Burden of Disease in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS), 2025, Vester

Dolphin

Senior Member (Voting Rights)
Comment: unfortunately the information that is freely available is not very informative in terms of the substance of this piece.


Abstract only
Volume 28, Issue 6, Supplement 1S77July 2025

EE81 Burden of Disease in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS)​

Patricia Vester, M.Sc.<a>1</a> ∙ Stefanos Boudouroglou-Walter, M.Sc.<a>1</a> ∙ Jonas Schreyögg, Prof. Dr.<a>2</a> ∙ Chantal Wieting, B.Sc.<a>1</a> ∙ Christine Blome, PD Dr.<a>1</a>
Affiliations & Notes
1University Medical Center Hamburg-Eppendorf (UKE), Hamburg, Germany
2Hamburg Center for Health Economics (HCHE), Hamburg, Germany


Show Outline

ME/CFS is a chronic neurological disease with the hallmark symptom of post-exertional malaise (PEM) alongside other symptoms such as fatigue, cognitive impairment, and pain. Its etiology is still unknown; the diagnosis relies on international consensus criteria. As no curative therapy exists, treatment focuses on symptom management. The prevalence in the US is estimated at 0.42% of the adult population with women being affected three times as often as men. As many Post-COVID patients meet the ME/CFS diagnostic criteria, a rise in prevalence is expected. Besides the severe symptoms, ME/CFS can lead to negative economic consequences. Therefore, this review aims to answer the question: What is known about the burden of ME/CFS?
 
Back
Top Bottom