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Coping With the Spectre of Cardiac Mortality

The Role of Genetic Testing

Bibliographic Data

ID5659504
AuthorsStefan Timmerman (0000-0002-4751-2893, Department of Sociology UCLA Los Angeles California USA), Will Schupmann (0000-0002-5937-8118, Department of Sociology UCLA Los Angeles California USA), Ruth Kaufman (0000-0001-8535-9730), Rebecca Kaufman (Department of Sociology UCLA Los Angeles California USA), A E Raz (0000-0001-6268-0409, Ben-Gurion University of the Negev), Aviad Raz (0000-0001-9794-5470, Department of Sociology Ben Gurion University Beersheba Israel)
Year2025
Volume47
Issue8
Pagese70107-e70107
Publication date2025-11-01
Peer ReviewedYes
Open AccessYes
TypeARTICLE
VenueSociology of Health & Illness (JOURNAL)
Journal identifiersISSN: 0141-9889 • E-ISSN: 1467-9566
PublisherWiley (PUBLISHER • GB)
DOI10.1111/1467-9566.70107
PMID41089045
OpenAlexW4415243616
LanguageEN
References cited45

A diagnosis of cardiovascular disease increases death awareness by raising the possibility of sudden death. Engaging sociological literature on patient experiences with terror management theory, we examine how patients diagnosed with cardiac disease turn to online communities to interpret the possibility of cardiac death. Drawing on 33 semi-structured interviews with individuals diagnosed with a cardiac condition and who have undergone genetic testing as part of its diagnosis or treatment, we find that respondents turn to biomedicine in the hope that medical interventions will prevent or postpone death. Respondents were motivated by anxiety to opt in genetic testing even if the results were unlikely to change diagnosis, treatment or prognosis. Genetic testing reinforced a biomedical world view where medical care can optimise the quality of life through prevention, including for their relatives. Their biological kin, however, refused to undergo genetic testing in absence of a cardiac diagnosis

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Highly citedNo

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