Department of Clinical Microbiology, Trinity College Dublingrid.8217.c, St James's Hospital Campus, Dublin, Ireland.
Department of Respiratory Medicine, St. James's Hospital, Dublin, Ireland.
Microbiol Spectr. 2022 Jun 29;10(3):e0234521. doi: 10.1128/spectrum.02345-21. Epub 2022 Apr 26.
The aim of this study was to evaluate the performance of Xpert MTB/RIF Ultra (Ultra) compared with its predecessor, Xpert MTB/RIF (Xpert), in the diagnosis of tuberculosis (TB) in a low TB incidence country. Retrospective analysis was performed on 689 clinical samples received between 2015 and 2018, on which Xpert was performed, and on 715 samples, received between 2018 and 2020, on which Ultra was performed. Samples were pulmonary ( = 830) and extrapulmonary ( = 574) in nature, and a total of 264 were culture positive for Mycobacterium tuberculosis complex (MTBC). The diagnostic performance of both assays was analyzed using culture as the reference standard. The sensitivity of Ultra for culture positive (smear positive and smear negative) MTBC samples, was 93.2% (110/118) compared with 82.2% (120/146) for Xpert ( = 0.0078). In smear negative-culture positive samples, Ultra had a sensitivity of 74.2% (23/31) versus 36.11% (13/36) for Xpert ( = 0.0018). Specificity of both assays was comparable at 94.8% (566/597) for Ultra and 95.8% (520/543) for Xpert ( = 0.4475). The sensitivity of Ultra and Xpert assays among exclusively pulmonary samples was 95.3% (82/86) and 90.3% (84/93), respectively ( = 0.1955), and 87.5% (28/32) and 67.9% (36/53), respectively, among extrapulmonary samples ( = 0.0426). Ultra showed improved performance compared with Xpert in a low TB incidence setting, particularly in smear negative and extrapulmonary MTBC disease. The specificity of Ultra was lower than Xpert, however, this was not statistically significant. The study demonstrates the improved sensitivity of the Ultra compared with the Xpert, particularly in smear negative TB disease, for both pulmonary and extrapulmonary samples in a low TB incidence setting. Cycle threshold (Ct) value for both assays was found to positively correlate with time to TB culture positivity, suggesting that Ct and semiquantitative results could be used as indicators of sample MTBC bacillary burden, and thus, perhaps, of transmission potential. This may have implications for the designation of patient isolation precautions.
本研究旨在评估 Xpert MTB/RIF Ultra(Ultra)在低结核病发病率国家的结核病(TB)诊断中的表现与前代产品 Xpert MTB/RIF(Xpert)相比。对 2015 年至 2018 年间接受 Xpert 检测的 689 份临床样本和 2018 年至 2020 年间接受 Ultra 检测的 715 份样本进行了回顾性分析。样本为肺源性(=830)和肺外源性(=574),共有 264 份结核分枝杆菌复合群(MTBC)培养阳性样本。使用培养作为参考标准分析两种检测方法的诊断性能。Ultra 对培养阳性(涂片阳性和涂片阴性)MTBC 样本的敏感性为 93.2%(110/118),而 Xpert 为 82.2%(120/146)(=0.0078)。在涂片阴性培养阳性样本中,Ultra 的敏感性为 74.2%(23/31),而 Xpert 为 36.11%(13/36)(=0.0018)。两种检测方法的特异性相当,Ultra 为 94.8%(566/597),Xpert 为 95.8%(520/543)(=0.4475)。纯肺样本中 Ultra 和 Xpert 检测的敏感性分别为 95.3%(82/86)和 90.3%(84/93)(=0.1955),肺外样本中分别为 87.5%(28/32)和 67.9%(36/53)(=0.0426)。Ultra 在低结核病发病率环境中的表现优于 Xpert,尤其是在涂片阴性和肺外 MTBC 疾病中。然而,Ultra 的特异性低于 Xpert,但这并不具有统计学意义。该研究表明,在低结核病发病率环境中,Ultra 与 Xpert 相比,在涂片阴性和肺外样本中均具有更高的敏感性,尤其在涂片阴性的结核病中。两种检测方法的循环阈值(Ct)值与结核培养阳性时间呈正相关,表明 Ct 和半定量结果可作为样本 MTBC 菌载量的指标,从而可能作为传播潜力的指标。这可能对指定患者隔离预防措施具有重要意义。