[日本癌症治疗中的共同决策]。

Q4 Medicine Japanese Journal of Cancer and Chemotherapy Pub Date : 2024-09-01
Etsuko Aruga
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引用次数: 0

摘要

过去,不仅是在癌症治疗中,父权制决策仍在继续。自此以后,病人的自我决定权取而代之。随着晚期护理规划概念的传播,医护人员和患者共同决策的重要性得到了认可。此外,在日本,家属也参与了这一过程,并发挥了关键作用。做决定有时是痛苦的,尤其是晚期癌症患者。当患者难以做出决定时,家人会为患者提供情感支持,并作为患者的代言人参与决策。此外,还提到了日本的障碍和应对方法。当患者抱有不切实际的希望时,医疗服务提供者可以表达他们的担忧,同时注意不要拒绝他们的愿望。痴呆症患者就是这样的人。对于回避决策的患者,评估其目前的身体疼痛症状和精神负担非常重要。痛苦会降低患者的精力,阻碍他们思考未来。未来的问题需要解决伦理方面的问题,并克服临床挑战。
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[Shared Decision-Making in Cancer Care of Japan].

Paternalistic decision-making continued in the past, not only in cancer care. It has since been replaced by self-determination by the patient. As the concept of advanced care planning has spread, the importance of shared decision-making between healthcare professionals and patients has been recognized. In addition, family participates in the process with Key Role in Japan. Decisions are sometimes painful, especially with advanced cancer. Families provide emotional support to the patient and participate in decision-making as an advocate when it is difficult to make decisions. Furthermore, barriers and coping with that in Japan are also mentioned. When patients have unrealistic hopes, healthcare providers can express their concerns while taking care not to deny their wishes. Patients with dementia are what they are. For patients who avoid decision-making, it is important to assess their current physical pain symptoms and emotional burden. Suffering reduces energy of the patient and can prevent thinking about the future. Future issues need to address ethical aspects and overcome clinical challenges.

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