[Determination of limit values for "safe driving" in street traffic with reference to centrally active drugs from the pharmacokinetic and pharmacodynamic viewpoint].

Blutalkohol Pub Date : 1993-05-01
H Schütz, G Weiler
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引用次数: 0

Abstract

When establishing threshold values for "driving under the influence of centrally acting compounds" it must be considered that many parameters have an important influence on the pharmacokinetic properties (e.g. volume of distribution, the elimination half-life, and the drug concentration in body fluids) and the pharmacodynamic action (e.g. impairment of skills related to driving). This article describes these inter-and intraindividual parameters from the pharmacokinetic (influence of body weight, age, gender, genetics, diseases, other compounds as ethanol and antacids, enzyme induction, enzyme inhibition, first-pass effects, pharmacokinetic interaction, chronopharmacokinetics, mode of application) and pharmacodynamic (tolerance, pharmacodynamic interaction, pharmacogenetic, chronopharmacodynamic, pathological alterations) point of view. The large variabilities clearly indicate, that preliminary threshold values should be chosen high enough to prevent prejudice of traffic participants. A "consensus value" could be established and continuously monitored by a commission. Beside this the high relevance of valid analytical investigations must be regarded.

[从药代动力学和药效学角度确定集中活性药物在道路交通中“安全驾驶”的极限值]。
在确定“在中枢作用化合物影响下驾驶”的阈值时,必须考虑到许多参数对药代动力学特性(例如分布体积、消除半衰期和体液中的药物浓度)和药效学作用(例如与驾驶有关的技能损害)有重要影响。本文从药代动力学(体重、年龄、性别、遗传、疾病、其他化合物如乙醇和抗酸剂的影响、酶诱导、酶抑制、首过效应、药代动力学相互作用、时药效学、应用方式)和药效学(耐受性、药效学相互作用、药效学、时药效学、病理改变)的角度描述了这些个体间和个体内的参数。较大的变量清楚地表明,初步阈值应选择足够高,以防止交通参与者的偏见。可以建立一个“协商一致值”,并由一个委员会持续监测。除此之外,必须考虑有效分析调查的高度相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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