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本文引用的文献

1
Wild-type MIC distributions and epidemiological cutoff values for caspofungin and Aspergillus spp. for the CLSI broth microdilution method (M38-A2 document).CLSI 肉汤微量稀释法(M38-A2 文件)中用于检测棘白菌素和曲霉菌属的野生型 MIC 分布和流行病学折点值。
Antimicrob Agents Chemother. 2011 Jun;55(6):2855-9. doi: 10.1128/AAC.01730-10. Epub 2011 Mar 21.
2
Wild-type MIC distributions and epidemiological cutoff values for the triazoles and six Aspergillus spp. for the CLSI broth microdilution method (M38-A2 document).CLSI 肉汤微量稀释法(M38-A2 文件)中三唑类药物和六种曲霉菌属的野生型 MIC 分布和流行病学折点值。
J Clin Microbiol. 2010 Sep;48(9):3251-7. doi: 10.1128/JCM.00536-10. Epub 2010 Jun 30.
3
Pharmacokinetics and pharmacodynamics of amphotericin B deoxycholate, liposomal amphotericin B, and amphotericin B lipid complex in an in vitro model of invasive pulmonary aspergillosis.两性霉素 B 去氧胆酸盐、脂质体两性霉素 B 和两性霉素 B 脂质复合物在侵袭性肺曲霉病体外模型中的药代动力学和药效学。
Antimicrob Agents Chemother. 2010 Aug;54(8):3432-41. doi: 10.1128/AAC.01586-09. Epub 2010 May 3.
4
Wild-type MIC distributions and epidemiological cutoff values for the echinocandins and Candida spp.棘白菌素类药物和念珠菌属的野生型 MIC 分布和流行病学折点值
J Clin Microbiol. 2010 Jan;48(1):52-6. doi: 10.1128/JCM.01590-09. Epub 2009 Nov 18.
5
Wild-type MIC distribution and epidemiological cutoff values for Aspergillus fumigatus and three triazoles as determined by the Clinical and Laboratory Standards Institute broth microdilution methods.根据临床和实验室标准协会的肉汤微量稀释方法,确定了烟曲霉野生型 MIC 分布和三种三唑类药物的流行病学截断值。
J Clin Microbiol. 2009 Oct;47(10):3142-6. doi: 10.1128/JCM.00940-09. Epub 2009 Aug 19.
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Patterns of susceptibility of Aspergillus isolates recovered from patients enrolled in the Transplant-Associated Infection Surveillance Network.从参加移植相关感染监测网络的患者中分离出的烟曲霉分离株的敏感性模式。
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7
Trends in invasive fungal infections, with emphasis on invasive aspergillosis.侵袭性真菌感染的趋势,重点是侵袭性曲霉病。
Clin Microbiol Infect. 2009 Jul;15(7):625-33. doi: 10.1111/j.1469-0691.2009.02929.x.
8
Species identification and antifungal susceptibility patterns of species belonging to Aspergillus section Nigri.黑曲霉组物种的物种鉴定及抗真菌药敏模式
Antimicrob Agents Chemother. 2009 Oct;53(10):4514-7. doi: 10.1128/AAC.00585-09. Epub 2009 Jul 27.
9
A long journey from minimum inhibitory concentration testing to clinically predictive breakpoints: deterministic and probabilistic approaches in deriving breakpoints.从最低抑菌浓度测试到临床预测断点的漫长历程:推导断点的确定性和概率性方法
Infection. 2009 Aug;37(4):296-305. doi: 10.1007/s15010-009-7108-9. Epub 2009 Jul 23.
10
In vitro activities of various antifungal drugs against Aspergillus terreus: Global assessment using the methodology of the European committee on antimicrobial susceptibility testing.多种抗真菌药物对土曲霉的体外活性:采用欧洲抗菌药物敏感性试验委员会方法进行的全球评估
Antimicrob Agents Chemother. 2009 Feb;53(2):794-5. doi: 10.1128/AAC.00335-08. Epub 2008 Dec 8.

CLSI 肉汤微量稀释法(M38-A2 文件)中两性霉素 B 和曲霉菌属的野生型 MIC 分布和流行病学折点值。

Wild-type MIC distributions and epidemiological cutoff values for amphotericin B and Aspergillus spp. for the CLSI broth microdilution method (M38-A2 document).

机构信息

VCU Medical Center, Richmond, Virginia, USA.

出版信息

Antimicrob Agents Chemother. 2011 Nov;55(11):5150-4. doi: 10.1128/AAC.00686-11. Epub 2011 Aug 29.

DOI:10.1128/AAC.00686-11
PMID:21876047
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3195003/
Abstract

Although clinical breakpoints have not been established for mold testing, epidemiological cutoff values (ECVs) are available for Aspergillus spp. versus the triazoles and caspofungin. Wild-type (WT) MIC distributions (organisms in a species-drug combination with no acquired resistance mechanisms) were defined in order to establish ECVs for six Aspergillus spp. and amphotericin B. Two sets (CLSI/EUCAST broth microdilution) of available MICs were evaluated: those for A. fumigatus (3,988/833), A. flavus (793/194), A. nidulans (184/69), A. niger (673/140), A. terreus (545/266), and A. versicolor (135/22). Three sets of data were analyzed: (i) CLSI data gathered in eight independent laboratories in Canada, Europe, and the United States; (ii) EUCAST data from a single laboratory; and (iii) the combined CLSI and EUCAST data. ECVs, expressed in μg/ml, that captured 95%, 97.5%, and 99% of the modeled wild-type population (CLSI and combined data) were as follows: for A. fumigatus, 2, 2, and 4; for A. flavus, 2, 4, and 4; for A. nidulans, 4, 4, and 4; for A. niger, 2, 2, and 2; for A. terreus, 4, 4, and 8; and for A. versicolor, 2, 2, and 2. Similar to the case for the triazoles and caspofungin, amphotericin B ECVs may aid in the detection of strains with acquired mechanisms of resistance to this agent.

摘要

虽然尚未建立用于霉菌检测的临床折点,但已有曲霉菌属与三唑类和卡泊芬净的流行病学切点值(ECV)。为了确定六种曲霉菌属和两性霉素 B 的 ECV,定义了野生型(WT)MIC 分布(在无获得性耐药机制的种-药物组合中的生物体)。评估了两套(CLSI/EUCAST 肉汤微量稀释法)可用 MIC:用于烟曲霉(3,988/833)、黄曲霉(793/194)、构巢曲霉(184/69)、黑曲霉(673/140)、土曲霉(545/266)和彩绒革盖菌(135/22)的 MIC。分析了三组数据:(i)在加拿大、欧洲和美国的八个独立实验室中收集的 CLSI 数据;(ii)来自单个实验室的 EUCAST 数据;以及(iii)CLSI 和 EUCAST 合并数据。以 μg/ml 表示的捕获了 95%、97.5%和 99%模型野生型群体(CLSI 和合并数据)的 ECV 如下:对于烟曲霉,分别为 2、2 和 4;对于黄曲霉,分别为 2、4 和 4;对于构巢曲霉,分别为 4、4 和 4;对于黑曲霉,分别为 2、2 和 2;对于土曲霉,分别为 4、4 和 8;对于彩绒革盖菌,分别为 2、2 和 2。与三唑类和卡泊芬净的情况类似,两性霉素 B 的 ECV 可能有助于检测对该药物具有获得性耐药机制的菌株。