Songkhla Munjit Na, Tantipong Hutsaya, Tongsai Sasima, Angkasekwinai Nasikarn
Chonburi Hospital, Thailand.
Division of Clinical Epidemiology, Department of Research and Development, Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Open Forum Infect Dis. 2019 Mar 15;6(4):ofz132. doi: 10.1093/ofid/ofz132. eCollection 2019 Apr.
Detection of mycobacterial lipoarabinomannan antigen in urine has emerged as a potential point-of-care test for diagnosis of tuberculosis. This study aimed to evaluate the accuracy of the lateral flow urine lipoarabinomannan (LF-LAM) assay for diagnosis of active tuberculosis among Thai adults with advanced human immunodeficiency virus (HIV) infection.
HIV-infected adult patients with CD4 cell counts ≤200/μL and symptoms suggestive of active tuberculosis were prospectively recruited from both inpatient and outpatient settings at Siriraj Hospital and Chonburi Hospital in Thailand during the study period from December 2015 to March 2017. Freshly collected urine samples were applied to the Alere Determine TB LAM Ag test strip using a grade 1 cutoff, according to the manufacturer's grading system. The diagnostic accuracy of the LF-LAM test was assessed against a microbiological reference standard (definite tuberculosis) or a composite reference standard (definite and probable tuberculosis).
Of the 280 patients who were included, 72 (25.7%) had definite and 65 (23.2%) had probable tuberculosis. Among patients with definite tuberculosis, the LF-LAM test yielded a sensitivity of 75.0% and a specificity of 76.0%. It had the highest sensitivity (90.5%) in HIV-infected patients with CD4 cell counts <50/μL. It yielded a lower sensitivity (61.3%) but a higher specificity (86.0%) when compared with the composite reference standard. Among the 20 patients (14%) with false-positive results, strong band intensity was observed mostly in complex infections. An incremental sensitivity of 11% was observed with use of acid-fast bacilli sputum smear or LF-LAM testing, compared with LF-LAM testing alone.
The LF-LAM test performed well in the diagnosis of active tuberculosis in selected patients with more advanced tuberculosis and coexisting HIV disease.
尿液中分枝杆菌脂阿拉伯甘露聚糖抗原的检测已成为一种潜在的用于结核病诊断的即时检测方法。本研究旨在评估侧向流动尿液脂阿拉伯甘露聚糖(LF-LAM)检测法在诊断晚期人类免疫缺陷病毒(HIV)感染的泰国成年人活动性结核病中的准确性。
在2015年12月至2017年3月的研究期间,从泰国诗里拉吉医院和春武里医院的住院和门诊环境中前瞻性招募CD4细胞计数≤200/μL且有活动性结核病症状的HIV感染成年患者。根据制造商的分级系统,将新鲜采集的尿液样本以1级临界值应用于Alere Determine TB LAM Ag测试条。LF-LAM检测的诊断准确性是相对于微生物学参考标准(确诊结核病)或综合参考标准(确诊和可能的结核病)进行评估的。
在纳入的280例患者中,72例(25.7%)确诊为结核病,65例(23.2%)可能患有结核病。在确诊结核病的患者中,LF-LAM检测的敏感性为75.0%,特异性为76.0%。在CD4细胞计数<50/μL的HIV感染患者中,其敏感性最高(90.5%)。与综合参考标准相比,其敏感性较低(61.3%),但特异性较高(86.0%)。在20例(14%)出现假阳性结果的患者中,大多在复杂感染中观察到强条带强度。与单独使用LF-LAM检测相比,使用抗酸杆菌痰涂片或LF-LAM检测观察到敏感性增加了11%。
LF-LAM检测在诊断患有更晚期结核病和并存HIV疾病的特定患者的活动性结核病中表现良好。