Views of Israeli healthcare professionals regarding communication of genetic variants of uncertain significance to patients

Alma Levin Fridman, Aviad Raz, Stefan Timmermans, Shiri Shkedi-Rafid

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

Abstract

While genomic medicine is becoming an important part of patient care with an ever-increasing diagnostic yield, communicating variants of uncertain clinical significance (VUSs) remains a major challenge. We draw on qualitative analysis of semi-structured interviews conducted in 2020 with 20 Israeli healthcare professionals and stakeholders involved in communicating the results of genome-wide sequencing to patients. Respondents described four main strategies of communicating VUSs to patients: preparing the patient pre-test for uncertainty; adapting the level of detail to the patient's needs; upgrading versus downgrading the VUS; and following up on the possible reclassification of VUSs. These strategies were expressed differently by physicians and genetic counselors, varying according to their specialty and perception of the patient's situation. We discuss the strategic management and communication of uncertain genomic test results with patients in the context of meeting patients' expectations and working toward genetic causality through genomic narration and designation.

Original languageEnglish
Pages (from-to)912-921
Number of pages10
JournalJournal of Genetic Counseling
Volume31
Issue number4
DOIs
StatePublished - 1 Aug 2022

Keywords

  • communication
  • genomic designation
  • uncertainty
  • variant classification
  • variant of uncertain significance

ASJC Scopus subject areas

  • Genetics(clinical)

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