英文摘要
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The ethical and legal doctrine of informed consent has a very strong metaphor that information is power. Therefore, it is believed (or at least claimed) that the power imbalance between doctor and patient caused by information asymmetry can be adjusted by empowering patients with physicians' duty to disclose. Nonetheless, clinical experiences often show that information does not necessarily bring about knowledge, and knowledge does not necessarily bring about right choices. While informed consent forms become ever lengthier, more and more people doubt such information-dumping really promotes patient autonomy.This paper asks a basic question: can a competent patient waive his/her right to autonomy? Is patient not only entitled but also obliged to autonomy? In more specific, can a patient/subject decline his/her right to know or/and right to make a choice and delegate it to the physician/researcher? Is autonomy in nature a right or a duty?This paper tries to answer these questions by exploring two scenarios: patients' informed waiver in a clinical setting and human subjects' blanket consent in a research setting. The author anatomizes the bioethical concept of autonomy into two identifiable rights: right to know and right to make a decision, both, I argued, under certain condition are waivable.
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