NOSOCOMIAL BREAKTHROUGH FUNGEMIA DURING ANTIFUNGAL PROPHYLAXIS OR EMPIRICAL ANTIFUNGAL THERAPY IN 41 CANCER-PATIENTS RECEIVING ANTINEOPLASTIC CHEMOTHERAPY - ANALYSIS OF ETIOLOGY RISK-FACTORS AND OUTCOME
V. Krcmery et al., NOSOCOMIAL BREAKTHROUGH FUNGEMIA DURING ANTIFUNGAL PROPHYLAXIS OR EMPIRICAL ANTIFUNGAL THERAPY IN 41 CANCER-PATIENTS RECEIVING ANTINEOPLASTIC CHEMOTHERAPY - ANALYSIS OF ETIOLOGY RISK-FACTORS AND OUTCOME, Journal of antimicrobial chemotherapy, 41(3), 1998, pp. 373-380
Forty-one episodes of breakthrough fungaemia occurring over a 7.5 year
period in the National and St Elizabeth's Cancer Institutes in Bratis
lava, Slovakia, were analysed. Five of them occurred during prophylaxi
s with fluconazole tone Torulopsis glabrata, one Hansenula anomala, tw
o Candida krusei and one Candida parapsilosis), ten with itraconazole
(three Trichosporon pullulans, one Trichosporon beigelii, one Cryptoco
ccus laurentii, three Candida albicans and two T. glabrata), 11 during
prophylaxis with ketoconazole (one Candida norvegenesis, one C. parap
silosis, one C. krusei, one Candida tropicalis, five C. albicans, one
Candida stellatoidea and one C. laurentii and 15 during empirical ther
apy with amphotericin B (ten C. albicans, two T. beigelii and three Ca
ndida lusitaniae). The most frequent risk factors for breakthrough fun
gaemia were neutropenia, previous therapy with multiple antibiotics an
d recent catheter insertion. Comparing these episodes with 38 non-brea
kthrough fungaemias (appearing at the same institute in the same perio
d) differences in certain risk factors were noted: breakthrough fungae
mias were more frequently observed in patients with acute leukaemia (3
9.0% vs 5.2%, P < 0.001), mucositis (34.2% vs 13.1%, P < 0.05), prophy
laxis with quinolones (58.5% vs 15.8%, P < 0.0001) and catheter-associ
ated infections (29.3% vs 2.6%, P < 0.003). In this subgroup overall m
ortality (36.6% vs 28.8%) or early attributable mortality (22.0% vs 23
.6%) were not significantly different.