Foundation for Innovative New Diagnostics, Geneva, Switzerland.
N Engl J Med. 2010 Sep 9;363(11):1005-15. doi: 10.1056/NEJMoa0907847. Epub 2010 Sep 1.
Global control of tuberculosis is hampered by slow, insensitive diagnostic methods, particularly for the detection of drug-resistant forms and in patients with human immunodeficiency virus infection. Early detection is essential to reduce the death rate and interrupt transmission, but the complexity and infrastructure needs of sensitive methods limit their accessibility and effect.
We assessed the performance of Xpert MTB/RIF, an automated molecular test for Mycobacterium tuberculosis (MTB) and resistance to rifampin (RIF), with fully integrated sample processing in 1730 patients with suspected drug-sensitive or multidrug-resistant pulmonary tuberculosis. Eligible patients in Peru, Azerbaijan, South Africa, and India provided three sputum specimens each. Two specimens were processed with N-acetyl-L-cysteine and sodium hydroxide before microscopy, solid and liquid culture, and the MTB/RIF test, and one specimen was used for direct testing with microscopy and the MTB/RIF test.
Among culture-positive patients, a single, direct MTB/RIF test identified 551 of 561 patients with smear-positive tuberculosis (98.2%) and 124 of 171 with smear-negative tuberculosis (72.5%). The test was specific in 604 of 609 patients without tuberculosis (99.2%). Among patients with smear-negative, culture-positive tuberculosis, the addition of a second MTB/RIF test increased sensitivity by 12.6 percentage points and a third by 5.1 percentage points, to a total of 90.2%. As compared with phenotypic drug-susceptibility testing, MTB/RIF testing correctly identified 200 of 205 patients (97.6%) with rifampin-resistant bacteria and 504 of 514 (98.1%) with rifampin-sensitive bacteria. Sequencing resolved all but two cases in favor of the MTB/RIF assay.
The MTB/RIF test provided sensitive detection of tuberculosis and rifampin resistance directly from untreated sputum in less than 2 hours with minimal hands-on time. (Funded by the Foundation for Innovative New Diagnostics.)
全球结核病控制受到缓慢、不敏感的诊断方法的阻碍,特别是在检测耐药形式和人类免疫缺陷病毒感染患者方面。早期发现对于降低死亡率和中断传播至关重要,但敏感方法的复杂性和基础设施需求限制了其可及性和效果。
我们评估了 Xpert MTB/RIF 的性能,这是一种用于结核分枝杆菌(MTB)和利福平(RIF)耐药性的自动化分子检测,具有完全集成的样本处理,涉及 1730 名疑似敏感或多药耐药性肺结核患者。秘鲁、阿塞拜疆、南非和印度的合格患者每人提供了三份痰标本。两份标本用 N-乙酰-L-半胱氨酸和氢氧化钠处理后,进行显微镜检查、固体和液体培养以及 MTB/RIF 检测,一份标本用于直接进行显微镜检查和 MTB/RIF 检测。
在培养阳性患者中,单次直接 MTB/RIF 检测可识别 561 例涂阳肺结核患者中的 551 例(98.2%)和 171 例涂阴肺结核患者中的 124 例(72.5%)。该检测在 609 例无结核病患者中的 604 例中具有特异性(99.2%)。在涂阴、培养阳性的肺结核患者中,增加第二个 MTB/RIF 检测可将敏感性提高 12.6 个百分点,第三个检测可提高 5.1 个百分点,总敏感性达到 90.2%。与表型药物敏感性检测相比,MTB/RIF 检测正确识别了 205 例利福平耐药菌中的 200 例(97.6%)和 514 例利福平敏感菌中的 504 例(98.1%)。测序解决了除两例外的所有病例,均支持 MTB/RIF 检测。
MTB/RIF 检测可直接从未经治疗的痰中在不到 2 小时内快速、敏感地检测结核病和利福平耐药性,所需人工操作时间最短。(由创新新诊断基金会资助)。