Aspergillus to zygomycetes: Causes, risk factors, prevention, and treatment of invasive fungal inections

被引:75
作者
Cornely, O. A. [1 ]
机构
[1] Klinikum Univ Koln, Innere Med Klin 1, D-50924 Cologne, Germany
关键词
D O I
10.1007/s15010-008-7357-z
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Invasive fungal infections (IFIs) are an important cause of morbidity and mortality, particularly in patients with underlying risk factors (e.g., neutropenia, cancer chemotherapy, transplantation, AIDS). Although Candida species remain a relevant cause of IFI, other organisms (particularly moulds) have become increasingly prevalent. In particular, Aspergillus species are the leading cause of mould infections although other moulds including Fusarium species and Zygomycetes are increasing in frequency, and are associated with a high mortality rate. Options available for the prevention and treatment of these infections include standard and liposomal formulations of amphotericin B, but toxicity concerns limit their use; fluconazole is effective for the prevention and treatment of candidiasis but its inactivity against moulds and increasing resistance are limiting factors. Newer azoles, particularly voriconazole and posaconazole, have an enhanced spectrum of activity that includes Candida species, Aspergillus species, Cryptococcus species, dimorphic fungi, Fusarium species, and, for posaconazole, Zygomycetes. Recent data suggest that these agents are highly effective in a variety of clinical settings. Echinocandins have good activity against Candida species and Aspergillus species but their spectrum generally does not include Fusanum species, Cryptococcus species, Trichosporon species, Zygomycetes, and dematiaceous moulds. While these agents are unlikely to exhibit cross-resistance with polyenes or azoles, they must be administered intravenously. Knowledge of the pathogenesis of IFIs and the activity, efficacy, and Limitations of available treatment options will allow the selection of an appropriate antifungal agent for individual patients.
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页码:296 / 313
页数:18
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共 202 条
[1]   Breakthrough trichosporonosis in patients with acute myeloid leukemia receiving micafungin [J].
Akagi, Tomoaki ;
Yamaguti, Kohei ;
Kawamura, Tizuko ;
Nakumura, Toshihiko ;
Kubo, Komei ;
Takemori, Hiromitu .
LEUKEMIA & LYMPHOMA, 2006, 47 (06) :1182-1183
[2]   Non-comparative evaluation of the safety of aerosolized amphotericin B lipid complex in patients undergoing allogeneic hematopoietic stem cell transplantation [J].
Alexander, BD ;
Ashley, ESD ;
Addison, RM ;
Alspaugh, JA ;
Chao, NJ ;
Perfect, J .
TRANSPLANT INFECTIOUS DISEASE, 2006, 8 (01) :13-20
[3]   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
[4]   Coccidioidomycosis in persons infected with HIV type 1 [J].
Ampel, NM .
CLINICAL INFECTIOUS DISEASES, 2005, 41 (08) :1174-1178
[5]   THE EMERGING ROLE OF FUSARIUM INFECTIONS IN PATIENTS WITH CANCER [J].
ANAISSIE, E ;
KANTARJIAN, H ;
RO, J ;
HOPFER, R ;
ROLSTON, K ;
FAINSTEIN, V ;
BODEY, G .
MEDICINE, 1988, 67 (02) :77-83
[6]   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
[7]   Prophylaxis and treatment of fungal infections associated with haematological malignancies [J].
Ascioglu, S ;
de Pauw, BE ;
Meis, JFGM .
INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 2000, 15 (03) :159-168
[8]   Salvage therapy with voriconazole for invasive fungal infections in patients failing or intolerant to standard antifungal therapy [J].
Baden, LR ;
Katz, JT ;
Fishman, JA ;
Koziol, C ;
DelVecchio, A ;
Doran, M ;
Rubin, RH .
TRANSPLANTATION, 2003, 76 (11) :1632-1637
[9]   Fluconazole versus itraconazole for Candida esophagitis in acquired immunodeficiency syndrome [J].
Barbaro, G ;
Barbarini, G ;
Calderon, W ;
Grisorio, B ;
Alcini, P ;
DiLorenzo, G .
GASTROENTEROLOGY, 1996, 111 (05) :1169-1177
[10]   Enhanced bioavailability of itraconazole in hydroxypropyl-β-cyclodextrin solution versus capsules in healthy volunteers [J].
Barone, JA ;
Moskovitz, BL ;
Guarnieri, J ;
Hassell, AE ;
Colaizzi, JL ;
Bierman, RH ;
Jessen, L .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1998, 42 (07) :1862-1865