Do in vitro susceptibility data predict the microbiologic response to amphotericin B?: Results of a prospective study of patients with Candida fungemia

被引:173
作者
Nguyen, MH
Clancy, CJ
Yu, VL
Yu, YC
Morris, AJ
Snydman, DR
Sutton, DA
Rinaldi, MG
机构
[1] Univ Florida, Coll Med, Dept Med, JHMHC, Gainesville, FL 32610 USA
[2] VA Med Ctr, Gainesville, FL USA
[3] Univ Pittsburgh, Med Ctr, Pittsburgh, PA USA
[4] VA Med Ctr, Pittsburgh, PA USA
[5] Duke Med Ctr, Durham, NC USA
[6] Tufts Med Ctr, Boston, MA USA
[7] Univ Texas, Hlth Sci Ctr, San Antonio, TX USA
关键词
D O I
10.1086/514193
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Outcome for 105 patients with candidemia treated with amphotericin B was correlated with amphotericin B in vitro susceptibility results, Thirty-three patients had microbiologic failure, which was defined as persistence of Candida in the bloodstream despite greater than or equal to 3 days of amphotericin B. Amphotericin B minimum inhibitory concentrations (MICs) were determined by the National Committee for Clinical Laboratory Standards methodology, After determination of MICs, the minimal lethal concentrations (MLCs) were determined. The isolates tested yielded a narrow range of amphotericin B MICs (0.06-2 mu g/mL); only 5% (5/105) exhibited MICs greater than or equal to 1 mu g/mL. The MLC range, on the other hand, was significantly broader (0.125 to >16 mu g/mL); 24% (25/105) exhibited MLCs greater than or equal to 1 mu g/mL. The strongest predictor for microbiologic failure was 48-h MLC (P < .001), followed by 24-h MLC (P = .03) and 48-h MIC (P = .11). A resistant break point for amphotericin B of >1 mu g/mL for MLC and greater than or equal to 1 mu g/mL for MIC could be inferred from this study.
引用
收藏
页码:425 / 430
页数:6
相关论文
共 9 条
[1]  
AMSTERDAM D, 1996, ANTIBIOTICS LAB MED, P103
[2]   AMPHOTERICIN-B SERUM CONCENTRATIONS DURING THERAPY [J].
FIELDS, BT ;
BATES, JH ;
ABERNATHY, RS .
APPLIED MICROBIOLOGY, 1970, 19 (06) :955-+
[3]  
*NAT COMM CLIN LAB, 1994, M27A NCCLS
[4]   THERAPEUTIC APPROACHES IN PATIENTS WITH CANDIDEMIA - EVALUATION IN A MULTICENTER, PROSPECTIVE, OBSERVATIONAL STUDY [J].
NGUYEN, MH ;
PEACOCK, JE ;
TANNER, DC ;
MORRIS, AJ ;
NGUYEN, ML ;
SNYDMAN, DR ;
WAGENER, MM ;
YU, VL .
ARCHIVES OF INTERNAL MEDICINE, 1995, 155 (22) :2429-2435
[5]   DETECTION OF AMPHOTERICIN B-RESISTANT CANDIDA ISOLATES IN A BROTH-BASED SYSTEM [J].
REX, JH ;
COOPER, CR ;
MERZ, WG ;
GALGIANI, JN ;
ANAISSIE, EJ .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1995, 39 (04) :906-909
[6]   ANTIFUNGAL SUSCEPTIBILITY TESTING [J].
REX, JH ;
PFALLER, MA ;
RINALDI, MG ;
POLAK, A ;
GALGIANI, JN .
CLINICAL MICROBIOLOGY REVIEWS, 1993, 6 (04) :367-381
[7]   ANTIFUNGAL SUSCEPTIBILITY TESTING OF ISOLATES FROM A RANDOMIZED, MULTICENTER TRIAL OF FLUCONAZOLE VERSUS AMPHOTERICIN-B AS TREATMENT OF NONNEUTROPENIC PATIENTS WITH CANDIDEMIA [J].
REX, JH ;
PFALLER, MA ;
BARRY, AL ;
NELSON, PW ;
WEBB, CD .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1995, 39 (01) :40-44
[8]   Development of interpretive breakpoints for antifungal susceptibility testing: Conceptual framework and analysis of in vitro in vivo correlation data for fluconazole, itraconazole, and Candida infections [J].
Rex, JH ;
Pfaller, MA ;
Galgiani, JN ;
Bartlett, MS ;
EspinelIngroff, A ;
Ghannoum, MA ;
Lancaster, M ;
Odds, FC ;
Rinaldi, MG ;
Walsh, TJ ;
Barry, AL .
CLINICAL INFECTIOUS DISEASES, 1997, 24 (02) :235-247
[9]   TRICHOSPORON-BEIGELII, AN EMERGING PATHOGEN RESISTANT TO AMPHOTERICIN-B [J].
WALSH, TJ ;
MELCHER, GP ;
RINALDI, MG ;
LECCIONES, J ;
MCGOUGH, DA ;
KELLY, P ;
LEE, J ;
CALLENDER, D ;
RUBIN, M ;
PIZZO, PA .
JOURNAL OF CLINICAL MICROBIOLOGY, 1990, 28 (07) :1616-1622