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Patient involvement in a scientific advisory process: Setting the research agenda for medical products

机译:患者参与科学咨询过程:设定医疗产品的研究议程

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Patient involvement in scientific advisory processes could lead to more societally relevant advice. This article describes a case study wherein the Health Council of the Netherlands involved patient groups in an advisory process with a predefined focus: setting a research agenda for medical products development. A four-phase approach was developed to stimulate needs-articulation concerning future medical products for a broad range of patient groups covering 15 disease domains. 119 (expert) patients and 92 non-patient representatives were consulted using interviews and focus groups. In a facilitated way, patients appeared capable and willing to provide input useful for an advisory process. A broad range of medical products was defined serving different purposes. This study showed two dilemmas: first, finding a balance between a predefined focus and being sufficiently broad to enable patients and patient representatives to contribute, and second, finding a balance between relevance for many patients groups and saturation of data for a lower number of patient groups. By taking the context of patients' daily life as starting point patient groups provided new insights. The predefined focus was sometimes perceived as constraining. The GR considered the articulated needs constructive and incorporated patients' input in their advice to the Minister of Health.
机译:患者参与科学咨询过程可能会导致更多与社会相关的建议。本文介绍了一个案例研究,其中荷兰卫生委员会以预先确定的重点将患者群体纳入了咨询过程:为医疗产品开发设定研究议程。开发了一种四阶段方法来激发对涉及15个疾病领域的广泛患者群体的未来医疗产品的需求表达。通过访谈和焦点小组咨询了119位(专家)患者和92位非患者代表。以一种便利的方式,患者似乎有能力并且愿意提供对咨询过程有用的输入。定义了用于不同目的的多种医疗产品。这项研究显示出两个难题:首先,在预定义的焦点和足够广泛的范围之间找到平衡,以使患者和患者代表能够做出贡献;其次,在许多患者组的相关性与较少数量的患者的数据饱和度之间找到平衡组。通过以患者的日常生活为背景,患者群体提供了新的见解。有时将预定义的焦点视为约束。遗传资源认为明确表达的需求具有建设性,并在向卫生部长的建议中纳入了患者的意见。

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