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本文引用的文献

1
Rapid microbiological tests for bloodstream infections due to multidrug resistant Gram-negative bacteria: therapeutic implications.快速微生物学检测多重耐药革兰氏阴性菌引起的血流感染:治疗意义。
Clin Microbiol Infect. 2020 Jun;26(6):713-722. doi: 10.1016/j.cmi.2019.09.023. Epub 2019 Oct 11.
2
Fosfomycin for treatment of multidrug-resistant pathogens causing urinary tract infection: A real-world perspective and review of the literature.磷霉素治疗多药耐药病原体引起的尿路感染:真实世界的视角和文献回顾。
Diagn Microbiol Infect Dis. 2019 Nov;95(3):114856. doi: 10.1016/j.diagmicrobio.2019.06.008. Epub 2019 Jun 24.
3
Efficacy and Safety of Meropenem-Vaborbactam Versus Best Available Therapy for the Treatment of Carbapenem-Resistant Enterobacteriaceae Infections in Patients Without Prior Antimicrobial Failure: A Post Hoc Analysis.美罗培南-维巴坦与最佳治疗方案治疗无前期抗菌失败碳青霉烯类耐药肠杆菌科感染患者的疗效和安全性:一项事后分析。
Adv Ther. 2019 Jul;36(7):1771-1777. doi: 10.1007/s12325-019-00981-y. Epub 2019 May 16.
4
Eravacycline: The Tetracyclines Strike Back.依拉环素:四环素类药物卷土重来。
Ann Pharmacother. 2019 Nov;53(11):1124-1135. doi: 10.1177/1060028019850173. Epub 2019 May 12.
5
Treatment of Infections Due to MDR Gram-Negative Bacteria.多重耐药革兰氏阴性菌感染的治疗
Front Med (Lausanne). 2019 Apr 16;6:74. doi: 10.3389/fmed.2019.00074. eCollection 2019.
6
Polymyxins: To Combine or Not to Combine?多粘菌素:联合还是不联合?
Antibiotics (Basel). 2019 Apr 10;8(2):38. doi: 10.3390/antibiotics8020038.
7
In vitro activity of imipenem-relebactam against non-MBL carbapenemase-producing Klebsiella pneumoniae isolated in Greek hospitals in 2015-2016.2015-2016 年在希腊医院分离的产非 MBL 碳青霉烯酶肺炎克雷伯菌的亚胺培南-雷利巴坦体外活性。
Eur J Clin Microbiol Infect Dis. 2019 Jun;38(6):1143-1150. doi: 10.1007/s10096-019-03517-y. Epub 2019 Mar 1.
8
Plazomicin for Infections Caused by Carbapenem-Resistant Enterobacteriaceae.普拉佐米星用于治疗耐碳青霉烯类肠杆菌科细菌引起的感染。
N Engl J Med. 2019 Feb 21;380(8):791-793. doi: 10.1056/NEJMc1807634.
9
Once-Daily Plazomicin for Complicated Urinary Tract Infections.每日 1 次普拉唑米星治疗复杂性尿路感染。
N Engl J Med. 2019 Feb 21;380(8):729-740. doi: 10.1056/NEJMoa1801467.
10
International Consensus Guidelines for the Optimal Use of the Polymyxins: Endorsed by the American College of Clinical Pharmacy (ACCP), European Society of Clinical Microbiology and Infectious Diseases (ESCMID), Infectious Diseases Society of America (IDSA), International Society for Anti-infective Pharmacology (ISAP), Society of Critical Care Medicine (SCCM), and Society of Infectious Diseases Pharmacists (SIDP).多黏菌素优化使用国际共识指南:获得美国临床药师协会(ACCP)、欧洲临床微生物学和传染病学会(ESCMID)、美国感染病学会(IDSA)、国际抗感染药理学会(ISAP)、重症医学学会(SCCM)和感染病药师学会(SIDP)认可。
Pharmacotherapy. 2019 Jan;39(1):10-39. doi: 10.1002/phar.2209.

如何管理耐碳青霉烯类肺炎克雷伯菌感染。

How to manage KPC infections.

作者信息

Bassetti Matteo, Peghin Maddalena

机构信息

Clinica Malattie Infettive, Azienda Ospedaliero-Universitaria "Santa Maria della Misericordia", Piazzale S. Maria della Misericordia, n. 15, Udine, 33100, Italy.

Department of Medicine, Infectious Diseases Clinic, University of Udine and Azienda Sanitaria Universitaria, Integrata di Udine, Udine, Italy.

出版信息

Ther Adv Infect Dis. 2020 May 14;7:2049936120912049. doi: 10.1177/2049936120912049. eCollection 2020 Jan-Dec.

DOI:10.1177/2049936120912049
PMID:32489663
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7238785/
Abstract

Carbapenemase-producing Enterobacteriaceae represent an increasing global threat worldwide and carbapenemase (KPC)-producing (KPC-KP) has become one of the most important contemporary pathogens, especially in endemic areas. Risk stratification and rapid diagnostics laboratory workflows are of paramount importance and indication for therapy of KPC-KP infection must be individualized according to the baseline characteristics of the patient and severity of infection. The optimal treatment of infection because of KPC-KP organisms is uncertain and antibiotic options are limited. The knowledge of the patient's pathophysiology, infection site, and application of the pharmacokinetic/pharmacodynamic principles on the basis of minimum inhibitory concentration (MIC) has progressively gained major relevance. Combination therapies including high-dose meropenem, colistin, fosfomycin, tigecycline, and aminoglycosides are widely used, with suboptimal results. In the past few years, new antimicrobials targeting KPC-KP have been developed and are now at various stages of clinical research. However, their optimal use should be guaranteed in the long term for delaying, as much as possible, the emergence of resistance. Strict infection control measures remain necessary. The aim of this review is to discuss the challenges in the management and treatment of patients with infections because KPC-KP and provide an expert opinion.

摘要

产碳青霉烯酶肠杆菌科细菌在全球范围内构成的威胁日益增加,产碳青霉烯酶(KPC)的肺炎克雷伯菌(KPC-KP)已成为当代最重要的病原体之一,尤其是在流行地区。风险分层和快速诊断实验室工作流程至关重要,KPC-KP感染的治疗指征必须根据患者的基线特征和感染严重程度进行个体化。因KPC-KP菌株引起的感染的最佳治疗方法尚不确定,抗生素选择有限。了解患者的病理生理学、感染部位以及基于最低抑菌浓度(MIC)应用药代动力学/药效学原理已逐渐变得至关重要。包括大剂量美罗培南、黏菌素、磷霉素、替加环素和氨基糖苷类药物的联合治疗被广泛使用,但效果欠佳。在过去几年中,已开发出针对KPC-KP的新型抗菌药物,目前正处于临床研究的不同阶段。然而,从长远来看,应确保其最佳使用,以尽可能延缓耐药性的出现。严格的感染控制措施仍然必要。本综述的目的是讨论KPC-KP感染患者管理和治疗中的挑战并提供专家意见。