What Happened to Consent? Rationalizing Its Breaches.
Harriet Washington's latest book, Carte Blanche: The Erosion of Medical Consent, examines several cases of exploitation within different U.S. populations involved in medical experimentation. She argues that "consent has been whittled away not by successful ethical argument or by persuasion but becau...
| Publicado en: | Hastings Center Report Vol. 52; no. 3; pp. 49 - 52 |
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| Autores principales: | , |
| Formato: | Artículo |
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Wiley-Blackwell
May2022
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| Acceso en línea: | Ver este registro en EBSCOhost |
| fields | @attributes: recordID: 1 pdfLink: plink: https://search.ebscohost.com/login.aspx?direct=true&db=ssf&AN=157693607&site=ehost-live header: @attributes: shortDbName: ssf uiTerm: 157693607 longDbName: Social Sciences Full Text (H.W. Wilson) uiTag: AN controlInfo: bkinfo: jinfo: jid: 00930334 HCR jtl: Hastings Center Report issn: 00930334 maglogo: Y pubinfo: dt: May2022 vid: 52 iid: 3 pid: 480 pub: Wiley-Blackwell artinfo: ui: 157693607 10.1002/hast.1396 ppf: 49 ppct: 3 formats: fmt: – @attributes: type: T – @attributes: type: P size: 377KB tig: atl: What Happened to Consent? Rationalizing Its Breaches. aug: au: Wilson, Yolonda Vinarcsik, Lou su: African Americans Health policy Human research subjects Racism Medical research Informed consent (Medical law) Military personnel Safety At-risk people sug: subj: African Americans Health policy Human research subjects Racism Medical research Informed consent (Medical law) Military personnel Administration of Public Health Programs Research and Development in the Physical, Engineering, and Life Sciences (except Biotechnology) Safety At-risk people keyword: bioethics exploitation health equity informed consent racism research ethics bioethics exploitation health equity informed consent racism research ethics ab: Harriet Washington's latest book, Carte Blanche: The Erosion of Medical Consent, examines several cases of exploitation within different U.S. populations involved in medical experimentation. She argues that "consent has been whittled away not by successful ethical argument or by persuasion but because the U.S. medical research system maintains subjects in a voiceless and uninformed state." Protections promised by the early medico‐legal ideal of consent were never universal, and exceptions favoring the aims of researchers over the well‐being of vulnerable groups have become the norm. Carte Blanche explores how ever‐growing categories of people are vulnerable to becoming unwitting subjects of medical research as consent is overridden in the name of emergencies, military utility, and scientific progress. pubtype: Academic Journal doctype: Article src: R language: English refInfo: copyright: @attributes: flag: N holdings: @attributes: islocal: N |
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