Impact of a Delirium Protocol on Deliriogenic Medication Use in Hospitalized Older Veterans.

Q2 Medicine Senior Care Pharmacist Pub Date : 2024-08-01 DOI:10.4140/TCP.n.2024.291
Alison M Weygint, Brandon LaMarr, Stephanie Lee
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Abstract

Background The Southern Arizona VA Health Care System (SAVAHCS) implemented a delirium prevention and treatment protocol in 2019. Objective The primary objective of this study was to determine if the implementation of a delirium protocol influenced deliriogenic medication use in hospitalized geriatric veterans. The secondary objectives were to compare the rates of delirium diagnosis, hospital length-of-stay, and rates of newly started deliriogenic medications during admission pre- and post-protocol. Methods This study was a retrospective, secondary data analysis study. Veterans 65 years of age and older who were admitted to an inpatient medical ward at the SAVAHCS for 24 hours or more between January 1, 2018 and December 31, 2018 (pre-protocol) or January 1, 2021 and December 31, 2021 (post-protocol) were included. Patients were excluded if they had a diagnosis of alcohol or benzodiazepine withdrawal upon admission. Results A total of 5491 patients were included in this study; 2940 (53.5%) in the pre-protocol group and 2551 (46.5%) in the post-protocol group. Patients received at least one deliriogenic medication during their admission in the post-protocol group (36.2%) compared with the pre-protocol group (34.1%), but there was no statistically significant difference (P = 0.098). There were also no significant differences in the rates of documentation of delirium as a diagnosis at discharge, hospital length-of-stay, or the rates of newly started deliriogenic medications during admission between the groups. Conclusion Implementation of a delirium prevention and treatment protocol at the SAVAHCS did not significantly impact the use of deliriogenic medications in hospitalized geriatric veterans.

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谵妄协议对住院老年退伍军人谵妄性药物使用的影响。
背景 南亚利桑那州退伍军人医疗保健系统(SAVAHCS)于 2019 年实施了谵妄预防和治疗方案。目标 本研究的首要目标是确定谵妄协议的实施是否会影响住院老年退伍军人的谵妄药物使用。次要目标是比较谵妄诊断率、住院时间以及入院前和入院后新开始使用致谵妄药物的比率。方法 本研究是一项回顾性二次数据分析研究。研究对象包括在 2018 年 1 月 1 日至 2018 年 12 月 31 日(协议前)或 2021 年 1 月 1 日至 2021 年 12 月 31 日(协议后)期间入住 SAVAHCS 住院病房 24 小时及以上的 65 岁及以上退伍军人。入院时诊断为酒精或苯二氮卓类药物戒断的患者排除在外。结果 本研究共纳入 5491 例患者,其中协议前组 2940 例(53.5%),协议后组 2551 例(46.5%)。与方案前组(34.1%)相比,方案后组(36.2%)患者在入院期间至少服用了一种脱利米松药物,但两者之间没有显著的统计学差异(P = 0.098)。此外,两组患者在出院时将谵妄作为诊断的记录率、住院时间或入院时新开始服用致谵妄药物的比例也无明显差异。结论 在SAVAHCS实施谵妄预防和治疗方案不会对住院老年退伍军人使用致谵妄药物产生明显影响。
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来源期刊
Senior Care Pharmacist
Senior Care Pharmacist PHARMACOLOGY & PHARMACY-
CiteScore
1.30
自引率
0.00%
发文量
160
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