首页> 外文期刊>Journal of Medical Microbiology: An Official Journal of the Pathological Society of Great Britain and Ireland >Comparison of susceptibility patterns using commercially available susceptibility testing methods performed on prevalent Candida spp.
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Comparison of susceptibility patterns using commercially available susceptibility testing methods performed on prevalent Candida spp.

机译:使用市售药敏试验方法对流行的假丝酵母菌进行药敏模式比较。

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The rising rates of invasive fungal infections caused by non-albicans Candida and the increasing emergence of antifungal resistance complicate the management of invasive candidiasis. Accurate and timely antifungal susceptibility testing is critical to targeting antifungal therapy. The purpose of this study was to compare commercially available susceptibility testing methods using prospectively collected Candida isolates. Susceptibility testing was performed on 74 Candida isolates collected from July 2014 to March 2015 using broth microdilution according to the Clinical and Laboratory Standards Institute method, Etest, Vitek 2 (YS-05) and Sensititre. Essential agreement and categorical agreement (CA) were assessed using the reference method. Of the 34 total blood isolates collected, Candida albicans comprised only 38?% (13) of the Candida spp. with Candidaglabrata being nearly as prevalent (29?%, 10). CA using Etest was 86?% for fluconazole, 72?% for caspofungin, 98?% for micafungin and 97?% for anidulafungin. Vitek 2 CA was 90?% for fluconazole and 98?% for caspofungin. Sensititre CA was 93?% for fluconazole, 98?% for caspofungin, 98?% for micafungin and 100?% for anidulafungin. Although our study tested a small population of Candida isolates, our results were variable by method. When implementing antifungal susceptibility testing, clinicians should be aware of the strengths and limitations of each testing method.
机译:由非白色念珠菌引起的侵袭性真菌感染率上升和抗真菌药耐药性的增加使侵袭性念珠菌病的管理复杂化。准确及时的抗真菌药敏试验对于靶向抗真菌治疗至关重要。这项研究的目的是比较使用前瞻性收集的念珠菌分离株的市售药敏试验方法。根据临床和实验室标准协会方法,Etest,Vitek 2(YS-05)和Sensititre,使用肉汤微量稀释法对2014年7月至2015年3月收集的74株念珠菌分离株进行了药敏试验。使用参考方法评估基本同意和绝对同意(CA)。在收集的34种血液分离物中,白色念珠菌仅占假丝酵母菌的38%(13)。与念珠菌几乎一样普遍(29%,10)。使用Etest的氟康唑的CA率为86%,卡泊芬净为72%,米卡芬净为98%,阿尼芬净为97%。氟康唑的Vitek 2 CA为90%,卡泊芬净为98%。氟康唑的敏感性CA为93%,卡泊芬净为98%,米卡芬净为98%,阿尼芬净为100%。尽管我们的研究测试了少量的念珠菌分离株,但我们的结果因方法而异。在进行抗真菌药敏试验时,临床医生应了解每种检测方法的优缺点。

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