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精神分裂症治疗中停用非典型抗精神病药物的风险。

Risk of discontinuation of atypical antipsychotic agents in the treatment of schizophrenia.

作者信息

Mullins C Daniel, Obeidat Nour A, Cuffel Brian J, Naradzay John, Loebel Antony D

机构信息

University of Maryland School of Pharmacy, 220 Arch Street, Baltimore, MD 21201, United States.

出版信息

Schizophr Res. 2008 Jan;98(1-3):8-15. doi: 10.1016/j.schres.2007.04.035. Epub 2007 Jun 26.

Abstract

OBJECTIVES

To compare discontinuation rates of atypical antipsychotic agents in patients with schizophrenia.

METHOD

Adult Maryland Medicaid patients with schizophrenia were categorized based on initial atypical antipsychotic drug received: aripiprazole (n=446); olanzapine (n=1705); quetiapine (n=1467); risperidone (n=1580); and ziprasidone (n=700). Discontinuation was measured using refill patterns, allowing 14-day gaps between refill dates. Using olanzapine as the reference drug, the hazard of discontinuation within the first year of follow-up was compared across atypicals using Cox proportional hazard models adjusted for demographic and clinical covariates. Sensitivity analysis tested the robustness of results by using different definitions of the index date.

RESULTS

At one-year follow-up, most patients discontinued their antipsychotic medication (90.4% adjusted mean discontinuation). The hazard ratio (HR) for discontinuing therapy in patients starting treatment on aripiprazole, risperidone, or ziprasidone was not significantly different from olanzapine [HR 1.047, 0.973 and 0.990, respectively]. Quetiapine was associated with significantly higher hazard of discontinuation [HR 1.130] than olanzapine. Covariates associated with significantly lower discontinuation were being male [HR 0.899], older age [HR 0.997] and being on concurrent medication when initiating therapy [HR 0.225]; having a previous hospitalization was associated with significantly higher discontinuation hazard [HR 1.276]. Results were robust in the sensitivity analysis.

CONCLUSIONS

Discontinuation rates were high at one-year follow-up and did not differ significantly for patients on aripiprazole, olanzapine, risperidone, or ziprasidone. The higher hazard of discontinuation associated with quetiapine when compared to olanzapine is consistent with that observed in Phase I of the Clinical Antipsychotic Trials of Intervention Effectiveness (CATIE).

摘要

目的

比较精神分裂症患者中使用非典型抗精神病药物的停药率。

方法

成年马里兰州医疗补助计划中患有精神分裂症的患者根据最初使用的非典型抗精神病药物进行分类:阿立哌唑(n = 446);奥氮平(n = 1705);喹硫平(n = 1467);利培酮(n = 1580);齐拉西酮(n = 700)。通过复诊模式来衡量停药情况,复诊日期之间允许有14天的间隔期。以奥氮平作为对照药物,使用经人口统计学和临床协变量调整的Cox比例风险模型,比较各种非典型药物在随访第一年的停药风险。敏感性分析通过使用不同的索引日期定义来检验结果的稳健性。

结果

在一年的随访中,大多数患者停用了抗精神病药物(调整后的平均停药率为90.4%)。开始使用阿立哌唑、利培酮或齐拉西酮治疗的患者停药的风险比(HR)与奥氮平相比无显著差异[分别为HR 1.047、0.973和0.990]。喹硫平与停药风险显著高于奥氮平相关[HR 1.130]。与停药率显著较低相关的协变量包括男性[HR 0.899]、年龄较大[HR 0.997]以及开始治疗时同时使用其他药物[HR 0.225];既往有住院史与停药风险显著较高相关[HR 1.276]。敏感性分析结果稳健。

结论

在一年的随访中停药率较高,使用阿立哌唑、奥氮平、利培酮或齐拉西酮的患者之间无显著差异。与奥氮平相比,喹硫平停药风险较高与干预有效性临床抗精神病药物试验(CATIE)第一阶段观察到的情况一致。

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