Risk of Bacteremia in Febrile Children and Young Adults With Sickle Cell Disease in a Multicenter Emergency Department Cohort

Abstract

ImportanceBacteremia is a major cause of morbidity and mortality in children and young adults with sickle cell disease (SCD), but among those presenting to the emergency department (ED) with fever, the absolute risk of, risk factors associated with, and outcomes of bacteremia are poorly defined.ObjectiveTo obtain contemporary data on the absolute risk of, risk factors associated with, and outcomes associated with bacteremia in children and young adults with SCD presenting to the ED with fever.Design, Setting, and ParticipantsA multicenter retrospective cohort study was conducted of individuals with SCD younger than 22 years (young adults) presenting to EDs within the Pediatric Health Information Systems database from January 1, 2016, to December 31, 2021, with fever (identified by diagnostic codes for fever or the collection of blood samples for cultures and intravenous antibiotic administration). Data analysis was performed from May 17 to December 15, 2022.Main Outcomes and MeasuresThe risk of bacteremia (defined by diagnostic coding) was identified in these children and young adults, and univariate analyses and multivariable regression were used to examine patient-level factors and bacteremia.ResultsA total of 35 548 encounters representing 11 181 individual patients from 36 hospitals were evaluated. The median age of the cohort was 6.17 (IQR, 2.36-12.11) years and 52.9% were male. Bacteremia was present in 405 encounters (1.1%, 95% CI, 1.05%-1.26%). A history of bacteremia, osteomyelitis, stroke, central line–associated bloodstream infection (CLABSI), central venous catheter, or apheresis was associated with the diagnosis of bacteremia, while age, sex, hemoglobin SC genotype, and race and ethnicity were not. In the multivariable analysis, individuals with a history of bacteremia (odds ratio [OR], 1.36; 95% CI, 1.01-1.83), CLABSI (OR, 6.39; 95% CI, 3.02-13.52), and apheresis (OR, 1.77; 95% CI, 1.22-2.55) had higher odds of bacteremia.Conclusions and RelevanceThe findings of this large cohort study suggest that bacteremia in children and young adults with SCD presenting with fever is rare. A history of invasive bacterial infection, CLABSI, or a central line appears to be associated with bacteremia, while age and SCD genotype are not.

Factors associated with adverse outcome among children with sickle cell disease admitted to the pediatric intensive care unit: an observational cohort

“…Sepsis in our population was rare (4%) and confirms the decreasing trend of severe infections in children with SCD thanks to prophylactic penicillin and vaccination [ 17 , 18 ]. In fact, in a recent multicenter retrospective cohort study that included patients with SCD younger than 22 years (young adults) presenting to emergency departments with fever found that bacteriemia was found only in 1.1% of patients (95% CI, 1.05-1.26%) [ 19 ].…”

Haematopoietic stem cell transplantation in children with sickle cell disease: Still to do?

“…Haemolysis, vaso-occlusion and vasopathies lead to acute chest crises, strokes and life-threatening bacterial infections, including meningitis, osteomyelitis and septic shock syndrome. 4 Because SCD families often belong to underprivileged populations, the management of such events is disrupting the fragile organisational structure and socioeconomical balance. 5,6 Blood transfusion and hydroxyurea are proven to avoid primary strokes.…”