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Experimental Human Pneumococcal Carriage
Published on: February 15, 2013
Predictors of occult pneumococcal bacteremia in young febrile children
N Kuppermann1, G R Fleisher, D M Jaffe
1Department of Internal Medicine, University of California, Davis School of Medicine, USA. nkuppermann@ucdavis.edu
Insights
In febrile children aged 3-36 months, higher temperature, younger age, and elevated absolute neutrophil count (ANC) predict occult pneumococcal bacteremia (OPB). These factors can guide targeted testing and treatment for OPB.
Area of Science:
- Pediatrics
- Infectious Diseases
- Clinical Microbiology
Background:
- Occult pneumococcal bacteremia (OPB) affects 2.5-3% of febrile children aged 3-36 months.
- Untreated OPB can lead to serious complications, including meningitis in 3-6% of cases.
Purpose of the Study:
- To identify independent predictors of OPB in young, febrile outpatients.
- To develop a predictive model for OPB using multivariable statistical methods.
Main Methods:
- A logistic regression model was derived and validated using data from 6,579 febrile outpatients (3-36 months old).
- Variables analyzed included age, temperature, clinical score, WBC count, absolute neutrophil count (ANC), and absolute band count (ABC).
Main Results:
- Multivariable analysis identified ANC, temperature, and age younger than 2 years as significant predictors of OPB.
- Higher ANC (≥10,000 cells/mm³) was associated with an 8.1% incidence of OPB, compared to 0.8% for lower ANC.
Conclusions:
- ANC, temperature, and younger age (<2 years) are independent predictors of OPB in febrile children.
- These findings can inform clinical strategies to optimize laboratory testing and antibiotic use for children at high risk of OPB.
Study Objective:
Occult pneumococcal bacteremia (OPB) occurs in 2.5% to 3% of highly febrile children 3 to 36 months of age, and 10% to 25% of untreated patients with OPB experience complications, including 3% to 6% in whom meningitis develops. The purpose of this study was to identify predictors of OPB among a large cohort of young, febrile children treated as outpatients using multivariable statistical methods.
Methods:
We derived and validated a logistic regression model for the prediction of OPB. We evaluated 6,579 outpatients 3 to 36 months of age with temperatures of 39 degrees C or higher who previously had been enrolled in a study of young febrile patients at risk of OPB in the emergency departments of 10 hospitals in the United States between 1987 and 1991; 164 patients (2.5%) had OPB. We randomly selected two thirds of this population for the derivation of the model and one third for validation. In the derivation set, we analyzed the univariate relationships of six variables with OPB: age, temperature, clinical score, WBC count, absolute neutrophil count (ANC), and absolute band count (ABC). All six variables were then entered into a logistic regression equation and those retaining statistical significance were considered to have an independent association with OPB.
Results:
Patients with OPB were younger, more frequently ill-appearing, and had higher temperatures, WBC, ANC, and ABC than patients without bacteremia. Only three variables, however, retained statistically significant associations with OPB in the multivariate analysis: ANC (Adjusted odds ratio [OR] 1.15 for each 1,000 cells/mm3 increase, 95% confidence interval [CI] 1.06, 1.25), temperature (adjusted OR 1.77 for each 1 degree C increase, 95% CI 1.21, 2.58), and age younger than 2 years (adjusted OR 2.43 versus patients 2 to 3 years old, 95% CI interval 1.11, 5.34). In the derivation set, 8.1% of patients with ANCs greater than or equal to 10,000 cell/mm3 had OPB (95% CI 6.3, 10.1%) versus .8% of patients with ANCs less than 10,000 cells/mm3 (95% CI .5, 1.2%). When tested on the validation set, the model performed similarly.
Conclusion:
Independent predictors of OPB in children 3 to 36 months of age with temperatures of 39 degrees C or higher treated as outpatients include ANC, temperature, and age younger than 2 years. These predictors may be used to develop clinical strategies to limit laboratory testing and antibiotic administration to those children at greatest risk of OPB.
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