Hasaneen Nadia A, Zaki Maysaa E, Shalaby Hala M, El-Morsi Ahmad S
Department of Thoracic Medicine, Mansoura University Hospital, Mansoura, Egypt.
Chest. 2003 Dec;124(6):2105-11. doi: 10.1378/chest.124.6.2105.
Tuberculous pleural effusion occurs in 30% of patients with tuberculosis (TB). Rapid diagnosis of a tuberculous pleural effusion would greatly facilitate the management of many patients. Polymerase chain reaction (PCR) has been used to detect Mycobacterium tuberculosis in pleural fluid with highly variable sensitivity.
To improve our laboratory diagnosis of tuberculous pleural effusion.
We applied PCR to detect DNA specific for M tuberculosis in 33 of the studied pleural biopsy specimens using an IS986-based primer that was specific for mycobacterium complex, and compared it to the results of pleural fluid and biopsy cultures performed on either Lowenstein-Jensen (LJ) medium or BACTEC 12B liquid medium (Becton Dickinson Microbiology Systems; Cockeysville, MD), Ziehl-Neelsen (ZN) staining, and histopathology in 45 patients with pleural effusion.
Of the 45 patients with pleural effusion who were studied, 26 patients received diagnoses of tuberculous pleural effusion that had been confirmed by either culture and or histopathology, 10 patients received diagnoses of exudative effusion due to causes other than TB, and 9 patients received diagnoses of transudative effusion. Histopathology of the pleural biopsy specimen had a sensitivity of 53.8%. The sensitivity of the ZN staining of pleural fluid and biopsy specimens was 0.0% and 3.8%, respectively. The sensitivity of the culture on both BACTEC 12B liquid medium and LJ medium was higher in pleural biopsy specimens (92.3%) than in pleural fluid specimens (15.4%; p > 0.001). The improvements of the BACTEC culture system improved and shortened the detection time of M tuberculosis in pleural biopsy specimens. PCR of pleural biopsy specimens had 90% sensitivity and 100% specificity. The positive predictive value and the negative predictive value for pleural biopsy specimen cultures were 100% and 90.5% vs 100% and 86.7% for pleural biopsy specimen PCRs.
The overall accuracy of PCR of pleural biopsy was similar to the results of pleural biopsy culture, however, PCR of the pleural biopsy was much faster in reaching diagnosis. PCR of pleural biopsy is a useful method when used in combination with the BACTEC culture system and histopathologic examination of pleural biopsy to reach a rapid diagnosis of tuberculous pleural effusion.
30%的肺结核(TB)患者会出现结核性胸腔积液。结核性胸腔积液的快速诊断将极大地便利许多患者的治疗。聚合酶链反应(PCR)已被用于检测胸腔积液中的结核分枝杆菌,但其敏感性差异很大。
改进我们对结核性胸腔积液的实验室诊断。
我们应用PCR,使用基于IS986的、对分枝杆菌属特异性的引物,检测33份研究的胸膜活检标本中结核分枝杆菌的特异性DNA,并将其与45例胸腔积液患者的胸腔积液和活检培养结果进行比较,这些培养分别在罗氏(LJ)培养基或BACTEC 12B液体培养基(Becton Dickinson微生物系统公司;马里兰州科基斯维尔)上进行,同时与萋-尼(ZN)染色及组织病理学结果进行比较。
在研究的45例胸腔积液患者中,26例被诊断为结核性胸腔积液,已通过培养和/或组织病理学证实;10例被诊断为非结核性原因导致的渗出性胸腔积液;9例被诊断为漏出性胸腔积液。胸膜活检标本的组织病理学敏感性为53.8%。胸腔积液和活检标本的ZN染色敏感性分别为0.0%和3.8%。胸膜活检标本在BACTEC 12B液体培养基和LJ培养基上培养的敏感性(92.3%)高于胸腔积液标本(15.4%;p>0.001)。BACTEC培养系统的改进提高并缩短了胸膜活检标本中结核分枝杆菌的检测时间。胸膜活检标本的PCR敏感性为90%,特异性为100%。胸膜活检标本培养的阳性预测值和阴性预测值分别为100%和90.5%,而胸膜活检标本PCR的阳性预测值和阴性预测值分别为100%和86.7%。
胸膜活检PCR的总体准确性与胸膜活检培养结果相似,然而,胸膜活检PCR在做出诊断方面要快得多。胸膜活检PCR与BACTEC培养系统及胸膜活检的组织病理学检查联合使用时,是快速诊断结核性胸腔积液的一种有用方法。