战略终局:姑息医学和法律

George P. Smith, Catholic U of America Columbus RPS Law Submitter
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摘要

本文分析了不通过使用遗嘱处置、医疗代理或其他预先医疗指示来规划或规划一个人的死亡的后果,这些指示规定了在生命的最后阶段要给予或拒绝的医疗过程。在缺乏这种性质的文书的情况下,司法部门往往陷入保健提供者和家庭成员之间的争议,他们对应该扩大的治疗或缓和护理的性质和程度持相反意见。传统上,为了解决这些冲突,法院采用了两种决策模式:最佳利益和替代判断。换句话说,法院试图确定——主要基于医学证据——什么对一个无法治愈的、没有能力的病人最有利,或者,如果他有能力做出目前的医疗决定,他会选择什么样的治疗方案。对于有能力的病人来说,在生命的最后阶段管理他的护理的最佳方法是行使他的普通法权利拒绝治疗。确定病人的生命价值是这两个模型的核心。对于无能的病人来说,确定和评估这些价值对于任何和所有有效的姑息治疗方法都是特别重要的。本文通过对英美法律框架的比较分析,认为在医生协助死亡缺乏明确的立法方向或司法认可的情况下,最明智、最富有同情心的临终关怀方法是通过更广泛地接受和应用医疗无用论来实现的。反过来,可以人道地通过使用深度镇静或姑息性镇静来加强这一原则,这种镇静被认为是有效的,在医学上是适当的,适用于难治性躯体和非躯体疼痛以及绝症期间的痛苦。事实上,这种做法与调整护理的伦理是一致的。邀请或继续医学上无效的治疗应被认为是完全错误的;因为,以这种方式行事不仅否认了人类有限的事实,而且给病人和其他受影响的第三方带来了不必要的努力、费用和情感创伤。当医生试图治疗无效的医疗条件时,这样的行为完全违背了医学伦理的基本原则之一——慈善。
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Strategizing the End-Game: Palliative Medicine and the Law
This paper analyzes the consequences of not strategizing or planning for one’s death by use of a testamentary disposition, health care proxy or other advance medical directive which sets out the course of medical treatment which is to be given or withheld during the end-stage of life. When instruments of this nature are absent, the judiciary is brought - all too often - into controversies among health care providers and family members who take opposing views regarding the nature and extent of therapeutic or palliative care which should be extended. Traditionally, in order to resolve these conflicts, two decision making models are utilized by the courts: best interests and substituted judgment. Stated otherwise, the courts attempt to ascertain - based largely upon medical evidence - what is in the best overall interests of an incurable, incompetent patient or, alternatively, what course of care such a patient would have chose if he were to be competent to make a present health care decision. For the competent patient, the best approach to managing his care at the end-stage of life is to exercise his common law right to refuse treatment. Determining patient life values are central to both of these two models. For the incompetent patient, ascertaining and evaluating these values is of particular consequence to any and all effective approaches to palliative care. This paper suggests, through a comparative analysis of British and the American legal frameworks, that - absent clear legislative direction or judicial recognition of physician assistance in dying - the most sensible and compassionate approach to end-stage care is to be realized by wider acceptance and application of the doctrine of medical futility. This doctrine can be strengthened, in turn, humanely, through use of deep or palliative sedation which is seen as efficacious and medically appropriate in cases of intractable somatic and non somatic pain and suffering during terminal illness. Indeed, such a practice is consistent with a ethic of adjusted care. To invite or continue medically futile treatment should be recognized as simply wrong; for, acting in such a manner not only denies the fact of human finitude, but it imposes unnecessary effort, expense, and emotional trauma on both the patient and other affected third parties. When physicians attempt to treat futile medical conditions, such actions are a total abnegation of one of the cardinal principles of medical ethics - beneficence.
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