Reasonable expectations of privacy in non-disclosure of familial genetic risk: What is it reasonable to expect?
Confidentiality
Genetic information
Non-disclosure
Privacy
Reasonable expectation of privacy
Journal
European journal of medical genetics
ISSN: 1878-0849
Titre abrégé: Eur J Med Genet
Pays: Netherlands
ID NLM: 101247089
Informations de publication
Date de publication:
May 2019
May 2019
Historique:
received:
03
07
2018
revised:
03
10
2018
accepted:
12
11
2018
pubmed:
7
12
2018
medline:
30
8
2019
entrez:
7
12
2018
Statut:
ppublish
Résumé
Where there is conflict between a patient's interests in non-disclosure of their genetic information to relatives and the relative's interest in knowing the information because it indicates their genetic risk, clinicians have customarily been able to protect themselves against legal action by maintaining confidence even if, professionally, they did not consider this to be the right thing to do. In ABC v St Georges Healthcare NHS Trust ([2017] EWCA Civ 336) the healthcare team recorded their concern about the wisdom of the patient's decision to withhold genetic risk information from his relative, but chose to respect what they considered to be an unwise choice. Even though professional guidance considers that clinicians have the discretion to breach confidence where they believe this to be justified, (Royal College of Physicians, Royal College of Pathologists and the British Society of Human Genetics, 2006; GMC, 2017) clinicians find it difficult to exercise this discretion in line with their convictions against the backdrop of the legal prioritisation of the duty to maintain confidence. Thus, the professional discretion is not being freely exercised because of doubts about the legal protection available in the event of disclosure. The reliance on consent as the legal basis for setting aside the duty of confidence often vetoes sharing information with relatives. This paper argues that an objective approach based on privacy, rather than a subjective consent-based approach, would give greater freedom to clinicians to exercise the discretion which their professional guidance affords.
Identifiants
pubmed: 30521983
pii: S1769-7212(18)30491-9
doi: 10.1016/j.ejmg.2018.11.013
pmc: PMC6588831
pii:
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
308-315Subventions
Organisme : Wellcome Trust
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 206194
Pays : United Kingdom
Informations de copyright
Copyright © 2018. Published by Elsevier Masson SAS.
Références
Am J Med Genet. 2002 Jul 15;110(4):324-31
pubmed: 12116205
Clin Genet. 2003 Oct;64(4):317-26
pubmed: 12974737
BMJ. 2004 Jul 17;329(7458):165-7
pubmed: 15258076
Eur J Hum Genet. 2005 May;13(5):556-62
pubmed: 15770225
Fam Cancer. 2006;5(1):103-16
pubmed: 16528614
Am J Nurs. 2009 Apr;109(4):65-9
pubmed: 19325321
J Community Genet. 2013 Apr;4(2):233-42
pubmed: 23319393
BMC Med Ethics. 2014 May 16;15:39
pubmed: 24885495
J Genet Couns. 2015 Aug;24(4):608-15
pubmed: 25400212
Genet Med. 2016 Apr;18(4):290-301
pubmed: 26110233
Med Law Rev. 2016 Winter;24(1):112-23
pubmed: 26433012
Hum Genet. 2016 Jan;135(1):109-20
pubmed: 26612611
J Med Ethics. 2016 Mar;42(3):174-9
pubmed: 26744307
J Med Ethics. 2016 Feb;42(2):89-94
pubmed: 26811487
BMJ Open. 2017 Feb 3;7(2):e012443
pubmed: 28159847
Med Law Int. 2017 Sep;17(3):158-182
pubmed: 28943725
Med Law Rev. 2018 Feb 1;26(1):51-72
pubmed: 28981744
Med Law Rev. 2018 Feb 1;26(1):125-133
pubmed: 29045720