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用于检测阿根廷人群结核病的商用酶联免疫吸附测定试剂盒的评估

Evaluation of commercial enzyme-linked immunosorbent assay kits for detection of tuberculosis in Argentinean population.

作者信息

Imaz María Susana, Comini Marcelo Alberto, Zerbini Elsa, Sequeira María Delfina, Latini Omar, Claus Juan Daniel, Singh Mahavir

机构信息

Instituto Nacional de Enfermedades Respiratorias "Emilio Coni," ANLIS "C Malbrán," Braunschweig, Germany.

出版信息

J Clin Microbiol. 2004 Feb;42(2):884-7. doi: 10.1128/JCM.42.2.884-887.2004.

Abstract

Pathozyme-Myco G (Myco G), M, A, and TB complex plus (Omega Diagnostics Ltd., Alloa, Scotland) were evaluated for the serological diagnosis of pulmonary tuberculosis (TB) in an Argentinean population. Sera from 58 patients with pulmonary TB, 24 subjects with pulmonary mycobacteriosis or mycoses (pulmonary MM group), and 45 subjects with other underlying disorders (control group) were analyzed. The sensitivities of the tests ranged from 29% (Myco M) to 82% (Myco G) in smear-positive patients (17 subjects) and from 29% (TB complex plus) to 49% (Myco G) in smear-negative patients (41 subjects). The specificities of the assays varied from 93% (Myco M) to 100% (Myco G and TB complex plus) in controls and from 62% (Myco A) to 96% (TB complex plus) in the pulmonary MM group. Overall, for the diagnosis of smear-negative patients, Myco G had the best characteristics, with a sensitivity of 49% and specificities of 100% for controls and 75% for the pulmonary MM group; after its combination with TB complex plus, its sensitivity improved to 59%. Nevertheless, despite its relatively poor capacity to discriminate between pulmonary TB and pulmonary MM, Myco G, alone or in combination with TB complex plus, would be a useful diagnostic tool for patients with suspected pulmonary TB living in areas where the relative prevalence of pulmonary MM was low.

摘要

对Pathozyme - Myco G(Myco G)、M、A和结核菌复合物加强版(Omega诊断有限公司,阿洛厄,苏格兰)进行评估,以用于阿根廷人群中肺结核(TB)的血清学诊断。分析了58例肺结核患者、24例患有肺部分枝杆菌病或真菌病的受试者(肺部MM组)以及45例患有其他基础疾病的受试者(对照组)的血清。在涂片阳性患者(17例受试者)中,检测的敏感性范围为29%(Myco M)至82%(Myco G);在涂片阴性患者(41例受试者)中,敏感性范围为29%(结核菌复合物加强版)至49%(Myco G)。检测的特异性在对照组中从93%(Myco M)至100%(Myco G和结核菌复合物加强版)不等,在肺部MM组中从62%(Myco A)至96%(结核菌复合物加强版)不等。总体而言,对于涂片阴性患者的诊断,Myco G具有最佳特征,对对照组的敏感性为49%,特异性为100%,对肺部MM组的特异性为75%;与结核菌复合物加强版联合使用后,其敏感性提高到59%。然而,尽管Myco G区分肺结核和肺部MM的能力相对较差,但单独使用或与结核菌复合物加强版联合使用时,对于生活在肺部MM相对患病率较低地区的疑似肺结核患者来说,它将是一种有用的诊断工具。

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