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PCV13 halves invasive pneumococcal disease incidence, but chronically ill still at risk

The introduction of the 13-valent pneumococcal conjugate vaccine has led to a significant decrease in the incidence of invasive pneumococcal disease in the general pediatric population but with a trend toward increasing incidence, particularly of nonvaccine serotypes, among children with comorbidities.

A study of Massachusetts public health surveillance data from before and after the introduction of the 13-valent vaccine (PCV13) showed a 49% decrease (168 vs. 85) in the absolute number of invasive pneumococcal disease cases in children aged under 5 years but a 17% increase in the proportion of cases in children with comorbidities such as chronic lung disease, malignancy, or immunosuppressive therapy. These changes are not considered statistically significant.

Dr. Pui-Ying Iroh Tam

"Routine vaccination with PCV13 may not be sufficient to reduce the risk of invasive disease in patients with comorbidity, and administering 23-valent pneumococcal polysaccharide vaccine to all children with comorbidity at the earliest acceptable age should be considered," wrote Dr. Pui-Ying Iroh Tam of the University of Minnesota Children’s Hospital, Minneapolis, and colleagues.

The prevalence of vaccine serotypes declined significantly (18%) in the first 2 years after introduction of PCV13, although serotype 19A remained the most common serotype even after the introduction of the vaccine, despite a significant decline in its prevalence, as reported online in the July 7 edition of Pediatrics (Pediatrics 2014 July 7 [doi: 10.1542/peds.2014-0473]).

The study was funded by the National Institutes of Health. One author received investigator-initiated grants from Pfizer for the study, while another author declared honoraria and grants from various pharmaceutical companies.

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The introduction of the 13-valent pneumococcal conjugate vaccine has led to a significant decrease in the incidence of invasive pneumococcal disease in the general pediatric population but with a trend toward increasing incidence, particularly of nonvaccine serotypes, among children with comorbidities.

A study of Massachusetts public health surveillance data from before and after the introduction of the 13-valent vaccine (PCV13) showed a 49% decrease (168 vs. 85) in the absolute number of invasive pneumococcal disease cases in children aged under 5 years but a 17% increase in the proportion of cases in children with comorbidities such as chronic lung disease, malignancy, or immunosuppressive therapy. These changes are not considered statistically significant.

Dr. Pui-Ying Iroh Tam

"Routine vaccination with PCV13 may not be sufficient to reduce the risk of invasive disease in patients with comorbidity, and administering 23-valent pneumococcal polysaccharide vaccine to all children with comorbidity at the earliest acceptable age should be considered," wrote Dr. Pui-Ying Iroh Tam of the University of Minnesota Children’s Hospital, Minneapolis, and colleagues.

The prevalence of vaccine serotypes declined significantly (18%) in the first 2 years after introduction of PCV13, although serotype 19A remained the most common serotype even after the introduction of the vaccine, despite a significant decline in its prevalence, as reported online in the July 7 edition of Pediatrics (Pediatrics 2014 July 7 [doi: 10.1542/peds.2014-0473]).

The study was funded by the National Institutes of Health. One author received investigator-initiated grants from Pfizer for the study, while another author declared honoraria and grants from various pharmaceutical companies.

The introduction of the 13-valent pneumococcal conjugate vaccine has led to a significant decrease in the incidence of invasive pneumococcal disease in the general pediatric population but with a trend toward increasing incidence, particularly of nonvaccine serotypes, among children with comorbidities.

A study of Massachusetts public health surveillance data from before and after the introduction of the 13-valent vaccine (PCV13) showed a 49% decrease (168 vs. 85) in the absolute number of invasive pneumococcal disease cases in children aged under 5 years but a 17% increase in the proportion of cases in children with comorbidities such as chronic lung disease, malignancy, or immunosuppressive therapy. These changes are not considered statistically significant.

Dr. Pui-Ying Iroh Tam

"Routine vaccination with PCV13 may not be sufficient to reduce the risk of invasive disease in patients with comorbidity, and administering 23-valent pneumococcal polysaccharide vaccine to all children with comorbidity at the earliest acceptable age should be considered," wrote Dr. Pui-Ying Iroh Tam of the University of Minnesota Children’s Hospital, Minneapolis, and colleagues.

The prevalence of vaccine serotypes declined significantly (18%) in the first 2 years after introduction of PCV13, although serotype 19A remained the most common serotype even after the introduction of the vaccine, despite a significant decline in its prevalence, as reported online in the July 7 edition of Pediatrics (Pediatrics 2014 July 7 [doi: 10.1542/peds.2014-0473]).

The study was funded by the National Institutes of Health. One author received investigator-initiated grants from Pfizer for the study, while another author declared honoraria and grants from various pharmaceutical companies.

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PCV13 halves invasive pneumococcal disease incidence, but chronically ill still at risk
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PCV13 halves invasive pneumococcal disease incidence, but chronically ill still at risk
Legacy Keywords
pneumococcal conjugate vaccine, pneumococcal disease, PCV13,
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pneumococcal conjugate vaccine, pneumococcal disease, PCV13,
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Major finding: The introduction of the 13-valent pneumococcal conjugate vaccine has led to a significant 49% decrease in the absolute number of invasive pneumococcal disease cases in children under 5 years, but with a trend toward increasing incidence, particularly of non-vaccine serotypes, among children with comorbidities.

Data source: Observational study using Massachusetts public health surveillance data from before and after the introduction of the 13-valent pneumococcal conjugate vaccine.

Disclosures: The study was funded by the National Institutes of Health. One author received investigator-initiated grants from Pfizer for the study, while another author declared honoraria and grants from pharmaceutical companies.