Bastien O, Boulieu R, Bleyzac N, Estanove S
DAR-Intensive Care Unit, Hôpital Cardiologique et Pneumologique, Lyon, France.
Intensive Care Med. 1994;20(1):47-8. doi: 10.1007/BF02425056.
Data is scarce concerning ganciclovir, used in CMV-related diseases in transplant patient with renal failure, especially when dialysis is necessary.
Prospective trial.
Intensive care unit in a university hospital, and pharmacy laboratory.
pharmacokinetics were obtained in 3 patients undergoing continuous veno-venous hemodialysis (CVVHD) (PAN 69).
HPLC measurements of plasmatic and ultrafiltrated ganciclovir were determined at 17 times intervals after a 5 mg/kg every 48 h dosage.
Peak and trough concentrations were respectively 16.1 +/- 2.4 and 5.5 +/- 0.5 mg/l, sieving coefficient 0.75-0.95, and volume of distribution at steady state 0.64 +/- 0.09 l/kg, half life (beta phase) 18.6 +/- 1.8 h. No direct toxicity, or CMV-related death occurred.
Plasma concentrations were higher than the ID 90. A dosage of 5 mg/kg/48 h of ganciclovir could be used during CVVHD, and ideally adjusted to monitoring of plasma drug levels.
关于更昔洛韦在肾衰竭移植患者巨细胞病毒相关疾病中的应用,尤其是在需要透析时的数据较少。
前瞻性试验。
大学医院的重症监护病房和药学实验室。
对3例接受持续静脉 - 静脉血液透析(CVVHD)的患者(PAN 69)进行药代动力学研究。
每48小时给予5mg/kg剂量后,在17个时间点通过高效液相色谱法测定血浆和超滤液中的更昔洛韦。
峰浓度和谷浓度分别为16.1±2.4和5.5±0.5mg/l,筛系数0.75 - 0.95,稳态分布容积0.64±0.09l/kg,半衰期(β相)18.6±1.8小时。未发生直接毒性反应或与巨细胞病毒相关的死亡。
血浆浓度高于90%抑制浓度。在CVVHD期间可使用每48小时5mg/kg的更昔洛韦剂量,并理想地根据血浆药物水平监测进行调整。