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结核病的实验室诊断:技术与药敏试验的进展

Laboratory diagnosis of tuberculosis: Advances in technology and drug susceptibility testing.

作者信息

Oommen Seema, Banaji Nandita

机构信息

Department of Microbiology, Pushpagiri Institute of Medical Sciences and Research Centre, Tiruvalla, Kerala, India.

Department of Microbiology, Indira Gandhi Medical College and Research Institute, Puducherry, India.

出版信息

Indian J Med Microbiol. 2017 Jul-Sep;35(3):323-331. doi: 10.4103/ijmm.IJMM_16_204.

DOI:10.4103/ijmm.IJMM_16_204
PMID:29063875
Abstract

There have been rapid technological advances in the detection of Mycobacterium tuberculosis and its drug susceptibility in clinical samples. These include advances in microscopic examination, in vitro culture and application of molecular techniques. The World Health Organization (WHO) has played a large role in evaluating these technologies for their efficacy and feasibility, especially in the developing countries. Amongst these, the Revised National Tuberculosis Control Programme (RNTCP), through its national network of designated microscopy centres and intermediate reference laboratories, has adopted certain technologies that are currently implemented in India. Advances in microscopy technology include fluorescent microscopy using light-emitting diode source, sodium hypochlorite microscopy and vital fluorescent staining of sputum smears. Automation of in vitro culture has markedly reduced the turnaround time (TAT), even in smear-negative samples, and permits simultaneous detection of resistant mutants. Molecular detection of drug resistance has further reduced the TAT, and the cartridge-based nucleic acid amplification test with its performance convenience and rapid results, appears poised to become the future of tuberculosis (TB) diagnosis in all settings, provided the cost of testing is reduced especially for use in private diagnostic settings. This article reviews technologies currently available for the diagnosis of TB, keeping in mind the WHO recommendations and the RNTCP practices. This is a thematic synthesis of data available on diagnosis in literature, preserving the conclusions of the primary studies.

摘要

在临床样本中检测结核分枝杆菌及其药物敏感性方面,技术取得了快速进展。这些进展包括显微镜检查、体外培养以及分子技术应用等方面。世界卫生组织(WHO)在评估这些技术的有效性和可行性方面发挥了重要作用,尤其是在发展中国家。其中,修订后的国家结核病控制规划(RNTCP)通过其指定显微镜中心和中间参考实验室的全国网络,采用了目前在印度实施的某些技术。显微镜技术的进展包括使用发光二极管光源的荧光显微镜、次氯酸钠显微镜以及痰涂片的活体荧光染色。体外培养的自动化显著缩短了周转时间(TAT),即使是涂片阴性样本也如此,并且能够同时检测耐药突变体。耐药性的分子检测进一步缩短了TAT,基于试剂盒的核酸扩增试验因其操作便捷和结果快速,似乎有望成为所有环境下结核病(TB)诊断的未来方法,前提是检测成本降低,特别是用于私人诊断机构。本文结合WHO的建议和RNTCP的实践,综述了目前可用于结核病诊断的技术。这是对文献中关于诊断的可用数据的主题综合,保留了主要研究的结论。

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