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首页> 外文期刊>Memorias do Instituto Oswaldo Cruz >Evaluation of rapid techniques for the detection of mycobacteria in sputum with scanty bacilli or clinically evident, smear negative cases of pulmonary and extra-pulmonary tuberculosis
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Evaluation of rapid techniques for the detection of mycobacteria in sputum with scanty bacilli or clinically evident, smear negative cases of pulmonary and extra-pulmonary tuberculosis

机译:快速检测痰中带有少量细菌或临床上明显的涂片阴性肺和肺外结核病例的分枝杆菌的技术评估

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The objective of the current study was to compare two rapid methods, the BBL Mycobacteria Growth Indicator Tube (MGITTM) and Biotec FASTPlaque TBTM (FPTB) assays, with the conventional L?wenstein-Jensen (LJ) media assay to diagnose mycobacterial infections from paucibacillary clinical specimens. For evaluation of the clinical utility of the BBL MGITTM and FPTB assays, respiratory tract specimens (n = 208), with scanty bacilli or clinically evident, smear negative cases and non-respiratory tract specimens (n = 119) were analyzed and the performance of each assay was compared with LJ media. MGIT and FPTB demonstrated a greater sensitivity (95.92% and 87.68%), specificity (94.59% and 98.78%), positive predictive value (94.91% and 99.16%) and negative predictive value (96.56% and 90.92%), respectively, compared to LJ culture for both respiratory tract and non-respiratory tract specimens. However, the FPTB assay was unable to detect nontuberculous mycobacteria and few Mycobacterium tuberculosis complex cases from paucibacillary clinical specimens. It is likely that the analytical sensitivity of FPTB is moderately low and may not be useful for the direct detection of tuberculosis in paucibacillary specimens. The current study concluded that MGIT was a dependable, highly efficient system for recovery of M. tuberculosis complexes and nontuberculous mycobacteria from both respiratory and non-respiratory tract specimens in combination with LJ media.
机译:本研究的目的是比较两种快速方法,即BBL分枝杆菌生长指示剂管(MGITTM)和Biotec FASTPlaque TBTM(FPTB)检测方法,与常规的L?wenstein-Jensen(LJ)培养基检测方法,以诊断来自脓杆菌的分枝杆菌感染临床标本。为了评估BBL MGITTM和FPTB分析的临床效用,对呼吸道标本(n = 208),细菌少或临床明显的涂片阴性病例和非呼吸道标本(n = 119)进行了分析,并对将每种测定与LJ培养基进行比较。 MGIT和FPTB分别显示出更高的敏感性(95.92%和87.68%),特异性(94.59%和98.78%),阳性预测值(94.91%和99.16%)和阴性预测值(96.56%和90.92%) LJ培养用于呼吸道和非呼吸道标本。但是,FPTB分析无法从脓疱性临床标本中检测出非结核分枝杆菌和少数结核分枝杆菌复杂病例。 FPTB的分析灵敏度可能会适度降低,可能无法直接用于检测脓杆菌标本中的结核病。当前的研究得出结论,MGIT是结合LJ培养基从呼吸道和非呼吸道标本中恢复结核分枝杆菌复合物和非结核分枝杆菌的可靠,高效的系统。

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