Kihara M, Ikeda Y, Takagi N, Fujita H, Shibata K, Masumori S, Shiratori K, Umemura S, Shionoiri H, Ishii M
Second Department of Internal Medicine, Yokohama Minami Kyousai Hospital, Japan.
Intensive Care Med. 1995 Apr;21(4):348-51. doi: 10.1007/BF01705414.
The pharmacokinetics of amikacin were studied in patients undergoing slow hemodialysis (HD).
Slow HD was performed at the dialysate flow rate of 30 ml/min. After a single intravenous dose of amikacin 5 mg/kg, pharmacokinetic variables were calculated by fitting individual concentration-time curves to a two-compartment open model.
6 critically ill patients with renal failure were entered into the study.
The volume of distribution was 0.35 +/- 0.03 l/kg. Total body clearance was 35.1 +/- 2.3 ml/min with an elimination half-life of 10.5 h. During a 10.5 h session of slow HD, the serum amikacin concentration decreased from the peak level of 21.3 +/- 1.2 mg/l to 7.2 +/- 0.9 mg/l.
Slow HD eliminate amikacin more efficiently than other types of slowly performed renal replacement therapy and had profound effects on the pharmacokinetics. Amikacin elimination by this approach should be taken into consideration for designing a dosage schedule during the treatment.
研究阿米卡星在接受缓慢血液透析(HD)患者中的药代动力学。
以30 ml/min的透析液流速进行缓慢血液透析。单次静脉注射5 mg/kg阿米卡星后,通过将个体浓度-时间曲线拟合至二室开放模型来计算药代动力学变量。
6例患有肾衰竭的危重症患者纳入本研究。
分布容积为0.35±0.03 l/kg。总体清除率为35.1±2.3 ml/min,消除半衰期为10.5小时。在10.5小时的缓慢血液透析过程中,血清阿米卡星浓度从峰值水平21.3±1.2 mg/l降至7.2±0.9 mg/l。
缓慢血液透析比其他类型的缓慢进行的肾脏替代治疗更有效地清除阿米卡星,并且对药代动力学有深远影响。在设计治疗期间的给药方案时应考虑通过这种方法清除阿米卡星。