Peters Evyn, Shamloo Arash, Lodhi Rohit J, Marcoux Gene, Jackson Kylie, Halayka Shawn, Balbuena Lloyd
Department of Psychiatry, University of Saskatchewan, Saskatoon, SK, Canada.
Department of Psychiatry, University of Western Ontario, London, ON, Canada.
Front Psychiatry. 2022 Jun 15;13:917361. doi: 10.3389/fpsyt.2022.917361. eCollection 2022.
Real world evidence about antipsychotics focuses on rehospitalization. Modeling the time course of pharmacotherapy would show patients' adherence to medications and physicians' adherence to medication guidelines. We aimed to calculate the cumulative time spent in second generation antipsychotics (SGAs), gaps, antipsychotic polypharmacy, and clozapine in discharged schizophrenia patients.
Hospitalization and pharmacy dispensing data from 2008-2018 in Manitoba, Saskatchewan, and British Columbia were linked and an electronic cohort ( = 2,997) was created (mean follow-up: 49 months, SD = 38). Cohort members were required to have a minimum of 6 weeks medicated with aripiprazole, olanzapine, paliperidone, quetiapine, risperidone, or ziprasidone.
The multistate model predicted that schizophrenia patients accumulated 44 months in SGA monotherapy, 4 months in polypharmacy, 11 months in medication gaps and 17 days in clozapine over a 5-year period. The majority of transitions were between SGA and medication gap. Accumulated time in medication gaps was seven times as much as in clozapine. Each 10% delay in SGA initiation post-discharge was associated with a 2, 1, and 6% higher risk for polypharmacy (95% CI: 1.01-1.02), gap (95% CI: 1.01-1.01), and clozapine (95% CI: 1.04-1.08), respectively.
Schizophrenia patients accumulated more time unmedicated and in polypharmacy compared to clozapine. Either treatment guidelines for schizophrenia are not followed, or real-world challenges hamper their implementation.
关于抗精神病药物的真实世界证据主要集中在再住院方面。对药物治疗的时间过程进行建模可以显示患者对药物的依从性以及医生对用药指南的依从性。我们旨在计算出院的精神分裂症患者使用第二代抗精神病药物(SGA)的累计时间、用药间隔、联合使用抗精神病药物的情况以及使用氯氮平的情况。
将2008年至2018年在马尼托巴省、萨斯喀彻温省和不列颠哥伦比亚省的住院和药房配药数据进行关联,并创建了一个电子队列(n = 2997)(平均随访时间:49个月,标准差 = 38)。队列成员需要至少使用阿立哌唑、奥氮平、帕利哌酮、喹硫平、利培酮或齐拉西酮治疗6周。
多状态模型预测,在5年的时间里,精神分裂症患者接受SGA单药治疗的累计时间为44个月,联合用药为4个月,用药间隔为11个月,使用氯氮平为17天。大多数转换发生在SGA和用药间隔之间。用药间隔的累计时间是使用氯氮平累计时间的7倍。出院后开始使用SGA每延迟10%,联合用药(95%置信区间:1.01 - 1.02)、用药间隔(95%置信区间:1.01 - 1.01)和使用氯氮平(95%置信区间:1.04 - 1.08)的风险分别增加2%、1%和6%。
与使用氯氮平相比,精神分裂症患者未用药和联合用药的时间更多。要么是未遵循精神分裂症的治疗指南,要么是现实世界中的挑战阻碍了这些指南的实施。