Subacute Sclerosing Panencephalitis: A Clinical, Radiological, and Outcome Study of 144 Cases

Jerry A George1, Venugopalan Y Vishnu1, Roopa Rajan1

  • 1Department of Neurology, All India Institute of Medical Sciences, New Delhi, India.

Abstract

Insights

Subacute sclerosing panencephalitis (SSPE) has a poor prognosis, with high mortality increasing over time. While short-term outcomes show some stabilization or improvement, long-term prognosis remains unfavorable for SSPE patients.

Area of Science:

  • Neurology
  • Infectious Diseases
  • Virology

Background:

  • Subacute sclerosing panencephalitis (SSPE) is a rare, progressive neurological disorder caused by persistent measles virus infection.
  • Literature primarily consists of small case series, limiting comprehensive understanding of SSPE's clinical spectrum and outcomes.

Purpose of the Study:

  • To delineate the clinical spectrum, radiological findings, and outcomes of SSPE patients.
  • To identify prognostic factors and compare childhood-onset versus late-onset SSPE.

Main Methods:

  • An observational study involving 144 SSPE patients (Dyken's criteria) between 2015-2022.
  • Data collection included clinical presentation, radiological features, functional outcomes (modified Rankin Scale), and follow-up duration.

Main Results:

  • Overall good outcome (mRS ≤3) was observed in 23.3% of patients, with 48% mortality.
  • Short-term follow-up showed stabilization in 31.3%, improvement in 28.1%, and worsening in 40.6%.
  • Good outcomes decreased with longer follow-up; late-onset SSPE exhibited distinct clinical and radiological features and higher mortality.

Conclusions:

  • Significant differences exist between childhood- and late-onset SSPE presentations.
  • The overall prognosis for SSPE is poor, with mortality increasing over extended follow-up periods.
  • Short-term outcomes were more favorable, suggesting potential for interventions; further research on immunomodulators is warranted.

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