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The Eradication of Rubella
Stanley A. Plotkin, MD;
Michael Katz, MD;
José F. Cordero, MD, MPH
JAMA. 1999;281:561-562.
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| Since this article does not have an abstract, we have provided the first 150 words of the full text and any section headings. |
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During 1963 to 1964, a pandemic of rubella swept across Europe and the United States, leaving in its wake at least 20,000 affected infants in this country alone.1 During the epidemic an expanded congenital rubella syndrome (CRS) was described, involving not only the classic triad of cataracts, cardiac abnormalities, and deafness, but also encephalitis, wasting, hepatitis, pneumonia, endocrinopathies, and other sequelae. This disaster supervened just after the first isolation of rubella virus in cell culture and stimulated efforts to develop a vaccine, which were successful by the end of the decade.
The initial strategy of vaccination of infants was only partly successful because transmission continued among adults.2 An alternative strategy focusing on vaccination of schoolgirls failed to provide sufficient population immunity.3 Consequently, current policy in the United States, and in most European countries,4 is to vaccinate all infants . . . [Full Text of this Article]
Author Affiliations: Pasteur Mérieux Connaught, Swiftwater, Pa, and Lyon, France (Dr Plotkin); the Department of Pediatrics, School of Medicine, University of Pennsylvania, Philadelphia (Dr Plotkin); the March of Dimes, Birth Defects Foundation, White Plains, NY (Dr Katz); and the Centers for Disease Control and Prevention, National Immunization Program, Atlanta, Ga (Dr Cordero).
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