Sandson Neil B, Cozza Kelly L, Armstrong Scott C, Eckermann Gabriel, Fischer Bernard A, Phillips Barnell
Psychosomatics. 2007 Mar-Apr;48(2):170-5. doi: 10.1176/appi.psy.48.2.170.
Clozapine is not a drug that is ever used casually. Patients generally are afflicted with severe illnesses and have demonstrated treatment resistance and/or intolerance to other therapeutic options before clozapine is seriously considered. When the clinical stakes are this high, it is especially important that physicians gain an appreciation for the various drug-drug interactions that can significantly increase or decrease clozapine blood levels; such pharmacokinetic changes can derail clozapine treatment by producing clozapine toxicity or loss of antipsychotic efficacy, respectively. The authors present a case series of five drug-drug interactions involving clozapine, each of which illustrates different mechanisms by which the metabolism of clozapine can be altered. Exploring these cases should help clinicians anticipate and avoid these undesirable drug-drug interactions.
氯氮平不是一种可以随意使用的药物。一般来说,患者患有严重疾病,并且在认真考虑使用氯氮平之前,已表现出对其他治疗方案的耐药性和/或不耐受性。当临床风险如此之高时,医生了解各种可能显著提高或降低氯氮平血药浓度的药物相互作用尤为重要;这种药代动力学变化可能分别通过产生氯氮平毒性或抗精神病疗效丧失而使氯氮平治疗失败。作者介绍了一系列涉及氯氮平的五种药物相互作用病例,每个病例都说明了氯氮平代谢可能被改变的不同机制。探究这些病例应有助于临床医生预见并避免这些不良的药物相互作用。