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Mortality in pediatric oncology and stem cell transplant patients with bloodstream infections
Daniel N Willis1, Mary Claire McGlynn2, Patrick J Reich3
1Department of Pediatrics, Division of Hematology/Oncology, Washington University School of Medicine, St. Louis Children's Hospital, St. Louis, MO, United States.
Insights
Bloodstream infections (BSI) significantly increase mortality risk in pediatric cancer patients. Preventing BSI is crucial for reducing deaths in this vulnerable population.
Area of Science:
- Pediatric Oncology
- Infectious Diseases
- Hematology
Background:
- Bloodstream infections (BSI) are a major cause of illness in pediatric oncology patients.
- The risk of death associated with BSI in this population is not well understood.
Purpose of the Study:
- To evaluate the risk of BSI and associated mortality in pediatric oncology and hematopoietic stem cell transplant (HSCT) patients.
- To identify risk factors for BSI and death in this cohort.
Main Methods:
- Retrospective analysis of inpatient data from pediatric oncology and HSCT patients over 9 years.
- Univariate and multivariable modeling to assess BSI and mortality risk.
- Examined variables including demographics, malignancy type, HSCT history, central line, and febrile neutropenia (FN).
Main Results:
- BSI occurred in 5.4% of admissions; risk factors included younger age, specific diagnoses (HLH, AML), ethnicity, and HSCT history.
- Mortality was significantly higher in patients with BSI (6.5%) compared to those without (0.7%).
- Febrile neutropenia (FN) in patients with BSI was associated with reduced mortality.
Conclusions:
- BSI is a significant contributor to mortality in pediatric oncology and HSCT patients.
- While demographics influence BSI risk, they do not impact mortality outcomes.
- Emphasizes the critical need for comprehensive BSI prevention strategies to reduce mortality.
Background:
Bloodstream infections (BSI) continue to represent a significant source of morbidity for pediatric oncology patients, however less is known regarding this population's risk of death. We sought to evaluate the risk of BSI and death at a large pediatric cancer center.
Methods:
We retrospectively collected inpatient data from pediatric oncology and hematopoietic stem cell transplant (HSCT) patients over a 9-year period. We performed univariate and multivariable modeling to assess risk of BSI and mortality examining the following variables: demographics, underlying malignancy, history of HSCT, central line type, and febrile neutropenia (FN).
Results:
During the study period, 6763 admissions from 952 patients met inclusion criteria. BSI occurred in 367 admissions (5.4%) from 231 unique individuals. Risk factors for BSI include younger age, diagnoses of hemophagocytic lymphohistiocytosis or acute myeloid leukemia, ethnicity, and history of HSCT. Mortality for those with BSI was 6.5%, compared to 0.7% without (OR 7.2, CI 4.1 - 12.7, p<0.0001). In patients with BSI, admissions with FN were associated with reduced mortality compared to admissions without FN (OR 0.21, CI 0.05 - 0.94, p=0.04). In both univariate and multivariable analysis, no other risk factor was significantly associated with mortality in patients with BSI.
Conclusion:
BSI is a significant source of mortality in pediatric oncology and HSCT patients. While demographic variables contribute to the risk of BSI, they did not influence mortality. These findings highlight the importance of BSI prevention to reduce the risk of death in pediatric oncology patients. Future studies should focus on comprehensive BSI prevention.
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