Journal article
Health, wellbeing, and prognosis of Australian adolescents with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS): A case-controlled follow-up study
EK Josev, RC Cole, A Scheinberg, K Rowe, L Lubitz, SJ Knight
Journal of Clinical Medicine | MDPI | Published : 2021
DOI: 10.3390/jcm10163603
Abstract
Background: The purpose of this study was to follow-up an Australian cohort of adolescents newly-diagnosed with ME/CFS at a tertiary paediatric ME/CFS clinic and healthy controls over a mean period of two years (range 1–5 years) from diagnosis. Objectives were to (a) examine changes over time in health and psychological wellbeing, (b) track ME/CFS symptomatology and fulfillment of paediatric ME/CFS diagnostic criteria over time, and (c) determine baseline predictors of ME/CFS criteria fulfilment at follow-up. Methods: 34 participants aged 13–18 years (25 ME/CFS, 23 controls) completed standardised questionnaires at diagnosis (baseline) and follow-up assessing fatigue, sleep quality and hygie..
View full abstractGrants
Awarded by Judith Jane Mason and Harold Stannett Williams Memorial Foundation
Funding Acknowledgements
This research was supported by ME Research UK (SCIO charity number SCO36942, http://www.meresearch.org.uk/, accessed on 9 August 2021). The Judith Jane Mason and Harold Stannett Williams Memorial Foundation (Mason Foundation, ABN96140017725), the Murdoch Children's Research Institute, the Royal Children's Hospital, and the Victorian Government's Operational Infrastructure Support Program. The APC was funded by the Mason Foundation.