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Effectiveness of seven-valent pneumococcal conjugate vaccine against invasive pneumococcal disease: a matched
Cynthia G Whitney1, Tamar Pilishvili, Monica M Farley
1Division of Bacterial and Mycotic Diseases, National Center for Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA. cwhitney@cdc.gov
Insights
The seven-valent pneumococcal conjugate vaccine effectively prevents invasive pneumococcal disease in children, even with varied vaccination schedules. This includes protection for both healthy and chronically ill children, highlighting vaccine versatility.
Area of Science:
- Immunology
- Pediatrics
- Epidemiology
Background:
- The introduction of the seven-valent pneumococcal conjugate vaccine (PCV7) in the USA led to varied vaccination schedules differing from clinical trial protocols.
- Assessing PCV7 effectiveness against diverse pneumococcal serotypes and various dosing regimens is crucial for public health.
Purpose of the Study:
- To evaluate the effectiveness of PCV7 against multiple pneumococcal serotypes.
- To determine the efficacy of recommended, catch-up, and incomplete vaccination schedules.
Main Methods:
- A case-control study identified invasive pneumococcal disease in children aged 3-59 months via CDC's Active Bacterial Core surveillance.
- Isolates were tested for serotype and antimicrobial susceptibility; three matched controls were selected per case.
- Conditional logistic regression calculated vaccine effectiveness, controlling for underlying conditions.
Main Results:
- Vaccine effectiveness was 96% in healthy children and 81% in those with coexisting disorders against vaccine serotypes.
- Effectiveness was 76% against penicillin-non-susceptible infections.
- PCV7 prevented disease from all seven vaccine serotypes and serotype 6A; varied schedules showed significant protection.
Conclusions:
- The seven-valent pneumococcal conjugate vaccine demonstrates efficacy in preventing invasive pneumococcal disease in both healthy and chronically ill children.
- PCV7 remains effective even when administered using non-standard vaccination schedules.
Background:
When seven-valent pneumococcal conjugate vaccine was introduced in the USA, many children were vaccinated on schedules that differed from those tested in clinical trials. Our aim was to assess the effectiveness of the vaccine against various pneumococcal serotypes, and to measure the effectiveness of the recommended dose schedule and of catch-up and incomplete schedules.
Methods:
Invasive disease, defined as isolation of pneumococcus from a sterile site, was identified in children aged 3-59 months through the US Centers for Disease Control and Prevention's Active Bacterial Core surveillance. We tested isolates for serotype and antimicrobial susceptibility. Three controls, matched for age and zip code were selected for each case. We calculated the matched odds ratio for vaccination using conditional logistic regression, controlling for underlying conditions. Vaccine effectiveness was calculated as one minus the adjusted matched odds ratio times 100%.
Findings:
We enrolled 782 cases and 2512 controls. Effectiveness of one or more doses against vaccine serotypes was 96% (95% CI 93-98) in healthy children and 81% (57-92) in those with coexisting disorders. It was 76% (63-85) against infections that were not susceptible to penicillin. Vaccination prevented disease caused by all seven vaccine serotypes, and by vaccine-related serotype 6A. Several schedules were more protective than no vaccination; three infant doses with a booster were more protective against vaccine-type disease than were three infant doses alone (p=0.0323).
Interpretation:
The seven-valent pneumococcal conjugate vaccine prevents invasive disease in both healthy and chronically ill children. The vaccine is effective when used with various non-standard schedules.
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