苯二氮卓类药物对急性缺血性卒中后医疗保险受益人死亡率的影响。

IF 2.4 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Madhav Sankaranarayanan, Maria A Donahue, Shuo Sun, Julianne D Brooks, Lee H Schwamm, Joseph P Newhouse, John Hsu, Deborah Blacker, Sebastien Haneuse, Lidia M V R Moura
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引用次数: 0

摘要

目的:尽管指南警告和关注死亡率增加,但66岁以上的急性缺血性卒中(AIS)幸存者仍然接受苯二氮卓类药物(BZDs)治疗。我们检查了老年医疗保险受益人在AIS后出院后30天内bzd对死亡率的相关影响。方法:我们分析了在AIS住院治疗前至少12个月登记的医疗保险受益人样本。我们的主要暴露是在出院后30天内发生BZD,其主要结局是出院后90天的死亡率风险差异(RDs),使用试验模拟方法来解决混淆(即克隆,加权,审查和反概率审查加权)。结果:47421例受益人中,826例(1.74%)在出院后30天开始BZD治疗,6392例(13.48%)在90天内死亡。中位年龄为79岁(IQR: 12),女性占55.3%,白人占82.9%,黑人占10.1%,西班牙裔占1.7%,亚裔占2.2%,美洲原住民占0.4%。标准化后(基于年龄、性别、种族/民族、住院时间和基线痴呆),90天死亡率风险显示RD为每1000例26例(95% CI: 22,33)。亚组分析显示,老年人群的RD较高,特别是86岁或以上的人群,RD为每1000人84个事件(95% CI: 73,106),基线痴呆患者的RD为每1000人87个事件(95% CI: 63,112)。结论:ais出院后30天内启动BZD与90天死亡风险增加相关,特别是在76岁及以上的老年人和基线痴呆患者中,突出了他们对BZD不良反应的脆弱性。简单的语言总结:这项研究着眼于开始服用苯二氮卓类药物(BZDs)如何影响老年人中风后的生存。bzd是通常用于治疗焦虑、失眠和癫痫的药物。这项研究的重点是66岁及以上的医疗保险患者,并确定出院后30天内服用BZDs是否会增加他们在90天内死亡的风险。该研究分析了47,000多名患者,选择了那些预后较好的患者,发现1.74%的患者在中风后开始服用bzd。在调整了年龄、性别、种族、住院时间和痴呆等因素后,我们发现,开始BZDs与更高的死亡风险相关。86岁及以上的患者和痴呆症患者的风险尤其高。该研究得出结论,给老年中风幸存者开bzd可能会大大增加死亡风险,尤其是对年龄最大和最脆弱的患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Benzodiazepine Initiation Effect on Mortality Among Medicare Beneficiaries Post-Acute Ischemic Stroke.

Purpose: Despite guideline warnings and concerns for increased mortality, acute ischemic stroke (AIS) survivors older than 66 years of age still receive benzodiazepines (BZDs). We examined the BZD-associated effect on mortality within 30 days post-discharge on survival among older Medicare beneficiaries after an AIS.

Methods: We analyzed a sample of Medicare beneficiaries enrolled for at least 12 months before hospitalization for AIS. Our primary exposure was BZD initiation within 30 days post-discharge, and its primary outcome was 90 days mortality risk differences (RDs) from discharge using trial emulation with methods to address confounding (i.e., cloning, weighting, censoring, and inverse-probability-of-censoring weighting).

Results: Of 47 421 beneficiaries, 826 (1.74%) initiated BZD 30 days post-discharge, and 6392 (13.48%) died within 90 days. The median age was 79 (IQR: 12), with 55.3% female, 82.9% White, 10.1% Black, 1.7% Hispanic, 2.2% Asian, and 0.4% American Native. After standardization (based on age, sex, race/ethnicity, length of stay, and baseline dementia), the 90-day mortality risk revealed an RD of 26 events per 1000 (95% CI: 22, 33). Subgroup analyses revealed higher RDs in older age groups, particularly those aged 86 or older, with an RD of 84 events per 1000 (95% CI: 73, 106), and for patients with baseline dementia, with an RD of 87 events per 1000 (95% CI: 63, 112).

Conclusion: Initiating BZDs within 30 days post-AIS discharge was associated with increased 90 days mortality risk, especially in older adults 76 years and older and those with baseline dementia, highlighting their vulnerability to BZD adverse effects.

Plain language summary: This study looked at how starting to take benzodiazepines (BZDs) affects survival in older adults after a stroke. BZDs are medications typically used for anxiety, insomnia, and seizures. The study focused on patients 66 years old and older on Medicare and determined whether taking BZDs within 30 days after leaving the hospital increased their risk of dying within 90 days. The study analyzed over 47,000 patients, selecting those with more favorable outcomes, and found that 1.74% began taking BZDs after their stroke. After adjusting for factors like age, gender, race, hospital stay, and dementia, we found that starting BZDs was associated with a higher risk of death. The risk was particularly high in patients 86 years and older and those with dementia. The study concluded that prescribing BZDs to older stroke survivors could substantially raise the risk of death, especially in the oldest and most vulnerable patients.

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来源期刊
CiteScore
4.80
自引率
7.70%
发文量
173
审稿时长
3 months
期刊介绍: The aim of Pharmacoepidemiology and Drug Safety is to provide an international forum for the communication and evaluation of data, methods and opinion in the discipline of pharmacoepidemiology. The Journal publishes peer-reviewed reports of original research, invited reviews and a variety of guest editorials and commentaries embracing scientific, medical, statistical, legal and economic aspects of pharmacoepidemiology and post-marketing surveillance of drug safety. Appropriate material in these categories may also be considered for publication as a Brief Report. Particular areas of interest include: design, analysis, results, and interpretation of studies looking at the benefit or safety of specific pharmaceuticals, biologics, or medical devices, including studies in pharmacovigilance, postmarketing surveillance, pharmacoeconomics, patient safety, molecular pharmacoepidemiology, or any other study within the broad field of pharmacoepidemiology; comparative effectiveness research relating to pharmaceuticals, biologics, and medical devices. Comparative effectiveness research is the generation and synthesis of evidence that compares the benefits and harms of alternative methods to prevent, diagnose, treat, and monitor a clinical condition, as these methods are truly used in the real world; methodologic contributions of relevance to pharmacoepidemiology, whether original contributions, reviews of existing methods, or tutorials for how to apply the methods of pharmacoepidemiology; assessments of harm versus benefit in drug therapy; patterns of drug utilization; relationships between pharmacoepidemiology and the formulation and interpretation of regulatory guidelines; evaluations of risk management plans and programmes relating to pharmaceuticals, biologics and medical devices.
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