National surveillance of nosocomial blood stream infection due to species of Candida other than Candida albicans:: Frequency of occurrence and antifungal susceptibility in the SCOPE program

被引:251
作者
Pfaller, MA
Jones, RN
Messer, SA
Edmond, MB
Wenzel, RP
机构
[1] Univ Iowa, Coll Med, Dept Pathol, Div Med Microbiol, Iowa City, IA 52242 USA
[2] Virginia Commonwealth Univ, Med Coll Virginia, Dept Internal Med, Richmond, VA 23298 USA
关键词
D O I
10.1016/S0732-8893(97)00192-2
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
A national surveillance program of nosocomial blood stream infections (BSI) in the USA between April 1995 and June 1996 revealed that Candida was the fourth lending cause of nosocomial BSI, accounting for 8% of all infections. Forty-eight percent of 379 episodes of candidemia were due to species other than Candida albicans. The rank order of non-C. albicans species was C. glabrata (20%) > C. tropicalis (11%) > C. parapsilosis (8%) > C. krusei (5%) > other Candida spp. (4%). The species distribution varied according to geographic region, with non-C. albicans species predominating in the Northeast (54%) and Southeast (53%) regions, and C. albicans predominating in the Northwest (60%) and Southwest (70%) regions. In vitro susceptibility studies demonstrated that 95% of Man-C. albicans isolates were susceptible to 5-fluorocytosine, and 84% and 75% were susceptible to fluconazole and itraconazole, respectively. Geographic variation in susceptibility to itraconazole, but not other agents, was observed. Isolates from the Northwest and Southeast regions were more frequently resistant to itraconazole (29-30%) than those from the Northeast and Southwest regions (17-18%). Molecular epidemiologic studies revealed possible nosocomial transmission (Foe medical centers). Continued surveillance for the presence of non-C. albicans species among hospitalized patients is recommended. (C) 1998 Elsevier Science Inc.
引用
收藏
页码:121 / 129
页数:9
相关论文
共 35 条
[1]   The epidemiology of hematogenous candidiasis caused by different Candida species [J].
AbiSaid, D ;
Anaissie, E ;
Uzun, O ;
Raad, I ;
Pinzcowski, H ;
Vartivarian, S .
CLINICAL INFECTIOUS DISEASES, 1997, 24 (06) :1122-1128
[2]  
AREVALO MP, 1994, J CHEMOTHERAPY, V6, P226
[3]   SECULAR TRENDS IN NOSOCOMIAL PRIMARY BLOOD-STREAM INFECTIONS IN THE UNITED-STATES, 1980-1989 [J].
BANERJEE, SN ;
EMORI, TG ;
CULVER, DH ;
GAYNES, RP ;
JARVIS, WR ;
HORAN, T ;
EDWARDS, JR ;
TOLSON, J ;
HENDERSON, T ;
MARTONE, WJ .
AMERICAN JOURNAL OF MEDICINE, 1991, 91 :S86-S89
[4]   CANDIDA-ALBICANS GENOTYPING IN STUDIES WITH PATIENTS WITH AIDS DEVELOPING RESISTANCE TO FLUCONAZOLE [J].
BARTDELABESSE, E ;
BOIRON, P ;
CARLOTTI, A ;
DUPONT, B .
JOURNAL OF CLINICAL MICROBIOLOGY, 1993, 31 (11) :2933-2937
[5]  
Cormican MG, 1996, J ANTIMICROB CHEMOTH, V38, P561
[6]   IN-VITRO SUSCEPTIBILITY OF FUNGAL ISOLATES OF CLINICALLY IMPORTANT SPECIMENS TO ITRACONAZOLE, FLUCONAZOLE AND AMPHOTERICIN-B [J].
DERMOUMI, H .
CHEMOTHERAPY, 1994, 40 (02) :92-98
[7]   AN OVERVIEW OF NOSOCOMIAL INFECTIONS, INCLUDING THE ROLE OF THE MICROBIOLOGY LABORATORY [J].
EMORI, TG ;
GAYNES, RP .
CLINICAL MICROBIOLOGY REVIEWS, 1993, 6 (04) :428-442
[8]   Epidemiology of nosocomial fungal infections [J].
Fridkin, SK ;
Jarvis, WR .
CLINICAL MICROBIOLOGY REVIEWS, 1996, 9 (04) :499-&
[9]   Can we agree on the treatment of candidiasis? Response [J].
Graybill, JR .
CLINICAL INFECTIOUS DISEASES, 1997, 25 (01) :60-62
[10]   PATTERNS OF IN-VITRO ACTIVITY OF ITRACONAZOLE AND IMIDAZOLE ANTIFUNGAL AGENTS AGAINST CANDIDA-ALBICANS WITH DECREASED SUSCEPTIBILITY TO FLUCONAZOLE FROM SPAIN [J].
MARTINEZSUAREZ, JV ;
RODRIGUEZTUDELA, JL .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1995, 39 (07) :1512-1516