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Ethical Concerns and Procedural Pathways for Patients Who are Incapacitated and Alone: Implications from a Qualitative Study for Advancing Ethical Practice

机译:丧失行为能力者和孤独者的伦理关注和程序途径:定性研究对推进伦理实践的启示

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摘要

Adults who are incapacitated and alone, having no surrogates, may be known as “unbefriended.” Decision-making for these particularly vulnerable patients is a common and vexing concern for healthcare providers and hospital ethics committees. When all other avenues for resolving the need for surrogate decision-making fail, patients who are incapacitated and alone may be referred for “public guardianship” or guardianship of last resort. While an appropriate mechanism in theory, these programs are often under-staffed and under-funded, laying the consequences of inadequacies on the healthcare system and the patient him or herself. We describe a qualitative study of professionals spanning clinical, court, and agency settings about the mechanisms for resolving surrogate consent for these patients and problems therein within the state of Massachusetts. Interviews found that all participants encountered adults who are incapacitated and without surrogates. Four approaches for addressing surrogate needs were: (1) work to restore capacity; (2) find previously unknown surrogates; (3) work with agencies to obtain surrogates; and (4) access the guardianship system. The use of guardianship was associated with procedural challenges and ethical concerns including delays in care, short term gains for long term costs, inabilities to meet a patient’s values and preferences, conflicts of interest, and ethical discomfort among interviewees. Findings are discussed in the context of resources to restore capacity, identify previously unknown surrogates, and establish improved surrogate mechanisms for this vulnerable population.
机译:丧失能力且独自一人而没有代孕的成年人可能被称为“未交朋友”。对于这些特别脆弱的患者而言,决策是医疗保健提供者和医院道德委员会普遍而烦恼的问题。当解决替代决策所需的所有其他途径均告失败时,无行为能力的患者可单独获得“公共监护权”或“最后监护权”。这些计划虽然在理论上是一种适当的机制,但通常人手不足且资金不足,这给医疗保健系统和患者(他或她自己)带来了不足的后果。我们描述了横跨临床,法院和代理机构的专业人员的定性研究,涉及解决这些患者的代理人同意及其在马萨诸塞州内的问题的机制。访谈发现,所有参与者都遇到了无行为能力且没有代孕的成年人。解决代理需求的四种方法是:(1)恢复容量的工作; (2)查找以前未知的代理人; (3)与代理机构合作以获取代理人; (4)访问监护系统。监护权的使用与程序上的挑战和道德上的顾虑相关联,包括护理延误,长期费用的短期收益,无法满足患者的价值观和喜好,利益冲突以及受访者的道德不适。在资源的背景下讨论了发现,以恢复能力,确定以前未知的替代物并建立针对该弱势群体的改进替代物机制。

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