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更昔洛韦在肾衰竭及持续血液透析期间的临床应用。

Clinical use of ganciclovir during renal failure and continuous hemodialysis.

作者信息

Bastien O, Boulieu R, Bleyzac N, Estanove S

机构信息

DAR-Intensive Care Unit, Hôpital Cardiologique et Pneumologique, Lyon, France.

出版信息

Intensive Care Med. 1994;20(1):47-8. doi: 10.1007/BF02425056.

Abstract

OBJECTIVE

Data is scarce concerning ganciclovir, used in CMV-related diseases in transplant patient with renal failure, especially when dialysis is necessary.

DESIGN

Prospective trial.

SETTING

Intensive care unit in a university hospital, and pharmacy laboratory.

PATIENTS

pharmacokinetics were obtained in 3 patients undergoing continuous veno-venous hemodialysis (CVVHD) (PAN 69).

INTERVENTIONS

HPLC measurements of plasmatic and ultrafiltrated ganciclovir were determined at 17 times intervals after a 5 mg/kg every 48 h dosage.

RESULTS

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.

CONCLUSION

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.

摘要

目的

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。

设计

前瞻性试验。

地点

大学医院的重症监护病房和药学实验室。

患者

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。

干预措施

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。

结果

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。

结论

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。

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