Evaluating the ability of patient reported outcome measures to represent the functional limitation of people living with myalgic encephalomyelitis/chronic fatigue syndrome
Author:
Affiliation:
1. School of Health and Social Wellbeing, UWE Bristol, Bristol, UK
2. Department of Psychology, Newman University, Birmingham, UK
3. Bristol M.E. Service, North Bristol NHS Trust, Bristol, UK
Publisher
Informa UK Limited
Subject
Behavioral Neuroscience,Public Health, Environmental and Occupational Health,Medicine (miscellaneous)
Link
https://www.tandfonline.com/doi/pdf/10.1080/21641846.2023.2175579
Reference27 articles.
1. Action for ME. Guide to welfare benefits and other support [Internet]. 2016–2022 [cited 2022 Aug 12]. Available from: https://www.actionforme.org.uk/uploads/pdfs/guide-to-benefits-factsheet-april-2016.pdf.
2. National Institute for Health and Care Excellence. Myalgic encephalomyelitis (or encephalopathy)/chronic fatigue syndrome: diagnosis and management. 2021.
3. Systematic review and meta-analysis of cognitive impairment in myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS)
4. Adaptation and validation of the Charlson Index for Read/OXMIS coded databases
5. A review and meta-synthesis of qualitative studies on Myalgic Encephalomyelitis/chronic fatigue syndrome
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