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Capacity for Preferences: Respecting Patients with Compromised Decision‐Making Respecting Patients with Compromised Decision‐Making

机译:偏好能力:尊重受损决策尊重患者的尊重患者

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Abstract When a patient lacks decision‐making capacity, then according to standard clinical ethics practice in the United States, the health care team should seek guidance from a surrogate decision‐maker, either previously selected by the patient or appointed by the courts. If there are no surrogates willing or able to exercise substituted judgment, then the team is to choose interventions that promote a patient's best interests. We argue that, even when there is input from a surrogate, patient preferences should be an additional source of guidance for decisions about patients who lack decision‐making capacity . Our proposal builds on other efforts to help patients who lack decision‐making capacity provide input into decisions about their care. For example, “supported,” “assisted,” or “guided” decision‐making models reflect a commitment to humanistic patient engagement and create a more supportive process for patients, families, and health care teams. But often, they are supportive processes for guiding a patient toward a decision that the surrogate or team believes to be in the patient's medical best interests. Another approach holds that taking seriously the preferences of such a patient can help surrogates develop a better account of what the patient's treatment choices would have been if the patient had retained decision‐making capacity; the surrogate then must try to integrate features of the patient's formerly rational self with the preferences of the patient's currently compromised self. Patients who lack decision‐making capacity are well served by these efforts to solicit and use their preferences to promote best interests or to craft would‐be autonomous patient images for use by surrogates. However, we go further: the moral reasons for valuing the preferences of patients without decision‐making capacity are not reducible to either best‐interests or (surrogate) autonomy considerations but can be grounded in the values of liberty and respect for persons. This has important consequences for treatment decisions involving these vulnerable patients .
机译:摘要患者当患者缺乏决策能力时,根据美国的标准临床伦理实践,医疗团队应寻求代理决策者的指导,以前由患者选择或由法院任命。如果没有愿意或能够锻炼替代判决的代理人,那么该团队是选择促进患者最佳利益的干预措施。我们认为,即使在来自代理商的意见时,患者偏好也应该是关于缺乏决策能力的患者的决策的额外指导来源。我们的提案建立了其他努力,帮助缺乏决策能力的患者提供有关他们护理的决定的投入。例如,“支持”,“辅助”或“引导”决策模型反映了对人文患者参与的承诺,为患者,家庭和医疗团队创造了更具支持性过程。但是,他们经常是支持患者决定代理人或团队认为处于患者的医疗最佳利益的决定的支持过程。另一种方法认为,这种患者的偏好可以帮助代理,更好地说明患者的治疗选择是患者是否保留了决策能力;然后,代理人必须尝试将患者以前合理的自身的特征与患者目前受损的自我的偏好集成。缺乏决策能力的患者通过这些努力征求并利用他们的偏好来促进最佳利益或工艺将是自主患者图像供代理人使用。然而,我们进一步进一步:对没有决策能力的患者偏好的道德原因不会降低最有利于最有利于或(代理人)的自主考虑因素,而是可以在自由的价值观和尊重人的基础上。这对涉及这些脆弱患者的治疗决策具有重要影响。

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