涂片镜检诊断肺结核在苏丹东部。

Tuberculosis Research and Treatment Pub Date : 2018-06-14 eCollection Date: 2018-01-01 DOI:10.1155/2018/8038137
Yassir A Shuaib, Eltahir A G Khalil, Ulrich E Schaible, Lothar H Wieler, Mohammed A M Bakheit, Saad E Mohamed-Noor, Mohamed A Abdalla, Susanne Homolka, Sönke Andres, Doris Hillemann, Knut Lonnroth, Elvira Richter, Stefan Niemann, Katharina Kranzer
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引用次数: 6

摘要

背景:在苏丹,与许多其他低收入和中等收入国家一样,结核病诊断主要依靠临床症状和涂片镜检。本研究的目的是调查痰涂片阳性对苏丹东部肺结核患者的阳性预测价值。方法:对2014年6 - 10月和2016年1 - 7月2例有结核症状患者的痰液进行直接Ziehl-Neelsen (ZN)染色及光镜检查。如果其中一个样本涂片阳性,则将两个样本合并,在-20°C保存,并送往德国国家参考实验室(NRL)。去污后,样品进行重复显微镜和培养。采用聚合酶链反应(PCR)对培养阴性/污染样品进行检测。结果:共调查样本383份。重复镜检阴性123例(32.1%),培养阳性31例。当PCR和培养结果一起考虑时,这一数字增加到80。培养阳性196份,其中结核分枝杆菌171份(87.3%),胞内分枝杆菌14份(7.1%),混合分枝杆菌11份(5.6%)。总体而言,15.6%(57/365)的样本没有结核分枝杆菌的证据,阳性预测值为84.4%。结论:在苏丹当地实验室和德国NRL进行的涂片显微镜检查结果不一致;此外,相当数量的样本没有结核分枝杆菌的证据。改善涂片镜检的质量控制和更具体的诊断对于避免可能的过度治疗至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Smear Microscopy for Diagnosis of Pulmonary Tuberculosis in Eastern Sudan.

Smear Microscopy for Diagnosis of Pulmonary Tuberculosis in Eastern Sudan.

Smear Microscopy for Diagnosis of Pulmonary Tuberculosis in Eastern Sudan.

Background: In Sudan, tuberculosis diagnosis largely relies on clinical symptoms and smear microscopy as in many other low- and middle-income countries. The aim of this study was to investigate the positive predictive value of a positive sputum smear in patients investigated for pulmonary tuberculosis in Eastern Sudan.

Methods: Two sputum samples from patients presenting with symptoms suggestive of tuberculosis were investigated using direct Ziehl-Neelsen (ZN) staining and light microscopy between June to October 2014 and January to July 2016. If one of the samples was smear positive, both samples were pooled, stored at -20°C, and sent to the National Reference Laboratory (NRL), Germany. Following decontamination, samples underwent repeat microscopy and culture. Culture negative/contaminated samples were investigated using polymerase chain reaction (PCR).

Results: A total of 383 samples were investigated. Repeat microscopy categorized 123 (32.1%) as negative, among which 31 were culture positive. This increased to 80 when PCR and culture results were considered together. A total of 196 samples were culture positive, of which 171 (87.3%), 14 (7.1%), and 11 (5.6%) were M. tuberculosis, M. intracellulare, and mixed species. Overall, 15.6% (57/365) of the samples had no evidence of M. tuberculosis, resulting in a positive predictive value of 84.4%.

Conclusions: There was a discordance between the results of smear microscopy performed at local laboratories in the Sudan and at the NRL, Germany; besides, a considerable number of samples had no evidence of M. tuberculosis. Improved quality control for smear microscopy and more specific diagnostics are crucial to avoid possible overtreatment.

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