Literature DB >> 28387784

Subacute Sclerosing Panencephalitis: The Devastating Measles Complication That Might Be More Common Than Previously Estimated.

Kristen A Wendorf1, Kathleen Winter1, Jennifer Zipprich1, Rob Schechter1, Jill K Hacker2, Chris Preas2, James D Cherry3, Carol Glaser4, Kathleen Harriman1.   

Abstract

BACKGROUND: Subacute sclerosing panencephalitis (SSPE) is a fatal complication of measles. We reviewed California cases from 1998-2015 to understand risk factors for SPPE and estimate incidence.
METHODS: SSPE cases had clinically compatible symptoms and measles antibody detection in cerebrospinal fluid (CSF) or medical record documentation of SSPE. Cases were identified though a state death certificate search, Centers for Disease Control and Prevention reports, or investigations for undiagnosed neurologic disease. Measles detection in CSF was performed by serology at the California Department of Public Health or at clinical laboratories.
RESULTS: Seventeen SSPE cases were identified. Males outnumbered females 2.4:1. Twelve (71%) cases had a history of measles-like illness; all 12 had illness prior to 15 months of age. Eight (67%) children were exposed to measles in California. SSPE was diagnosed at a median age of 12 years (3-35 years), with a latency period of 9.5 years (2.5-34 years). Among measles cases reported to CDPH during 1988-1991, the incidence of SSPE was 1:1367 for children <5 years, and 1:609 for children <12 months at time of measles disease.
CONCLUSIONS: SSPE cases in California occurred at a high rate among unvaccinated children, particularly those infected during infancy. Protection of unvaccinated infants requires avoidance of travel to endemic areas, or early vaccination prior to travel at age 6-11 months. Clinicians should be aware of SSPE in patients with compatible symptoms, even in older patients with no specific history of measles infection. SSPE demonstrates the high human cost of "natural" measles immunity. Published by Oxford University Press for the Infectious Diseases Society of America 2017. This work is written by (a) US Government employee(s) and is in the public domain in the US.

Entities:  

Keywords:  SSPE; measles; subacute sclerosing panencephalitis

Mesh:

Substances:

Year:  2017        PMID: 28387784     DOI: 10.1093/cid/cix302

Source DB:  PubMed          Journal:  Clin Infect Dis        ISSN: 1058-4838            Impact factor:   9.079


  27 in total

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Review 6.  Measles virus persistence and its consequences.

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Review 7.  Measles Vaccine.

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Journal:  Viral Immunol       Date:  2017-12-19       Impact factor: 2.257

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9.  Genetic characterization of measles virus genotype D6 subacute sclerosing panencephalitis case, Alberta, Canada.

Authors:  K Pabbaraju; K Fonseca; S Wong; M W Koch; J T Joseph; G A Tipples; R Tellier
Journal:  J Neurovirol       Date:  2018-10-05       Impact factor: 2.643

10.  Adult-Onset Subacute Sclerosing Panencephalitis With a 30-Year Latent Period.

Authors:  Brandon B Holmes; Jessamyn Conell-Price; Collin J Kreple; Davin Ashraf; John Betjemann; Nicole Rosendale
Journal:  Neurohospitalist       Date:  2019-08-18
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