改善药物处方相关的结果对于高风险药物过渡的弱势老年人 (IMPROVE-IT HRM):一个试点随机试验协议
Anne Holbrook1,2,3, Dan Perri4,5, Mitch Levine4,6
1Division of Clinical Pharmacology and Toxicology, Department of Medicine, McMaster University, Hamilton, ON, Canada. holbrook@mcmaster.ca.
Pilot and feasibility studies
|April 10, 2024
概括
这项研究评估了临床药理和毒理学 (CPT) 药物管理干预措施,用于经常住院治疗的老年人. 该干预旨在减少药物治疗问题和改善护理过渡,其结果可能为更大的国家试验提供信息.
科学领域:
- 老年医学 老年医学
- 临床药理学 临床药理学
- 患者安全 患者安全
背景情况:
- 经常住院和多药治疗的老年人面临药物不良事件的高风险.
- 在这个人群中,高风险药物加剧了严重药物相关问题的可能性.
- 目前的护理缺口需要创新的方法来管理弱势老年人的药物管理.
研究的目的:
- 评估临床药理和毒理 (CPT) 药物管理干预措施对高风险老年人的可行性.
- 确定CPT干预是否可以减少住院期间和之后的药物治疗问题.
- 评估干预对护理协调,生活质量和医疗保健利用的影响.
主要方法:
- 实用试点随机试验与1:1分配和盲目的结果评估.
- 纳入标准:65岁以上的成年人,>2天内科住院,之前住院,≥5种慢性药物,包括≥1种高风险药物.
- 干预包括住院患者药物标识,患者协商的处方优先级,出院协调,护理圈沟通和两次出院后的虚拟访问.
主要成果:
- 可行性结果包括招聘率,参与者保留率和干预成本.
- 临床结局侧重于药物治疗问题的数量在干预后得到改善.
- 二次结果评估了护理过渡协调,患者报告的生活质量和医疗保健利用情况.
结论:
- 有希望的可行性和临床结果可以支持使用国家平台进行最终试验.
- 专业临床药理学和毒理学专业知识的虚拟交付提供了一个可扩展的解决方案.
- 该干预措施有可能大大提高药物安全性,患者的治疗结果和老年护理的成本效益.
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