硬化腹水患者中的药代动力学。

Pharmacokinetics of ceftazidime in patients with liver cirrhosis and ascites.

作者信息

el Touny M, el Guinaidy M A, Abd el Barry M, Osman L, Sabbour M S

机构信息

Department of Internal Medicine, Ain-Shams University, Heliopolis, Cairo, Egypt.

出版信息

J Antimicrob Chemother. 1991 Jul;28(1):95-100. doi: 10.1093/jac/28.1.95.

Abstract

The pharmacokinetics of ceftazidime were studied in 18 male individuals, including six healthy volunteers and 12 patients with liver cirrhosis and ascites. Each participant received 1 g of ceftazidime as a single intravenous bolus injection. The elimination half-life was longer in cirrhotic than in control patients (5.40 +/- 1.02 h) vs. (1.98 +/- 0.24 h), P less than 0.01; probably due to slow return from the ascitic compartment. Nevertheless, total body clearance did not differ significantly between the two groups (81.4 +/- 30.3 ml/h/kg vs. 83.6 +/- 24.9 ml/h/kg). Dose reduction is not necessary when treating systemic infection in cirrhotics. Ceftazidime attained a concentration of 1 microgram/ml in the ascitic fluid in most patients 15 to 30 min after the injection, and maintained this level, which is higher than the MIC90 of Enterobacteriaceae, for 24 h. An intravenous bolus injection of 1 g ceftazidime every 24 h is sufficient to treat patients with spontaneous bacterial peritonitis caused by a susceptible organism other than Pseudomonas aeruginosa.

摘要

对18名男性个体进行了头孢他啶的药代动力学研究,其中包括6名健康志愿者和12名肝硬化腹水患者。每位受试者接受1克头孢他啶单次静脉推注。肝硬化患者的消除半衰期长于对照组患者(5.40±1.02小时 vs. 1.98±0.24小时),P<0.01;这可能是由于腹水腔室的药物返回缓慢所致。然而,两组之间的总体清除率没有显著差异(81.4±30.3毫升/小时/千克 vs. 83.6±24.9毫升/小时/千克)。治疗肝硬化患者的全身感染时无需减少剂量。大多数患者在注射后15至30分钟,头孢他啶在腹水中达到1微克/毫升的浓度,并维持该水平24小时,该浓度高于肠杆菌科细菌的MIC90。每24小时静脉推注1克头孢他啶足以治疗由除铜绿假单胞菌以外的敏感生物体引起的自发性细菌性腹膜炎患者。

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