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Assessment of Accuracy of Identification of Pathogenic Yeasts in Microbiology Laboratories in the United Kingdom

机译:英国微生物实验室中病原菌鉴定的准确性评估

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Rapid, accurate identification of yeast isolates from clinical samples has always been important given their innately variable antifungal susceptibility profiles. Recently, this has become paramount with the proposed introduction of species-specific interpretive breakpoints for MICs obtained in yeast antifungal susceptibility tests (M. A. Pfaller, D. Andes, D. J. Diekema, A. Espinel–Ingroff, D. Sheehan, and CLSI Subcommittee for Antifungal Susceptibility Testing, Drug Resist. Updat. 13:180–195, 2010). Here, we present the results of a 12-month evaluation of the accuracy of identifications that accompany yeast isolates submitted to the Mycology Reference Laboratory (United Kingdom) for either confirmation of identity or susceptibility testing. In total, 1,781 yeast isolates were analyzed, and the robustness of prior identifications obtained in microbiology laboratories throughout the United Kingdom was assessed using a combination of culture on chromogenic agar, morphology on cornmeal agar, and molecular identification by pyrosequencing. Over 40% of isolates (755) were submitted without any suggested identification. Of those isolates with a prior identification, 100 (9.7%) were incorrectly identified. Error rates ranged from 5.2% (for organisms submitted for antifungal susceptibility testing) to 18.2% (for organisms requiring confirmation of identity) and varied in a strictly species-specific manner. At least 50% of identification errors would be likely to affect interpretation of MIC data, with a possible impact on patient management. In addition, 2.3% of submitted cultures were found to contain mixtures of at least two yeast species. The vast majority of mixtures had gone undetected in the referring laboratory and would have impacted the interpretation of antifungal susceptibility profiles and patient management. Some of the more common misidentifications are discussed according to the identification method employed, with suggestions for avoiding such misinterpretations.
机译:鉴于其天生具有可变的抗真菌药敏性,从临床样品中快速,准确地鉴定酵母分离株一直很重要。最近,这对于提议引入针对酵母抗真菌药敏试验中获得的MIC的物种特定解释性断裂点至关重要(MA Pfaller,D.Andes,DJ Diekema,A.Espinel-Ingroff,D.Sheehan和CLSI抗真菌小组委员会药敏测试,抗药性更新。13:180-195,2010年)。在这里,我们介绍了为期12个月的鉴定准确性的评估结果,该鉴定与酵母菌分离物一起提交给了Mycology Reference Laboratory(英国)以确认身份或进行药敏测试。总共分析了1,781个酵母菌分离物,并结合了生色琼脂上的培养物,玉米面琼脂上的形态学和焦磷酸测序进行分子鉴定的组合,评估了在英国整个微生物学实验室获得的先前鉴定结果的可靠性。超过40%的分离株(755)提交时没有任何建议的鉴定。在那些事先有鉴定的菌株中,有100株(9.7%)被错误鉴定。错误率的范围从5.2%(对于提交用于抗真菌药敏试验的生物)到18.2%(对于需要确认身份的生物),并且严格按照特定于物种的方式变化。至少有50%的识别错误可能会影响MIC数据的解释,并可能影响患者管理。此外,发现2.3%提交的培养物中含有至少两种酵母菌的混合物。绝大多数混合物在推荐实验室中未被发现,并且会影响抗真菌药敏性和患者管理的解释。根据所采用的识别方法,讨论了一些较常见的误识别,并提出了避免这种误解的建议。

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