| Risk Factors
Subacute sclerosing panencephalitis (SSPE) is a condition that affects the brain and spine. It is a gradual break down of nerve cells from constant swelling.
When left untreated, SSPE almost always leads to death.
Central Nervous System
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SSPE is caused either by an altered form of the
virus or an abnormal immune response to measles. It occurs anywhere from 2-10 years after contracting measles.
SSPE is more common in male, and in those aged 5-15 years old. Other factors that may increase your chance of SSPE include:
- Measles infection in infancy
- Not being vaccinated against measles
- Arabs and Sephardic Jews have an incidence that is 6 times higher than Ashkenazi Jews.
- Caucasians have a 4-fold higher incidence than African Americans in the United States.
Symptoms of SSPE may include:
- Abnormal behavior
- Loss of intellectual abilities
- Memory loss
- Involuntary movements
- Inability to walk
- Speech impairment with poor understanding
- Difficulty swallowing
- Loss of consciousness
Your doctor will ask about your symptoms and medical history. A physical exam will be done.
Tests may include blood tests and an electrocardiogram
Imaging tests to evaluate bodily structures may include:
Talk with your doctor about the best treatment plan. Treatment options include:
With advanced disease, tube feedings and nursing care may be necessary.
Anticonvulsant medications can reduce some symptoms of SSPE. In addition, there is some evidence that certain medications may help stabilize the disease and/or delay its progression.
The best way to prevent SSPE is to get immunized to avoid contracting measles. The measles vaccine is generally given at 12-15 months of age and again at 4-6 or 11-12 years. If you have not been vaccinated, avoid contact with people who are infected with measles until all of their symptoms are gone.