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欧盟东部地区的耐多药结核病:较短的疗程是例外还是常规?

Multidrug-resistant TB in Eastern region of the EU: is the shorter regimen an exception or a rule?

机构信息

Blizard Institute, Queen Mary, University of London, London, UK.

Department of Infectious Diseases, Imperial College London, London, UK.

出版信息

Thorax. 2017 Sep;72(9):850-852. doi: 10.1136/thoraxjnl-2016-209841. Epub 2017 Feb 16.

DOI:10.1136/thoraxjnl-2016-209841
PMID:28209653
Abstract

WHO recently recommended the use of a shorter multidrug-resistant TB (MDR-TB) regimen under programmatic conditions. We assessed eligibility for this regimen in a cohort of 737 adult patients with MDR-TB from Latvia, Lithuania, Estonia and Bucharest city recruited in 2007 and 2009. Only 4.2% of the patients were eligible for this regimen. Ethambutol (64%), pyrazinamide resistance (58%) and previous exposure to second-line TB drugs were major reasons for non-eligibility. High-level resistance to isoniazid is expected due to widespread prevalence of mutations. In Eastern Europe, the use of the shorter regimen might be an exception rather than a rule.

摘要

世卫组织最近建议在规划条件下使用更短的耐多药结核病(MDR-TB)方案。我们在 2007 年和 2009 年招募的来自拉脱维亚、立陶宛、爱沙尼亚和布加勒斯特的 737 名耐多药结核病成人患者队列中评估了该方案的适用性。只有 4.2%的患者符合该方案的条件。乙胺丁醇(64%)、吡嗪酰胺耐药(58%)和以前接触二线结核病药物是不合格的主要原因。由于突变的广泛流行,预计异烟肼的高水平耐药是不可避免的。在东欧,使用更短的方案可能是例外情况,而不是常规情况。

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