临床决策支持系统对老年患者抗胆碱能负荷随时间变化的影响:SADP-Antichol 研究。

IF 2 Q3 PHARMACOLOGY & PHARMACY
Pharmacy Pub Date : 2024-10-30 DOI:10.3390/pharmacy12060162
Grégoire Delvallée, Lisa Mondet, Chloé Cornille, Guillaume Deschasse, Aurélie Lenglet
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引用次数: 0

摘要

目的:抗胆碱能药物可导致老年人发生不良事件(AE)。临床决策支持系统(CDSS)可以检测出抗胆碱能负荷较高的处方。我们最初的假设是,通过将 CDSS 与药剂师干预策略相结合,可以减少抗胆碱能药物负荷。本研究的目的是评估这一组合对住院老年人抗胆碱能负荷随时间推移而变化的影响:这项前瞻性单中心研究分为两个为期 6 周的阶段。在干预期,药剂师分析 CDSS 对 30 种目标抗胆碱能药物发出的警报,并决定是否进行药剂师干预。对照期为标准护理期。研究的主要终点是发出警报与出院之间的抗胆碱能药物负荷δ;次要终点是抗胆碱能药物不良事件(AEs)的发生率:在生成的 144 个警报中,有 87 个被认为是相关的(干预期 36 个,对照期 51 个)。实验期和对照期的抗胆碱能负荷δ之间存在明显差异(1.61 对 0.67,P 值 = 0.0115)。在 87 次警报的目标药物(n = 94)中,46.8% 用于抗组胺药,21.3% 用于地氯雷他定。在药剂师发出的 36 次干预中,19 次(52.8%)被接受。处方最多的药物类别是抗组胺类药物(7 人),处方最多的药物是阿米替林(5 人)。在这87名警报患者中,抗胆碱能药物负荷与AEs数量之间的相关性无统计学意义(p = 0.887)。影响周围神经系统最常见的 AE 是便秘(28.6%),影响中枢神经系统最常见的 AE 是精神错乱(29.9%):我们的研究结果表明,与常规护理相比,将特定的 CDSS 规则与药剂师介导的风险管理程序相结合,可以进一步减少住院老年人的抗胆碱能负荷。抗胆碱能药物负荷的减少是否会影响外周和中枢抗胆碱能药物不良反应的发生率,进而影响这些患者的健康,还有待进一步确定。
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 a Clinical Decision Support System on the Change over Time in the Anticholinergic Load in Geriatric Patients: The SADP-Antichol Study.

Purpose: Anticholinergic drugs can cause adverse events (AEs) in older adults. Clinical decision support systems (CDSSs) can detect prescriptions with a high anticholinergic load. Our starting hypothesis was that the anticholinergic load could be reduced by combining a CDSS with a strategy for generating pharmacist interventions. The objective of the present study was to assess the impact of this combination on the change over time in the anticholinergic load in hospitalized older adults.

Methods: This prospective, single-centre study was divided into two 6-week periods. During the interventional period, a pharmacist analyzed the alerts generated by the CDSS for 30 targeted anticholinergic drugs and decided whether to issue a pharmacist intervention. A control period corresponds to standard care. The primary endpoint of the study is the delta of the anticholinergic load between the alert and hospital discharge; the secondary endpoint is the incidence of anticholinergic adverse events (AEs).

Results: Of the 144 alerts generated, 87 were considered to be relevant (36 in the interventional period and 51 in the control period). A significant difference was observed between the delta anticholinergic load between the experimental and control periods (1.61 vs. 0.67, p-value = 0.0115). For the targeted drugs (n = 94) over the 87 alerts, 46.8% were for antihistamines and 21.3% were for desloratadine. Of the 36 pharmacist interventions sent by the pharmacist, 19 (52.8%) were accepted. The most deprescribed drug class was the antihistamine class (n = 7), and the most deprescribed drug was amitriptyline (n = 5). Among these 87 patients with alerts, the correlation between the anticholinergic load and the number of AEs was not statistically significant (p = 0.887). The most common AE affecting the peripheral nervous system was constipation (28.6%), and the most common AE affecting the central nervous system was confusion (29.9%).

Conclusions: Our results showed that the combination of specific CDSS rules with pharmacist-mediated risk management procedures could further reduce the anticholinergic load in hospitalized older adults, relative to routine care. It remains to be determined whether this reduction in the anticholinergic load has an impact on the incidence of peripheral and central anticholinergic AEs, and thus the health of these patients.

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来源期刊
Pharmacy
Pharmacy PHARMACOLOGY & PHARMACY-
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