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布雷哌唑在痴呆症患者中的使用情况以及6个月死亡率、住院率和急诊就诊率的真实世界证据。

Real-World Evidence of Brexpiprazole Use and 6-Month Mortality, Hospitalization, and Emergency Department Visits Among Persons With Dementia.

作者信息

Zissimopoulos Julie, Thunell Johanna, Jacobson Mireille, Haye Sidra, Tysinger Bryan, Ferido Patricia, Joyce Geoffrey

机构信息

Health Policy and Management, University of Southern California, Los Angeles.

Schaeffer Center, University of Southern California, Los Angeles.

出版信息

Neurology. 2025 Aug 12;105(3):e213717. doi: 10.1212/WNL.0000000000213717. Epub 2025 Jul 3.

Abstract

BACKGROUND AND OBJECTIVES

Alzheimer disease and other dementias are accompanied by depression and agitation and other behavioral and neuropsychiatric symptoms. In 2023, brexpiprazole became the first antipsychotic approved by the US Food and Drug Administration to treat agitation in persons with Alzheimer disease, but, like all atypical antipsychotics, it includes a black box warning of an increased risk of mortality among persons with dementia. This study provides real-world evidence of mortality in a heterogeneous sample of brexpiprazole users to understand effects in the population.

METHODS

We used a 100% sample of Medicare claims data Parts A, B, and D from 2014 to 2023. Our sample was limited to beneficiaries with diagnosed dementia, who were continuously enrolled for at least 2 years and were new users of the atypical antipsychotics brexpiprazole or aripiprazole in a given year. We used matching and logistic regression to estimate the relationship between incident use of brexpiprazole, compared with aripiprazole, and mortality, emergency department (ED) visits, and hospitalization within 6 months.

RESULTS

Among the 41,871 beneficiaries with dementia, 71.7% of brexpiprazole and 69.7% of aripiprazole users were women with a mean age of 75.7 and 78.0 years, respectively. Among persons living with dementia (PLWD), 6-month mortality was statistically lower among new users of brexpiprazole based on estimates from logistic regression and a matched sample of new users of brexpiprazole or aripiprazole (OR 0.49, [95% CI 0.37-0.65]).There was no statistical difference between the incident use of brexpiprazole and aripiprazole use for ED visits or hospitalization within 6 months of use initiation. Adjustment for potential unobserved confounding used two-stage least squares estimation and found no statistically significant differences in six-month mortality, ED visits, or hospitalizations between the 2 groups.

DISCUSSION

Brexpiprazole use is not associated with differential mortality risk compared with aripiprazole use among PLWD. Brexpiprazole offers a treatment option which is important given the heterogeneity of effects of antipsychotics on persons. A two-stage least squares method is used to eliminate bias on estimates because of observed and unobserved differences between the 2 groups, but the small sample size is a limitation.

CLASSIFICATION OF EVIDENCE

This study provides Class III evidence that brexpiprazole does not increase the risk of mortality at 6 months compared with aripiprazole in PLWD.

摘要

背景与目的

阿尔茨海默病和其他痴呆症伴有抑郁、激越及其他行为和神经精神症状。2023年,布瑞哌唑成为美国食品药品监督管理局批准的首个用于治疗阿尔茨海默病患者激越症状的抗精神病药物,但是,与所有非典型抗精神病药物一样,它有一个黑框警告,提示痴呆症患者死亡风险增加。本研究提供了布瑞哌唑使用者异质性样本的真实世界死亡率证据,以了解其在总体人群中的影响。

方法

我们使用了2014年至2023年医疗保险A、B和D部分索赔数据的100%样本。我们的样本仅限于诊断为痴呆症的受益人,他们连续登记至少2年,且在某一年是非典型抗精神病药物布瑞哌唑或阿立哌唑的新使用者。我们使用匹配和逻辑回归来估计与阿立哌唑相比,布瑞哌唑的起始使用与6个月内死亡率、急诊就诊和住院之间的关系。

结果

在41,871名痴呆症受益人中,布瑞哌唑使用者的71.7%和阿立哌唑使用者的69.7%为女性,平均年龄分别为75.7岁和78.0岁。基于逻辑回归估计和布瑞哌唑或阿立哌唑新使用者的匹配样本,痴呆症患者中,布瑞哌唑新使用者的6个月死亡率在统计学上较低(比值比0.49,[95%置信区间0.37 - 0.65])。在开始使用药物后的6个月内,布瑞哌唑和阿立哌唑的起始使用在急诊就诊或住院方面没有统计学差异。对潜在未观察到的混杂因素进行调整时使用了两阶段最小二乘法估计,发现两组在6个月死亡率、急诊就诊或住院方面没有统计学显著差异。

讨论

与阿立哌唑相比,在痴呆症患者中使用布瑞哌唑与不同的死亡风险无关。鉴于抗精神病药物对个体影响的异质性,布瑞哌唑提供了一种治疗选择。使用两阶段最小二乘法来消除由于两组之间观察到的和未观察到的差异对估计值造成的偏差,但小样本量是一个局限性。

证据分类

本研究提供了III类证据,表明在痴呆症患者中,与阿立哌唑相比,布瑞哌唑在6个月时不会增加死亡风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5020/12226927/a12ddb2865ec/WNL-2024-105218f1.jpg

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