Literature DB >> 6491557

The 'right' not to know.

D E Ost.   

Abstract

There is a common view in medical ethics that the patient's right to be informed entails, as well, a correlative right not to be informed, i.e., to waive one's right to information. This paper argues, from a consideration of the concept of autonomy as the foundation for rights, that there can be no such 'right' to refuse relevant information, and that the claims for such a right are inconsistent with both deontological and utilitarian ethics. Further, the right to be informed is shown to be a mandatory right (though not a welfare right); persons are thus seen to have both a right and a duty to be informed. Finally, the consequences of this view are addressed: since the way in which we conceptualize our problems tends to determine the actions we take to resolve them, it is important properly to conceptualize patients' requests not to be informed. There may be many reasons for acting in accord with such a request, but it is a mistake to conceptualize one's act as 'respecting a right possessed by persons'.

Entities:  

Keywords:  Analytical Approach; Philosophical Approach; Professional Patient Relationship

Mesh:

Year:  1984        PMID: 6491557     DOI: 10.1093/jmp/9.3.301

Source DB:  PubMed          Journal:  J Med Philos        ISSN: 0360-5310


  12 in total

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2.  Informed consent for clinical treatment: a psychologist speaks for patients.

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Journal:  Health Care Anal       Date:  1996-02

3.  The role of beneficence in clinical genetics: non-directive counseling reconsidered.

Authors:  M Yarborough; J A Scott; L K Dixon
Journal:  Theor Med       Date:  1989-06

4.  Consent to epistemic interventions: a contribution to the debate on the right (not) to know.

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Journal:  Med Health Care Philos       Date:  2016-03

5.  The Ethics of General Population Preventive Genomic Sequencing: Rights and Social Justice.

Authors:  Clair Morrissey; Rebecca L Walker
Journal:  J Med Philos       Date:  2018-01-12

6.  Looking for Trouble: Preventive Genomic Sequencing in the General Population and the Role of Patient Choice.

Authors:  Gabriel Lázaro-Muñoz; John M Conley; Arlene M Davis; Marcia Van Riper; Rebecca L Walker; Eric T Juengst
Journal:  Am J Bioeth       Date:  2015       Impact factor: 11.229

7.  Should cancer patients be informed about their diagnosis and prognosis? Future doctors and lawyers differ.

Authors:  Bernice S Elger; T W Harding
Journal:  J Med Ethics       Date:  2002-08       Impact factor: 2.903

8.  Free Choice and Patient Best Interests.

Authors:  Emma C Bullock
Journal:  Health Care Anal       Date:  2016-12

9.  The right not to know: an autonomy based approach.

Authors:  R Andorno
Journal:  J Med Ethics       Date:  2004-10       Impact factor: 2.903

10.  The right not to know and the obligation to know.

Authors:  Ben Davies
Journal:  J Med Ethics       Date:  2020-04-29       Impact factor: 5.926

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