Moore T D, Bechtel T P, Ayers L W
Am J Hosp Pharm. 1981 Oct;38(10):1496-9.
The relationship between serum concentrations and cerebrospinal fluid (CSF) concentrations of cefazolin, and the association between these concentrations and neurotoxic reactions, were investigated. Samples of serum and spinal fluid were drawn simultaneously from six patients at the steady state on various dosages of cefazolin sodium for different conditions. The dose, dosing interval, number of doses, results of renal function tests, and signs of neurotoxicity, such as muscle twitches, confusion, and seizures, were recorded. The concentrations of cefazolin in the serum and CSF, total serum protein, and percent albumin were determined. Five of the six patients given multiple doses of cefazolin sodium had notable CSF accumulation of the drug (11.3 +/- 2.7% of the serum concentration). Three patients experienced generalized focal-motor seizures during their therapy. Neurotoxicity was found to be associated with renal dysfunction and multiple-dose therapy leading to serum concentrations greater than 360 micrograms/ml and CFS concentrations greater than 34 micrograms/ml. Cefazolin will penetrate into the CSF in patients receiving multiple-dose therapy of the drug. To avoid neurotoxicity, careful attention should be paid to the recommended dosage regimens, the impact of renal dysfunction on drug clearance should be recognized, and serum assays should be performed when necessary.
研究了头孢唑林的血清浓度与脑脊液(CSF)浓度之间的关系,以及这些浓度与神经毒性反应之间的关联。在不同情况下,从六名接受不同剂量头孢唑林钠且处于稳态的患者中同时采集血清和脑脊液样本。记录剂量、给药间隔、给药次数、肾功能测试结果以及神经毒性体征,如肌肉抽搐、意识模糊和癫痫发作。测定血清和脑脊液中头孢唑林的浓度、血清总蛋白以及白蛋白百分比。接受多次剂量头孢唑林钠治疗的六名患者中有五名出现药物在脑脊液中的明显蓄积(为血清浓度的11.3±2.7%)。三名患者在治疗期间发生全身性局灶性运动性癫痫发作。发现神经毒性与肾功能不全以及多次给药治疗导致血清浓度大于360微克/毫升和脑脊液浓度大于34微克/毫升有关。接受该药物多次给药治疗的患者中,头孢唑林可穿透进入脑脊液。为避免神经毒性,应仔细关注推荐的给药方案,认识到肾功能不全对药物清除的影响,并在必要时进行血清检测。