CDC: Interim guidance for use of 23-valent pneumococcal polysaccharide vaccine during novel influenza A (H1N1) outbreak

Wednesday, June 10, 2009

CDC: Interim guidance for use of 23-valent pneumococcal polysaccharide vaccine during novel influenza A (H1N1) outbreak

Objective

To provide interim guidance on which groups should be vaccinated with the 23-valent pneumococcal polysaccharide vaccine (PPSV23) to prevent pneumococcal infections during the outbreak of novel influenza A(H1N1).



Background

Influenza predisposes individuals to bacterial community-acquired pneumonia. During the 20th century influenza pandemics, secondary bacterial pneumonia was an important cause of illness and death and Streptococcus pneumoniae (pneumococcus) was reported as the most common etiology. Severe pneumococcal pneumonia associated with inter-pandemic influenza also has been reported, and S. pneumoniae remains a leading cause of vaccine-preventable illness and death in the United States. The current novel influenza A (H1N1) outbreak is evolving rapidly, and CDC continues to compile key information regarding risk of influenza, severity of illness and attack rate of secondary bacterial pneumonia among influenza patients. At this time, however, the role of pneumococcal infections among severe cases of novel influenza A (H1N1), such as those requiring hospitalization, is unclear.

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