Bogaerts Jonathan M K, Warmerdam Laurie A, Achterberg Wilco P, Gussekloo Jacobijn, Poortvliet Rosalinde K E
Department of Public Health and Primary Care, Leiden University Medical Center, Leiden, the Netherlands.
Department of Public Health and Primary Care, Leiden University Medical Center, Leiden, the Netherlands; University Network for the Care sector South Holland, Leiden University Medical Center, Leiden, the Netherlands.
J Am Med Dir Assoc. 2023 Apr;24(4):541-547.e2. doi: 10.1016/j.jamda.2023.02.017. Epub 2023 Mar 13.
The benefit-risk ratio of many interventions remains unclear in older adults with dementia. Efforts for more representative trial inclusion are made; however, recruiting and particularly gaining informed consent remains complex. For research participation, dementia compels the designation of a legal guardian (LG) to give proxy consent. To advance future trial development, we aimed to provide more insights into the factors that affect the proxy decision-making process in dementia research.
A qualitative analysis of semi-structured interviews about proxy decision-making on participation in dementia research.
LGs of nursing home residents that gave (n = 19) and refrained from giving (n = 18) proxy consent for a clinical trial (the Danton study) in the Netherlands.
Verbatim transcripts were thematically analyzed by using a preliminary deductive framework with room for induction of additional emerging themes, being an overall abductive approach. Based on that theme list, related factors of the decision-making process were grouped into overarching levels and merged into a step-by-step process.
When discussing proxy decision-making on the participation of an older adult with dementia in a clinical trial, LGs described interconnected factors on the level of the study and patient. Past experiences and attitudes of the LG influenced the weighing of these study- and patient-related factors, leading to a preliminary decision. Other proxies and treating health care professionals (HCPs) were named as important other stakeholders of the decision-making process.
When giving proxy consent for research participation, LGs weigh study- and patient-related factors, leading to an initial benefit-risk evaluation. This weighing process is influenced by LG-related factors and can be modulated by other proxies or treating HCPs, leading to a definitive decision. Although insights into these underlying mechanisms could facilitate the proxy decision-making process for both LGs and researchers, treating HCPs could act as an independent party.
在患有痴呆症的老年人中,许多干预措施的利弊比率仍不明确。人们正在努力使试验纳入更具代表性的人群;然而,招募受试者,尤其是获得知情同意仍然很复杂。对于参与研究而言,痴呆症迫使指定一名法定监护人(LG)来给予代理同意。为推动未来试验的发展,我们旨在更深入地了解影响痴呆症研究中代理决策过程的因素。
对关于参与痴呆症研究的代理决策的半结构化访谈进行定性分析。
荷兰一家养老院居民的法定监护人,其中19人给予了(参与一项临床试验(丹顿研究)的)代理同意,18人未给予代理同意。
使用一个初步的演绎框架对逐字记录进行主题分析,该框架为归纳其他新出现的主题留出了空间,这是一种总体的归纳推理方法。基于该主题列表,将决策过程的相关因素归为总体层次,并合并为一个逐步的过程。
在讨论痴呆症老年患者参与临床试验的代理决策时,法定监护人描述了研究层面和患者层面相互关联的因素。法定监护人过去的经历和态度影响了对这些与研究和患者相关因素的权衡,从而做出初步决策。其他代理人和主治医护人员被认为是决策过程中的重要其他利益相关者。
在给予参与研究的代理同意时,法定监护人会权衡与研究和患者相关的因素,从而进行初步的利弊评估。这个权衡过程受法定监护人相关因素的影响,并可能受到其他代理人或主治医护人员的调节,从而做出最终决策。尽管深入了解这些潜在机制有助于法定监护人和研究人员的代理决策过程,但主治医护人员可以作为独立一方发挥作用。