Genetic variants with discordant classifications: An assessment of genetic counselor attitudes and practices. Issue 1 (17th August 2022)
- Record Type:
- Journal Article
- Title:
- Genetic variants with discordant classifications: An assessment of genetic counselor attitudes and practices. Issue 1 (17th August 2022)
- Main Title:
- Genetic variants with discordant classifications: An assessment of genetic counselor attitudes and practices
- Authors:
- Lahiri, Sayoni
Reys, Brian
Wunder, Julia
Pirzadeh‐Miller, Sara - Abstract:
- Abstract: Discordant variant classifications (DVCs) can impact patient care and pose challenges for clinicians. A survey‐based study was conducted to examine genetic counselor (GC) attitudes and practices related to DVCs. Most GCs (202/229, 88%) in the study provide direct patient care across clinical specialties; review patients' genetic test results to determine if reported genetic variants have DVCs (176/202, 88%); and inform patients of known DVCs that impact medical management (165/202, 82%). DVC review, which takes 41 min (range: 5–240) on average per week, is typically prompted by the identification of a variant of uncertain significance (VUS) (160/176, 90%) and is primarily conducted using public databases (176/176, 100%). While most GCs felt it would not be ethical to knowingly provide different medical management recommendations to patients with the same genetic variant (152/229, 66%), they also stated they would rely on the variant classification on the test report (141/229, 61%) and/or the patient's personal/family history (188/229, 82%) to determine which classification to follow if a DVC is identified. Both factors are patient‐specific and, inherently, could lead to differing recommendations. When posed with a hypothetical scenario in which two patients have the same genetic variant, but test reports show a DVC (pathogenic vs VUS), most GCs (179/229, 78.2%) stated they would make the same recommendation for both patients regardless of management guidelines.Abstract: Discordant variant classifications (DVCs) can impact patient care and pose challenges for clinicians. A survey‐based study was conducted to examine genetic counselor (GC) attitudes and practices related to DVCs. Most GCs (202/229, 88%) in the study provide direct patient care across clinical specialties; review patients' genetic test results to determine if reported genetic variants have DVCs (176/202, 88%); and inform patients of known DVCs that impact medical management (165/202, 82%). DVC review, which takes 41 min (range: 5–240) on average per week, is typically prompted by the identification of a variant of uncertain significance (VUS) (160/176, 90%) and is primarily conducted using public databases (176/176, 100%). While most GCs felt it would not be ethical to knowingly provide different medical management recommendations to patients with the same genetic variant (152/229, 66%), they also stated they would rely on the variant classification on the test report (141/229, 61%) and/or the patient's personal/family history (188/229, 82%) to determine which classification to follow if a DVC is identified. Both factors are patient‐specific and, inherently, could lead to differing recommendations. When posed with a hypothetical scenario in which two patients have the same genetic variant, but test reports show a DVC (pathogenic vs VUS), most GCs (179/229, 78.2%) stated they would make the same recommendation for both patients regardless of management guidelines. One‐third (52/179, 29.1%) cited patient‐specific factors, such as personal/family history, would impact their recommendations. Disagreements about whether the pathogenic or VUS classification should be used to make medical management recommendations were noted. Differing practices and opinions on how to manage patients with DVCs, as well as the fact that most GCs (209/229, 91.3%) have consulted with colleagues on this matter, highlight the need for more professional guidance to ensure equitable patient care. … (more)
- Is Part Of:
- Journal of genetic counseling. Volume 32:Issue 1(2023)
- Journal:
- Journal of genetic counseling
- Issue:
- Volume 32:Issue 1(2023)
- Issue Display:
- Volume 32, Issue 1 (2023)
- Year:
- 2023
- Volume:
- 32
- Issue:
- 1
- Issue Sort Value:
- 2023-0032-0001-0000
- Page Start:
- 100
- Page End:
- 110
- Publication Date:
- 2022-08-17
- Subjects:
- attitudes -- discordant -- ethics -- genetic counselors -- genetic testing -- medical management -- variant classification
Genetic counseling -- Periodicals
616.042 - Journal URLs:
- https://onlinelibrary.wiley.com/journal/15733599 ↗
http://www.springer.com/gb/ ↗ - DOI:
- 10.1002/jgc4.1626 ↗
- Languages:
- English
- ISSNs:
- 1059-7700
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4989.700000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 25761.xml