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Updated: Jun 16, 2026

Experimental Human Pneumococcal Carriage
Published on: February 15, 2013
Effect of heptavalent pneumococcal conjugate vaccination on invasive pneumococcal disease in preterm born infants
Simon Rückinger1, Mark van der Linden, Rüdiger von Kries
1Division of Epidemiology, Ludwig-Maximilians-University of Munich, Institute of Social Pediatrics and Adolescent Medicine, Germany. simon.rueckinger@med.uni-muenchen.de
Insights
7-valent pneumococcal conjugate vaccination (PCV7) effectively protects preterm infants from invasive pneumococcal disease (IPD). This study shows PCV7 significantly reduced IPD rates in preterm infants, supporting timely vaccination.
Area of Science:
- Pediatrics
- Immunology
- Public Health
Background:
- Limited data exists on the effectiveness of 7-valent pneumococcal conjugate vaccination (PCV7) in protecting preterm infants from invasive pneumococcal disease (IPD).
- Previous randomized trials involved small numbers of preterm infants, necessitating further evidence.
Purpose of the Study:
- To evaluate the impact of PCV7 on invasive pneumococcal disease (IPD) rates in preterm infants in Germany.
- To compare IPD occurrence in preterm and general infant populations before and after PCV7 introduction.
Main Methods:
- Active, prospective surveillance of IPD in children in Germany.
- Comparison of IPD incidence in preterm and all infants born in 2000 versus 2007.
Main Results:
- A significant reduction in IPD rates was observed in the overall infant population (15.0 to 8.5 per 100,000).
- A comparable reduction in IPD notification rates was seen in preterm infants (26.1 to 16.7 per 100,000).
- Preterm infants diagnosed with IPD were largely unvaccinated or incompletely vaccinated.
Conclusions:
- PCV7 demonstrates effective protection for preterm infants against IPD.
- Recommendations support vaccinating preterm infants according to their chronological age.
Background:
Evidence for protection of preterm born infants from invasive pneumococcal disease (IPD) by 7-valent pneumococcal conjugate vaccination (PCV7) is relatively sparse. Data from randomized trials is based on relatively small numbers of preterm born children.
Methods:
We report data from active prospective surveillance of IPD in children in Germany. The cohorts of preterm born children in 2000 and 2007 and the respective whole birth cohorts are compared regarding occurrence of IPD.
Results:
After introduction of PCV7 we observed a reduction in the rate of IPD in preterm born infants comparing the 2000 and 2007 birth cohort. The rate of IPD among the whole birth cohorts was reduced from 15.0 to 8.5 notifications per 100,000 (P < .001). The impact among the preterm birth cohort was comparable: A reduction in notification rate from 26.1 to 16.7 per 100,000 comparing the 2000 with the 2007 preterm birth cohort (P = .39). Preterm born infants with IPD were either unvaccinated or vaccinated delayed or incomplete.
Conclusions:
This adds to evidence that PCV7 also protects preterm born infants effectively from IPD. Preterm born infants should receive pneumococcal vaccination according to their chronological age.
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