Volume 40, Issue 2 pp. 93-98

Ciprofloxacin and amoxicillin as continuation treatment of febrile neutropenia in pediatric cancer patients

Julie R. Park MD

Corresponding Author

Julie R. Park MD

Pediatric Hematology/Oncology, Children's Hospital and Regional Medical Center, University of Washington, Seattle, Washington

Pediatric Hematology/Oncology, Children's Hospital and Regional Medical Center, 4800 Sand Point Way NE, CH29, Seattle WA 98105.Search for more papers by this author
James Coughlin MD

James Coughlin MD

Pediatric Hematology/Oncology, Children's Hospital and Regional Medical Center, University of Washington, Seattle, Washington

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Douglas Hawkins MD

Douglas Hawkins MD

Pediatric Hematology/Oncology, Children's Hospital and Regional Medical Center, University of Washington, Seattle, Washington

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Debra L. Friedman MD

Debra L. Friedman MD

Pediatric Hematology/Oncology, Children's Hospital and Regional Medical Center, University of Washington, Seattle, Washington

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Jane L. Burns MD

Jane L. Burns MD

Pediatric Infectious Disease, Children's Hospital and Regional Medical Center, University of Washington, Seattle, Washington

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Thomas Pendergrass MD, MSPH

Thomas Pendergrass MD, MSPH

Pediatric Hematology/Oncology, Children's Hospital and Regional Medical Center, University of Washington, Seattle, Washington

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First published: 29 November 2002
Citations: 22

This work was performed at Children's Hospital and Regional Medical Center, Seattle, Washington.

Presented in part at the meeting of the American Society of Pediatric Hematology Oncology/SIOP, 1999, Montreal, Canada.

Abstract

Background

The empiric administration of anti-microbial therapy significantly reduces the morbidity and mortality associated with febrile neutropenic episodes in oncology patients. Outpatient empiric antibiotic therapy can be safely administered to a subset of febrile neutropenic patients at low risk for clinical complications.

Procedure

Pediatric cancer patients presenting with febrile neutropenia after non-myeloablative chemotherapy and who met institutional criteria for early hospital discharge following a minimum of 48-hr inpatient empiric intravenous ceftazidime were eligible for the study. The feasibility and efficacy of an outpatient continuation therapy of oral ciprofloxacin (CPR) 25–30 mg/kg/day divided BID and amoxicillin (AMX) 30–50 mg/kg/day divided TID was assessed.

Results

Thirty febrile neutropenic episodes in 26 patients were treated with outpatient oral CPR/AMX therapy. Oral CPR/AMX therapy was feasible in 28 (93%) and efficacious in 26 (87%) of treatment episodes. CPR/AMX was discontinued due to abdominal pain and diarrhea (n = 2), recurrent fever (n = 3), or gastrointestinal bleeding (n = 1). No patient developed new bacteremia or cardiopulmonary decompensation. Bone/joint pain or gastrointestinal symptoms occurred in 27% of treatment episodes. Duration of neutropenia, lower absolute neutrophil count (ANC) (< 100/mm3) at start of oral antibiotic therapy and active malignant disease were associated with failure of oral antibiotic therapy.

Conclusions

It is feasible to administer oral CPR/AMX as continuation antibiotic therapy for a selected subgroup of febrile neutropenic episodes defined after initial hospitalization and empiric antibiotic therapy. Prospectively randomized trials will be required to analyze adequately the efficacy of an oral CPR/AMX outpatient antibiotic regimen for treatment of febrile neutropenia in pediatric oncology patients. Med Pediatr Oncol 2003;40:93–98. © 2003 Wiley-Liss, Inc.

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