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Published on: February 23, 2014
The aetiology of paediatric bloodstream infections changes after pneumococcal vaccination and group B streptococcus
Joachim Luthander1,2, Rutger Bennet1, Christian G Giske3
1Paediatric Infectious Diseases Unit, Paediatric Emergency Department, Astrid Lindgren's Children Hospital, Stockholm, Sweden.
Insights
Pneumococcal conjugate vaccination and intrapartum antibiotics significantly reduced bloodstream infections and early-onset sepsis in children. Staphylococcus aureus is now a key pathogen requiring targeted therapy.
Area of Science:
- Pediatric Infectious Diseases
- Vaccinology
- Antimicrobial Resistance
Background:
- Bloodstream infections (BSIs) and early-onset sepsis (EOS) pose significant risks to children.
- Group B Streptococcus (GBS) and Streptococcus pneumoniae are common causes of pediatric BSIs and sepsis.
- Antimicrobial resistance is a growing global health concern.
Purpose of the Study:
- To evaluate the impact of pneumococcal conjugate vaccination (PCV) and risk-based intrapartum antibiotic prophylaxis (IAP) on BSIs and EOS.
- To monitor trends in clinically relevant antimicrobial resistance in pediatric bloodstream infections.
Main Methods:
- Retrospective analysis of 3986 positive blood cultures from children up to 17 years old.
- Data collected from a pediatric hospital in Stockholm, Sweden, before and after the introduction of PCV and risk-based IAP in 2007-2008.
- Monitoring of bacterial pathogens and their antimicrobial susceptibility patterns.
Main Results:
- Significant decline in Streptococcus pneumoniae BSIs (42% overall, 62% in healthy children <36 months).
- Marked reduction in early-onset sepsis due to group B Streptococcus (60%).
- Staphylococcus aureus and Gram-negative bacteria emerged as dominant pathogens; overall antimicrobial resistance remained low.
Conclusions:
- PCV and risk-based IAP are effective in reducing BSIs and EOS.
- Current empirical antibiotic strategies should consider Staphylococcus aureus for invasive bacterial infections in children.
Aim:
This study explored the incidence and aetiology of bloodstream infections after patients received the pneumococcal conjugate vaccination and a risk-based intrapartum antibiotic prophylaxis against early onset sepsis caused by group B streptococcus. We also monitored clinically relevant antimicrobial resistance.
Method:
We studied 3986 positive blood cultures from children up to 17 years of age at a paediatric hospital in Stockholm, Sweden, using data from medical records before and after the initiatives, to reduce early onset sepsis, were introduced in 2007 and 2008.
Results:
Bloodstream infections caused by Streptococcus pneumoniae declined by 42% overall (5.6 to 3.2/100 000) and by 62% in previously healthy children under 36 months of age (24.2 to 9.2/100 000). Early onset sepsis caused by group B streptococcus declined by 60% (0.5 to 0.2/1000 live born children). Bacterial meningitis caused by these bacteria decreased by 70%. Staphylococcus aureus and various Gram-negative bacteria became the dominant pathogens, in both previously healthy children and those with underlying disease. Overall, antimicrobial resistance remained low between the two 5-year study periods.
Conclusion:
Pneumococcal conjugate vaccination and risk-based intrapartum antibiotic prophylaxis against group B streptococcus effectively decreased the incidence of bloodstream infections. Empirical antibiotic therapy should target Staphylococcus aureus in both community and hospital-acquired invasive bacterial infections.
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