"Duty to Recontact" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
The ethical and/or legal obligation of a health provider or researcher to communicate with a former patient or research subject about advances in research relevant to a treatment or to a genetic or other diagnostic test provided earlier, or about proposed new uses of blood or tissue samples taken in the past for another purpose.
Descriptor ID |
D033002
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MeSH Number(s) |
F01.829.401.650.505 I01.880.604.583.166 N03.706.535.247
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Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Duty to Recontact".
Below are MeSH descriptors whose meaning is more specific than "Duty to Recontact".
This graph shows the total number of publications written about "Duty to Recontact" by people in this website by year, and whether "Duty to Recontact" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2018 | 0 | 1 | 1 |
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Below are the most recent publications written about "Duty to Recontact" by people in Profiles.
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What do cancer genetic providers want us to know about variant reclassification and recontact that we are not asking? A thematic analysis of open-ended survey responses. Cancer. 2024 Nov 15; 130(22):3926-3934.
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Practices and Views of US Oncologists and Genetic Counselors Regarding Patient Recontact After Variant Reclassification: Results of a Nationwide Survey. JCO Precis Oncol. 2023 06; 7:e2300079.
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Continued access to investigational brain implants. Nat Rev Neurosci. 2018 06; 19(6):317-318.