Prophylaxis, empirical therapy, or pre-emptive therapy of fungal infections in immunocompromised patients: which is better for whom?

被引:16
作者
Leather, HL [1 ]
Wingard, JR [1 ]
机构
[1] Univ Florida, Coll Med, Dept Pharm, Gainesville, FL 32610 USA
关键词
D O I
10.1097/00001432-200208000-00003
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Immunocompromised patients are at risk of developing fungal infections. Over time, the incidence of fungal infections and the spectrum of causative organisms have changed. In addition, treatment strategies in this high-risk population have also changed. Traditional approaches (using polyene-based therapy and older azoles), including empirical treatment strategies, have evolved to include prophylaxis in populations at the greatest risk. These strategies, although effective against Candida species, have not really impacted infections caused by Aspergillus spp. With the recent approval of antifungal agents with demonstrated activity against Aspergillus and other mould infections, there is hope for better outcomes in the treatment of established infections. Several agents, with activity against Aspergillus, have been shown to be effective in the empirical setting. The role of these new antifungal agents in the prophylactic setting remains unknown at present, but the potential for reducing Aspergillus infections is promising and requires ongoing study. The other area of significant research in fungal infections has been the search for accurate, non-invasive, rapid diagnostic tests. Over the past year, several publications have indicated that early diagnosis is possible in immunocompromised patients. These new diagnostics have paved the way for a new strategy, called pre-emptive therapy, enabling infected patients to be identified at an earlier stage of infection. This strategy will permit targeted antifungal therapy in those at greatest risk, and will avoid unnecessary, potentially toxic therapy in those not infected. Validations of the various techniques show promise and are reviewed in this paper.
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页码:369 / 375
页数:7
相关论文
共 51 条
[1]  
Aliff TB, 2001, BLOOD, V98, p327A
[2]   A randomized, double-blind, double-dummy, multicenter trial of voriconazole and fluconazole in the treatment of esophageal candidiasis in immunocompromised patients [J].
Ally, R ;
Schürmann, D ;
Kreisel, W ;
Carosi, G ;
Aguirrebengoa, K ;
Dupont, B ;
Hodges, M ;
Troke, P ;
Romero, AJ .
CLINICAL INFECTIOUS DISEASES, 2001, 33 (09) :1447-1454
[3]  
[Anonymous], 2000, MMWR Recomm Rep, V49, P1
[4]   Randomized, double-blind, Multicenter study of caspofungin versus amphotericin B for treatment of oropharyngeal and esophageal candidiases [J].
Arathoon, EG ;
Gotuzzo, E ;
Noriega, LM ;
Berman, RS ;
DiNubile, MJ ;
Sable, CA .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (02) :451-457
[5]   In vitro synergy of caspofungin and amphotericin B against Aspergillus and Fusarium spp. [J].
Arikan, S ;
Lozano-Chiu, M ;
Paetznick, V ;
Rex, JH .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (01) :245-247
[6]   Defining opportunistic invasive fungal infections in immunocompromised patients with cancer and hematopoietic stem cell transplants: An international consensus [J].
Ascioglu, S ;
Rex, JH ;
de Pauw, B ;
Bennett, JE ;
Bille, J ;
Crokaert, F ;
Denning, DW ;
Donnelly, JP ;
Edwards, JE ;
Erjavec, Z ;
Fiere, D ;
Lortholary, O ;
Maertens, J ;
Meis, JF ;
Patterson, TF ;
Ritter, J ;
Selleslag, D ;
Shah, PM ;
Stevens, DA ;
Walsh, TJ .
CLINICAL INFECTIOUS DISEASES, 2002, 34 (01) :7-14
[7]  
Baran J, 2001, SCAND J INFECT DIS, V33, P137, DOI 10.1080/003655401750065544
[8]   Mortality and costs of acute renal failure associated with amphotericin B therapy [J].
Bates, DW ;
Su, L ;
Yu, DT ;
Chertow, GM ;
Seger, DL ;
Gomes, DRJ ;
Dasbach, EJ ;
Platt, R .
CLINICAL INFECTIOUS DISEASES, 2001, 32 (05) :686-693
[9]   Intravenous and oral itraconazole versus intravenous amphotericin B deoxycholate as empirical antifungal therapy for persistent fever in neutropenic patients with cancer who are receiving broad-spectrum antibacterial therapy - A randomized, controlled trial [J].
Boogaerts, M ;
Winston, DJ ;
Bow, EJ ;
Garber, G ;
Reboli, AC ;
Schwarer, AP ;
Novitzky, N ;
Boehme, A ;
Chwetzoff, E ;
De Beule, K .
ANNALS OF INTERNAL MEDICINE, 2001, 135 (06) :412-422
[10]   Invasive aspergillosis in allogeneic stem cell transplant recipients: Increasing antigenemia is associated with progressive disease [J].
Boutboul, F ;
Alberti, C ;
Leblanc, T ;
Sulahian, A ;
Gluckman, E ;
Derouin, F ;
Ribaud, P .
CLINICAL INFECTIOUS DISEASES, 2002, 34 (07) :939-943