2020
DOI: 10.1186/s12910-020-0452-0
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Ethical values supporting the disclosure of incidental and secondary findings in clinical genomic testing: a qualitative study

Abstract: Background: Incidental findings (IFs) and secondary findings (SFs), being results that are unrelated to the diagnostic question, are the subject of an important debate in the practice of clinical genomic medicine. Arguments for reporting these results or not doing so typically relate to the principles of autonomy, nonmaleficence and beneficence. However, these principles frequently conflict and are insufficient by themselves to come to a conclusion. This study investigates empirically how ethical principles ar… Show more

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Cited by 19 publications
(19 citation statements)
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“…A consideration when using WES or WGS, which include genes not associated with the phenotypes, is the potential for incidental or secondary findings not related to the clinical reason for undertaking the test. The ethical considerations surrounding the return of incidental or secondary findings have been extensively discussed elsewhere 36,37 . Particular consideration is required when children or infants are involved and/or when the test is being used as a screening tool 38,39 .…”
Section: Incidental Findings In Genomic Testingmentioning
confidence: 99%
“…A consideration when using WES or WGS, which include genes not associated with the phenotypes, is the potential for incidental or secondary findings not related to the clinical reason for undertaking the test. The ethical considerations surrounding the return of incidental or secondary findings have been extensively discussed elsewhere 36,37 . Particular consideration is required when children or infants are involved and/or when the test is being used as a screening tool 38,39 .…”
Section: Incidental Findings In Genomic Testingmentioning
confidence: 99%
“…Ряд европейских специалистов по биоэтике рассматривают обязательное сообщение незапрошенной генетической информации или ее сообщение по умолчанию как форму «технологического патернализма». Такое ущемление «права не знать» они связывают с произвольным сужением понятий рационального выбора и блага (Saelaert et. al., 2020).…”
Section: благо автономия и индивидуальное право не знатьunclassified
“…In the context of secondary findings from diagnostic exome or genome sequencing, the American College of Medical Genetics and Genomics (ACMG) proposed disclosing genomic variants that confer risk for diseases with well‐established effective medical interventions (i.e., medically actionable results) (Green et al, 2013; Kalia et al, 2017). However, no such formal guidance exists for the research setting, despite a growing consensus to report results that may impact clinical care (Botkin, Mancher, Busta, & Downey, 2018; Knoppers, Zawati, & Senecal, 2015; Saelaert, Mertes, Moerenhout, De Baere, & Devisch, 2020). Furthermore, as more research groups push to sequence larger and more inclusive cohorts (Ilori et al, 2020; Mapes et al, 2020; Van Hout et al, 2020), there is a growing need for guidance on how to accurately and efficiently identify and report clinically relevant findings to research participants.…”
Section: Introductionmentioning
confidence: 99%