School of Pharmacy and Pharmacology, University of Tasmania, Hobart, Australia.
Faculty of Health, University of Canberra, Australia.
Ann Pharmacother. 2021 Apr;55(4):530-542. doi: 10.1177/1060028020949125. Epub 2020 Aug 10.
To investigate mortality and hospitalization outcomes associated with medication misadventure (including medication errors [MEs], such as the use of potentially inappropriate medications [PIMs], and adverse drug events [ADEs]) among people with cognitive impairment or dementia.
Ovid MEDLINE, Ovid EMBASE, Ovid International Pharmaceutical Abstracts, Cumulative Index to Nursing and Allied Health Literature, and Cochrane Central Register of Controlled Trials were searched from inception to December 2019.
Relevant studies using any study design were included. Reviewers independently performed critical appraisal and extracted relevant data.
The systematic review included 10 studies that reported the outcomes of mortality or hospitalization associated with medication misadventure, including PIMs (n=5), ADEs (n=2), a combination of MEs and ADEs (n=2), and drug interactions (n=1). Five studies examining the association between PIMs and mortality/hospitalization were included in the meta-analyses. Exposure to PIMs was not associated with either mortality (odds ratio [OR]=1.36; 95%CI=0.79-2.35) or hospitalization (OR=1.02; 95%CI=0.83-1.26). In contrast, single studies indicated that ADEs with cholinesterase inhibitors were associated with mortality and hospitalization.
Individuals with cognitive impairment or dementia are at increased risk of medication misadventure; based on relatively limited published data, this does not necessarily translate to increased mortality and hospitalization.
Overall, medication misadventure was not associated with mortality or hospitalization in people with cognitive impairment or dementia, noting the limited number of studies, difficulty in controlling potential confounding variables, and that most studies focus on PIMs.
调查认知障碍或痴呆患者药物误用(包括药物错误[ME],如使用潜在不适当药物[PIM]和药物不良事件[ADE])与死亡率和住院结局的关联。
从建库到 2019 年 12 月,检索了 Ovid MEDLINE、Ovid EMBASE、Ovid 国际药学文摘、护理学及相关健康文献累积索引和 Cochrane 对照试验中心注册库。
纳入了使用任何研究设计的相关研究。审查员独立进行了批判性评价并提取了相关数据。
系统综述包括 10 项研究,报告了与药物误用相关的死亡率或住院率的结果,包括 PIMs(n=5)、ADEs(n=2)、ME 和 ADE 的组合(n=2)和药物相互作用(n=1)。有 5 项研究纳入了 PIMs 与死亡率/住院率之间的关联的荟萃分析。暴露于 PIMs 与死亡率(比值比[OR]=1.36;95%置信区间[CI]=0.79-2.35)或住院率(OR=1.02;95%CI=0.83-1.26)无关。相比之下,个别研究表明,与胆碱酯酶抑制剂相关的 ADE 与死亡率和住院率相关。
认知障碍或痴呆患者发生药物误用的风险增加;根据相对有限的已发表数据,这并不一定意味着死亡率和住院率增加。
总体而言,认知障碍或痴呆患者的药物误用与死亡率或住院率无关,这需要注意研究数量有限、难以控制潜在混杂变量以及大多数研究都集中在 PIMs 上。