"Patient Participation" 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.
Patient involvement in the decision-making process in matters pertaining to health.
Descriptor ID |
D010358
|
MeSH Number(s) |
F01.100.150.750.500.620 F01.145.488.887.500.620 N02.421.143.262.300 N03.540.245.360.300 N05.300.150.800.500.620
|
Concept/Terms |
Patient Participation Rates- Patient Participation Rates
- Participation Rate, Patient
- Participation Rates, Patient
- Patient Participation Rate
|
Below are MeSH descriptors whose meaning is more general than "Patient Participation".
Below are MeSH descriptors whose meaning is more specific than "Patient Participation".
This graph shows the total number of publications written about "Patient Participation" by people in this website by year, and whether "Patient Participation" 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 |
---|
2004 | 0 | 2 | 2 |
2006 | 1 | 0 | 1 |
2007 | 2 | 1 | 3 |
2008 | 0 | 1 | 1 |
2009 | 0 | 1 | 1 |
2011 | 0 | 2 | 2 |
2012 | 2 | 0 | 2 |
2014 | 1 | 1 | 2 |
2015 | 1 | 0 | 1 |
2016 | 0 | 2 | 2 |
2017 | 4 | 0 | 4 |
2018 | 0 | 1 | 1 |
2019 | 5 | 1 | 6 |
2020 | 3 | 1 | 4 |
2021 | 0 | 1 | 1 |
2024 | 1 | 0 | 1 |
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Below are the most recent publications written about "Patient Participation" by people in Profiles.
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Patient Perspectives on a Decision Aid for Systemic Lupus Erythematosus: Insights and Future Considerations. J Rheumatol. 2024 Aug 01; 51(8):798-803.
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Leveraging patient-reported outcomes (PROs) in patients with pancreatic cancer: The Pancreatic Cancer Action Network (PanCAN) online patient registry experience. Cancer Med. 2021 10; 10(20):7152-7161.
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Treatment Decision Making and Financial Toxicity in Women With Metastatic Breast Cancer. Clin Breast Cancer. 2021 02; 21(1):37-46.
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A Pilot Study Determining Comprehension and the Acceptability of a Cancer Research Study Website for Cancer Patients and Caregivers. J Cancer Educ. 2020 06; 35(3):589-598.
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Importance of quality-of-life priorities and preferences surrounding treatment decision making in patients with cancer and oncology clinicians. Cancer. 2020 08 01; 126(15):3534-3541.
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Lupus patient decisions about clinical trial participation: a qualitative evaluation of perceptions, facilitators and barriers. Lupus Sci Med. 2020; 7(1):e000360.
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Neurochemical supplementation in patients with depressed levels of participation after brain tumor surgery: Rationale and preliminary results. J Clin Neurosci. 2020 Jan; 71:93-96.
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Strategies for Developing and Sustaining Patient and Community Advisory Groups: Lessons from the State Networks of Colorado Ambulatory Practices and Partners (SNOCAP) Consortium of Practice-Based Research Networks. J Am Board Fam Med. 2019 Sep-Oct; 32(5):663-673.
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Narratives and Stories: Novel Approaches to Improving Patient-Facing Information Resources and Patient Engagement. Stud Health Technol Inform. 2019 Aug 09; 265:175-180.
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The Influence of Patient Identification and Narrative Transportation on Intentions to Participate in Cancer Research. J Cancer Educ. 2019 Aug; 34(4):725-734.