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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.
Background And Objectives:
Subacute sclerosing panencephalitis (SSPE) is a progressive encephalitis caused by persistent measles virus infection and is mostly described as small case series in literature. We aimed to describe the clinical spectrum, radiological features, outcomes, and prognostic factors in patients with SSPE and provide a comparison of childhood- versus late-onset disease.
Methods:
An observational study was conducted in a tertiary hospital in India, documenting the spectrum and functional outcome [modified Rankin Scale (mRS)] of patients with SSPE.
Results:
We enrolled 144 patients (35 prospective and 109 retrospective, mean age: 16.7 ± 5.0 years, 79.9% males) of SSPE (Dyken's criteria), who presented between 2015 and 2022. Overall, we found good outcome (mRS ≤3) in 23.3% of cases and mortality in 48% (follow-up: n = 73/144, range 6-95 months). Short-term follow-up (prospective group, 32/35) revealed stabilization (no improvement or worsening of mRS) in 31.3% of patients, improvement of mRS grade in 28.1% patients, and worsening in 40.6% of patients. Intrathecal interferon was prescribed in majority of these cases, and 65.6% (21/32) were compliant to therapy. Frequency of good outcome reduced with longer follow-up duration (34.4% when followed up to 11 months, 22.2% for a follow-up duration of 24-60 months, and 10% for duration longer than 60 months). The studied outcome predictors were not statistically significant. Late-onset cases were different from childhood-onset cases with respect to some clinical features [more focal deficits ( P = 0.043), less-frequent seizures ( P = 0.003)], radiological features [more frequent cortical lesions ( P = 0.44) and cerebral atrophy ( P = 0.52)], and mortality [late-onset cases: 55.2% vs. childhood-onset cases: 33.3% ( P = 0.08)].
Conclusion:
We found differences in the presentation of childhood- versus late-onset disease. Overall, the prognosis was not good, with increasing mortality observed with increasing duration of follow-up. Short-term outcomes were better. Future studies can look at the effect of immunomodulators on long-term outcomes in a larger sample size.
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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