痴呆患者使用布雷哌唑与6个月死亡率、住院率和急诊科就诊的真实世界证据

IF 7.7 1区 医学 Q1 CLINICAL NEUROLOGY
Neurology Pub Date : 2025-08-12 Epub Date: 2025-07-03 DOI:10.1212/WNL.0000000000213717
Julie Zissimopoulos, Johanna Thunell, Mireille Jacobson, Sidra Haye, Bryan Tysinger, Patricia Ferido, Geoffrey Joyce
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引用次数: 0

摘要

背景与目的:阿尔茨海默病和其他痴呆伴发抑郁、躁动等行为和神经精神症状。2023年,brexpiprazole成为美国食品和药物管理局(fda)批准的首个用于治疗阿尔茨海默病患者躁动的抗精神病药物,但与所有非典型抗精神病药物一样,brexpiprazole也有一个黑框警告,警告痴呆症患者死亡风险增加。本研究提供了真实世界的死亡率的证据,在一个异质样本brexpiprazole使用者了解在人群中的影响。方法:我们使用2014年至2023年医疗保险索赔数据a、B和D部分的100%样本。我们的样本仅限于诊断为痴呆的受益人,他们连续入组至少2年,并且在给定年份是非典型抗精神病药物brexpiprazole或aripiprazole的新使用者。我们使用匹配和逻辑回归来估计brexpiprazole(与阿立哌唑相比)与死亡率、急诊(ED)访问量和6个月内住院率之间的关系。结果:在41871名痴呆患者中,71.7%的brexpiprazole使用者和69.7%的aripiprazole使用者是女性,平均年龄分别为75.7岁和78.0岁。在痴呆症患者(PLWD)中,根据逻辑回归和新使用brexpiprazole或aripiprazole的匹配样本估计,brexpiprazole的6个月死亡率在统计学上较低(or 0.49, [95% CI 0.37-0.65])。brexpiprazole与阿立哌唑在开始使用后6个月内用于急诊科或住院的发生率无统计学差异。使用两阶段最小二乘估计对潜在的未观察到的混淆进行调整,发现两组之间6个月死亡率、急诊科就诊或住院率没有统计学上的显著差异。讨论:与使用阿立哌唑相比,在PLWD中使用布雷哌唑与死亡风险差异无关。Brexpiprazole提供了一种重要的治疗选择,考虑到抗精神病药物对人的影响的异质性。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而导致的估计偏差,但样本量小是一个限制。证据分类:本研究提供的III级证据表明,与阿立哌唑相比,brexpiprazole不会增加PLWD患者6个月死亡风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Real-World Evidence of Brexpiprazole Use and 6-Month Mortality, Hospitalization, and Emergency Department Visits Among Persons With Dementia.

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.

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来源期刊
Neurology
Neurology 医学-临床神经学
CiteScore
12.20
自引率
4.00%
发文量
1973
审稿时长
2-3 weeks
期刊介绍: Neurology, the official journal of the American Academy of Neurology, aspires to be the premier peer-reviewed journal for clinical neurology research. Its mission is to publish exceptional peer-reviewed original research articles, editorials, and reviews to improve patient care, education, clinical research, and professionalism in neurology. As the leading clinical neurology journal worldwide, Neurology targets physicians specializing in nervous system diseases and conditions. It aims to advance the field by presenting new basic and clinical research that influences neurological practice. The journal is a leading source of cutting-edge, peer-reviewed information for the neurology community worldwide. Editorial content includes Research, Clinical/Scientific Notes, Views, Historical Neurology, NeuroImages, Humanities, Letters, and position papers from the American Academy of Neurology. The online version is considered the definitive version, encompassing all available content. Neurology is indexed in prestigious databases such as MEDLINE/PubMed, Embase, Scopus, Biological Abstracts®, PsycINFO®, Current Contents®, Web of Science®, CrossRef, and Google Scholar.
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