Kerwin Robert
Institute of Psychiatry, King's College, London, UK.
CNS Drugs. 2007;21(4):267-78. doi: 10.2165/00023210-200721040-00002.
Clozapine is one of the original atypical antipsychotics. It was withdrawn from the market in 1974 because of haematological safety concerns, but since 1989 has enjoyed a renaissance for the management of treatment-resistant schizophrenia under systems where case registration allows regular haematological monitoring. Clozapine continues to show enduring superiority across many aspects of the clinical pharmacology of the treatment of schizophrenia, e.g. it has specific anti-suicidal properties and recent broader trials have shown continuing superiority in wide groups of patients. This article considers some of the arguments for unshackling clozapine from its current license for schizophrenia (its superiority overall in treatment-resistant schizophrenia, its potential for use in first-episode patients, and its anti-suicidal potential), and tries to synthesise these into some of the national guidelines available for the treatment of schizophrenia.
氯氮平是最早的非典型抗精神病药物之一。由于血液学安全性问题,它于1974年退出市场,但自1989年以来,在病例登记允许定期进行血液学监测的系统下,它在难治性精神分裂症的治疗中再度兴起。氯氮平在精神分裂症治疗的临床药理学的许多方面继续显示出持久的优越性,例如它具有特定的抗自杀特性,最近更广泛的试验表明在广泛的患者群体中它持续具有优越性。本文探讨了一些关于解除氯氮平目前用于精神分裂症的许可限制的观点(它在难治性精神分裂症中的总体优越性、其在首发患者中的使用潜力以及其抗自杀潜力),并试图将这些观点整合到一些现有的精神分裂症治疗国家指南中。