Fan Lin, Zhang Qing, Cheng Liping, Liu Zhibing, Ji Xiaobing, Cui Zhenling, Ju Jingliang, Xiao Heping
Tuberculosis Center for Diagnosis and Treatment, Shanghai Pulmonary Hospital, Tongji University School of Medicine, Shanghai 200433, China.
Shanghai Key Laboratory of Tuberculosis, Shanghai Pulmonary Hospital, Tongji University School of Medicine, Shanghai 200433, China.
Chin Med J (Engl). 2014;127(10):1863-7.
Early detection of pulmonary tuberculosis (PTB) is a big challenge in smear negative and sputum scarce patients in China. Simultaneous amplification and testing methods for detection of the Mycobacterium tuberculosis (MTB) complex (SAT-TB assay) is a novel molecular technique established in our hospital. This method has a high sensitivity and specificity in the lab. In this study, the clinical diagnostic performance of this method in smear-negative or sputum-scarce PTB suspects was investigated and evaluated.
Two hundred smear negative and 80 sputum-scarce patients were recruited in this study. Samples that included sputum or bronchial washing fluid were collected and sent for both bacteria culture and SAT-TB assay. Diagnosis for these patients was based on the comprehensive evaluation of chestX- ray/CT study, histology examination, lab results, and treatment response. Sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV) for each diagnostic test were investigated and calculated using confirmed tuberculosis (TB) and non-TB cases. The time required for detection of MTB was also measured for each method.
Ninety-two patients (33%) were diagnosed as definitive TB, 112 patients (40%) were probable PTB, and 76 (27%) were non-TB. The sensitivity, specificity, PPV, and NPV of SAT-TB in smear-negative PTB suspects were 93% (95% CI, 84%-98%), 98% (95% CI, 90%-100%), 98% (95% CI, 91%-100%), and 93% (95% CI, 83%-98%). In sputum scarce PTB suspects, the sensitivity, specificity, PPV, and NPV of the SAT-TB assay on bronchial washing fluids were 90% (95% CI, 74%-98%), 100% (95% CI, 85%-100%), 100% (95% CI, 88%-100%), and 88% (95% CI, 69%-97%). The accuracy of the SAT-TB assay is consistent with the bacteria culture assay. The median time required for detecting MTB in the SAT-TB assay was 0.5 day, which was much faster than bacteria culture (28 days).
The SAT-TB assay is a fast and accurate method for the detection of MTB. It can be widely applied in the clinic and be an asset in early detection and management of PTB suspects, especially in those patients who are smear negative or sputum scarce.
在中国,早期发现肺结核(PTB)对于涂片阴性和痰量少的患者是一项重大挑战。同时扩增检测结核分枝杆菌(MTB)复合群的方法(SAT-TB检测法)是我院建立的一种新型分子技术。该方法在实验室中具有高灵敏度和特异性。本研究对该方法在涂片阴性或痰量少的PTB疑似患者中的临床诊断性能进行了调查和评估。
本研究招募了200例涂片阴性和80例痰量少的患者。收集包括痰液或支气管冲洗液在内的样本,送去进行细菌培养和SAT-TB检测。这些患者的诊断基于胸部X线/CT检查、组织学检查、实验室结果和治疗反应的综合评估。使用确诊的结核病(TB)和非TB病例调查并计算每种诊断测试的灵敏度、特异性、阳性预测值(PPV)和阴性预测值(NPV)。还测量了每种方法检测MTB所需的时间。
92例患者(33%)被诊断为确诊TB,112例患者(40%)可能为PTB,76例(27%)为非TB。SAT-TB在涂片阴性PTB疑似患者中的灵敏度、特异性、PPV和NPV分别为93%(95%CI,84%-98%)、98%(95%CI,90%-100%)、98%(95%CI,91%-100%)和93%(95%CI,83%-98%)。在痰量少的PTB疑似患者中,SAT-TB检测支气管冲洗液的灵敏度、特异性、PPV和NPV分别为90%(95%CI,74%-98%)、100%(95%CI,85%-100%)、100%(95%CI,88%-100%)和88%(95%CI,69%-97%)。SAT-TB检测法的准确性与细菌培养检测法一致。SAT-TB检测法检测MTB所需的中位时间为0.5天,比细菌培养(28天)快得多。
SAT-TB检测法是一种快速、准确的MTB检测方法。它可广泛应用于临床,有助于早期发现和管理PTB疑似患者,尤其是涂片阴性或痰量少的患者。