Related Experiment Videos
Cefepime and mortality in pediatric acute myelogenous leukemia: a retrospective cohort study
Brian T Fisher1, Richard Aplenc, Russell Localio
1Division of Infectious Diseases, The Children's Hospital of Philadelphia, and Department of Pediatrics, University of Pennsylvania School of Medicine, Philadelphia, PA 19104, USA. fisherbria@email.chop.edu
Insights
Cefepime use in pediatric acute myelogenous leukemia (AML) patients did not increase mortality risk compared to other beta-lactam antibiotics. This study found no significant difference in survival rates for children treated with cefepime.
Area of Science:
- Pediatric Oncology
- Infectious Diseases
- Pharmacology
Background:
- The U.S. Food and Drug Administration (FDA) warned of potential cefepime risks in 2009.
- Pediatric acute myelogenous leukemia (AML) patients frequently experience fever, requiring antibiotics like cefepime.
- This study investigates cefepime's association with mortality in pediatric AML.
Purpose of the Study:
- To evaluate the association between cefepime exposure and all-cause in-hospital mortality in pediatric AML patients.
- To compare cefepime's safety profile against other beta-lactam antibiotics in this vulnerable population.
Main Methods:
- Retrospective cohort study utilizing the Pediatric Health Information System database.
- Examined exposure to cefepime, ceftazidime, antipseudomonal penicillin, and carbapenems within the first year of AML diagnosis.
- Employed Cox regression analysis, adjusting for clinical and demographic factors, with analysis split into 0-3 and >3-12 month periods.
Main Results:
- No significant differences in hazard ratios for mortality were observed between cefepime and ceftazidime, antipseudomonal penicillin, or carbapenems in either the 0-3 month or >3-12 month periods.
- Hazard ratios (HR) and 95% confidence intervals (CI) showed no increased risk for cefepime across comparisons and timeframes.
Conclusions:
- Cefepime exposure within 30 days of death did not elevate mortality risk in pediatric AML patients.
- The findings suggest cefepime is a safe alternative to other beta-lactam antibiotics in this patient group.
Background:
Based on 2 meta-analyses, the Food and Drug Administration issued a communication in 2009 regarding the potential risk of death in patients treated with cefepime. Pediatric patients with acute myelogenous leukemia (AML) have frequent episodes of fever necessitating the use of antibiotics such as cefepime. We evaluated the association of cefepime and other beta-lactam antibiotic exposures with all cause in-hospital mortality in pediatric AML patients.
Methods:
We performed a retrospective cohort study using the Pediatric Health Information System, an inpatient database. Exposure to cefepime, ceftazidime, antipseudomonal penicillin, and carbapenems was evaluated for each 30-day period within the first year from AML diagnosis. Cox regression analysis was used to compute hazard ratios (HR) for death adjusting for demographics, clinical variables, and clustering by hospital. The final analysis used 2 distinct time periods (0-3 months and >3-12 months) to account for variation in proportional hazards over time.
Results:
No differences between the HRs for mortality were observed for the time period of 0 to 3 months (cefepime vs. ceftazadime: HR=1.33, 95% CI: 0.70-2.52; cefepime vs. antipseudmonal penicillin: HR=0.86, 95% CI: 0.34-2.13; and cefepime vs. carbapenems: HR=1.08, 95% CI: 0.50-2.35) or the time period of >3 to 12 months after diagnosis (cefepime vs. ceftazadime: HR=1.29, 95% CI: 0.53-3.15; cefepime vs. antipseudomonal penicillin: HR=1.08, 95% CI: 0.44-2.66; and cefepime vs. carbapenems: HR=1.03, 95% CI: 0.45-2.33).
Conclusions:
In this cohort of pediatric AML patients, cefepime exposure in the 30 days preceding death did not result in an increased mortality risk when compared with ceftazidime, antipseudomonal penicillins, or carbapenems.
Related Concept Videos
Pharmacokinetics in Pediatric Patients: Drug Excretion
Pharmacokinetics in Pediatric Patients: Drug Metabolism
Acute Pyelonephritis II: Diagnostic Studies and Management