Demotes-Mainard F, Albin H, Ragnaud J M, Gin H, Vincon G, Aubertin J
Service de Pharmacologie Clinique, Hôpital Pellegrin, Bordeaux, France.
Pathol Biol (Paris). 1988 Feb;36(2):155-8.
The role of fever on cefotaxime disposition was studied in ten hyperthermic patients. Each subject received intravenously 1 g of cefotaxime on two separated occasions, first when the body temperature was more than 39 degrees C then during a basal state (37 degrees C). Blood samples were taken over 12 hours and urine was collected for 24 hours after injection. After dosing cefotaxime and its metabolite by high performance liquid chromatography, the pharmacokinetic parameters were calculated, especially: plasma and renal clearance, volume of distribution at steady state, area under the curve, and elimination half-life. There is no significant difference in cefotaxime and desacetylcefotaxime disposition between these two states. Hyperthermia has no influence on pharmacokinetics of this cephalosporin.
在十名高热患者中研究了发热对头孢噻肟处置的作用。每位受试者在两个不同时间静脉注射1克头孢噻肟,第一次是在体温高于39摄氏度时,然后是在基础状态(37摄氏度)下。注射后采集12小时的血样,并收集24小时的尿液。通过高效液相色谱法测定头孢噻肟及其代谢物的含量后,计算药代动力学参数,特别是:血浆清除率和肾脏清除率、稳态分布容积、曲线下面积以及消除半衰期。在这两种状态下,头孢噻肟和去乙酰头孢噻肟的处置没有显著差异。高热对这种头孢菌素的药代动力学没有影响。