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评价 Genotype® MTBDRplus assay 作为耐药性调查的工具。

Evaluation of the Genotype® MTBDRplus assay as a tool for drug resistance surveys.

机构信息

Microbiology Department, Institute of Tropical Medicine, Antwerp, Belgium.

出版信息

Int J Tuberc Lung Dis. 2011 Jul;15(7):959-65. doi: 10.5588/ijtld.10.0515.

Abstract

SETTING

A national tuberculosis (TB) drug resistance survey in Tanzania.

OBJECTIVE

To compare the performance of the Genotype® MTBDRplus line-probe assay (LPA) on smear-positive sputum specimens with conventional culture and isoniazid (INH) plus rifampicin (RMP) drug susceptibility testing (DST).

DESIGN

Mycobacterium tuberculosis isolates tested at the Tanzanian Central TB Reference Laboratory (CTRL) were submitted for quality assurance of phenotypic DST to its supranational reference laboratory (SRL), together with ethanol-preserved sputum specimens for LPA DST.

RESULTS

Only 321 samples could be tested using LPA; of these, three were identified as being non-tuberculous mycobacteria using CTRL DST. Both tests had 269 sets with interpretable results. CTRL DST yielded almost the same number of interpretable results as LPA, with 90% concordance (κ = 0.612, P < 0.001). Five (1.9%) multidrug-resistant (MDR) strains, 46 (17.1%) resistant to INH only and 0 RMP only, were found by CTRL DST. For the LPA, these results were respectively 5 (1.9%), 26 (9.7%) and 2 (0.7%). With SRL DST as the gold standard, LPA was more accurate than CTRL DST for RMP, but missed almost half the INH-resistant samples.

CONCLUSION

LPA applied directly on ethanol-preserved sputum specimens was similar to phenotypic DST in terms of yield of interpretable results. Although probably more accurate for RMP and MDR-TB, it appears to seriously underestimate INH resistance. Considering speed, easy and safe specimen transportation and low infrastructure requirements, LPA DST from sputum can be recommended for surveys in resource-poor settings.

摘要

背景

坦桑尼亚全国结核病(TB)耐药性调查。

目的

比较 Genotype® MTBDRplus 线探针分析(LPA)在痰涂片阳性标本中的表现与常规培养和异烟肼(INH)加利福平(RMP)药物敏感性测试(DST)。

设计

在坦桑尼亚中央结核病参考实验室(CTRL)测试的结核分枝杆菌分离株与保存于乙醇中的痰标本一起提交给其超国家参考实验室(SRL),以进行表型 DST 的质量保证,用于 LPA DST。

结果

只有 321 个样本可以用 LPA 进行测试;其中,3 个样本经 CTRL DST 鉴定为非结核分枝杆菌。两种测试都有 269 组具有可解释的结果。CTRL DST 产生的可解释结果数量与 LPA 几乎相同,一致性为 90%(κ=0.612,P<0.001)。CTRL DST 发现 5 株(1.9%)耐多药(MDR)株、46 株(17.1%)仅耐 INH 和 0 株仅耐 RMP。对于 LPA,这些结果分别为 5(1.9%)、26(9.7%)和 2(0.7%)。以 SRL DST 为金标准,LPA 对 RMP 的准确性高于 CTRL DST,但几乎错过了一半的 INH 耐药样本。

结论

直接应用于乙醇保存的痰标本的 LPA 在可解释结果的产量方面与表型 DST 相似。尽管可能对 RMP 和 MDR-TB 更准确,但它似乎严重低估了 INH 耐药性。考虑到速度、简便和安全的标本运输以及低基础设施要求,从资源匮乏的环境中推荐使用 LPA 进行 DST。

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