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Updated: Apr 25, 2026

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Fever in children with sickle cell disease: are all fevers equal?
Bashar Sami Shihabuddin1, Catherine Ann Scarfi2
1Division of Pediatric Emergency Medicine, Department of Pediatrics, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma; The Children's Hospital of Oklahoma at OU Medical Center, Oklahoma City, Oklahoma.
Insights
Bacteremia is rare in febrile children with sickle cell disease (SCD). This suggests delayed antibiotic use and close follow-up may be safe alternatives to immediate treatment in these patients.
Area of Science:
- Pediatric Hematology
- Infectious Diseases
- Emergency Medicine
Background:
- Sepsis is a leading cause of death in sickle cell disease (SCD).
- Current practice involves immediate antibiotics for febrile children with SCD after blood cultures.
- This study investigates the necessity of this standard approach.
Purpose of the Study:
- To determine the rate of bacteremia in febrile pediatric patients with SCD.
- To identify predictors of bacteremia, including vital signs and diagnostic data.
Main Methods:
- Retrospective chart review of 307 pediatric patients with SCD presenting with fever.
- Inclusion criteria: age 0-20 years, SCD diagnosis, fever, and blood culture performed.
- Data collected included descriptive, visit-specific, and diagnostic information.
Main Results:
- Only 6 out of 307 patients (2%) had a positive blood culture.
- One true pathogen, Streptococcus pneumoniae, was identified (0.33% incidence).
- No significant difference in vital signs or diagnostics was found between patients with positive and negative blood cultures.
Conclusions:
- The incidence of bacteremia in febrile children with SCD is low.
- Delayed antibiotic administration with close follow-up is a potential alternative strategy.
- This approach may reduce unnecessary antibiotic exposure in this vulnerable population.
Background:
Sepsis is the most common cause of mortality in sickle cell disease (SCD). Empiric antibiotic administration after obtaining blood cultures in febrile children with SCD has been a standard practice parameter.
Objective:
Our primary objective was to calculate the rate of bacteremia in febrile pediatric patients with SCD. Our secondary objective was to establish whether vital signs or diagnostics predict bacteremia in these patients.
Methods:
We conducted a retrospective chart review of patients with SCD who presented to an urban pediatric emergency department in Newark, NJ between January 1, 2001 and June 30, 2011 with the chief complaint of fever. Patients between the ages of 0 and 20 years with SCD who presented with the chief complaint of fever and who had a blood culture performed were included. Descriptive data, visit-specific data, and diagnostic data were collected.
Results:
Charts of 307 patients were included. Six patients had a positive blood culture, one of which was considered a true pathogen (Streptococcus pneumoniae) (0.33%; 95% confidence interval 0.06%-1.86%). There was no statistical significance between the means of visit-specific and diagnostic data of patients with positive blood cultures and those with negative blood cultures.
Conclusions:
The incidence of bacteremia in febrile children with SCD presenting to the emergency department is low. Close follow-up within 24 hours and delayed antibiotic administration can be a plausible alternative treatment option in this population.
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