Drew J. Winston, MD; Anita Pakrasi, RN; Ronald W. Busuttil, MD, PhD
Acknowledgments: The authors thank Dr. Marcia Levenstein, Dr. Lichen Teng, and Paul Schwartz of Pfizer, Inc., for performing statistical analyses; Dr. David Bruckner and the staff of the UCLA clinical microbiology laboratories for technical assistance; Ed Arriola and the staff of the UCLA pharmacy service for administrative assistance; and Katharine Fry for preparation of the manuscript. They also thank the UCLA liver transplant physicians and nurses for their assistance and for care of patients during the study.
Grant Support: By a research grant from Pfizer, Inc., the Joanne Barr Foundation, and the Dumont Foundation.
Requests for Reprints: Drew J. Winston, MD, Room 42-121 CHS, Department of Medicine, UCLA Medical Center, Los Angeles, CA 90095. For reprint orders in quantities exceeding 100, please contact the Reprints Coordinator; phone, 215-351-2657; e-mail, email@example.com.
Current Author Addresses: Dr. Winston: Room 42-121 CHS, Department of Medicine, UCLA Medical Center, Los Angeles, CA 90095.
Ms. Pakrasi and Dr. Busuttil: The Dumont-UCLA Transplant Center, Room 77-120 CHS, UCLA Medical Center, Los Angeles, CA 90095.
Among persons who receive solid organ transplants, liver transplant recipients have the highest incidence of invasive fungal infection; however, no antifungal prophylaxis has been proven to be effective.
To evaluate the efficacy and safety of prophylactic fluconazole in liver transplant recipients.
Randomized, double-blind, placebo-controlled trial.
University-affiliated transplantation center.
212 liver transplant recipients who received fluconazole (400 mg/d) or placebo until 10 weeks after transplantation.
Fungal colonization, proven superficial or invasive fungal infection, drug-related side effects, and death.
Fungal colonization increased in patients who received placebo (from 60% to 90%) but decreased in patients who received fluconazole (from 70% to 28%). Proven fungal infection occurred in 45 of 104 placebo recipients (43%) but in only 10 of 108 fluconazole recipients (9%) (P < 0.001). Fluconazole prevented both superficial infection (29 of 104 placebo recipients became infected [28%] compared with 4 of 108 fluconazole recipients [4%]; P < 0.001) and invasive infection (24 of 104 placebo recipients became infected [23%] compared with 6 of 108 fluconazole recipients [6%]; P < 0.001). Fluconazole prevented infection by most Candida species, except C. glabrata. However, infection and colonization by organisms intrinsically resistant to fluconazole did not seem to increase. Fluconazole was not associated with any hepatotoxicity. Patients receiving fluconazole had higher serum cyclosporine levels and more adverse neurologic events (headaches, tremors, or seizures in 13 fluconazole recipients compared with 3 placebo recipients; P = 0.01). Although the overall mortality rate was similar in both groups (12 of 108 [11%] in the fluconazole group compared with 15 of 104 [14%] in the placebo group; P > 0.2), fewer deaths related to invasive fungal infection were seen in the fluconazole group (2 of 108 patients [2%]) than in the placebo group (13 of 104 patients [13%]) (P = 0.003).
Prophylactic fluconazole after liver transplantation decreases fungal colonization, prevents superficial and invasive fungal infections, and has no appreciable hepatotoxicity. Although fluconazole prophylaxis is associated with fewer deaths from fungal infection, it does not improve overall survival. Patients receiving prophylactic fluconazole require close monitoring of serum cyclosporine levels to avoid neurologic toxicity.
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Winston DJ, Pakrasi A, Busuttil RW. Prophylactic Fluconazole in Liver Transplant Recipients: A Randomized, Double-Blind, Placebo-Controlled Trial. Ann Intern Med. 1999;131:729–737. doi: 10.7326/0003-4819-131-10-199911160-00003
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Published: Ann Intern Med. 1999;131(10):729-737.
Gastroenterology/Hepatology, Liver Disease, Liver Transplantation.
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Print ISSN: 0003-4819 | Online ISSN: 1539-3704
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