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Bloodstream Infections in Children With Sickle Cell Disease: 2010-2019
Marianne E Yee1,2, Kristina W Lai1, Nitya Bakshi1,2
1Aflac Cancer and Blood Disorders Center.
Insights
Bloodstream infections (BSIs) remain a significant risk for children with sickle cell disease (SCD). Key pathogens include Streptococcus pneumoniae, with higher BSI odds in those with sickle cell anemia genotypes and chronic transfusions.
Area of Science:
- Pediatric Infectious Diseases
- Hematology
- Epidemiology
Background:
- Children with sickle cell disease (SCD) face a heightened risk of bloodstream infections (BSIs) due to functional asplenia.
- While immunizations and antibiotic prophylaxis have decreased invasive bacterial infections, current data on BSIs in pediatric SCD patients are scarce.
Purpose of the Study:
- To conduct a contemporary analysis of bloodstream infections (BSIs) in children with sickle cell disease (SCD).
- To identify the incidence, common pathogens, and associated risk factors for BSIs in this vulnerable pediatric population.
Main Methods:
- A retrospective cohort study analyzed blood cultures from children under 18 with SCD between 2010 and 2019.
- Exclusion criteria included contaminant organisms and repeated cultures. Incidence rates and multivariate logistic regression were used to assess risk factors.
Main Results:
- 156 BSI episodes occurred in 144 patients, with an average incidence rate of 0.89 per 100 person-years.
- Common pathogens were Streptococcus pneumoniae, Streptococcus viridans group, Escherichia coli, Staphylococcus aureus, Bordetella holmesii, Haemophilus influenzae, and Salmonella species.
- Sickle cell anemia genotypes (OR 1.88) and chronic transfusions (OR 2.66) increased BSI odds, while hydroxyurea (OR 0.57) decreased them.
Conclusions:
- Bloodstream infections (BSIs) continue to pose a significant threat to children with sickle cell disease (SCD).
- Understanding the current incidence, risk factors, and spectrum of pathogens is crucial for effective prevention and empirical treatment strategies in pediatric SCD patients.
Background:
Children with sickle cell disease (SCD) are at increased risk for bloodstream infections (BSIs), mainly because of functional asplenia. Immunizations and antibiotic prophylaxis have reduced the prevalence of invasive bacterial infections, but contemporary analysis of BSI in children with SCD is limited.
Methods:
We conducted a retrospective cohort study of children aged <18 years with SCD who had blood cultures collected at our institution from 2010 to 2019 to identify BSI. Probable contaminant organisms were identified and not included as BSI. We calculated the annual incidence of BSI at our institution with 95% confidence intervals (CIs) and used multivariate logistic regression to evaluate associations.
Results:
There were 2694 eligible patients with 19 902 blood cultures. Excluding repeated cultures and contaminant cultures, there were 156 BSI episodes in 144 patients. The median age at BSI was 7.5 years. The average incidence rate of BSI was 0.89 per 100 person-years (95% CI 0.45-1.32). The most common pathogens were Streptococcus pneumoniae (16.0%), Streptococcus viridans group (9.0%), Escherichia coli (9.0%), Staphylococcus aureus (7.7%), Bordetella holmesii (7.7%), Haemophilus influenzae (7.1%), and Salmonella species (6.4%). Odds of BSI were higher with sickle cell anemia genotypes (odds ratio [OR] 1.88; 95% CI 1.20-2.94) and chronic transfusions (OR 2.66; 95% CI 1.51-4.69) and lower with hydroxyurea (OR 0.57; 95% CI 0.39-0.84).
Conclusions:
BSI remains a risk for children with SCD. Overall incidence, risk factors, and spectrum of pathogens are important considerations to guide prevention and empirical treatment of suspected infection in SCD.
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