Challenges and practical solutions for managing secondary genomic findings in primary care

Primary care providers will increasingly be tasked with managing most secondary findings from genomic sequencing, but literature exploring their capacity to manage findings beyond conventional genetic testing is limited. This study aimed to explore primary care providers’ challenges and potential so...

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Veröffentlicht in:European journal of medical genetics 2022-01, Vol.65 (1), p.104384-104384, Article 104384
Hauptverfasser: Sebastian, Agnes, Carroll, June C., Vanstone, Meredith, Clausen, Marc, Kodida, Rita, Reble, Emma, Mighton, Chloe, Shickh, Salma, Aronson, Melyssa, Eisen, Andrea, Elser, Christine, Lerner-Ellis, Jordan, Kim, Raymond H., Bombard, Yvonne
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container_end_page 104384
container_issue 1
container_start_page 104384
container_title European journal of medical genetics
container_volume 65
creator Sebastian, Agnes
Carroll, June C.
Vanstone, Meredith
Clausen, Marc
Kodida, Rita
Reble, Emma
Mighton, Chloe
Shickh, Salma
Aronson, Melyssa
Eisen, Andrea
Elser, Christine
Lerner-Ellis, Jordan
Kim, Raymond H.
Bombard, Yvonne
description Primary care providers will increasingly be tasked with managing most secondary findings from genomic sequencing, but literature exploring their capacity to manage findings beyond conventional genetic testing is limited. This study aimed to explore primary care providers’ challenges and potential solutions for managing secondary findings. Providers were recruited in two groups. Group 1 providers had a patient in their practice who received secondary findings and all potential group 1 providers were invited to participate. Group 2 providers were provided with the secondary findings of a hypothetical patient and were purposefully sampled for maximal variation in sex, practice setting, and geographic location. Providers were interviewed about their challenges and solutions managing secondary findings from a patient in their practice or a hypothetical patient. Using interpretive description methodology, transcripts were analysed thematically complemented by constant comparison. Out of the fifty-five providers invited, 15 family physicians participated across community and academic settings in Ontario, Canada (range 6–40 years in practice; 10/15 female). Providers described a responsibility to manage secondary findings, but limited capacity for this, describing practice, knowledge, and technical challenges. Providers expressed concern that compared to other incidental findings, secondary genomic findings might be reported directly to patients and result in longer-term anxiety. Potential solutions were a structured letter with categorized results and summary tables highlighting key secondary findings with follow-up recommendations and resources, as well as electronic medical records (EMRs) that store and integrate genomic information for prescribing or referrals. These solutions were deemed essential to address knowledge and technical challenges faced by primary care physicians and ultimately promote clinical utility of secondary findings.
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Providers described a responsibility to manage secondary findings, but limited capacity for this, describing practice, knowledge, and technical challenges. Providers expressed concern that compared to other incidental findings, secondary genomic findings might be reported directly to patients and result in longer-term anxiety. Potential solutions were a structured letter with categorized results and summary tables highlighting key secondary findings with follow-up recommendations and resources, as well as electronic medical records (EMRs) that store and integrate genomic information for prescribing or referrals. 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subjects Adult
Aged
Clinical utility
Female
Genetic testing
Genomics
Humans
Incidental Findings
Male
Middle Aged
Physician's Role
Physicians, Primary Care
Primary care physicians
Primary Health Care
Whole exome sequencing
Whole Genome Sequencing
title Challenges and practical solutions for managing secondary genomic findings in primary care
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