奥氮平
药理学
治疗药物监测
抗精神病药
治疗指标
CYP1A2
生物利用度
抗精神病药
治疗窗口
医学
非定型抗精神病薬
精神分裂症(面向对象编程)
药品
内科学
细胞色素P450
新陈代谢
精神科
作者
Zoubir Djerada,Georges Brousse,Philippe Niel,Pierre‐Michel Llorca,Alain Eschalier,Danièle Bentué‐Ferrer,Fréderic Libert
出处
期刊:Therapie
[Elsevier BV]
日期:2015-07-28
卷期号:78 (5): S75-S80
被引量:3
标识
DOI:10.2515/therapie/2015040
摘要
Olanzapine, atypical antipsychotic, is used to treat schizophrenia and bipolar disorder. Its therapeutic drug monitoring (TDM) is quite commonly done. Olanzapine is well absorbed orally (bioavailability: 85 %), with peak plasma occurring between 4 and 6hours after oral administration. It is extensively metabolized by different hepatic enzymes (including CYP1A2 and CYP2D6 isoforms) to a large number of inactive metabolites, and its half-life is between 30 and 60hours. No specific therapeutic range, or threshold concentration could not be a consensus, but the higher intra- and interindividual variability, as well as the existence of studies suggesting a correlation between circulating concentrations of olanzapine and occurrence of therapeutic relapse or toxic phenomena appear to justify the STP for this molecule. Given these data, the interest of the STP was evaluated for this molecule to: recommended with therapeutic window of 20μg/L to 80μg/L.
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