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首页> 外文期刊>Journal of Krishna Institute of Medical Sciences University. >Comparison of the VITEK 2 Yeast Antifungal Susceptibility Testing with CLSI Broth Microdilution Reference Method for Testing Four Antifungal Drugs against Candida species Isolated from Blood Samples.
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Comparison of the VITEK 2 Yeast Antifungal Susceptibility Testing with CLSI Broth Microdilution Reference Method for Testing Four Antifungal Drugs against Candida species Isolated from Blood Samples.

机译:将VITEK 2酵母抗真菌药敏试验与CLSI肉汤微稀释参考方法进行比较,以测试四种抗真菌药物针对从血样中分离出的念珠菌。

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Background: Although the patients in the IntensiveCare Unit (ICU) are at risk for candidemia resulting incomplication, rapid diagnosis of aetiologic agent willreduce the delay in initiating the appropriate therapywith adequate dosage of antifungals thus improvingthe outcome. Due to reduced susceptibility of nonalbicansCandida species to antifungal agents; testingthe antifungal susceptibility pattern has becomeimportant both epidemiologically and for patientmanagement. Aim and Objectives: To compare theVITEK 2 Yeast antifungal susceptibility testing withClinical and Laboratory Standards Institute (CLSI)Broth Microdilution (BMD) reference method againstisolates of Candida species and assess the CategoricalAgreement (CA) and errors. Material and Methods:Candida species isolated from blood samples ofpatients admitted under Medical and Surgical ICU ofKrishna Hospital and Medical Research Centre, Karadwere subjected to antifungal susceptibility testing byCLSI reference BMD and VITEK 2 method. Results:Compared to the reference BMD method, the VITEK 2system yielded highly reproducible and accurate MICresults and excellent overall categorical agreement at100% for amphotericin B, flucytosine, fluconazole,and voriconazole against C. albicans, C. tropicalis, C.krusei, C. parapsilosis, C. lusitaniae and C.guillermondii except C. rugosa and C. glabrata.Conclusion: The VITEK 2 method demonstratedexcellent reproducibility and standardization. Itprovides a fully automated method for fungalidentification, determining the MICs against Candidaspp. based on spectrophotometry, thus eliminating theinherent bias of manual MIC determination.
机译:背景:尽管重症监护病房(ICU)的患者有患上念珠菌血症并发并发症的风险,但快速诊断成因药物会减少开始采用适当剂量的抗真菌药物进行适当治疗的延迟,从而改善结果。由于非白色念珠菌对抗真菌剂的敏感性降低;测试抗真菌药性在流行病学和患者管理上都变得很重要。目的和目的:比较VITEK 2酵母抗真菌药敏试验与临床和实验室标准协会(CLSI)肉汤微稀释(BMD)参考方法对假丝酵母菌的分离物,并评估分类协议(CA)和错误。材料与方法:从卡拉德克里希纳医院和医学研究中心的医学和外科ICU入院的患者血液样本中分离出的念珠菌物种,通过CLSI参考BMD和VITEK 2方法进行了抗真菌药敏试验。结果:与参考BMD方法相比,VITEK 2系统可针对两性念珠菌B,氟胞嘧啶,氟康唑和伏立康唑对白念珠菌,热带热带念珠菌,克鲁斯酵母,C.krusei和C的结果进行重现和准确的MIC检测,并获得100%的优异总体分类一致性。结论:VITEK 2方法具有极好的可重复性和标准化性。它提供了一种用于真菌鉴定的全自动方法,可确定针对假丝酵母的MIC。基于分光光度法,从而消除了手动MIC测定的固有偏差。

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