[诊断广泛耐药结核分枝杆菌的抗结核药敏试验的外部质量评价]。

Kekkaku : [Tuberculosis] Pub Date : 2016-11-01
Satoshi Mitarai, Hiroyuki Yamada, Akio Aono, Kinuyo Chikamatsu, Takeshi Higuchi, Yuriko Igarashi, Akiko Takaki
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引用次数: 0

摘要

【目的】2015年5月,我国传染病防治法进行了修订,根据世界卫生组织对广泛耐药m.b rtb (XDR-TB)的定义,改变了结核分枝杆菌作为感染性病原体的分类定义。为了评估广泛耐药结核的诊断能力,我们对抗结核药敏试验(DST)进行了外部质量评价(EQA)。[方法]将已知药敏的结核分枝杆菌10株送入各参与实验室。评估的药物有异烟肼(INH)、利福平(RFP)、链霉素(SM)、乙胺丁醇(EB)、左氧氟沙星(LVFX)和卡那霉素(KM)。采用各常规方法行DST,并与司法诊断结果进行比较。计算每种药物的敏感性、特异性、总体一致性(效率)和kappa系数。此外,还评估了多药耐药结核(MDR-TB)和广泛耐药结核(XDR-TB)的诊断准确性。[结果]共有88个机构(包括67家医院、16家商业实验室和5家公共卫生实验室)参与了EQA。2个实验室提交2组结果,共分析90组独立数据集。INH、RFP和LVFX的效率均在95%以上,而SM、EB和KM各有2株,效率均在95%以下。其中菌株1和菌株2对SM的效率分别为72.2%和71.1%。这个错误主要是在某个测试套件中发现的。如果以INH和RFP的敏感性和特异性均≥95%为及格分,则本研究对MDR-TB的诊断准确率为92.2%(83/90)。在与INH、RFP、LVFX和KM标准相同的情况下,XDR-TB的检漏率为79.7%(63/79)。【讨论】当前研究对广泛耐药结核病的诊断能力不足。良好的病例管理和病原体控制需要更高的准确性。政府可能需要进行持续的环境质量保证和相关的补救措施。
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[EXTERNAL QUALITY ASSESSMENT OF ANTI-TUBERCULOSIS DRUG SUSCEPTIBILITY TESTING FOR DIAGNOSING EXTENSIVELY DRUG-RESISTANT MYCOBACTERIUM TUBERCULOSIS].

[Objective] The infectious disease control law has been amended in May 2015, and the category definition of Mycobacterium tuberculosis as infectious pathogen has been changed, following the definition of extensively drug-resistant M.tuberculosis (XDR-TB) by World Health Organization. To assess the diagnostic capacity of XDR-TB, we conducted an external quality assessment (EQA) for the anti-tuberculosis drug susceptibility testing (DST). [Method] A total of 10 M.tuberculosis strains with known drug susceptibility were sent to each participating laboratory. The drugs assessed were isoniazid (INH), rifampicin (RFP), streptomycin (SM), ethambutol (EB), levofloxacin (LVFX), and kanamycin (KM). DST was performed using each routine method(s), and the results were compared with the judicial diagnoses. The sensitivity, specificity, overall agreement (effi- ciency) and kappa coefficient were calculated for each drug tested. In addition, the diagnostic accuracy of multidrug-resis- tant M. tuberculosis (MDR-TB) and XDR-TB was assessed. [Results] A total of 88 institutes including 67 hospitals, 16 commercial laboratories, and 5 public health laboratories par- ticipated in the EQA. With 2 laboratories submitting 2 sets of results, a total of 90 independent data sets were analyzed. As for INH, RFP and LVFX, the efficiency was over 95%, but we found two strains each for SM, EB and KM with the efficiency less than 95%. Especially, strain 1 and strain 2 showed efficiency of 72.2% and 71.1% to SM, respectively. This error was mainly found in a certain test kit. If we consider the passing score as showing ≥95 % sensitivity and specificity both to INH and RFP, the diagnostic accuracy of MDR-TB was 92.2% (83/90) in this study. With the same criteria to INH, RFP, LVFX and KM, that of XDR-TB was 79.7% (63/79). [Discussion] The diagnostic capacity of XDR-TB was not sufficient in the current study. Good case management and pathogen control requires higher accuracy. The government may need to conduct a constant EQA and relevant remedial actions.

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