Pollak P Timothy, Shafer Steven L
Department of Medicine, Suite 406 Bethune Building, Queen Elizabeth II HSC, Dalhousie University, Victoria General Site, 1278 Tower Road, Halifax, Nova Scotia, Canada B3H 2Y9.
J Clin Pharmacol. 2004 Feb;44(2):141-9. doi: 10.1177/0091270003262106.
Massive drug overdoses provide a unique opportunity to observe human pharmacokinetic data not otherwise ethically available. They can also provide practical examples for teaching thoughtful application of the principles of clinical pharmacology. Following a case of clozapine overdose in which onset of toxicity was delayed by 72 hours, a probable explanation was found in an exploration of three cases with unusual concentration-time profiles and revealed unexpected implications for the management of clozapine overdoses. The authors systematically addressed the possible mechanisms proposed in the literature for an unusual plateau in concentrations observed in three clozapine overdoses. The effects that the most commonly suggested explanations (i.e., delayed absorption and saturated or impaired metabolism) would have on both clozapine and norclozapine concentrations were then modeled using the data available from those three cases to provide an objective illustration for comparison. This exercise was then used as a teaching seminar, leading students through the steps required to reach a logical explanation for the observed delayed toxicity and to consider the implications for therapy. Delayed absorption best predicted the sustained serum clozapine and norclozapine concentrations observed in three cases, and modeling suggests that much of the drug remains in the gut, available for absorption for days following an overdose. As a seminar, the exercise provides students with a practical example of the value of systematically ruling out possible explanations by considering what effects various pharmacokinetic alterations would have on observed data. Absorption following massive clozapine overdose appears fundamentally different from that with conventional dosing. This suggests a potential for delayed or prolonged toxicity, extending well beyond the time frame predicted by its half-life, unless aggressive and sustained efforts are applied to remove clozapine from the gut. Data from drug overdoses provide opportunities to explore unusual aspects of pharmacokinetics, better understand future overdoses of the same agent, and present excellent material for teaching. A seminar illustrating the role that thoughtful application of pharmacologic principles had in addressing this case is now used to introduce the clinical aspects of pharmacology to students at our institutions.
大量药物过量提供了一个独特的机会来观察人体药代动力学数据,而这些数据在其他情况下从伦理角度是无法获取的。它们还能为讲授临床药理学原理的审慎应用提供实际案例。在一例氯氮平过量病例中,毒性发作延迟了72小时,通过对三例具有异常浓度 - 时间曲线的病例进行探究,找到了一个可能的解释,并揭示了氯氮平过量处理方面的意外影响。作者系统地探讨了文献中提出的关于三例氯氮平过量中观察到的异常浓度平台期的可能机制。然后,利用这三例病例的现有数据,对最常提出的解释(即吸收延迟和代谢饱和或受损)对氯氮平和去甲氯氮平浓度的影响进行建模,以提供一个客观的比较示例。这个练习随后被用作一个教学研讨会,引导学生逐步得出对观察到的延迟毒性的合理解释,并考虑对治疗的影响。吸收延迟最能预测三例病例中观察到的氯氮平和去甲氯氮平血清浓度持续存在的情况,建模表明,过量用药后,大量药物仍留在肠道中,数天内可供吸收。作为一个研讨会,这个练习为学生提供了一个实际例子,展示了通过考虑各种药代动力学改变对观察数据的影响来系统排除可能解释的价值。大量氯氮平过量后的吸收似乎与常规给药有根本不同。这表明存在延迟或延长毒性的可能性,远远超出其半衰期预测的时间范围,除非采取积极持续的措施从肠道中清除氯氮平。药物过量的数据提供了探索药代动力学异常方面、更好地理解同一药物未来过量情况以及提供优秀教学材料的机会。一个说明审慎应用药理学原理在处理该病例中所起作用的研讨会,现在被用于向我们院校的学生介绍药理学的临床方面。