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由药剂师主导的减药方案以提高老年髋部骨折患者的用药安全性。

Pharmacist-led deprescribing to improve medication safety in older patients with hip fractures.

作者信息

Hu Tingting, Wang Yu, Wu Renzheng, Zhang Zhongyin, Tian Fangyuan

机构信息

Department of Pharmacy, West China Hospital, Sichuan University, Chengdu, China.

Department of Pharmacy, West China Hospital, National Clinical Research Center for Geriatrics, Sichuan University, Chengdu, China.

出版信息

BMC Geriatr. 2025 Aug 8;25(1):602. doi: 10.1186/s12877-025-06250-8.

DOI:10.1186/s12877-025-06250-8
PMID:40781701
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12333155/
Abstract

OBJECTIVES

Older patients with hip fractures face a patient safety threat due to multimorbidity, polypharmacy, potentially inappropriate medications (PIMs), and adverse drug reactions (ADRs, refer to adverse and unrelated reactions to drugs administered at normal doses for the prevention, diagnosis, treatment of diseases, or regulation of physiological functions). Therefore, optimizing drug therapy through drug review and prescription intervention is essential. The primary aim of this study was to assess the efficacy of pharmacist intervention in mitigating ADRs in older inpatients with hip fractures.

METHODS

This study employed a cross-sectional design. It included patients aged 75 years or older who were hospitalized for hip fractures and received multi-disciplinary treatment (MDT) between December 2021 and March 2024. Intervention comprised clinical pharmacist-led drug reviews focusing on PIMs and recommendations for minimizing any unnecessary medications during hospitalization. If the pharmacist-led intervention was accepted by the MDT, the inpatients were regarded as the intervention group; otherwise, they were regarded as the control group. The 2023 AGS/Beers criteria was utilized to assess the PIM status of inpatients with hip fractures. Medscape was used to evaluate drug-drug interactions (DDIs). Quantitative ADRs indicators, including hypoglycemia and hypotension, were assessed via the monitoring of biochemical parameters. Qualitative ADRs indicators, such as rash and delirium, were evaluated based on the observation of patients' clinical manifestations. Causality between drugs and ADRs was systematically assessed based on the standardized criteria established by the WHO-UMC (Uppsala Monitoring Center), and multivariate logistic regression was employed to identify the risk factors associated ADRs. The primary outcome was a significant reduction in the incidence of ADRs. Secondary outcomes included decreases in the prevalence of PIMs and the incidence of serious DDIs.

RESULTS

A total of 106 inpatients were included in the analysis. Following pharmacist-led drug review and deprescribing intervention, the mean number of prescribed medicines in the intervention group was significantly less than that in the control group [8.89 (SD, 2.20) vs. 11.38 (SD, 2.99), P < 0.01]. Additionally, the mean number of PIMs was significantly lower in the intervention group compared to the control group [1.11 (SD, 0.93) vs. 1.82 (SD, 1.30), P = 0.01]. Furthermore, the incidence of ADRs in the intervention group was significantly lower than that in the control group [17.14% (n = 6) vs. 69.01% (n = 49), P < 0.01]. The logistic regression further demonstrated that renal insufficiency (OR: 3.44, 95% CI: 1.22, 9.70, P = 0.02) was the independent risk factor for ADRs in older inpatients with hip fractures, and pharmacist-led deprescribing intervention significantly reduced the incidence of ADRs (OR: 0.14, 95% CI: 0.04, 0.48, P = 0.02).

CONCLUSIONS

The clinical pharmacist-led deprescribing intervention, designed to reduce the use of PIMs not only significantly decreased the number of prescribed drugs, but also markedly reduced the incidence of ADRs among older inpatients with hip fractures.

