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本文引用的文献

1
WHO recommendations for multidrug-resistant tuberculosis.
Lancet. 2016 Nov 5;388(10057):2234. doi: 10.1016/S0140-6736(16)32071-2.
2
WHO recommendations for multidrug-resistant tuberculosis - Authors' reply.世界卫生组织关于耐多药结核病的建议——作者回复。
Lancet. 2016 Nov 5;388(10057):2234-2235. doi: 10.1016/S0140-6736(16)31465-9.
3
Eligibility for the Shorter Multidrug-Resistant Tuberculosis Regimen: Ambiguities in the World Health Organization Recommendations.较短疗程耐多药结核病治疗方案的适用标准:世界卫生组织建议中的模糊之处
Am J Respir Crit Care Med. 2016 Oct 15;194(8):1028-1029. doi: 10.1164/rccm.201605-1080LE.
4
Population-based resistance of Mycobacterium tuberculosis isolates to pyrazinamide and fluoroquinolones: results from a multicountry surveillance project.基于人群的结核分枝杆菌分离株对吡嗪酰胺和氟喹诺酮类药物的耐药性:一项多国监测项目的结果
Lancet Infect Dis. 2016 Oct;16(10):1185-1192. doi: 10.1016/S1473-3099(16)30190-6. Epub 2016 Jul 7.
5
An update on repurposed medications for the treatment of drug-resistant tuberculosis.用于治疗耐多药结核病的重新利用药物的最新情况。
Expert Rev Clin Pharmacol. 2016 Oct;9(10):1331-1340. doi: 10.1080/17512433.2016.1208562. Epub 2016 Jul 18.
6
WHO recommendations on shorter treatment of multidrug-resistant tuberculosis.世界卫生组织关于缩短耐多药结核病治疗疗程的建议。
Lancet. 2016 Jun 18;387(10037):2486-7. doi: 10.1016/S0140-6736(16)30729-2.
7
Multicenter Noninferiority Evaluation of Hain GenoType MTBDRplus Version 2 and Nipro NTM+MDRTB Line Probe Assays for Detection of Rifampin and Isoniazid Resistance.Hain GenoType MTBDRplus v2版和尼康NTM+MDRTB线性探针检测法检测利福平及异烟肼耐药性的多中心非劣效性评估
J Clin Microbiol. 2016 Jun;54(6):1624-1630. doi: 10.1128/JCM.00251-16. Epub 2016 Apr 13.
8
Tuberculosis--advances in development of new drugs, treatment regimens, host-directed therapies, and biomarkers.结核病——新药物、治疗方案、宿主导向疗法和生物标志物的研究进展。
Lancet Infect Dis. 2016 Apr;16(4):e34-46. doi: 10.1016/S1473-3099(16)00070-0.
9
Drug Resistance Mechanisms in Mycobacterium tuberculosis.结核分枝杆菌耐药机制。
Antibiotics (Basel). 2014 Jul 2;3(3):317-40. doi: 10.3390/antibiotics3030317.
10
Short-course treatment for multidrug-resistant tuberculosis: the STREAM trials.耐多药结核病的短程治疗:STREAM试验
Eur Respir Rev. 2016 Mar;25(139):29-35. doi: 10.1183/16000617.0080-2015.

《检测与治疗:实施耐多药结核病新方案的影响》。

Of Testing and Treatment: Implications of Implementing New Regimens for Multidrug-Resistant Tuberculosis.

机构信息

Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.

DST/NRF Centre of Excellence for Biomedical Tuberculosis Research and SAMRC Centre for Tuberculosis Research, Division of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, Stellenbosch University, Tygerberg, South Africa; and.

出版信息

Clin Infect Dis. 2017 Oct 1;65(7):1206-1211. doi: 10.1093/cid/cix486.

DOI:10.1093/cid/cix486
PMID:29554229
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5850434/
Abstract

A novel, shorter-course regimen for treating multidrug-resistant (MDR) tuberculosis was recently recommended by the World Health Organization. However, the most appropriate use of drug susceptibility testing (DST) to support this regimen is less clear. Implementing countries must therefore often choose between using a standardized regimen despite high levels of underlying drug resistance or require more stringent DST prior to treatment initiation. The former carries a high likelihood of exposing patients to de facto monotherapy with a critical drug class (fluoroquinolones), whereas the latter could exclude large groups of patients from their most effective treatment option. We discuss the implications of this dilemma and argue for an approach that will integrate DST into the delivery of any novel antimicrobial regimen, without excessively stringent requirements. Such guidance could make the novel MDR tuberculosis regimen available to most patients while reducing the risk of generating additional drug resistance.

摘要

世界卫生组织最近推荐了一种新的、疗程更短的治疗耐多药(MDR)结核病方案。然而,支持该方案最恰当的药物敏感性测试(DST)应用方法尚不清楚。因此,实施国家必须在使用标准化方案(尽管存在高水平的基础耐药性)或在开始治疗前进行更严格的 DST 之间做出选择。前者极有可能导致患者实际上接受关键药物类别(氟喹诺酮类)的单药治疗,而后者则可能将大量患者排除在最有效的治疗方案之外。我们讨论了这一两难困境的影响,并主张采取一种方法,将 DST 纳入任何新的抗菌治疗方案的实施中,而不会有过于严格的要求。这种指导意见可以使大多数患者获得新型耐多药结核病方案,同时降低产生额外耐药性的风险。