Bergmann J S, Yuoh G, Fish G, Woods G L
Department of Pathology, University of Texas Medical Branch, Galveston, Texas 77555-0740, USA.
J Clin Microbiol. 1999 May;37(5):1419-25. doi: 10.1128/JCM.37.5.1419-1425.1999.
The reliability of the enhanced Amplified Mycobacterium Tuberculosis Direct Test (E-MTD; Gen-Probe, Inc., San Diego, Calif.) for rapid diagnosis of pulmonary tuberculosis (TB) was evaluated by testing 1, 004 respiratory specimens from 489 Texas prison inmates. Results were compared to those of mycobacterial culture (BACTEC TB 460 and Middlebrook 7H11 biplates), smear for acid-fast bacilli (AFB; auramine O), and clinical course. After chart review, three patients (nine specimens) who were on antituberculosis therapy before the study began were excluded from final analysis. Of the remaining 995 specimens, 21 were AFB smear positive: 13 grew Mycobacterium tuberculosis complex (MTBC), 6 grew nontuberculous mycobacteria, and 2 (from two patients diagnosed with TB and started on therapy after the study began) were culture negative. Twenty-eight specimens (20 patients) were positive for MTBC by culture and E-MTD. Seven specimens (seven patients) were positive by culture alone; three were from patients who had other E-MTD-positive specimens, two were false-positive cultures, and two were false-negative E-MTD results. Eight specimens were positive by E-MTD only; four specimens (four patients) were false-positive E-MTD results, and four specimens were from two patients with earlier E-MTD-positive specimens that grew MTBC. Thus, there were 22 patients with TB (10 smear positive and 12 smear negative). The sensitivity and specificity of the AFB smear for diagnosis of TB, by patient, were 45.5 and 98.9%, respectively. After resolving discrepancies, these same values for E-MTD were 90.9 and 99.1% overall, 100 and 100% for the smear-positive patients, and 83.3 and 99.1% for the smear-negative patients. Excluding the one smear-negative patient whose E-MTD-negative, MTBC culture-positive specimen contained inhibitory substances, the sensitivity of E-MTD was 95.2% overall and 90.9% in smear-negative patients. The specificity and positive predictive value of E-MTD can be improved, without altering other performance characteristics, by modifying the equivocal zone recommended by the manufacturer. These data suggest that E-MTD is a reliable method for rapid diagnosis of pulmonary TB, irrespective of the AFB smear result. Guidelines for the most appropriate use of E-MTD with smear-negative patients are needed.
通过检测489名得克萨斯州监狱囚犯的1004份呼吸道标本,对增强型结核分枝杆菌直接检测法(E-MTD;Gen-Probe公司,加利福尼亚州圣地亚哥)用于快速诊断肺结核(TB)的可靠性进行了评估。将结果与分枝杆菌培养(BACTEC TB 460和Middlebrook 7H11双平板)、抗酸杆菌涂片(AFB;金胺O)及临床病程的结果进行比较。在查阅病历后,将研究开始前正在接受抗结核治疗的3名患者(9份标本)排除在最终分析之外。在其余的995份标本中,21份AFB涂片阳性:13份培养出结核分枝杆菌复合群(MTBC),6份培养出非结核分枝杆菌,2份(来自两名在研究开始后被诊断为TB并开始治疗的患者)培养阴性。28份标本(20名患者)通过培养和E-MTD检测MTBC呈阳性。7份标本(7名患者)仅培养阳性;3份来自有其他E-MTD阳性标本的患者,2份为培养假阳性,2份为E-MTD检测假阴性。8份标本仅E-MTD检测阳性;4份标本(4名患者)为E-MTD检测假阳性,4份标本来自两名早期E-MTD检测阳性且培养出MTBC的患者。因此,有22名患者患有TB(10名涂片阳性和12名涂片阴性)。AFB涂片诊断TB的患者敏感性和特异性分别为45.5%和98.9%。解决差异后,E-MTD的总体敏感性和特异性分别为90.9%和99.1%,涂片阳性患者为100%和100%,涂片阴性患者为83.3%和99.1%。排除一名涂片阴性患者(其E-MTD检测阴性、MTBC培养阳性的标本含有抑制物质)后,E-MTD的总体敏感性为95.2%,涂片阴性患者为90.9%。通过修改制造商推荐的可疑区域,可在不改变其他性能特征的情况下提高E-MTD的特异性和阳性预测值。这些数据表明,无论AFB涂片结果如何,E-MTD都是快速诊断肺结核的可靠方法。需要制定针对涂片阴性患者最合理使用E-MTD的指南。