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Public support for healthcare-mediated disclosure of hereditary cancer risk information: Results from a population-based survey in Sweden.

Andreas AnderssonCarolina HawranekAnna ÖfverholmHans EhrencronaKalle GrillSenada HajdarevicBeatrice MelinEmma ThamBarbro Numan HellquistAnna Rosén
Published in: Hereditary cancer in clinical practice (2020)
In this study a majority of respondents wanted to be informed about a potential hereditary risk of CRC and preferred healthcare professionals to communicate this information. The two presented levels of CRC lifetime risk did not significantly affect the interest in being informed. Our data offer insights into the needs and preferences of the Swedish population, providing a rationale for developing complementary healthcare-assisted communication pathways to realise the full potential of targeted prevention of hereditary CRC.
Keyphrases
  • healthcare
  • health information
  • human health
  • clinical trial
  • cross sectional
  • electronic health record
  • big data
  • risk assessment
  • machine learning
  • climate change
  • data analysis