Division of Pharmacy Practice and Administrative Sciences, College of Pharmacy, University of Cincinnati Medical Center, 3225 Eden Ave., Cincinnati, OH 45267, USA.
Psychiatr Serv. 2012 Nov;63(11):1080-8. doi: 10.1176/appi.ps.201100443.
Antipsychotic drug therapy is the cornerstone of treatment of persons with schizophrenia. Because most antipsychotics are metabolized by the hepatic cytochrome P450 system, concomitant use of an antipsychotic and medications that are competitively metabolized by the same system may cause a potentially harmful drug-drug interaction. This study used a large state's Medicaid claims database to examine the proportion of patients exposed to such interactions and the risk factors associated with exposure.
Claims from January 2000 through December 2003 for adult patients with a diagnosis of schizophrenia and at least one prescription for an antipsychotic (N=27,909) were examined for pairs of medications identified as potentially causing moderate or severe adverse drug effects. Logistic regression models were estimated to determine potential risk factors associated with exposure to the interaction pairs.
A total of 6,417 (23%) patients were exposed to 14,213 potentially harmful interactions; 4,725 patients had at least one exposure from the same pharmacy, and 4,032 patients were exposed by the same physician. The greatest number of exposures (N=1,353) to potentially harmful combinations involved olanzapine and haloperidol. Patients prescribed risperidone were most likely to be exposed to an interaction (13.1%), followed by patients prescribed olanzapine (10.3%), quetiapine (3.3%), and clozapine (3.2%). A higher risk of exposure was associated with being female (odds ratio [OR]=.94), being white (OR=1.43), having depression (OR=1.21), or having impulse-control disorder (OR=1.98).
Interventions by physicians and pharmacies to reduce the prescribing and dispensing of potentially harmful pairs of medications to patients with schizophrenia are recommended.
抗精神病药物治疗是精神分裂症患者治疗的基石。由于大多数抗精神病药物是通过肝细胞色素 P450 系统代谢的,因此同时使用一种抗精神病药物和通过同一系统竞争代谢的药物可能会导致潜在的有害药物相互作用。本研究使用一个大型州的医疗补助索赔数据库,检查了接触这种相互作用的患者比例以及与接触相关的危险因素。
对 2000 年 1 月至 2003 年 12 月期间有精神分裂症诊断且至少有一份抗精神病药物处方的成年患者的索赔进行了检查,以确定可能导致中度或重度药物不良反应的药物对。使用逻辑回归模型来确定与接触相互作用药物对相关的潜在危险因素。
共有 27909 名患者(23%)接触了 14213 种潜在有害的相互作用;4725 名患者在同一家药店至少有一种暴露,4032 名患者由同一名医生暴露。涉及奥氮平和氟哌啶醇的潜在有害组合暴露最多(N=1353)。处方利培酮的患者最有可能接触到相互作用(13.1%),其次是奥氮平(10.3%)、喹硫平(3.3%)和氯氮平(3.2%)。女性(比值比[OR] =.94)、白人(OR=1.43)、患有抑郁症(OR=1.21)或患有冲动控制障碍(OR=1.98)与接触风险增加相关。
建议医生和药房采取干预措施,减少精神分裂症患者潜在有害药物对的处方和配药。