The long-term risk of tuberculosis among individuals with Xpert Ultra "trace" screening results: a longitudinal follow-up study.

Joowhan Sung, Mariam Nantale, Annet Nalutaaya, Patrick Biché, James Mukiibi, Joab Akampurira, Rogers Kiyonga, Francis Kayondo, Michael Mukiibi, Caitlin Visek, Caleb E Kamoga, David W Dowdy, Achilles Katamba, Emily A Kendall
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Abstract

Background: Systematic screening for tuberculosis using Xpert Ultra generates "trace" results of uncertain significance. Additional microbiological testing in this context is often negative, but untreated individuals might still progress to culture-positive disease. We aimed to estimate the two-year risk of tuberculosis among screening participants with trace-positive sputum.

Methods: We screened 31,505 people for tuberculosis in Uganda using sputum Xpert Ultra as an initial test, through event-based and door-to-door screening. We enrolled 128 participants with trace-positive sputum (PWTS), 139 Ultra-negative controls into a prospective cohort, and 110 Ultra-positive (>trace) controls for cross-sectional comparison. All participants underwent extensive initial evaluation, and untreated PWTS and negative controls were followed with re-testing for up to 24 months. We estimated cumulative hazards of tuberculosis among PWTS versus negative controls, using two definitions of tuberculosis: one incorporating clinician judgment (primary) and one based strictly on microbiological results (secondary). We then compared hazards between subgroups of PWTS.

Findings: Of 128 PWTS, 79 (62%) were male and 19 (15%) HIV-positive. Forty-five (35%) PWTS were recommended for treatment upon enrollment, eight lost to follow-up within three months, and 75 followed for median 706 (interquartile range 344-714) days, of whom 19 were recommended for treatment during follow-up. The cumulative hazard of tuberculosis among PWTS not treated at baseline was 0.24 (95% confidence interval: 0.15-0.40) at one year and 0.33 (0.21-0.54) at two years, versus 0.03 (0.01-0.10) at two years for negative controls. Hazards were similar for microbiologically defined tuberculosis (0.36 [0.22-0.58] at 2 years). Tuberculosis diagnosis during follow-up was strongly associated with abnormal baseline chest X-ray (hazard ratio 14.6 [3.3-63.8]) but not with baseline symptoms.

Interpretation: Individuals with trace-positive sputum during screening have a substantial two-year risk of tuberculosis, even when extensive initial evaluations do not confirm disease. Treatment should be considered for most screening participants with trace-positive sputum and abnormal chest imaging.

Funding: National Institutes of Health and Gates Foundation.

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Xpert Ultra“痕量”筛查结果的个体患结核病的长期风险:一项纵向随访研究
背景:使用 Xpert Ultra 对结核病进行系统筛查会产生意义不确定的 "微量 "结果。在这种情况下,额外的微生物检测通常是阴性的,但有微量结果的人可能患有早期疾病或结核病风险升高:方法:我们在乌干达用 Xpert Ultra 进行了结核病筛查,纳入了痕量阳性结果者和 Ultra 阴性对照者。我们对初次广泛评估时未发现结核病的参与者进行了随访,并在痕量结果出现后的 1、3 和 6 个月以及所有参与者出现痕量结果后的 12 和 24 个月进行了重复检测。我们估算了肺结核发病的累积特异性病因危险度,考虑了包括临床医生判断在内的肺结核定义和严格基于微生物学结果的定义。我们比较了痰液为超痕量和超阴性的参与者,以及痰液为超痕量的参与者亚组:在筛查结果为痕量阳性的 129 名参与者中,有 45 人(35%)在注册时被建议接受治疗,8 人在三个月内失去了随访机会。其余 76 名参与者的随访天数中位数为 697 天(四分位数间距为 179-714 天),其中 20 人(26%)被建议接受结核病治疗。临床医生定义的肺结核发病累积危险度在一年时为 26%(95% 置信区间:14-38%),两年时为 35%(19-52%),而对照组在两年时为 2%(0-5%)。微生物学定义的结核病发病风险与对照组相似。肺结核与基线胸部 X 光片异常密切相关(危险比为 15.0 [3.4-65.1]),但与基线症状无关:解释:筛查期间痰液呈痕量阳性的人,尤其是胸部X光检查异常的人,在随后的两年中患结核病的风险很大:研究背景:美国国立卫生研究院:本研究之前的证据:结核病研究的最新进展已将疾病框架从潜伏结核病与活动性结核病的二元分类法转变为疾病状态的连续统一体。这些研究还使人们对早期结核病的动态病程有了更好的了解,随着时间的推移,早期结核病既可能发展为培养阳性疾病,也可能自然消退。Xpert MTB/RIF Ultra("Ultra")的 "微量 "检测结果有时会被认为是假阳性,因为这些人随后在其他诊断检测中检测结果为阴性。然而,其中一些人可能患有早期结核病,但低于现有诊断检测的检测阈值,随着时间的推移,可能发展为微生物可检测的疾病。为了研究这个问题,我们在 PubMed 上搜索了截至 2025 年 2 月 7 日发表的研究,搜索时使用了 "结核病 "和("Xpert 或 "Xpert Ultra" 或 "Ultra")以及 "痕量 "等词,并查阅了相关搜索结果的参考文献列表。两项使用 Xpert Ultra 作为对有症状或胸部 X 光片异常者进行确诊检测的患病率调查发现,20% 和 46% 的痕量阳性痰培养呈阳性。在乌干达进行的一项研究中,Ultra 被用作初筛检测,结果显示只有 14% 的痕量阳性患者痰培养呈阳性。然而,此前没有任何研究对系统筛查中 Ultra 检测结果呈痕量阳性但微生物学检测结果为阴性且未开始接受治疗的患者的结核病发病率进行过前瞻性研究:在这项研究中,我们对 Ultra 检测结果呈痕量阳性、但经过大量诊断检测后仍未开始治疗的患者进行了长达两年的重复检测。在随访期间,约有 25% 的人患上了肺结核,2 年的累计肺结核发病率高达 35%(95% 置信区间为 19-52%)。入组时胸部 X 光片正常者罹患肺结核的风险明显较低。在入组时报告症状的人与未报告症状的人患肺结核的风险相似:本研究中观察到的微量结果显示肺结核的高发病率支持为大多数在肺结核筛查中得到微量结果的人提供治疗。这些结果还表明,X 射线是指导痰液呈微量阳性者做出治疗决策的有用工具。
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