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使用商用聚合酶链反应试剂盒检测临床标本中的结核分枝杆菌复合群

Detection of Mycobacterium tuberculosis complex in clinical specimens by a commercial polymerase chain reaction kit.

作者信息

Stauffer F, Mutschlechner R, Hasenberger P, Stadlbauer S, Schinko H

机构信息

Federal Public Health Laboratory, Vienna, Austria.

出版信息

Eur J Clin Microbiol Infect Dis. 1995 Dec;14(12):1046-51. doi: 10.1007/BF01590937.

Abstract

A total of 722 respiratory and 86 nonrespiratory specimens obtained from 456 patients were tested for detection of Mycobacterium tuberculosis complex by a commercial polymerase chain reaction (PCR) kit (Amplicor, Roche Diagnostic Systems) and the results compared with those of microscopy and culture (solid and radiometric media). Respiratory and nonrespiratory specimens were analysed separately. Of the respiratory specimens, 54 were positive for Mycobacterium tuberculosis complex both in the PCR and in culture, five were positive in the PCR but negative in culture, and eight were positive in culture but negative in the PCR. Four cultures were positive for mycobacteria other than Mycobacterium tuberculosis; none of these gave a positive result in the commercial test. Resolution of discrepant results was performed by analysis of patients' clinical data. For respiratory specimens the sensitivity of the commercial test was 87.6%, the specificity 99.6%, the positive predictive value 96.6%, and the negative predictive value 98.7%. For nonrespiratory specimens the sensitivity was 60%, whereas the specificity ranged as high as 98.6%. For this group the positive predictive value was 85.7% and the negative predictive value 94.9%. When respiratory specimens are used, the commercial PCR test for detection of Mycobacterium tuberculosis complex, with its high sensitivity and specificity, is a good complementary diagnostic tool for rapid diagnosis of bronchopulmonary tuberculosis in a routine mycobacterial laboratory.

摘要

从456例患者身上获取了722份呼吸道标本和86份非呼吸道标本,使用商用聚合酶链反应(PCR)试剂盒(Amplicor,罗氏诊断系统公司)检测结核分枝杆菌复合群,并将结果与显微镜检查和培养(固体培养基和放射性测量培养基)结果进行比较。呼吸道标本和非呼吸道标本分别进行分析。在呼吸道标本中,54份在PCR和培养中均为结核分枝杆菌复合群阳性,5份在PCR中为阳性但培养中为阴性,8份在培养中为阳性但PCR中为阴性。4份培养物为非结核分枝杆菌阳性;这些在商业检测中均未得出阳性结果。通过分析患者的临床数据来解决结果不一致的问题。对于呼吸道标本,商业检测的敏感性为87.6%,特异性为99.6%,阳性预测值为96.6%,阴性预测值为98.7%。对于非呼吸道标本,敏感性为60%,而特异性高达98.6%。该组的阳性预测值为85.7%,阴性预测值为94.9%。当使用呼吸道标本时,用于检测结核分枝杆菌复合群的商业PCR检测具有高敏感性和特异性,是常规分枝杆菌实验室快速诊断支气管肺结核的良好补充诊断工具。

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