Oral amphotericin B for the prevention of Candida bloodstream infection in critically ill children
- PMID: 16474259
- DOI: 10.1097/01.PCC.0000200946.30263.B6
Oral amphotericin B for the prevention of Candida bloodstream infection in critically ill children
Abstract
Objectives: To determine the efficacy of oral amphotericin B for the prevention of Candida bloodstream infection in the pediatric intensive care unit.
Design: Retrospective, nonrandomized, historic-control study.
Setting: Multidisciplinary pediatric intensive care unit at a university-affiliated children's medical center.
Patients: Study group included all patients admitted to the pediatric intensive care unit from January 1, 1998, to December 31, 1999, who required mechanical ventilation and who were admitted for >7 days. The control group included all patients admitted for >7 days who needed mechanical ventilation from January 1, 1994, to December 31, 1997.
Interventions: Oral amphotericin B suspension, 50 mg every 8 hrs, administered to all study group patients soon after initiation of mechanical ventilation and terminating after weaning.
Measurements: The rates of Candida bloodstream infection were compared between the study and control groups.
Main results: Candida species were isolated from blood cultures in 5 of 185 (2.1%) and 21 of 196 (10.7%) patients in the study and control groups, respectively (p= .0038). There was also a statistically significant (p= .017) decrease in Candida bloodstream infection rate in all patients admitted to the pediatric intensive care unit for >7 days during the study period compared with the Candida bloodstream infection rate during the control period.
Conclusion: Prophylactic administration of oral amphotericin B may lead to a significant decrease in the rate of Candida bloodstream infection in ventilated pediatric intensive care unit patients.
Comment in
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Candidal bloodstream infection: will prevention work?Pediatr Crit Care Med. 2006 Mar;7(2):184-5. doi: 10.1097/01.PCC.0000209188.83340.DE. Pediatr Crit Care Med. 2006. PMID: 16531952 No abstract available.
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