开发药物审查干预措施,将医院药剂师调派到初级保健中心
Sara Sommer Holst1, Johanne Mølby Hansen1, Susanne Kaae2
1Department of Clinical Pharmacology, Copenhagen University Hospital Bispebjerg, DK-2400 Copenhagen, Denmark.
Exploratory research in clinical and social pharmacy
|October 14, 2024
概括
这项研究开发了一种由医院临床药剂师领导的一般实践新药评价 (MR) 干预措施. 该过程确保了透明度和可行性,以改善多药房患者的治疗结果.
科学领域:
- 医疗保健服务研究 医疗服务研究
- 临床药房实践 临床药房实践
- 一般实践管理的管理.
背景情况:
- 药物评价 (MRs) 已被证明可以改善多药患者的治疗结果.
- 在一般实践中,特别是在医院临床药剂师领导下,MR的表现需要进一步调查.
- 描述像MR这样复杂干预的发展对于透明度和防止研究浪费至关重要.
研究的目的:
- 概述了用于一般医疗的新型MR干预的开发过程.
- 确保干预设计的透明度和可转移性.
- 解决医院临床药剂师在初级保健机构领导的了解MR的需要.
主要方法:
- 采用了循序渐进的方法,遵循医学研究理事会的框架.
- 该过程包括通过文献搜索,专家咨询和一般实践中的试点测试来起草干预方案.
- 评估了定量MR数据,以评估可行性和完善干预.
主要成果:
- 影响干预成功的四个关键主题出现了:全科医生资源,患者参与,实施挑战和跨学科合作.
- 这些主题为试点评估提供了信息,导致了干预的完善.
- 该研究确定了在现实环境中成功实施的关键因素.
结论:
- 成功开发了一种复杂,可行的药物审查干预措施.
- 该干预有效地利用临床药剂师在一般实践中,整合医院临床药剂师的专业知识.
- 这种方法提供了一种可转移的模型,用于提高初级保健中的药物管理.
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