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O consentimento informado é um termo técnico usado pela primeira vez pelo advogado, Paul G. Gebhard, em um caso de negligência médica no tribunal dos Estados Unidos em 1957. [ 10] Ao traçar sua história, alguns estudiosos sugeriram traçar a história da verificação de qualquer uma dessas práticas: [ 11]:54.
2 de mar. de 2017 · Informed consent, which is ethically essential in most clinical research, respects persons’ rights to decide whether participation in the research is compatible with their interests, including...
Informed consent is a principle in medical ethics, medical law and media studies, that a patient must have sufficient information and understanding before making decisions about their medical care.
5 de jun. de 2023 · Informed consent is the process in which a health care provider educates a patient about the risks, benefits, and alternatives of a given procedure or intervention. The patient must be competent to make a voluntary decision about whether to undergo the procedure or intervention.
- 2023/06/05
2 de abr. de 2020 · A chapter from a handbook of research ethics and scientific integrity that explores the origin, meaning, and forms of informed consent in different fields and contexts of research. It analyzes the challenges and changes in the understanding of the principle of informed consent due to scientific and ethical developments.
7 de mar. de 2024 · Informed consent is a communication process between patients and healthcare providers that involves understanding diagnosis, treatment options, and risks. Learn when and how informed consent is required, and what to do if you have questions or concerns.
Informed consent to medical treatment is fundamental in both ethics and law. Patients have the right to receive information and ask questions about recommended treatments so that they can make well-considered decisions about care.
