Subacute sclerosing panencephalitis natural history: Difference between revisions
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{{Subacute sclerosing panencephalitis}} | {{Subacute sclerosing panencephalitis}} | ||
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==Complications== | ==Complications== | ||
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[[Category:Viral diseases]] | [[Category:Viral diseases]] | ||
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Latest revision as of 18:53, 18 September 2017
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Subacute sclerosing panencephalitis Microchapters |
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Differentiating Subacute sclerosing panencephalitis from other Diseases |
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Diagnosis |
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Treatment |
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Subacute sclerosing panencephalitis natural history On the Web |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Complications
Prior to death, there may be:
Prognosis
- Death usually occurs within 3 years.
- If the diagnosis is made during stage 1 of the SSPE infection then it is possible to cure the disease. However, once SSPE progresses to stage 2 then it is universally fatal in all occurrences.
- The standard rate of decline spans anywhere between 1–3 years after the onset of the infection.
- The progression of each stage is unique to the sufferer and cannot be predicted although the pattern or symptoms/signs can be.
- Although the prognosis is bleak for SSPE past stage 1, it should be noted that there is a 5% remission rate — this may be either a full remission or an improvement in condition giving a longer progression period or at least a longer period with the less severe symptoms.
- Regardless of the stage that the infection is at, treatment with inosine pranobex combined with interferon can give up to a 50% remission/improvement rate.