Detection of Bacterial and Yeast Species with the Bactec 9120 Automated System with Routine Use of Aerobic, Anaerobic, and Fungal Media

被引:29
作者
Chiarini, Alfredo [1 ,2 ]
Palmeri, Angelo [1 ]
Amato, Teresa [2 ]
Immordino, Rita [2 ]
Distefano, Salvatore [1 ,2 ]
Giammanco, Anna [1 ,2 ]
机构
[1] Univ Palermo, Dept Sci Hlth Promot, Div Microbiol, I-90127 Palermo, Italy
[2] Microbiol Lab, AOUP Paolo Giaccone, Palermo, Italy
关键词
D O I
10.1128/JCM.01014-08
中图分类号
Q93 [微生物学];
学科分类号
071005 [微生物学]; 100705 [微生物与生化药学];
摘要
During the period 2006 and 2007, all blood cultures required by four units at high infective risk and most of those required by other units of the University Hospital of Palermo, Palermo, Italy were performed using a Bactec 9120 automated blood culture system with a complete set of Plus Aerobic/F, Plus Anaerobic/F, and Mycosis IC/F bottles. The aim of the study was to enable the authors to gain firsthand experience of the culture potentialities of the three different media, to obtain information regarding the overall and specific recovery of bacteria and yeasts from blood cultures in the hospital, and to reach a decision as to whether and when to utilize anaerobic and fungal bottles. Although very few bloodstream infections (1.8%) were associated with obligate anaerobes, the traditional routine use of anaerobic bottles was confirmed because of their usefulness, not only in the detection of anaerobes, but also in that of gram-positive cocci and fermentative gram-negative bacilli. In this study, Mycosis IC/F bottles detected 77.4% of all the yeast isolates, 87.0% of yeasts belonging to the species Candida albicans, and 45.7% of nonfermentative gram-negative bacilli resistant to chloramphenicol and tobramycin. In order to improve the diagnosis of fungemia in high-risk patients, the additional routine use of fungal bottles was suggested when, as occurred in the intensive-care unit and in the hematology unit of the University Hospital of Palermo, high percentages of bloodstream infections are associated with yeasts, and/or antibiotic-resistant bacteria and/or multiple bacterial isolates capable of inhibiting yeast growth in aerobic bottles.
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页码:4029 / 4033
页数:5
相关论文
共 23 条
[1]
Epidemiology and outcome of nosocomial and community-onset bloodstream infection [J].
Diekema, DJ ;
Beekmann, SE ;
Chapin, KC ;
Morel, KA ;
Munson, E ;
Doern, GV .
JOURNAL OF CLINICAL MICROBIOLOGY, 2003, 41 (08) :3655-3660
[2]
DORSHER CW, 1991, REV INFECT DIS, V13, P633
[3]
Optimum detection times for bacteria and yeast species with the BACTEC 9120 aerobic blood culture system:: Evaluation for a 5-year period in a Turkish university hospital [J].
Durmaz, G ;
Us, T ;
Aydinli, A ;
Kiremitci, A ;
Kiraz, N ;
Akgün, Y .
JOURNAL OF CLINICAL MICROBIOLOGY, 2003, 41 (02) :819-821
[4]
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
[5]
Epidemiology and susceptibility profile of blood culture isolates in an intensive care unit (2002-2005) [J].
Elouennass, M. ;
Sahnoun, I. ;
Zrara, A. ;
Bajjou, T. ;
Elhamzaoui, S. .
MEDECINE ET MALADIES INFECTIEUSES, 2008, 38 (01) :18-24
[6]
Comparison of BACTEC PLUS blood culture media to BacT/Alert FA blood culture media for detection of bacterial pathogens in samples containing therapeutic levels of antibiotics [J].
Flayhart, Diane ;
Borek, Anita P. ;
Wakefield, Teresa ;
Dick, James ;
Carroll, Karen C. .
JOURNAL OF CLINICAL MICROBIOLOGY, 2007, 45 (03) :816-821
[7]
Fricker-Hidalgo HN, 2004, J CLIN MICROBIOL, V42, P1855, DOI 10.1128/JCM.42.4.1855-1856.2004
[8]
GROWTH-INHIBITION OF PATHOGENIC YEASTS BY PSEUDOMONAS-AERUGINOSA IN-VITRO - CLINICAL IMPLICATIONS IN BLOOD CULTURES [J].
GRILLOT, R ;
PORTMANNCOFFIN, V ;
AMBROISETHOMAS, P .
MYCOSES, 1994, 37 (9-10) :343-347
[9]
DETECTION OF FUNGEMIA OBSCURED BY CONCOMITANT BACTEREMIA - INVITRO AND INVIVO STUDIES [J].
HOCKEY, LJ ;
FUJITA, NK ;
GIBSON, TR ;
ROTROSEN, D ;
MONTGOMERIE, JZ ;
EDWARDS, JE .
JOURNAL OF CLINICAL MICROBIOLOGY, 1982, 16 (06) :1080-1085
[10]
Horvath LL, 2004, J CLIN MICROBIOL, V42, P1855