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Implementing patient-reported outcome measures in palliative care clinical practice: A systematic review of facilitators and barriers

机译:在姑息治疗临床实践中实施患者报告的结局指标:对促进因素和障碍的系统评价

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Background: Many patient-reported outcome measures have been developed in the past two decades, playing an increasingly important role in palliative care. However, their routine use in practice has been slow and difficult to implement. Aim: To systematically identify facilitators and barriers to the implementation of patient-reported outcome measures in different palliative care settings for routine practice, and to generate evidence-based recommendations, to inform the implementation process in clinical practice. Design: Systematic literature review and narrative synthesis. Data Sources: Medline, PsycInfo, Cumulative Index to Nursing and Allied Health Literature, Embase and British Nursing Index were systematically searched from 1985. Hand searching of reference lists for all included articles and relevant review articles was performed. Results: A total of 3863 articles were screened. Of these, 31 articles met the inclusion criteria. First, data were integrated in the main themes: facilitators, barriers and lessons learned. Second, each main theme was grouped into either five or six categories. Finally, recommendations for implementation on outcome measures at management, health-care professional and patient levels were generated for three different points in time: preparation, implementation and assessment/improvement. Conclusions: Successful implementation of patient-reported outcome measures should be tailored by identifying and addressing potential barriers according to setting. Having a coordinator throughout the implementation process seems to be key. Ongoing cognitive and emotional processes of each individual should be taken into consideration during changes. The educational component prior to the implementation is crucial. This could promote ownership and correct use of the measure by clinicians, potentially improving practice and the quality of care provided through patient-reported outcome measure data use in clinical decision-making.
机译:背景:在过去的二十年中,已经开发了许多患者报告的结局指标,在姑息治疗中发挥着越来越重要的作用。但是,它们在实践中的常规使用速度慢且难以实现。目的:系统地确定在常规姑息治疗的不同姑息治疗环境中实施患者报告的结局指标的促进因素和障碍,并生成基于证据的建议,以告知临床实践实施过程。设计:系统的文献综述和叙事综合。数据来源:自1985年以来系统地检索了Medline,PsycInfo,护理和相关健康文献的累积索引,Embase和英国护理指数。对包括在内的所有文章和相关评论文章进行了手工检索。结果:共筛选3863篇文章。其中,有31条符合纳入标准。首先,将数据整合到主要主题中:促进者,障碍和经验教训。第二,每个主要主题分为五个或六个类别。最后,针对三个不同的时间点,提出了在管理,保健专业人员和患者层面上关于成果措施的实施建议:准备,实施和评估/改进。结论:应根据情况确定并解决潜在障碍,以量身定制成功执行患者报告的结局指标的措施。在整个实施过程中拥有协调员似乎是关键。在更改期间,应考虑到每个人正在进行的认知和情感过程。实施之前的教育内容至关重要。这可以提高临床医生的所有权并正确使用该措施,从而可能通过在临床决策中使用患者报告的结局指标数据来改善实践和护理质量。

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