关于改善欧洲各地强迫数据收集的专家意见:一个概念绘图研究
Jakub Lickiewicz1, Simone Agnes Efkemann2, Tonje Lossius Husum3
1Department of Psychology, Faculty of Health Sciences, Jagiellonian University Medical College, Krakow, Poland.
Frontiers in psychiatry
|June 13, 2024
概括
关于心理健康胁迫的标准化数据收集对于监测减少计划至关重要. 专家们优先考虑可靠的数据和全国性的注册,尽管欧洲的数据共享面临可行性挑战.
科学领域:
- 心理健康研究 心理健康研究
- 公共卫生政策 公共卫生政策
- 医疗保健中的人权.
背景情况:
- 强迫在心理健康护理中很普遍,影响了患者的权利.
- 需要标准化数据来监测强制减少努力.
- 很少有国家对强迫数据保持可访问的注册表.
研究的目的:
- 收集有关欧洲强制数据收集系统可行的战略的专家意见.
- 确定促进,开发和实施综合胁迫数据收集的方法.
- 为减少强迫行为建立国家和国际基准.
主要方法:
- 来自27个欧洲国家的59名专家参与的概念绘图方法.
- 专家们生成,排序和评分相关性和可行性的策略.
- 参与者是欧盟COST行动FOSTREN倡议的成员.
主要成果:
- 41个策略被组织成七个集群,在两个更高阶域内.
- 关键策略包括"收集可靠的数据"",实施全国性的登记",以及"对不同强制措施的平等理解".
- 相关性通常被评为高于可行性;国家组之间没有发现显著差异.
结论:
- 收集可靠的数据和建立全国性的注册表是非常相关的策略.
- 专家认为,欧洲共享数据库和立法统一的可能性较低.
- 关于心理健康胁迫的国际基准测试策略存在共识.
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