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[癌症治疗中的生物伦理问题与原则]

[Bioethical issues and principles in cancer treatment].

作者信息

Hoshino K

机构信息

Kyoto University.

出版信息

Gan To Kagaku Ryoho. 1992 Mar;19(3):281-5.

PMID:1543355
Abstract

Bioethics was established as a new area of interdisciplinary studies focusing on human conduct in the field of the life sciences and health care in the light of moral values and principles in the 1960's and the beginning of the 1970's. Physicians abiding by classical medical ethics based upon the Oath of Hippocrates became subject to criticism because they behaved paternalistically in relation to their patients and provided medical treatment dogmatically without adequate explanation concerning conditions and diagnoses of patients' diseases, what kinds of treatments they were to receive and the possible benefits and risks thereof, along with their prognoses. During the patients' rights' movement, law suits against paternalistic physicians increased in number and the courts tried to establish ethical and legal principles for judgments in law suits using the Ethical Code of Neurenberg (1947) as an excellent model. The legal principles established as "informed consent" include obligations of physicians to provide their patients with adequate explanation and truth-telling, and the rights of patients to autonomy, choice, self-determination, and to give consent to physicians. Besides these rights, patients also have the right to put their veto on their own rights. In such cases, truth-telling by physicians, who believe in truth-telling, such as the disclosure of the diagnosis of cancer to these patients, can legally result in infringement of the patient's rights. It is important for physicians to respect the wishes and opinions of patients based on their own values and not to insist on personal dogmatic opinions. The disclosure of cancer diagnosis to terminal patients is certainly one of the most difficult procedures in medical practice and requires profound medical experience and bioethical insight.

摘要

生物伦理学作为一个新的跨学科研究领域,于20世纪60年代和70年代初依据道德价值观和原则,聚焦于生命科学与医疗保健领域中的人类行为而确立。遵循基于希波克拉底誓言的传统医学伦理的医生受到了批评,因为他们对患者表现出家长式作风,在未充分解释患者疾病的状况和诊断、患者将接受何种治疗及其可能的益处和风险以及预后的情况下,教条地提供医疗服务。在患者权利运动期间,针对家长式作风医生的诉讼数量增加,法院试图以《纽伦堡法典》(1947年)为典范,确立用于法律诉讼判决的伦理和法律原则。确立为“知情同意”的法律原则包括医生有义务向患者提供充分解释并告知真相,以及患者享有自主、选择、自我决定和同意医生治疗的权利。除了这些权利,患者还有权对自己的权利行使否决权。在这种情况下,信奉告知真相的医生如实告知,比如向这些患者披露癌症诊断,在法律上可能会导致侵犯患者权利。医生尊重基于患者自身价值观的愿望和意见,而不是坚持个人的教条观点,这一点很重要。向晚期患者披露癌症诊断无疑是医疗实践中最困难的程序之一,需要深厚的医学经验和生物伦理洞察力。

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