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Pneumococcal Vaccine Adds More Protection
(February 25, 2010) - The Food and Drug Administration (FDA) has given the OK to a stronger, more powerful vaccine for pneumococcal disease. (Read about "Immunizations") It almost doubles the number of bacteria (Read about "Microorganisms") targeted by the vaccine. Prevnar 13, is a pneumococcal 13-valent conjugate vaccine for infants and young children ages 6 weeks through 5 years. Prevnar 13 will be the successor to Prevnar, the pneumococcal 7-valent conjugate vaccine licensed by the FDA in 2000 to prevent invasive pneumococcal disease (IPD) and otitis media. (Read about "Otitis Media") The new vaccine extends the protection to six additional types of the disease causing bacteria.
Prevnar 13 is approved for the prevention of invasive disease caused by 13 different serotypes of the bacterium Streptococcus pneumoniae. It also is approved for the prevention of otitis media caused by the seven serotypes shared with Prevnar. The bacterium can cause infections of the blood, middle ear, and the covering of the brain and spinal cord, as well as pneumonia. (Read about "Encephalitis & Meningitis" "Pneumonia")
"Although the rates of invasive pneumococcal disease have declined dramatically, there are still children in the United States who are suffering with this serious illness," said Karen Midthun, M.D., acting director of the FDA's Center for Biologics Evaluation and Research. "The availability of Prevnar 13 will help prevent pneumococcal disease caused by the six additional serotypes."
The seven Streptococcus pneumoniae serotypes against which Prevnar is directed accounted for about 80 percent of IPD in young children in North America at the time that the vaccine was licensed. With the use of Prevnar, by 2007 the overall rate of IPD caused by these seven serotypes in children less than 5 years old was reduced by 99 percent. However, at that time, it was also shown that of the remaining invasive pneumococcal disease in this age group, 62 percent are caused by the six additional serotypes that will be included in Prevnar 13.
The vaccine is administered in a four-dose schedule given at 2, 4, 6 and 12-15 months of age.
Note: Statements and conclusions of study authors that are published here are solely those of the study authors and do not necessarily reflect this hospital's policy or position. This hospital makes no representation or warranty as to their accuracy or reliability.
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By printing and/or reading this article, you agree that you accept all terms and conditions of use, as specified online.