Subacute sclerosing panencephalitis natural history: Difference between revisions
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{{Subacute sclerosing panencephalitis}} | {{Subacute sclerosing panencephalitis}} | ||
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{{CMG}} | {{CMG}} | ||
==Complications== | |||
Prior to death, there may be: | |||
*Behavior changes | |||
*[[Dementia (patient information)|Dementia]] | |||
*[[Stupor]] and [[coma]] | |||
*[[Seizures]] and subsequent injuries | |||
==Prognosis== | ==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 | *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. | |||
==References== | ==References== | ||
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{{WikiDoc Sources}} | {{WikiDoc Sources}} | ||
[[Category:Needs overview]] | |||
[[Category:Needs content]] | [[Category:Needs content]] | ||
[[Category:Disease]] | [[Category:Disease]] | ||
[[Category:Neurology]] | [[Category:Neurology]] | ||
[[Category:Neurological disorders]] | [[Category:Neurological disorders]] | ||
[[Category:Viral diseases]] | [[Category:Viral diseases]] | ||
[[Category:Inflammations]] | [[Category:Inflammations]] | ||
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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Subacute sclerosing panencephalitis natural history On the Web |
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Blogs on Subacute sclerosing panencephalitis natural history |
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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.