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Section 3. Summaries of Infectious Diseases
Measles
Clinical Manifestations
Etiology
Epidemiology
Diagnostic Tests
Treatment
Isolation of the Hospitalized Patient
Control Measures
CLINICAL MANIFESTATIONS: Measles is an acute disease characterized by fever, cough, coryza, conjunctivitis, an erythematous maculopapular rash, and pathognomonic enanthemas (Koplik spots). Complications such as otitis media, bronchopneumonia, laryngotracheobronchitis (croup), and diarrhea occur commonly in young children. Acute encephalitis, which often results in permanent brain damage, occurs in approximately 1 of every 1000 cases. Death, predominantly resulting from respiratory and neurologic complications, occurs in 1 to 3 of every 1000 cases reported in the United States. Case fatality rates are increased in children younger than 5 years of age and immunocompromised children, including children with leukemia, human immunodeficiency virus (HIV) infection, and severe malnutrition. Sometimes the characteristic rash does not develop in immunocompromised patients.
Subacute sclerosing panencephalitis (SSPE), a rare degenerative central nervous system disease characterized by behavioral and intellectual deterioration and seizures that develop years after the original infection, is a result of a persistent measles virus infection. Widespread measles immunization has led to the virtual disappearance of SSPE in the United States.
ETIOLOGY: Measles virus is an RNA virus with 1 serotype, classified as a member of the genus Morbillivirus in the Paramyxoviridae family.
EPIDEMIOLOGY: The only natural hosts of measles virus are humans. Measles is transmitted by direct contact with infectious droplets or, less commonly, by airborne spread. In temperate areas, the peak incidence of infection usually occurs during late winter and spring. In the prevaccine era, most cases of measles in the United States occurred in preschool and young school-aged children, and few people remained susceptible by age 20 years. The childhood and adolescent immunization program in the United States has resulted in a greater than 99% decrease . . . [Go to Full Text]
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This topic has been referenced by these articles:
- Chalmers, I.
(2002). Why We Need to Know Whether Prophylactic Antibiotics Can Reduce Measles-Related Morbidity. Pediatrics
109: 312-315
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(2001). Varicella Vaccine Question. Pediatrics
107: 612-612
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(2002). The Dummies' Guide to Risk-Benefit Analysis of Vaccines. Pediatrics
110: 193-193
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- Pelton, S. I.
(2004). The Decline in Invasive Pneumococcal Disease. Pediatrics
113: 617-618
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- Dayan, G. H., Ortega-Sanchez, I. R., LeBaron, C. W., Quinlisk, M. P., and the Iowa Measles Response Team,
(2005). The Cost of Containing One Case of Measles: The Economic Impact on the Public Health Infrastructure--Iowa, 2004. Pediatrics
116: e1-e4
[Abstract]
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- Perez, E. E., Bokszczanin, A., McDonald-McGinn, D., Zackai, E. H., Sullivan, K. E.
(2003). Safety of Live Viral Vaccines in Patients With Chromosome 22q11.2 Deletion Syndrome (DiGeorge Syndrome/Velocardiofacial Syndrome). Pediatrics
112: e325-325
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- Krugman, S., Giles, J. P., Jacobs, A. M., Friedman, H.
(1963). STUDIES WITH A FURTHER ATTENUATED LIVE MEASLES-VIRUS VACCINE. Pediatrics
31: 919-928
[Abstract]
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(2003). Response to Immunization With Measles, Tetanus, and Haemophilus influenzae Type b Vaccines in Children Who Have Human Immunodeficiency Virus Type 1 Infection and Are Treated With Highly Active Antiretroviral Therapy. Pediatrics
111: e641-644
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(2002). Prevalence of Anti-Gelatin IgE Antibodies in People With Anaphylaxis After Measles-Mumps-Rubella Vaccine in the United States. Pediatrics
110: e71-71
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(1963). POLIOMYELITIS FOLLOWING RECENT MEASLES. Pediatrics
31: 929-935
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(2001). No Evidence for A New Variant of Measles-Mumps-Rubella-Induced Autism. Pediatrics
108: e58-58
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(2000). Morbidity Among Human Immunodeficiency Virus-1-Infected and -Uninfected African Children. Pediatrics
106: 77e-77
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- Halsey, N. A., Hyman, S. L., the Conference Writing Panel,
(2001). Measles-Mumps-Rubella Vaccine and Autistic Spectrum Disorder: Report From the New Challenges in Childhood Immunizations Conference Convened in Oak Brook, Illinois, June 12-13, 2000. Pediatrics
107: 84e-84
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- Meissner, H. C., Strebel, P. M., Orenstein, W. A.
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- Leitch, R., Halsey, N., Hyman, S. L.
(2002). MMR--Separate Administration--Has It Been Done?. Pediatrics
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(2005). Live Attenuated Influenza Vaccine, Trivalent, Is Safe in Healthy Children 18 Months to 4 Years, 5 to 9 Years, and 10 to 18 Years of Age in a Community-Based, Nonrandomized, Open-Label Trial. Pediatrics
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- Bellamy, C.
(2004). International Pediatric Congress. Pediatrics
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- Miller, L. C., Comfort, K., Kelly, N.
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- Posfay-Barbe, K. M., Heininger, U., Aebi, C., Desgrandchamps, D., Vaudaux, B., Siegrist, C.-A.
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- Stiehm, E. R.
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- Virtanen, M., Peltola, H., Paunio, M., Heinonen, O. P.
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- Nilsson, A., De Milito, A., Engstrom, P., Nordin, M., Narita, M., Grillner, L., Chiodi, F., Bjork, O.
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