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Published on: February 23, 2014
Emergence of vaccine-related pneumococcal serotypes as a cause of bacteremia
Andrew P Steenhoff1, Samir S Shah, Adam J Ratner
1Division of Infectious Diseases, The Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA. steenhoff@email.chop.edu
Insights
The heptavalent pneumococcal conjugate vaccine (PCV7) reduced pneumococcal bacteremia by 57% in children. However, penicillin resistance and bacteremia from related serotypes increased post-vaccination.
Area of Science:
- Pediatric Infectious Diseases
- Vaccinology
- Microbiology
Background:
- The heptavalent pneumococcal conjugate vaccine (PCV7) significantly reduced invasive pneumococcal disease in US children.
- The impact of non-PCV7 serotypes on pediatric pneumococcal bacteremia post-licensure remains understudied.
Purpose of the Study:
- To evaluate the impact of PCV7 on pediatric pneumococcal bacteremia incidence and serotype distribution.
- To assess changes in antibiotic resistance patterns and the emergence of non-PCV7 serotypes.
Main Methods:
- Retrospective analysis of bacteremia episodes (Streptococcus pneumoniae, other respiratory pathogens) in children (<18 years) from 1999-2005.
- Comparison of serotype distribution and antibiotic resistance between pre- and post-PCV7 introduction periods.
Main Results:
- Pneumococcal bacteremia incidence decreased by 57% post-PCV7 introduction.
- Bacteremia caused by vaccine serotypes dropped significantly (85% to 34%), while non-vaccine serotypes showed no significant change.
- Penicillin non-susceptibility increased from 25% to 39%; bacteremia due to vaccine-related serotypes rose from 6% to 35%.
Conclusions:
- PCV7 introduction led to a substantial decrease in overall pneumococcal bacteremia.
- Increased penicillin resistance and a rise in bacteremia due to vaccine-related serotypes were observed post-PCV7 introduction.
Background:
The heptavalent pneumococcal conjugate vaccine (PCV7) has decreased the incidence of invasive pneumococcal disease among children in the United States. In the postlicensure period, the impact of non-PCV7 serotypes against pediatric pneumococcal bacteremia is unknown.
Methods:
Episodes of bacteremia due to Streptococcus pneumoniae and other respiratory pathogens (ORP), namely Neisseria meningitidis, Haemophilus influenzae, and Moraxella catarrhalis, were identified in children <18 years old at the Children's Hospital of Philadelphia from January 1999 to May 2005. For pneumococci, serotype distribution and antibiotic resistance were compared.
Results:
A total of 188 episodes of pneumococcal bacteremia and 55 episodes of ORP bacteremia were identified. By comparing data from 1999-2000 with data from 2001 to May 2005, we found that the incidence of pneumococcal bacteremia decreased by 57%. The incidence of bacteremia caused by ORPs was unchanged; 1.43 episodes (95% confidence interval [CI], 0.84-2.29 episodes) to 1.25 (95% CI, 0.88-1.71) per 10,000 emergency department visits. Vaccine serotypes caused 85% of episodes of bacteremia in 1999-2000, compared with 34% of episodes of bacteremia in 2001 to May 2005 (P<.01). The percentage of isolates nonsusceptible to penicillin increased from 25% to 39% (P<.05). The percentage of episodes of pneumococcal bacteremia caused by vaccine-related serotypes--those of the same serogroup but not of the same serotype as PCV7--increased from 6% of episodes in the prelicensure period to 35% of episodes in the postlicensure period (P<.01). Rates of serotype pneumococcal bacteremia caused by nonvaccine serotypes were not statistically different between the 2 periods.
Conclusions:
The overall incidence of pneumococcal bacteremia decreased by 57% after the introduction of PCV7. During the postlicensure period, there were significant decreases in the incidence of pneumococcal bacteremia caused by vaccine serotypes; however, rates of penicillin resistance and bacteremia due to vaccine-related serotypes increased.
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