老年人中潜在有害的药物-药物相互作用:综述

Lisa E. Hines PharmD , John E. Murphy PharmD
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引用次数: 248

摘要

背景:由于与年龄相关的生理变化、与衰老相关的疾病风险增加以及随之而来的药物使用增加,老年患者容易受到药物相互作用的影响。目的:本叙述性综述的目的是描述严格设计的观察性队列研究和病例对照研究的结果,这些研究评估了老年患者的特定药物相互作用。方法检索PubMed和国际药学文摘数据库中过去10年(2000年12月- 2010年12月)用相关医学主题词发表的英文研究(年龄;80岁及以上;以及药物相互作用)和搜索词(药物相互作用和老年人)。搜索策略被保存并重复到2011年9月,以确保确定最新的相关发表文章。通过检索已确定研究的综述文章和参考文献列表,发现了其他文章。如果研究是观察性队列研究或病例对照研究,报告了特定的药物不良反应,包括年龄≥65岁的患者,并评估了临床有意义的终点,则纳入研究。如果研究采用不太严格的观察设计,评估了药代动力学/药效学特性,评估了药物-营养物质或药物-疾病相互作用或用于治疗益处的药物组合的相互作用(例如,双重抗血小板治疗),或证据不确定,则排除研究。结果17项研究符合纳入标准。16项研究报告了与不良药物相互作用相关的老年人住院风险升高。药物相互作用包括:血管紧张素转换酶(ACE)抑制剂和保钾利尿剂、ACE抑制剂或血管紧张素受体阻滞剂和磺胺甲恶唑/甲氧苄啶、苯二氮卓类或唑吡坦和相互作用药物、钙通道阻滞剂和大环内酯类抗生素、地高辛和大环内酯类抗生素、锂和环利尿剂或ACE抑制剂、苯妥英和磺胺甲恶唑/甲氧苄啶、磺酰脲类和抗菌剂、茶碱和环丙沙星、华法林和抗菌剂或非甾体抗炎药。一项研究报告说,在接受他莫昔芬治疗的妇女中,帕罗西汀暴露与乳腺癌相关死亡的风险有关。结论:几项基于人群的研究报告了老年患者药物相互作用的显著危害。需要提高认识并采取干预措施,以减少接触和尽量减少与潜在有害药物组合有关的风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Potentially Harmful Drug–Drug Interactions in the Elderly: A Review

Background

Elderly patients are vulnerable to drug interactions because of age-related physiologic changes, an increased risk for disease associated with aging, and the consequent increase in medication use.

Objective

The purpose of this narrative review was to describe findings from rigorously designed observational cohort and case-control studies that have assessed specific drug interactions in elderly patients.

Methods

The PubMed and International Pharmaceutical Abstracts databases were searched for studies published in English over the past 10 years (December 2000–December 2010) using relevant Medical Subject Headings terms (aged; aged, 80 and over; and drug interactions) and search terms (drug interaction and elderly). Search strategies were saved and repeated through September 2011 to ensure that the most recent relevant published articles were identified. Additional articles were found using a search of review articles and reference lists of the identified studies. Studies were included if they were observational cohort or case-control studies that reported specific adverse drug interactions, included patients aged ≥65 years, and evaluated clinically meaningful end points. Studies were excluded if they used less rigorous observational designs, assessed pharmacokinetic/pharmacodynamic properties, evaluated drug-nutrient or drug-disease interactions or interactions of drug combinations used for therapeutic benefit (eg, dual antiplatelet therapy), or had inconclusive evidence.

Results

Seventeen studies met the inclusion criteria. Sixteen studies reported an elevated risk for hospitalization in older adults associated with adverse drug interactions. The drug interactions included: angiotensin-converting enzyme (ACE) inhibitors and potassium-sparing diuretics, ACE inhibitors or angiotensin receptor blockers and sulfamethoxazole/trimethoprim, benzodiazepines or zolpidem and interacting medications, calcium channel blockers and macrolide antibiotics, digoxin and macrolide antibiotics, lithium and loop diuretics or ACE inhibitors, phenytoin and sulfamethoxazole/trimethoprim, sulfonylureas and antimicrobial agents, theophylline and ciprofloxacin, and warfarin and antimicrobial agents or nonsteroidal anti-inflammatory drugs. One study reported the risk for breast cancer-related death as a function of paroxetine exposure among women treated with tamoxifen.

Conclusions

Several population-based studies have reported significant harm associated drug interactions in elderly patients. Increased awareness and interventions aimed at reducing exposure and minimizing the risks associated with potentially harmful drug combinations are needed.

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来源期刊
American Journal Geriatric Pharmacotherapy
American Journal Geriatric Pharmacotherapy GERIATRICS & GERONTOLOGY-PHARMACOLOGY & PHARMACY
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