为治疗阿片类药物治疗持续疼痛的人设计初级保健药剂师主导的审查:多方法定性研究
Charlotte Woodcock1, Nicola Cornwall2, Lisa Dikomitis3
1Centre for Musculoskeletal Health Research, School of Medicine, Keele University, Keele, UK c.woodcock@keele.ac.uk.
BJGP open
|April 17, 2024
概括
减少治疗慢性疼痛的阿片类药物使用的患者面临着由期望和药剂师关系影响的障碍和促进者. 这项定性研究确定了有效的药剂师主导审查的关键组成部分,以支持减少阿片类药物的使用.
科学领域:
- 药理学和疼痛管理
- 质量健康研究 质量健康研究
- 行为科学 行为科学
背景情况:
- 处方阿片类药物治疗持续的非癌症疼痛缺乏长期证据,并带有风险.
- 对不适当的阿片类药物使用需要有效的干预措施.
研究的目的:
- 探索患者对阿片类药物减少障碍和促进者的观点.
- 为了确定药剂师领导的初级保健审查的最佳组件和交付特征.
主要方法:
- 使用半结构面试 (n=15) 和在线论坛 (n=31) 在英国初级保健中的定性研究.
- 理论领域框架 (TDF) 指导数据收集和主题分析.
- 行为改变技术被绘制为识别审查组件.
主要成果:
- 在13个TDF领域中确定了32个子主题 (障碍/促进者),形成了6个总体主题.
- 关键主题包括患者的期望,药剂师与患者的关系和参与.
- 将主题映射到21种行为改变技术中,为PROMPPT审查定义了17个组件和5个交付特征.
结论:
- 为设计药剂师领导的PROMPPT审查来减少阿片类药物的生成证据.
- 未来的研究将评估PROMPPT审查和相关药剂师培训的可行性和可接受性.
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