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本文引用的文献

1
Reliability of nucleic acid amplification for detection of Mycobacterium tuberculosis: an international collaborative quality control study among 30 laboratories.用于检测结核分枝杆菌的核酸扩增的可靠性:30个实验室的一项国际合作质量控制研究
J Clin Microbiol. 1996 Oct;34(10):2522-5. doi: 10.1128/jcm.34.10.2522-2525.1996.
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Diagnostic mycobacteriology: where are we today?诊断分枝杆菌学:我们如今处于什么境地?
J Clin Microbiol. 1996 Aug;34(8):1873-6. doi: 10.1128/jcm.34.8.1873-1876.1996.
3
Detection of Mycobacterium tuberculosis in respiratory specimens by strand displacement amplification of DNA.通过DNA链置换扩增检测呼吸道标本中的结核分枝杆菌。
J Clin Microbiol. 1996 Apr;34(4):860-5. doi: 10.1128/jcm.34.4.860-865.1996.
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Amplification of rRNA for assessment of treatment response of pulmonary tuberculosis patients during antimicrobial therapy.通过扩增核糖体RNA评估肺结核患者抗菌治疗期间的治疗反应。
J Clin Microbiol. 1996 Jul;34(7):1745-9. doi: 10.1128/JCM.34.7.1745-1749.1996.
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Evaluation of Roche Amplicor PCR assay for Mycobacterium tuberculosis.罗氏Amplicor聚合酶链反应检测法用于结核分枝杆菌检测的评估
J Clin Microbiol. 1996 Jan;34(1):134-9. doi: 10.1128/jcm.34.1.134-139.1996.
6
Evaluation of Gen-Probe Amplified Mycobacterium Tuberculosis Direct Test and Roche PCR-microwell plate hybridization method (AMPLICOR MYCOBACTERIUM) for direct detection of mycobacteria.评估Gen-Probe分枝杆菌结核直接检测法和罗氏聚合酶链反应-微孔板杂交法(AMPLICOR分枝杆菌检测法)用于直接检测分枝杆菌。
J Clin Microbiol. 1996 Jan;34(1):130-3. doi: 10.1128/jcm.34.1.130-133.1996.
7
Utility of PCR in diagnosing pulmonary tuberculosis.聚合酶链反应在诊断肺结核中的应用。
J Clin Microbiol. 1996 Jun;34(6):1407-11. doi: 10.1128/jcm.34.6.1407-1411.1996.
8
Clinical evaluation of the Roche AMPLICOR PCR Mycobacterium tuberculosis test for detection of M. tuberculosis in respiratory specimens.罗氏AMPLICOR聚合酶链反应检测结核分枝杆菌试验在呼吸道标本中检测结核分枝杆菌的临床评估。
J Clin Microbiol. 1996 May;34(5):1083-5. doi: 10.1128/jcm.34.5.1083-1085.1996.
9
Evaluation of Amplicor MTB test as adjunct to smears and culture for direct detection of Mycobacterium tuberculosis in the French Caribbean.评估Amplicor MTB检测法作为涂片和培养的辅助手段用于直接检测法属加勒比地区结核分枝杆菌的效果。
J Clin Microbiol. 1996 May;34(5):1065-8. doi: 10.1128/jcm.34.5.1065-1068.1996.
10
Strand displacement amplification and the polymerase chain reaction for monitoring response to treatment in patients with pulmonary tuberculosis.链置换扩增和聚合酶链反应用于监测肺结核患者的治疗反应
J Infect Dis. 1996 Apr;173(4):934-41. doi: 10.1093/infdis/173.4.934.

与罗氏Amplicor聚合酶链反应(PCR)及培养法相比,链置换扩增法在检测痰标本中分枝杆菌的诊断价值。

Diagnostic value of the strand displacement amplification method compared to those of Roche Amplicor PCR and culture for detecting mycobacteria in sputum samples.

作者信息

Ichiyama S, Ito Y, Sugiura F, Iinuma Y, Yamori S, Shimojima M, Hasegawa Y, Shimokata K, Nakashima N

机构信息

Department of Clinical Laboratory Medicine, Nagoya University Hospital, Nagoya University School of Medicine, Japan.

出版信息

J Clin Microbiol. 1997 Dec;35(12):3082-5. doi: 10.1128/jcm.35.12.3082-3085.1997.

DOI:10.1128/jcm.35.12.3082-3085.1997
PMID:9399498
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC230126/
Abstract

We compared the ability of the semiautomated BDProbeTec-SDA system, which uses the strand displacement amplification (SDA) method, with that of the Roche Amplicor-PCR system and the Septi-Chek AFB culture system to directly detect Mycobacterium tuberculosis complex (MTB) and other mycobacteria in sputum samples. A total of 530 sputum samples from 299 patients were examined in this study. Of the 530 samples, 129 were culture positive for acid-fast bacilli with the Septi-Chek AFB system; 95 for MTB, 29 for M. avium-M. intracellulare complex (MAC), and 5 for other mycobacteria. The BDProbeTec-SDA system detected 90 of the 95 samples culture positive for MTB (sensitivity, 94.7%), and the Amplicor-PCR system detected 85 of the 95 samples culture positive for MTB (sensitivity, 89.5%). The specificity of each system, based on the clinical diagnosis, was 99.8% for SDA and 100% for PCR, respectively. Among the 29 samples culture positive for MAC, the BDProbeTec-SDA system detected MAC in 24 samples (sensitivity, 82.8%), whereas the Amplicor-PCR system detected MAC in 23 samples (sensitivity, 79.3%). The specificities of the systems were 98.3 and 100%, respectively. The high degrees of sensitivity and specificity of the BDProbeTec-SDA system suggest that it should be very useful in clinical laboratories for the rapid detection of mycobacteria in sputum samples.

摘要

我们比较了采用链置换扩增(SDA)方法的半自动BDProbeTec - SDA系统、罗氏Amplicor - PCR系统和Septi - Chek AFB培养系统直接检测痰液样本中结核分枝杆菌复合群(MTB)及其他分枝杆菌的能力。本研究共检测了来自299例患者的530份痰液样本。在这530份样本中,Septi - Chek AFB系统检测出129份耐酸杆菌培养阳性;其中95份为MTB阳性,29份为鸟分枝杆菌 - 胞内分枝杆菌复合群(MAC)阳性,5份为其他分枝杆菌阳性。BDProbeTec - SDA系统检测出95份MTB培养阳性样本中的90份(敏感性为94.7%),Amplicor - PCR系统检测出95份MTB培养阳性样本中的85份(敏感性为89.5%)。基于临床诊断,各系统的特异性分别为SDA 99.8%,PCR 100%。在29份MAC培养阳性样本中,BDProbeTec - SDA系统检测出24份MAC(敏感性为82.8%),而Amplicor - PCR系统检测出23份MAC(敏感性为79.3%)。各系统的特异性分别为98.3%和100%。BDProbeTec - SDA系统的高灵敏度和特异性表明,它在临床实验室快速检测痰液样本中的分枝杆菌方面应非常有用。