Freeman D J, Oyewumi L K
Department of Medicine, University of Western Ontario, London, Canada.
Clin Pharmacokinet. 1997 Feb;32(2):93-100. doi: 10.2165/00003088-199732020-00001.
Clozapine is an atypical antipsychotic medication with proven efficacy in the management of refractory schizophrenia. It is also recommended for patients who do not tolerate the extrapyramidal adverse effects of traditional antipsychotic medications. However, the therapeutic promise of clozapine has been limited by a higher incidence of agranulocytosis. Currently, plasma clozapine concentrations are not routinely used in clinical management. Therapeutic effects are monitored empirically during a 6 to 8 week titration period in which the dosage is raised to 300 to 450 mg/day. Clozapine nevertheless fulfils a number of criteria which make it a candidate for therapeutic monitoring. These include an identifiable therapeutic range, an unpredictable dose-concentration relationship between patients, a potential for clinically relevant pharmacokinetic interaction with other drugs and a high probability of patient noncompliance. The therapeutic threshold plasma concentration appears to be about 400 micrograms/L. Concentrations above 1000 micrograms/L increase the risk of adverse effects on the central nervous system (confusion, delirium and generalised seizures). There is no evidence to link increased concentrations of clozapine or its metabolite to the development of agranulocytosis. We conclude that therapeutic drug monitoring can play a useful role in the clinical management of patients treated with clozapine. The clinician is advised to primarily use clinical judgement during dosage escalation, but intermittent monitoring is recommended to quickly optimise a therapeutic dosage for each patient. At steady state, occasional measurements could be made when clinical signs indicate possible toxicity or lack of effect (possibly caused by a lack of compliance or drug interaction). Long term monitoring would, in our view, not be necessary.
氯氮平是一种非典型抗精神病药物,在难治性精神分裂症的治疗中已证实具有疗效。对于不能耐受传统抗精神病药物锥体外系不良反应的患者,也推荐使用氯氮平。然而,氯氮平的治疗前景因粒细胞缺乏症发生率较高而受到限制。目前,血浆氯氮平浓度在临床管理中并非常规使用。在6至8周的滴定期内根据经验监测治疗效果,在此期间剂量逐渐增加至300至450毫克/天。尽管如此,氯氮平满足多项标准,使其成为治疗监测的候选药物。这些标准包括可识别的治疗范围、患者之间不可预测的剂量-浓度关系、与其他药物发生临床相关药代动力学相互作用的可能性以及患者不依从的高概率。治疗阈值血浆浓度似乎约为400微克/升。浓度高于1000微克/升会增加对中枢神经系统产生不良反应(意识模糊、谵妄和全身性癫痫发作)的风险。没有证据表明氯氮平或其代谢产物浓度升高与粒细胞缺乏症的发生有关。我们得出结论,治疗药物监测在氯氮平治疗患者的临床管理中可发挥有益作用。建议临床医生在剂量增加过程中主要运用临床判断,但建议进行间歇性监测,以便迅速为每位患者优化治疗剂量。在稳态时,如果临床体征表明可能存在毒性或无效果(可能由不依从或药物相互作用引起),可偶尔进行测量。我们认为,无需进行长期监测。