住院对社区痴呆症患者问题药物使用的影响。

W James Deardorff, Bocheng Jing, Matthew E Growdon, Leah J Blank, Tasce Bongiovanni, Kristine Yaffe, W John Boscardin, Kenneth S Boockvar, Michael A Steinman
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引用次数: 0

摘要

背景:对于痴呆症患者(PWD)来说,住院治疗经常会造成混乱,部分原因是由于谵妄、疼痛和失眠等并发症而使用了可能有问题的药物。我们试图确定住院对住院后数月内问题药物处方的影响:我们纳入了健康与退休研究(Health and Retirement Study)中年龄≥66 岁、在 2008-2018 年期间住院治疗的社区残疾人。我们将有问题的药物定义为对认知有负面影响的药物(强抗胆碱能药/镇静催眠药)、2019 年 Beers 标准中的药物以及 STOPP-V2 中的药物。为了捕捉持久的变化,我们对入院前 4 周(基线)和入院后 4 个月的问题药物进行了比较。我们使用了泊松分布的广义线性混合模型,并对年龄、性别、合并症数量、入院前的慢性药物和时间点进行了调整:在 1,475 名残疾人中,504 人符合住院条件(中位数年龄为 84 岁(IQR=79-90),66% 为女性,17% 为黑人)。从基线到住院后的时间点,问题药物略有增加,但未达到统计学意义(调整后平均值为 1.28 vs. 1.40,差异为 0.12 (95% CI -0.03, 0.26),P=0.12)。不同用药领域和某些亚组的结果一致。在一个预先指定的亚组中,服用 "结论"、"结论"、"结论 "和 "结论 "的患者的住院治疗率很小,且无统计学意义:住院对残疾人长期问题药物使用的影响较小且无统计学意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impact of Hospitalizations on Problematic Medication Use Among Community-Dwelling Persons With Dementia.

Background: Hospitalizations are frequently disruptive for persons with dementia (PWD) in part due to the use of potentially problematic medications for complications such as delirium, pain, and insomnia. We sought to determine the impact of hospitalizations on problematic medication prescribing in the months following hospitalization.

Methods: We included community-dwelling PWD in the Health and Retirement Study aged ≥66 with a hospitalization from 2008 to 2018. We characterized problematic medications as medications that negatively affect cognition (strongly anticholinergics/sedative-hypnotics), medications from the 2019 Beers criteria, and medications from STOPP-V2. To capture durable changes, we compared problematic medications 4 weeks prehospitalization (baseline) to 4 months posthospitalization period. We used a generalized linear mixed model with Poisson distribution adjusting for age, sex, comorbidity count, prehospital chronic medications, and timepoint.

Results: Among 1 475 PWD, 504 had a qualifying hospitalization (median age 84 (IQR = 79-90), 66% female, 17% Black). There was a small increase in problematic medications from the baseline to posthospitalization timepoint that did not reach statistical significance (adjusted mean 1.28 vs 1.40, difference 0.12 (95% CI -0.03, 0.26), p = .12). Results were consistent across medication domains and certain subgroups. In one prespecified subgroup, individuals on <5 prehospital chronic medications showed a greater increase in posthospital problematic medications compared with those on ≥5 medications (p = .04 for interaction, mean increase from baseline to posthospitalization of 0.25 for those with <5 medications (95% CI 0.05, 0.44) vs. 0.06 (95% CI -0.12, 0.25) for those with ≥5 medications).

Conclusions: Hospitalizations had a small, nonstatistically significant effect on longer-term problematic medication use among PWD.

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