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Published on: September 18, 2013
Prophylactic Levofloxacin Use in Oncology and Hematopoietic Stem Cell Transplants for Children Under 2 Years of Age
Ali Goldensoph1, Jane Mauro1, Jean Freudenthal1
1Department of Pharmacy, Children's Mercy Hospital (CMH), Kansas City, MO.
Insights
Levofloxacin (LVX) prophylaxis showed similar efficacy against bacteremia in infants under 6 months and older children with leukemia or undergoing stem cell transplant. Further research is needed to confirm safety and efficacy in this vulnerable population.
Area of Science:
- Pediatric Oncology
- Infectious Diseases
- Pharmacology
Background:
- Levofloxacin (LVX) is used for prophylaxis in pediatric patients with hematologic malignancies or after hematopoietic stem cell transplantation (HSCT).
- Limited data exists on LVX efficacy and safety in infants under 6 months compared to older children in these high-risk groups.
Purpose of the Study:
- To evaluate the efficacy and safety of levofloxacin prophylaxis in infants under 6 months compared to older children (6 months to 2 years) undergoing treatment for acute myeloid leukemia (AML), relapsed acute lymphoblastic leukemia (rALL), infant ALL (iALL), Down syndrome with ALL (DS ALL), or HSCT.
Main Methods:
- A retrospective chart review was conducted at Children's Mercy Hospital from April 2019 to September 2024.
- Data from 79 patient encounters receiving LVX prophylaxis were analyzed for bacteremia, febrile neutropenia, and adverse drug reactions.
- Statistical analysis compared outcomes between infants under 6 months and older children.
Main Results:
- Bacteremia occurred in 9% of encounters, with no significant difference between the age groups (P=0.643).
- While some secondary outcomes like antibiotic exposure duration and liver enzyme elevations differed, clinical significance was limited by baseline differences.
- No differences were observed in febrile neutropenia, total LVX exposure, or time to first fever.
- One isolate of Streptococcus mitis showed resistance to LVX.
Conclusions:
- This preliminary study suggests comparable efficacy of LVX prophylaxis against bacteremia in young infants and older children with hematologic conditions.
- Further research with larger cohorts is necessary to confirm these findings and assess long-term safety in vulnerable pediatric populations.
- The emergence of LVX resistance in one isolate warrants ongoing surveillance.
Abstract:
This study evaluates the efficacy and safety of levofloxacin (LVX) prophylaxis against bacteremia and febrile neutropenia in infants under 6 months of age compared with those 6 months to 2 years old with acute myeloid leukemia (AML), relapsed acute lymphoblastic leukemia (rALL), infant ALL (iALL), Down syndrome with ALL (DS ALL), or undergoing hematopoietic stem cell transplantation (HSCT). A retrospective chart review was conducted at Children's Mercy Hospital, Kansas City, MO (April 2019 to September 2024), including 79 encounters from patients receiving LVX prophylaxis. Data were collected on occurrences of bacteremia, febrile neutropenia, and adverse drug reactions. Bacteremia occurred in 9% of patient encounters with no significant difference between the infants under 6 months and the older age group ( P =0.643). Secondary outcomes of total duration of treatment antibiotic exposure and increases in liver enzymes were statistically different between groups. However, based on underlying differences in baseline characteristics, the results do not support definitive clinical significance. Other secondary outcomes, including febrile neutropenia, total LVX exposure, and time to first fever, showed no difference between groups. Of 7 positive blood cultures, susceptibility testing for LVX was performed for one culture isolate of Streptococcus mitis , and it was resistant to LVX. This preliminary data indicates that further research is needed in this underexplored topic to confirm these findings with larger patient populations and explore long-term safety in this vulnerable population.
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