Literature DB >> 34234303

Disclosure of genetic information to family members: a systematic review of normative documents.

Amicia Phillips1, Pascal Borry2, Ine Van Hoyweghen3, Danya F Vears2,4,5.   

Abstract

PURPOSE: Findings from genomic sequencing can have important implications for patients and family members. Yet, when a patient does not consent to the disclosure of genetic information to relatives, it is unclear how health-care professionals (HCPs) should balance their responsibilities toward patients and their family members and whether breaches in confidentiality are warranted.
METHODS: We conducted a systematic review of normative documents to understand how HCPs should discuss and facilitate family disclosure, and what should be done in cases where the patient does not consent to disclosure.
RESULTS: We analyzed 35 documents from advisory committees at the national, European, and international level. We identified discrepancies regarding the recommended role of HCPs in disclosure. While almost all normative documents supported the disclosure of genetic information without patient consent in limited conditions, the conditions for disclosure were often not well defined. Documents provided varying degrees of information regarding what actions HCPs must take in such situations.
CONCLUSION: Our findings present concerns regarding the ability of these normative documents to guide HCPs' decision making around the disclosure of genetic information to family members. Clearer guidance outlining the responsibilities and acceptability of disclosure is necessary to facilitate disclosure of genetic information to family members.
© 2021. The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics.

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Mesh:

Year:  2021        PMID: 34234303     DOI: 10.1038/s41436-021-01248-0

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  17 in total

1.  Genetic Test Results and Disclosure to Family Members: Qualitative Interviews of Healthcare Professionals' Perceptions of Ethical and Professional Issues in France.

Authors:  Diane D' Audiffret Van Haecke; Sandrine de Montgolfier
Journal:  J Genet Couns       Date:  2015-10-19       Impact factor: 2.537

Review 2.  Communicating genetic information in families--a review of guidelines and position papers.

Authors:  Laura E Forrest; Martin B Delatycki; Loane Skene; MaryAnne Aitken
Journal:  Eur J Hum Genet       Date:  2007-03-28       Impact factor: 4.246

Review 3.  Ending a Diagnostic Odyssey: Family Education, Counseling, and Response to Eventual Diagnosis.

Authors:  Donald Basel; Julie McCarrier
Journal:  Pediatr Clin North Am       Date:  2017-02       Impact factor: 3.278

4.  Essential elements of genetic cancer risk assessment, counseling, and testing: updated recommendations of the National Society of Genetic Counselors.

Authors:  Bronson D Riley; Julie O Culver; Cécile Skrzynia; Leigha A Senter; June A Peters; Josephine W Costalas; Faith Callif-Daley; Sherry C Grumet; Katherine S Hunt; Rebecca S Nagy; Wendy C McKinnon; Nancie M Petrucelli; Robin L Bennett; Angela M Trepanier
Journal:  J Genet Couns       Date:  2011-12-02       Impact factor: 2.537

5.  To tell or not to tell: barriers and facilitators in family communication about genetic risk.

Authors:  K Forrest; S A Simpson; B J Wilson; E R van Teijlingen; L McKee; N Haites; E Matthews
Journal:  Clin Genet       Date:  2003-10       Impact factor: 4.438

Review 6.  Disclosing genetic information to family members without consent: Five Australian case studies.

Authors:  Jane Tiller; Gemma Bilkey; Rebecca Macintosh; Sarah O'Sullivan; Stephanie Groube; Marili Palover; Nicholas Pachter; Mark Rothstein; Paul Lacaze; Margaret Otlowski
Journal:  Eur J Med Genet       Date:  2020-08-14       Impact factor: 2.708

7.  Approaching confidentiality at a familial level in genomic medicine: a focus group study with healthcare professionals.

Authors:  Sandi Dheensa; Angela Fenwick; Anneke Lucassen
Journal:  BMJ Open       Date:  2017-02-03       Impact factor: 2.692

8.  Limitations and Pitfalls of Using Family Letters to Communicate Genetic Risk: a Qualitative Study with Patients and Healthcare Professionals.

Authors:  Sandi Dheensa; Anneke Lucassen; Angela Fenwick
Journal:  J Genet Couns       Date:  2017-11-01       Impact factor: 2.537

9.  Using a genetic test result in the care of family members: how does the duty of confidentiality apply?

Authors:  Michael Parker; Anneke Lucassen
Journal:  Eur J Hum Genet       Date:  2018-04-27       Impact factor: 4.246

10.  Genetic testing for Lynch syndrome: family communication and motivation.

Authors:  Celine H M Leenen; Mariska den Heijer; Conny van der Meer; Ernst J Kuipers; Monique E van Leerdam; Anja Wagner
Journal:  Fam Cancer       Date:  2016-01       Impact factor: 2.375

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  3 in total

1.  Comparing the attitudes of physicians and non-physicians toward communicating a patient's BRCA1 mutation to a first-degree relative against a patient's wishes.

Authors:  Jane E Zebrack; Wei Yang; Matthew Milone; Max J Coppes
Journal:  J Community Genet       Date:  2022-05-21

Review 2.  Informing relatives of their genetic risk: an examination of the Belgian legal context.

Authors:  Amicia Phillips; Thomas Bronselaer; Pascal Borry; Ine Van Hoyweghen; Danya F Vears; Laurent Pasquier; Stefaan Callens
Journal:  Eur J Hum Genet       Date:  2022-01-08       Impact factor: 5.351

3.  The Communication Chain of Genetic Risk: Analyses of Narrative Data Exploring Proband-Provider and Proband-Family Communication in Hereditary Breast and Ovarian Cancer.

Authors:  Carla Pedrazzani; Monica Aceti; Reka Schweighoffer; Andrea Kaiser-Grolimund; Nicole Bürki; Pierre O Chappuis; Rossella Graffeo; Christian Monnerat; Olivia Pagani; Manuela Rabaglio; Maria C Katapodi; Maria Caiata-Zufferey
Journal:  J Pers Med       Date:  2022-07-29
  3 in total

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