信息如何影响帕金森病患者:对文献的全面审查
Elisabeth Kurpershoek1,2,3,4, Leonie N C Visser2,3,4,5,6, Arjan Malekzadeh7
1Neurology, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
Journal of Parkinson's disease
|July 12, 2024
概括
患有帕金森病的患者需要信息来管理他们的病情. 这次审查发现,虽然患者重视信息,但需要更多的研究来了解它如何影响他们的结果.
科学领域:
- 神经学 神经学
- 卫生沟通健康沟通
- 患者教育 患者教育
背景情况:
- 帕金森病 (PD) 患者需要足够的信息来进行有效的自我管理.
- 信息提供对PD患者结果的影响仍未得到充分研究.
研究的目的:
- 对PD特定信息 (内容,时间,交付,来源) 与患者结果之间的关系进行范围审查.
- 综合现有的关于信息如何影响帕金森病患者体验和幸福感的文献.
主要方法:
- 在MEDLINE,Embase和PsychInfo进行了全面的文献搜索,截至2024年4月.
- 从报告原始数据的40个获取的出版物中提取和合成了数据.
主要成果:
- 患者的结果被分类为信息评估,身体功能,心理社会福祉和生活质量.
- 患者普遍欣赏提供的信息,研究强调需要量身定制的信息传递.
- 研究设计和结果的变化阻止了关于信息与结果关系的最终结论.
结论:
- 该审查确定了帕金森病患者如何获取信息,但强调了信息影响的系统研究中的差距.
- 未来的研究应该调查当前的临床信息提供,确定有益的额外信息,并探索有效的调整策略.
- 优化信息传递有可能更有效地赋予帕金森病患者权力.
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