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预测血浆氟哌啶醇浓度的药代动力学方案。

Pharmacokinetic protocol for predicting plasma haloperidol concentrations.

作者信息

Miller D D, Perry P J, Kelly M W, Coryell W H, Arndt S V

机构信息

Department of Psychiatry, College of Medicine, University of Iowa, Iowa City.

出版信息

J Clin Psychopharmacol. 1990 Jun;10(3):207-12.

PMID:2376619
Abstract

The accurate prediction of steady-state plasma haloperidol concentrations was successfully accomplished by obtaining two blood samples following a 20 mg test dose (kinetic method). Prediction of steady-state concentrations on the basis of a mg/kg/day dosage (dose method), although equally precise, generated significantly less information concerning the variance between observed and predicted haloperidol plasma concentrations. Both predictive methods were less precise when the daily doses exceeded 0.47 mg/kg/day. Fifty percent (6/12 patients) of the haloperidol plasma concentrations were underpredicted if this threshold was exceeded. This finding may suggest the possibility of dose-dependent pharmacokinetics with haloperidol in some patients.

摘要

通过给予20毫克试验剂量后采集两份血样(动力学方法),成功实现了对稳态血浆氟哌啶醇浓度的准确预测。基于毫克/千克/天剂量(剂量方法)预测稳态浓度,虽然同样精确,但关于观察到的和预测的氟哌啶醇血浆浓度之间的差异所产生的信息要少得多。当日剂量超过0.47毫克/千克/天时,两种预测方法的精确性均降低。如果超过此阈值,50%(6/12例患者)的氟哌啶醇血浆浓度会被低估。这一发现可能提示在某些患者中氟哌啶醇存在剂量依赖性药代动力学的可能性。

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