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换用鲁拉西酮或喹硫平后精神分裂症患者的住院结局:一项美国索赔数据库分析

Hospitalization outcomes in patients with schizophrenia after switching to lurasidone or quetiapine: a US claims database analysis.

作者信息

Newcomer John W, Ng-Mak Daisy, Rajagopalan Krithika, Loebel Antony

机构信息

Charles E. Schmidt College of Medicine, Florida Atlantic University, Boca Raton, FL, USA.

GHEOR, Sunovion Pharmaceuticals Inc., Marlborough, MA, USA.

出版信息

BMC Health Serv Res. 2018 Apr 4;18(1):243. doi: 10.1186/s12913-018-3020-2.

Abstract

BACKGROUND

This study compared hospital admission rates among adult patients with schizophrenia who switched to antipsychotic monotherapy with lurasidone or quetiapine.

METHODS

This retrospective cohort study used U.S.-based Truven Health MarketScan® Medicaid Multi-State Database (April 2010 through December 2012) and MarketScan® Commercial Claims and Encounters Database (April 2010 through October 2013). Continuous enrollment for 6-months before and after medication initiation was required. Treatment episodes ended after 6-months post lurasidone or quetiapine initiation, a 60-day treatment gap, or initiation of another antipsychotic. Length of treatment episodes (i.e., treatment duration) was compared using a t-test. All-cause, mental-health, and schizophrenia-related hospitalization rates, as well as costs, were compared between lurasidone- and quetiapine-treated patients using multivariable generalized linear models that adjusted for background characteristics.

RESULTS

Quetiapine (n = 435) compared to lurasidone (n = 238) treatment was associated with increased all-cause (21% vs 13%, p < 0.05) and mental health-related hospitalizations (20% vs 12%, p < 0.05), but similar rates of schizophrenia-related hospitalizations (14% vs. 10%, p = 0.14). After adjusting for baseline covariates, quetiapine had 64% higher likelihood of all-cause hospitalizations (OR [odds ratio] = 1.64, 95% confidence interval [CI] 1.05-2.57, p = 0.03), 74% higher likelihood of mental health-related hospitalizations (OR = 1.74, 95% CI 1.11-2.75, p = 0.02), and a similar likelihood of schizophrenia-related hospitalization (OR = 1.35, 95% CI 0.82-2.22, p = 0.24). For those with hospital admissions, adjusted all-cause admission costs were higher for quetiapine when compared with lurasidone in both the Medicaid ($22,036 vs. $15,424, p = 0.17) and commercial populations ($23,490 vs. $20,049, p = 0.61). These differences were not significant. The length of treatment episodes was significantly shorter for quetiapine than lurasidone (115.4 vs 123.1 days, p < 0.05).

CONCLUSIONS

In this retrospective claims database study, patients with schizophrenia who were switched to lurasidone had significantly fewer all-cause and mental health-related hospitalizations and similar rates of schizophrenia-related hospitalization compared with those switched to quetiapine. Patients switching to lurasidone had a significantly longer treatment duration rate than those switching to quetiapine. These results may reflect differences in efficacy or tolerability between lurasidone and quetiapine.

摘要

背景

本研究比较了换用鲁拉西酮或喹硫平进行抗精神病药物单药治疗的成年精神分裂症患者的住院率。

方法

这项回顾性队列研究使用了美国的Truven Health MarketScan® 医疗补助多州数据库(2010年4月至2012年12月)和MarketScan® 商业保险理赔与病历数据库(2010年4月至2013年10月)。要求在药物起始前和起始后连续登记6个月。鲁拉西酮或喹硫平起始后6个月、60天的治疗间隔或开始使用另一种抗精神病药物后,治疗疗程结束。使用t检验比较治疗疗程的长度(即治疗持续时间)。使用调整了背景特征的多变量广义线性模型,比较了接受鲁拉西酮和喹硫平治疗的患者的全因、心理健康和精神分裂症相关的住院率以及费用。

结果

与鲁拉西酮(n = 238)治疗相比,喹硫平(n = 435)治疗与全因住院率增加(21% 对13%,p < 0.05)和心理健康相关住院率增加(20% 对12%,p < 0.05)相关,但精神分裂症相关住院率相似(14% 对10%,p = 0.14)。在调整基线协变量后,喹硫平全因住院的可能性高64%(比值比[OR] = 1.64,95%置信区间[CI] 1.05 - 2.57,p = 0.03),心理健康相关住院的可能性高74%(OR = 1.74,95% CI 1.11 - 2.75,p = 0.02),精神分裂症相关住院的可能性相似(OR = 1.35,95% CI 0.82 - 2.22,p = 0.24)。对于那些有住院治疗的患者,在医疗补助人群(22,036美元对15,424美元,p = 0.17)和商业保险人群(23,490美元对20,049美元,p = 0.61)中,调整后的喹硫平全因住院费用均高于鲁拉西酮。这些差异不显著。喹硫平的治疗疗程长度显著短于鲁拉西酮(115.4天对123.1天,p < 0.05)。

结论

在这项回顾性保险理赔数据库研究中,与换用喹硫平的精神分裂症患者相比,换用鲁拉西酮的患者全因和心理健康相关住院显著减少,精神分裂症相关住院率相似。换用鲁拉西酮的患者治疗持续时间率显著长于换用喹硫平的患者。这些结果可能反映了鲁拉西酮和喹硫平在疗效或耐受性方面的差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dcbc/5885302/821bd35a2b45/12913_2018_3020_Fig1_HTML.jpg

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