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Current Fungal Infection Reports最新文献

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Skin Infections Caused by Emerging Candida Species 新出现的念珠菌引起的皮肤感染
IF 1.4 Q3 INFECTIOUS DISEASES Pub Date : 2020-03-27 DOI: 10.1007/s12281-020-00380-9
V. M. Espinosa-Hernández, Verónica Morales-Pineda, E. Martínez-Herrera
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引用次数: 5
Coccidioidomycosis in Children and Adolescents: an Update 儿童和青少年球虫病的最新进展
IF 1.4 Q3 INFECTIOUS DISEASES Pub Date : 2020-03-12 DOI: 10.1007/s12281-020-00381-8
M. Maza-Morales, M. Rivas-Calderón, E. Barrón-Calvillo, M. García-Romero
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引用次数: 2
Extrapolating Antifungal Animal Data to Humans - Is it reliable? 将抗真菌动物数据推断给人类--可靠吗?
IF 1.4 Q3 INFECTIOUS DISEASES Pub Date : 2020-03-01 Epub Date: 2020-01-16 DOI: 10.1007/s12281-020-00370-x
Victoria M Stevens, Scott W Mueller, Paul M Reynolds, Robert MacLaren, Tyree H Kiser

Purpose of review: This article aimed to review animal models of antifungals and identifies human literature to assess if the extrapolation of results is reliable.

Recent findings: Animal studies have helped identify AUC/MIC targets for new drugs and formulations such as isavuconazole and delayed release posaconazole that have translated to successful outcomes in humans. Models have also been influential in the identification of possible combination therapies for the treatment of aspergillosis, such as voriconazole and echinocandins. However, challenges are endured with animal models when it comes to replicating the pharmacokinetics of humans which has been exemplified with the newest itraconazole formulation. Additionally, animal models have displayed a survival benefit with the use of iron chelators and amphotericin for mucormycosis which was not demonstrated in humans.

Summary: Animal models have been a staple in the development and optimization of antifungal agents. They afford the ability to investigate uncommon diseases, such as invasive fungal infections, that would otherwise take years and many resources to complete. Although there are many benefits of animal models there are also shortcomings. This is why the reliability of extrapolating data from animal models to humans is often scrutinized.

综述目的:本文旨在回顾抗真菌药物的动物模型,并对人类文献进行鉴定,以评估外推结果是否可靠:动物研究有助于确定新药和新制剂(如异武康唑和缓释泊沙康唑)的AUC/MIC目标,从而在人体中取得成功。在确定治疗曲霉菌病的可能联合疗法(如伏立康唑和棘菌素)方面,动物模型也发挥了重要作用。然而,动物模型在复制人体药代动力学方面面临挑战,最新的伊曲康唑制剂就是一个例子。此外,动物模型在使用铁螯合剂和两性霉素治疗粘孢子菌病时显示出了生存优势,而这在人类身上并未得到证实。动物模型能够研究侵袭性真菌感染等不常见疾病,否则将需要数年时间和大量资源才能完成。虽然动物模型有很多优点,但也有不足之处。因此,从动物模型向人类推断数据的可靠性经常受到审查。
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引用次数: 0
Applying Pharmacogenomics to Antifungal Selection and Dosing: Are We There Yet? 将药物基因组学应用于抗真菌选择和给药:我们做到了吗?
IF 1.4 Q3 INFECTIOUS DISEASES Pub Date : 2020-03-01 Epub Date: 2020-01-16 DOI: 10.1007/s12281-020-00371-w
Matthew A Miller, Yee Ming Lee

Purpose of review: This review summarizes recent literature for applying pharmacogenomics to antifungal selection and dosing, providing an approach to implementing antifungal pharmacogenomics in clinical practice.

Recent findings: The Clinical Pharmacogenetics Implementation Consortium published guidelines on CYP2C19 and voriconazole, with recommendations to use alternative antifungals or adjust voriconazole dose with close therapeutic drug monitoring (TDM). Recent studies demonstrate an association between CYP2C19 phenotype and voriconazole levels, clinical outcomes, and adverse events. Additionally, CYP2C19-guided preemptive dose adjustment demonstrated benefit in two prospective studies for prophylaxis. Pharmacokinetic-pharmacodynamic modeling studies have generated proposed voriconazole treatment doses based on CYP2C19 phenotypes, with further validation studies needed.

