Clinical and microbiologic outcomes of quinolone prophylaxis in children with acute myeloid leukemia
Susanna Felsenstein1, Etan Orgel, Teresa Rushing
1From the *Division of Infectious Diseases, Children's Hospital Los Angeles, University of Southern California; †Children's Center for Cancer and Blood Diseases, University of Southern California; and ‡Department of Pharmacy, Children's Hospital Los Angeles, Los Angeles, CA.
Insights
Ciprofloxacin prophylaxis (CPx) did not alter overall bacteremia rates in pediatric acute myeloid leukemia (AML) patients. While reducing Gram-negative infections, CPx increased viridans streptococci bacteremia, warranting further research.
Area of Science:
- Pediatric Oncology
- Infectious Diseases
- Hematology
Background:
- Intensified pediatric acute myeloid leukemia (AML) treatment improves survival but increases infection risks.
- Ciprofloxacin prophylaxis (CPx) was adopted for pediatric AML based on adult and transplant data.
- The study evaluated the real-world impact of CPx in pediatric AML.
Purpose of the Study:
- To assess the effect of ciprofloxacin prophylaxis (CPx) on infection rates and outcomes in pediatric acute myeloid leukemia (AML).
- To compare fever, neutropenia, infection spectrum, antibiotic use, and mortality before and after CPx implementation.
Main Methods:
- Retrospective comparison of pediatric AML patients before and after CPx implementation.
- Analysis included chemotherapy courses, fever and neutropenia episodes, infection types, and mortality.
- Data on antibiotic use and supportive care were also collected.
Main Results:
- CPx did not significantly alter the incidence of febrile episodes, infectious episodes, fever duration, antibiotic treatment duration, or mortality.
- CPx significantly decreased Gram-negative rod infections (13.4% to 4.7%) but increased viridans streptococci bacteremia (12% to 28%).
- Overall bacteremia rates remained similar (35.9% pre-CPx vs. 31.5% post-CPx).
Conclusions:
- Ciprofloxacin prophylaxis (CPx) did not change overall bacteremia incidence or impact fever patterns and supportive care needs in pediatric AML.
- The findings suggest CPx did not provide the expected benefit in reducing overall bacteremia.
- Further investigation into extended-spectrum quinolone prophylaxis for pediatric AML is supported.
Background:
Intensifying treatment for pediatric acute myeloid leukemia (AML) has improved survival, with infections now being a leading cause of morbidity. Because quinolone prophylaxis is effective in adults with AML and in transplant populations, ciprofloxacin prophylaxis (CPx) was introduced as the standard for pediatric AML. We report here the impact of CPx in this population.
Methods:
Prevalence of fever and neutropenia, frequency and pathogen spectrum of infections, antibiotic use, supportive care and mortality before and after implementation of CPx were retrospectively compared in children with AML.
Results:
The cohort included 35 patients with de novo and 10 with relapsed AML, who together underwent 153 chemotherapy courses. Fever and neutropenia resulting in the use of empiric antibiotics occurred in 90% of chemotherapy courses (137/153); this was associated with proven bacteremia in 26%. The use of CPx did not change the incidence of febrile or infectious episodes, number of days of fever or antibiotic treatment or mortality. CPx was associated with a significant decrease in infections caused by Gram-negative rods (13.4% vs 4.7%) but a concomitant significant increase in bacteremia caused by viridans streptococci (12% vs 28%), resulting in no significant overall difference in the incidence of bacteremia between the 2 groups (35.9% vs 31.5%).
Conclusions:
CPx neither alter the incidence of overall bacteremia nor change the pattern of fever or use of supportive care. Our experience supports further investigation into the use of extended-spectrum quinolone prophylaxis during therapy for pediatric AML.
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