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. 2011 Jan 25;2(1):e00309-10.
doi: 10.1128/mBio.00309-10.

Impact of pneumococcal conjugate vaccination of infants on pneumonia and influenza hospitalization and mortality in all age groups in the United States

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Impact of pneumococcal conjugate vaccination of infants on pneumonia and influenza hospitalization and mortality in all age groups in the United States

Lone Simonsen et al. mBio. .

Abstract

A seven-valent pneumococcal conjugate vaccine (PCV7) introduced in the United States in 2000 has been shown to reduce invasive pneumococcal disease (IPD) in both vaccinated children and adults through induction of herd immunity. We assessed the impact of infant immunization on pneumococcal pneumonia hospitalizations and mortality in all age groups using Health Care Utilization Project State Inpatient Databases (SID) for 1996 to 2006 from 10 states; SID contain 100% samples of ICD9-coded hospitalization data for the selected states. Compared to a 1996-1997 through 1998-1999 baseline, by the 2005-2006 season, both IPD and pneumococcal pneumonia hospitalizations and deaths had decreased substantially in all age groups, including a 47% (95% confidence interval [CI], 38 to 54%) reduction in nonbacteremic pneumococcal pneumonia (ICD9 code 481 with no codes indicating IPD) in infants <2 years old and a 54% reduction (CI, 53 to 56%) in adults ≥65 years of age. A model developed to calculate the total burden of pneumococcal pneumonia prevented by infant PCV7 vaccination in the United States from 2000 to 2006 estimated a reduction of 788,838 (CI, 695,406 to 875,476) hospitalizations for pneumococcal pneumonia. Ninety percent of the reduction in model-attributed pneumococcal pneumonia hospitalizations occurred through herd immunity among adults 18 years old and older; similar proportions were found in pneumococcal disease mortality prevented by the vaccine. In the first seasons after PCV introduction, when there were substantial state differences in coverage among <5-year-olds, states with greater coverage had significantly fewer influenza-associated pneumonia hospitalizations among children, suggesting that PCV7 use also reduces influenza-attributable pneumonia hospitalizations.

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Figures

FIG 1
FIG 1
Rate ratio versus season, comparing a three-season pre-PCV7 introduction baseline outcome rate to those of subsequent seasons for all 10 study states combined and for (A) children under 2 years of age and (B) adults ≥65 years old.
FIG 2
FIG 2
Representative plots of rates of all-cause pneumonia (ICD9 codes 480 to 486, grey) and model attributions for RSV-related pneumonia (green), pneumococcal pneumonia (red), and influenza virus-related pneumonia (light blue). Data shown are from New Jersey for (A) children under 2 years of age and (B) adults ≥65 years old; panel C shows the proportion of all-cause pneumonia attributed by our model to the pneumococcus.
FIG 3
FIG 3
Scatterplots of state hospitalization RRs (season/baseline) versus state PCV coverage for the 1999–2000 through the 2003–2004 seasons for (A) attributed influenza-related pneumonia among those <2 years old and (B) attributed influenza-related pneumonia among those ≥65 years old. The lines represent exponential fits to the data from each season, showing the trend. An asterisk next to the year in each panel indicates a significant trend.

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