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Views of Israeli healthcare professionals regarding communication of genetic variants of uncertain significance to patients
Author(s) -
Levin Fridman Alma,
Raz Aviad,
Timmermans Stefan,
ShkediRafid Shiri
Publication year - 2022
Publication title -
journal of genetic counseling
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.867
H-Index - 52
eISSN - 1573-3599
pISSN - 1059-7700
DOI - 10.1002/jgc4.1560
Subject(s) - qualitative research , genetic testing , narrative , context (archaeology) , health care , genetic counseling , perception , medicine , specialty , causality (physics) , test (biology) , psychology , nursing , family medicine , genetics , sociology , paleontology , social science , linguistics , philosophy , physics , quantum mechanics , neuroscience , economics , biology , economic growth
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.