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Myalgic encephalomyelitis / chronic fatigue syndrome

Last updated: August 11, 2025

Summarytoggle arrow icon

Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a multisystem condition characterized by severe fatigue that is not relieved by rest, postexertional malaise, and unrefreshing sleep. The cause is not completely understood, but possible factors include genetic predisposition, history of infections, and immune abnormalities. The diagnosis is based on clinical features and confirmed using diagnostic criteria. Other causes of fatigue and malaise should be excluded based on clinical evaluation and/or diagnostic testing. There is currently no curative treatment. Management is focused on alleviating symptoms (e.g., improving quality of sleep), educating patients on energy management, and providing supportive care. In most patients, symptoms improve with management, but complete resolution is rare.

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Epidemiologytoggle arrow icon

Epidemiological data refers to the US, unless otherwise specified.

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Etiologytoggle arrow icon

The etiology of ME/CFS is not completely understood. Factors possibly involved include the following:

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Clinical featurestoggle arrow icon

Clinical features of ME/CFS are typically exacerbated by physical activity or stress. [15]

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Diagnosistoggle arrow icon

Approach [15][16]

A thorough clinical evaluation is crucial, as other potentially treatable causes of fatigue and malaise may manifest similarly to ME/CFS. [15][16]

2015 Institute of Medicine diagnostic criteria for CFS [2][17]

Approx. 50% of patients with postacute COVID-19 syndrome meet the diagnostic criteria for ME/CFS. [15]

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Differential diagnosestoggle arrow icon

The differential diagnoses listed here are not exhaustive.

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Managementtoggle arrow icon

General principles [15]

  • There is currently no curative treatment.
  • Therapy focuses on symptom management and supportive care to maximize quality of life.
  • Educate patients on self-management strategies.
  • Identify and treat comorbid conditions (e.g., fibromyalgia, mood disorders, irritable bowel syndrome).
  • Consider referral to a specialist ME/CFS clinic for patients with severe or complex features. [15]

Approach to exercise should be carefully planned based on the patient's symptoms and energy limits to avoid postexertional malaise and sustained functional deterioration. [15][16]

Patient education [15][16]

  • Self-management strategies (e.g., activity pacing)
    • Goal: to balance periods of activity and rest to avoid postexertional malaise and reduce the risk of deterioration
    • Patient instructions
      • Determine an individual activity baseline (i.e., physical, cognitive, emotional, and social) that minimizes symptoms.
      • Avoid exceeding the activity baseline.
      • Schedule rest periods throughout the day (e.g., before challenging activities).
      • Consider using activity diaries and/or tracking devices (e.g., mobile heart-rate monitor) to monitor activity and symptoms.
  • Response to symptom deterioration: Instruct patients to decrease energy expenditure until symptoms return to baseline.
  • Lifestyle changes, e.g.:

Symptom deterioration is often triggered by infections and/or exertion and can occur despite good energy management.

Symptom management and supportive care [15]

Provide individualized care and consider specialist referral for patients with complex or severe features.

Intolerance to pharmacological treatment is common in patients with ME/CFS. [15]

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Prognosistoggle arrow icon

  • Long-term prognosis of ME/CFS is variable.
  • In most patients, symptoms improve with management, but complete resolution of symptoms is rare. [16]
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