Prognosis
Symptoms of myasthenia gravis usually progress to maximum severity within 3 years. After 3 years, patients usually stabilize or improve. Infants with transient neonatal MG may develop acute respiratory failure within a few weeks after birth.
Advances in medical care have reduced the mortality rate from respiratory failure in MG patients to approximately 3%. Patients over the age of 40, those with a short history of severe disease, and those with thymoma have a worse prognosis.
Prevention
Myasthenia gravis cannot be prevented, but avoiding the following triggers may help patients prevent exacerbations:
- Emotional stress
- Exposure to extreme temperatures
- Fever
- Illness (e.g., respiratory infection, pneumonia, tooth abscess)
- Low levels of potassium in the blood (hypokalemia; caused by diuretics, frequent vomiting)
- Medications (e.g., muscle relaxants, anticonvulsants, certain antibiotics)
- Overexertion