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Identifiant d'origine
QE42
Libellé préféré
consentement éclairé
informed consentLibellé catégorie
Consentement éclairéInformed consentNote de contenu Q-Code
autorisation volontaire, donnée par un patient ou par le sujet d’une recherche qui comprend parfaitement les risques encourus, à la réalisation de procédures diagnostiques ou d'investigation, y compris le traitement médical ou chirurgical. (MeSH) voluntary authorization, by a patient or research subject, with full comprehension of the risks involved, for diagnostic or investigative procedures, and for medical and surgical treatment. (MeSH)Contenu conceptuel Q-Code
Presumed Consent . An institutional policy of granting authority to health personnel to perform procedures on patients or to remove organs from cadavers for transplantation unless an objection is registered by family members or by the patient prior to death. This also includes emergency care of minors without prior parental consent (MeSH)Informed Consent ; Voluntary authorization, by a patient or research subject, with full comprehension of the risks involved, for diagnostic or investigative procedures, and for medical and surgical treatment.(MeSH)Informed consent: the process of making a free and informed decision (such as to participate in research). Individuals who provide informed consent must be legally competent and have enough decision-making capacity to consent to research. Research regulations specify the types of information that must be disclosed to the subject. (NIEHgloss)Informed consent; Voluntary consent given by a subject or a responsible proxy (e.g., a parent) for participation in a study, immunization program, treatment regimen, etc., after being informed of the purpose, methods, procedures, potential benefits and potential harms, and, when relevant, the degree of uncertainty about such outcomes. The essential criteria of informed consent are that the subject has both knowledge and comprehension, that consent is freely given without duress or undue influence, and that the right of withdrawal at any time is clearly communicated to the subject (Dicepid)Involuntary Treatment : Procedures, surgery, or other treatment without consent of person or persons receiving treatment (MeSH 2018) Involuntary Treatment, Psychiatric : Treatment of persons with MENTAL DISORDERS without the persons' consent. (MeSH 2018)CUI UMLS
C0021430
Référence bibliographique
Citation
Hueston WJ, Mainous AG, Weiss BD, Macaulay AC, Hickner J, Sherwood RA, null, null. Protecting participants in family medicine research: a consensus statement on improving research integrity and participants' safety in educational research, community-based participatory research, and practice network research. Family medicine. 2006; 38(2): 116-20. Available from: http://www.ncbi.nlm.nih.gov/pubmed/16450233
Kubiak R. The right to information. Anaesthesiology intensive therapy. 2014; 46(3): 180-94. Available from: http://www.ncbi.nlm.nih.gov/pubmed/25078772
Lawal YZ, Garba ES, Ogirima MO, Dahiru IL, Maitama MI, Abubakar K. The doctrine of informed consent in surgical practice. Annals of African medicine. 2011; 10(1): 1-5. Available from: http://www.ncbi.nlm.nih.gov/pubmed/21311147
Tam NT, Huy NT, Thoa le TB, Long NP, Trang NT, Hirayama K, Karbwang J. Participants' understanding of informed consent in clinical trials over three decades: systematic review and meta-analysis. Bulletin of the World Health Organization. 2015; 93(3): 186-98H. Available from: http://www.ncbi.nlm.nih.gov/pubmed/25883410
Thistlethwaite J, Evans R, Tie RN, Heal C. Shared decision making and decision aids - a literature review. Australian family physician. 2006; 35(7): 537-40. Available from: http://www.ncbi.nlm.nih.gov/pubmed/16820831
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