Comparison of fungemia caused by Candida and non-Candida rare yeasts: a retrospective study from a tertiary care hospital

被引:1
作者
Oz, Yasemin [1 ]
Yilmaz, Mustafa [1 ]
Bulduk, Tuba [2 ,4 ]
Basayigit, Mehmet [1 ]
Gunduz, Eren [2 ]
Metintas, Selma [3 ]
机构
[1] Eskisehir Osmangazi Univ, Med Fac, Dept Microbiol, TR-26040 Eskisehir, Turkiye
[2] Eskisehir Osmangazi Univ, Med Fac, Dept Hematol, TR-26040 Eskisehir, Turkiye
[3] Eskisehir Osmangazi Univ, Med Fac, Dept Publ Hlth, TR-26040 Eskisehir, Turkiye
[4] Gulhane Educ & Training Hosp, Dept Hematol, Ankara, Turkiye
关键词
Candida; candidemia; fungemia; non-Candida; rare yeast;
D O I
10.1093/mmy/myae037
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Although Candida species are the most common cause of fungemia, non-Candida rare yeasts (NCY) have been increasingly reported worldwide. Although the importance of these yeast infections is recognized, current epidemiological information about these pathogens is limited, and they have variable antifungal susceptibility profiles. In this study, we aimed to evaluate the clinical characteristics for fungemia caused by NCY by comparing with candidemia. The episodes of NCY fungemia between January 2011 and August 2023 were retrospectively evaluated in terms of clinical characteristics, predisposing factor, and outcome. In addition, a candidemia group, including patients in the same period was conducted for comparison. Antifungal susceptibility tests were performed according to the reference method. A total of 85 patients with fungemia episodes were included: 25 with NCY fungemia and 60 with candidemia. Fluconazole had high minimal inhibitory concentration (MIC) values against almost all NCY isolates. The MIC values for voriconazole, posaconazole, and amphotericin B were <= 2 mu g/ml, and for caspofungin and anidulafungin were >= 1 mu g/ml against most of isolates. Hematological malignancies, immunosuppressive therapy, neutropenia and prolonged neutropenia, polymicrobial bacteremia/fungemia, preexposure to antifungal drugs, and breakthrough fungemia were associated with NCY fungemia, whereas intensive care unit admission, diabetes mellitus, urinary catheters, and total parenteral nutrition were associated with candidemia. In conclusion, the majority of fungemia due to NCY species was the problem, particularly in hematology units and patients with hematological malignancy. Preexposure to antifungal drugs likely causes a change in the epidemiology of fungemia in favor of non-albicans Candida and/or NCY. Among all fungemia episodes, hematological malignancies, immunosuppressive therapy, neutropenia, and preexposure to antifungals were risk factors for non-Candida yeast fungemia; diabetes mellitus, urinary catheters, and total parenteral nutrition were risks for candidemia.
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