Risk-based fluconazole prophylaxis of Candida bloodstream infection in a medical intensive care unit

被引:20
作者
Faiz, S. [1 ,2 ]
Neale, B. [2 ]
Rios, E. [2 ]
Campos, T. [2 ]
Parsley, E. [2 ]
Patel, B. [2 ]
Ostrosky-Zeichner, L. [2 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Houston, TX 77030 USA
[2] Univ Texas Houston, Sch Med, Houston, TX USA
关键词
PLACEBO-CONTROLLED TRIAL; ILL SURGICAL-PATIENTS; CRITICALLY-ILL; INVASIVE CANDIDIASIS; ANTIFUNGAL AGENTS; DOUBLE-BLIND; EPIDEMIOLOGY; METAANALYSIS; MULTICENTER; MORTALITY;
D O I
10.1007/s10096-008-0666-4
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Candida bloodstream infection (CBSI) accounted for 50% of bloodstream infections in our medical intensive care unit (MICU) in 2004. Our objective was to evaluate a risk-based fluconazole prophylaxis program. CBSI incidence, patient demographics, and unit metrics were retrospectively reviewed for 2004. Starting on January 2005, patients meeting pre-specified criteria were placed on risk-based fluconazole prophylaxis and their outcomes, adverse events, and unit metrics were prospectively collected. The inclusion criteria were based on a clinical prediction rule and included an MICU stay greater than 72 h, broad-spectrum antibiotics, and central venous catheter, along with at least two of the following: mechanical ventilation for at least 48 h, any type of dialysis, parenteral nutrition, pancreatitis, systemic steroids, or other systemic immunosuppressive agents. For 2004, the unit had nine CBSI, corresponding to a rate of 3.4 CBSI/1,000 line-days. Four cases were caused by C. albicans, four by C. glabrata, and one by C. tropicalis. The mean +/- standard deviation (SD) APACHE II score for these patients was 25 +/- 9. In 2005, a total of 36 patients (2.6% of all unit admissions) received prophylaxis and the unit had two CBSI, corresponding to a rate of 0.79 CBSI/1,000 line-days. One patient had C. albicans and the other had C. tropicalis. The mean +/- SD APACHE II score for these patients was 21 +/- 8. The mean +/- SD duration of fluconazole prophylaxis was 8 +/- 6 days. Fluconazole was discontinued in two patients due to non-severe adverse events (acute eosinophilia, elevated transaminases). The attributable cost of CBSI in the unit in 2004 was $63,000 per episode. The total cost for the 36 courses of fluconazole was $6,000. When comparing the 2004 CBSI patients and the 2005 prophylaxis patients, we found similar acuity, demographics, and risk factors, with no differences in MICU or hospital mortality or length of stay. Risk-based fluconazole prophylaxis in an MICU with a high incidence of CBSI was safe and cost-effective when applied to a limited number of patients and produced a significant decrease in the incidence of this disease.
引用
收藏
页码:689 / 692
页数:4
相关论文
共 17 条
[1]   Risk factors for candidal bloodstream infections in surgical intensive care unit patients: The NEMIS Prospective Multicenter Study [J].
Blumberg, HM ;
Jarvis, WR ;
Soucie, JM ;
Edwards, JE ;
Patterson, JE ;
Pfaller, MA ;
Rangel-Frausto, MS ;
Rinaldi, MG ;
Saiman, L ;
Wiblin, RT ;
Wenzel, RP .
CLINICAL INFECTIOUS DISEASES, 2001, 33 (02) :177-186
[2]   Nosocomial bloodstream infections in United States hospitals: A three-year analysis [J].
Edmond, MB ;
Wallace, SE ;
McClish, DK ;
Pfaller, MA ;
Jones, RN ;
Wenzel, RP .
CLINICAL INFECTIOUS DISEASES, 1999, 29 (02) :239-244
[3]   Fluconazole prophylaxis prevents intra-abdominal candidiasis in high-risk surgical patients [J].
Eggimann, P ;
Francioli, P ;
Bille, J ;
Schneider, R ;
Wu, MM ;
Chapuis, G ;
Chiolero, R ;
Pannatier, A ;
Schilling, J ;
Geroulanos, S ;
Glauser, MP ;
Calandra, T .
CRITICAL CARE MEDICINE, 1999, 27 (06) :1066-1072
[4]   Epidemiology of Candida species infections in critically ill non-immunosuppressed patients [J].
Eggimann, P ;
Garbino, J ;
Pittet, D .
LANCET INFECTIOUS DISEASES, 2003, 3 (11) :685-702
[5]   Prevention of severe Candida infections in nonneutropenic, high-risk, critically ill patients:: a randomized, double-blind, placebo-controlled trial in patients treated by selective digestive decontamination [J].
Garbino, J ;
Lew, DP ;
Romand, JA ;
Hugonnet, S ;
Auckenthaler, R ;
Pittet, D .
INTENSIVE CARE MEDICINE, 2002, 28 (12) :1708-1717
[6]   Attributable mortality of nosocomial candidemia, revisited [J].
Gudlaugsson, O ;
Gillespie, S ;
Lee, K ;
Berg, JV ;
Hu, JF ;
Messer, S ;
Herwaldt, L ;
Pfaller, M ;
Diekema, D .
CLINICAL INFECTIOUS DISEASES, 2003, 37 (09) :1172-1177
[7]   Antifungal agents: mechanisms of action [J].
Odds, FC ;
Brown, AJP ;
Gow, NAR .
TRENDS IN MICROBIOLOGY, 2003, 11 (06) :272-279
[8]   Multicenter retrospective development and validation of a clinical prediction rule for nosocomial invasive candidiasis in the intensive care setting [J].
Ostrosky-Zeichner, L. ;
Sable, C. ;
Sobel, J. ;
Alexander, B. D. ;
Donowitz, G. ;
Kan, V. ;
Kauffman, C. A. ;
Kett, D. ;
Larsen, R. A. ;
Morrison, V. ;
Nucci, M. ;
Pappas, P. G. ;
Bradley, M. E. ;
Major, S. ;
Zimmer, L. ;
Wallace, D. ;
Dismukes, W. E. ;
Rex, J. H. .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 2007, 26 (04) :271-276
[9]   A prospective observational study of candidemia: Epidemiology, therapy, and influences on mortality in hospitalized adult and pediatric patients [J].
Pappas, PG ;
Rex, JH ;
Lee, J ;
Hamill, RJ ;
Larsen, RA ;
Powderly, W ;
Kauffman, CA ;
Hyslop, N ;
Mangino, JE ;
Chapman, S ;
Horowitz, HW ;
Edwards, JE ;
Dismukes, WE .
CLINICAL INFECTIOUS DISEASES, 2003, 37 (05) :634-643
[10]   Double-blind placebo-controlled trial of fluconazole to prevent candidal infections in critically ill surgical patients [J].
Pelz, RK ;
Hendrix, CW ;
Swoboda, SM ;
Diener-West, M ;
Merz, WG ;
Hammond, J ;
Lipsett, PA .
ANNALS OF SURGERY, 2001, 233 (04) :542-548