Summary: Sufficient evidence is available for implementing CYP2C19-guided voriconazole selection and dosing among select patients at risk for invasive fungal infections. The institution needs appropriate infrastructure for pharmacogenomic testing, integration of results in the clinical decision process, with TDM confirmation of goal trough achievement, to integrate antifungal pharmacogenomics into routine clinical care.

综述目的:本文综述了近年来药物基因组学在抗真菌药物选择和给药方面的研究进展,为临床应用药物基因组学治疗抗真菌药物提供了思路。最近的发现:临床药理学实施联盟发布了CYP2C19和伏立康唑的指南,建议使用替代抗真菌药物或在密切治疗药物监测(TDM)的同时调整伏立康唑剂量。最近的研究表明CYP2C19表型与伏立康唑水平、临床结果和不良事件之间存在关联。此外,cyp2c19引导的预防性剂量调整在两项前瞻性研究中显示出益处。基于CYP2C19表型的药代动力学-药效学建模研究产生了伏立康唑治疗剂量建议,需要进一步的验证研究。摘要:有足够的证据支持在有侵袭性真菌感染风险的患者中实施cyp2c19指导的伏立康唑选择和给药。该机构需要适当的药物基因组学检测基础设施,在临床决策过程中整合结果,通过实现TDM确认目标,将抗真菌药物基因组学整合到常规临床护理中。
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引用次数: 9
Should Etest MICs for Yeasts Be Categorized by Reference (BPs/ECVs) or by Etest (ECVs) Cutoffs as Determinants of Emerging Resistance? 酵母的测试mic是否应按参考值(bp / ecv)分类,还是按测试值(ecv)截止值作为新出现耐药性的决定因素进行分类?
IF 1.4 Q3 INFECTIOUS DISEASES Pub Date : 2020-02-20 DOI: 10.1007/s12281-020-00378-3
A. Espinel-Ingroff, E. Dannaoui
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引用次数: 4
Molecular Characterization of Coccidioides spp. Strains Isolated from Patients in the Argentine Republic 从阿根廷共和国患者身上分离的球虫菌株的分子特征
IF 1.4 Q3 INFECTIOUS DISEASES Pub Date : 2020-02-04 DOI: 10.1007/s12281-020-00372-9
A. Motter, M. C. López-Joffre, A. Toranzo, D. Salas, M. Viale, Flavia Vivot, A. Hevia, R. Abrantes, Julián Fernández, C. Canteros, R. Suárez-Alvarez
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引用次数: 0
Diagnosis, Burden and Mortality of Pneumocystis jirovecii Pneumonia in Venezuela 委内瑞拉乙氏肺囊虫肺炎的诊断、负担和死亡率
IF 1.4 Q3 INFECTIOUS DISEASES Pub Date : 2020-01-31 DOI: 10.1007/s12281-020-00377-4
M. Panizo, G. Ferrara, N. Garcia, Xiomara Moreno, T. Navas, E. Calderón
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引用次数: 0
Could Fungicides Lead to Azole Drug Resistance in a Cross-Resistance Manner among Environmental Cryptococcus Strains? 杀菌剂是否会导致环境隐球菌交叉耐药?
IF 1.4 Q3 INFECTIOUS DISEASES Pub Date : 2020-01-30 DOI: 10.1007/s12281-020-00373-8
J. P. F. Takahashi, L. M. Feliciano, D. Santos, S. Ramos, R. A. Oliveira, D. Attili-Angelis, Nadia Regina Rodrigues, J. Sampaio, M. dos Anjos Martins, M. Melhem
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引用次数: 7
Nucleic Acid Tools for Invasive Fungal Disease Diagnosis 用于侵袭性真菌疾病诊断的核酸工具
IF 1.4 Q3 INFECTIOUS DISEASES Pub Date : 2020-01-21 DOI: 10.1007/s12281-020-00374-7
P. White, A. Alanio, M. Cruciani, R. Gorton, L. Millon, V. Rickerts, R. Barnes, J. Donnelly, J. Loeffler
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引用次数: 11
An Approach to Suspected Invasive Fungal Infection in Patients with Hematologic Malignancy and HCT Recipients with Persistent Neutropenic Fever Despite Mold-Active Prophylaxis 血液恶性肿瘤患者和HCT接受者持续中性粒细胞减少热疑似侵袭性真菌感染的方法,尽管有霉菌活性预防
IF 1.4 Q3 INFECTIOUS DISEASES Pub Date : 2020-01-21 DOI: 10.1007/s12281-020-00375-6
Erica J. Stohs, A. Zimmer
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引用次数: 5
期刊
Current Fungal Infection Reports
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