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Estimating the Risk of Subacute Sclerosing Panencephalitis After Measles in Okinawa, Japan, 1986-2007
Yusuke Kobayashi1,2, Takuri Takahashi1, Kyomi Hirayasu3
1Department of Infectious Disease Surveillance, National Institute of Infectious Diseases, Japan Institute for Health Security, Tokyo, Japan.
Background:
Subacute sclerosing panencephalitis (SSPE) is a rare, fatal, late complication of measles that develops years after infection, particularly following measles in early childhood. In Japan, measles incidence has declined markedly after improved vaccination coverage and verification elimination; however, recent SSPE epidemiology remains poorly characterized.
Methods:
SSPE cases were identified from the Intractable Disease Treatment Research Project, the Research Project on the Treatment of Children with Specified Chronic Diseases, and Okinawa-specific publications. Measles-related outpatient visits (1986-2007) were estimated by public health center jurisdiction using annual pediatric sentinel surveillance reports and outpatient visit volumes from the Static Survey of Medical Institutions. Ratio estimation with finite population correction was applied.
Results:
Seventeen SSPE cases were identified, 71% in males. SSPE onset occurred during 1994-2009, at a mean age of 8.1 years. The year of measles infection was known for 14 cases, most frequently 1990. For risk estimation, 16 infections occurring during 1986-2007 were included. SSPE risk was estimated as one per 3944 estimated measles-related outpatient visits (95% CI: 1054-6995). In 1990, SSPE risk was one per 1828 outpatient visits (95% CI: 836-2820). Among infants aged < 1 year, SSPE risk was one per 910 outpatient visits (95% CI: 416-1403).
Conclusions:
Estimating denominators for medically attended measles cases from sentinel surveillance enabled quantification of SSPE risk during historical outbreaks in Okinawa. The higher risk during infancy emphasizes the long-term consequences of measles transmission and the need to maintain high measles vaccination coverage.
Insights
Subacute sclerosing panencephalitis (SSPE) risk is higher in infants following measles infection. Maintaining high measles vaccination coverage is crucial to prevent this rare but fatal neurological complication.
Area of Science:
- Neurology
- Infectious Diseases
- Public Health
Background:
- Subacute sclerosing panencephalitis (SSPE) is a rare, fatal neurological complication of measles, particularly following childhood infection.
- While measles incidence has decreased due to vaccination, recent SSPE epidemiology requires further characterization.
Purpose of the Study:
- To quantify the risk of SSPE following measles infection in Okinawa.
- To assess the impact of measles infection timing on SSPE risk.
Main Methods:
- Identified SSPE cases from national research projects and local publications.
- Estimated measles-related outpatient visits using pediatric sentinel surveillance and medical institution data (1986-2007).
- Applied ratio estimation with finite population correction to calculate SSPE risk.
Main Results:
- Seventeen SSPE cases were identified, predominantly in males, with onset between 1994-2009.
- The estimated overall SSPE risk was 1 per 3944 measles-related outpatient visits.
- Infants under one year old faced a significantly higher risk (1 per 910 outpatient visits).
Conclusions:
- Quantifying SSPE risk is feasible using sentinel surveillance data for medically attended measles cases.
- The elevated risk in infants highlights the severe long-term consequences of measles.
- Sustaining high measles vaccination coverage is essential to mitigate SSPE incidence.
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