"Informed Consent" 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.
Voluntary authorization, by a patient or research subject, with full comprehension of the risks involved, for diagnostic or investigative procedures, and for medical and surgical treatment.
| Descriptor ID |
D007258
|
| MeSH Number(s) |
I01.880.604.473.650.718 I01.880.604.583.427 N03.706.437.650.312 N03.706.535.489
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Informed Consent".
Below are MeSH descriptors whose meaning is more specific than "Informed Consent".
This graph shows the total number of publications written about "Informed Consent" by people in this website by year, and whether "Informed Consent" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1998 | 0 | 1 | 1 |
| 2002 | 0 | 1 | 1 |
| 2003 | 0 | 1 | 1 |
| 2005 | 0 | 1 | 1 |
| 2007 | 0 | 1 | 1 |
| 2008 | 1 | 0 | 1 |
| 2009 | 0 | 1 | 1 |
| 2010 | 0 | 1 | 1 |
| 2011 | 0 | 1 | 1 |
| 2012 | 0 | 2 | 2 |
| 2013 | 1 | 1 | 2 |
| 2014 | 0 | 1 | 1 |
| 2016 | 1 | 0 | 1 |
| 2019 | 0 | 1 | 1 |
| 2020 | 0 | 1 | 1 |
| 2021 | 1 | 0 | 1 |
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Below are the most recent publications written about "Informed Consent" by people in Profiles.
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Zelen design clinical trials: why, when, and how. Trials. 2021 Aug 17; 22(1):541.
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Integrating Personalized Medicine With Population Health Management: The Path Forward. JAMA. 2020 Aug 18; 324(7):631-632.
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Integrating stakeholder feedback in translational genomics research: an ethnographic analysis of a study protocol's evolution. Genet Med. 2020 06; 22(6):1094-1101.
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Conducting Clinical Research in Post-acute and Long-term Nursing Home Care Settings: Regulatory Challenges. J Am Med Dir Assoc. 2019 07; 20(7):798-803.
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Researching the Appropriateness of Care in the Complementary and Integrative Health Professions Part 5: Using Patient Records: Selection, Protection, and Abstraction. J Manipulative Physiol Ther. 2019 06; 42(5):327-334.
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Online Education and e-Consent for GeneScreen, a Preventive Genomic Screening Study. Public Health Genomics. 2017; 20(4):235-246.
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Public Attitudes toward Consent and Data Sharing in Biobank Research: A Large Multi-site Experimental Survey in the US. Am J Hum Genet. 2017 Mar 02; 100(3):414-427.
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Who Gets to Decide? Radiology. 2016 Feb; 278(2):635-6.
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Seeking worldwide professional consensus on the principles of end-of-life care for the critically ill. The Consensus for Worldwide End-of-Life Practice for Patients in Intensive Care Units (WELPICUS) study. Am J Respir Crit Care Med. 2014 Oct 15; 190(8):855-66.
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Practical barriers and ethical challenges in genetic data sharing. Int J Environ Res Public Health. 2014 Aug 15; 11(8):8383-98.