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f611/12333155/7a763ac5c4b0/12877_2025_6250_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f611/12333155/7a763ac5c4b0/12877_2025_6250_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f611/12333155/7a763ac5c4b0/12877_2025_6250_Fig1_HTML.jpg
摘要

目的

老年髋部骨折患者因多种疾病共存、多种药物联用、潜在不适当用药(PIMs)及药物不良反应(ADRs,指在正常剂量下用于预防、诊断、治疗疾病或调节生理功能的药物所产生的不良且不相关的反应)而面临患者安全威胁。因此,通过药物审查和处方干预优化药物治疗至关重要。本研究的主要目的是评估药师干预对减轻老年髋部骨折住院患者药物不良反应的疗效。

方法

本研究采用横断面设计。纳入2021年12月至2024年3月期间因髋部骨折住院并接受多学科治疗(MDT)的75岁及以上患者。干预措施包括由临床药师主导的针对潜在不适当用药的药物审查,以及关于尽量减少住院期间任何不必要药物的建议。如果药师主导的干预措施被多学科治疗团队接受,住院患者被视为干预组;否则,他们被视为对照组。采用2023年美国老年医学会/Beers标准评估髋部骨折住院患者的潜在不适当用药情况。利用Medscape评估药物相互作用(DDIs)。通过监测生化参数评估低血糖和低血压等定量药物不良反应指标。基于对患者临床表现的观察评估皮疹和谵妄等定性药物不良反应指标。根据世界卫生组织乌普萨拉监测中心(WHO-UMC)制定的标准化标准系统评估药物与药物不良反应之间的因果关系,并采用多因素逻辑回归分析确定与药物不良反应相关的危险因素。主要结局是药物不良反应发生率显著降低。次要结局包括潜在不适当用药患病率的降低和严重药物相互作用发生率的降低。

结果

共有106名住院患者纳入分析。在药师主导的药物审查和减药干预后,干预组的平均用药数量显著少于对照组[8.89(标准差, 2.20)对11.38(标准差, 2.99),P < 0.01]。此外,干预组的潜在不适当用药平均数量显著低于对照组[1.11(标准差, 0.93)对1.82(标准差, 1.30),P = 0.01]。此外,干预组的药物不良反应发生率显著低于对照组[17.14%(n = 6)对69.01%(n = 49),P < 0.01]。逻辑回归进一步表明,肾功能不全(比值比:3.44,95%置信区间:1.22, 9.70,P = 0.02)是老年髋部骨折住院患者发生药物不良反应的独立危险因素,药师主导的减药干预显著降低了药物不良反应的发生率(比值比:0.14,95%置信区间:0.04, 0.48,P = 0.02)。

结论

由临床药师主导的减药干预旨在减少潜在不适当用药的使用,不仅显著减少了用药数量,还显著降低了老年髋部骨折住院患者的药物不良反应发生率。

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本文引用的文献

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Impact of Chinese criteria on potentially inappropriate medication use in China.中国标准对中国潜在不适当用药的影响。
J Glob Health. 2025 Feb 7;15:04063. doi: 10.7189/jogh.15.04063.
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Polypharmacy and anticholinergic burden scales in older adults: a cross-sectional study among psychiatric outpatients in a tertiary care hospital.老年人的多重用药和抗胆碱能负担量表:一项针对三级医院精神科门诊患者的横断面研究。
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Building an Evidence Base for Deprescribing in the Setting of Polypharmacy.
建立多重用药背景下减药的证据基础。
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Reducing Central Nervous System-Active Medications to Prevent Falls and Injuries Among Older Adults: A Cluster Randomized Clinical Trial.减少中枢神经系统活性药物以预防老年人跌倒和受伤:一项集群随机临床试验。
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A deprescribing programme aimed to optimise blood glucose-lowering medication in older people with type 2 diabetes mellitus, the OMED2-study: the study protocol for a randomised controlled trial.一项旨在优化 2 型糖尿病老年患者血糖降低药物的停药方案(OMED2 研究):一项随机对照试验的研究方案。
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Polypharmacy and Elevated Risk of Severe Adverse Events in Older Adults Based on the Korea Institute of Drug Safety and Risk Management-Korea Adverse Event Reporting System Database.基于韩国药物安全和风险管理研究所-韩国不良事件报告系统数据库,老年人的多种药物治疗与严重不良事件风险升高有关。
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