IGRA试验和TST在波兰克拉科夫危险人群中诊断潜伏性结核感染和预测结核的比较

Katarzyna Kruczak, Mariusz Duplaga, Marek Sanak, Adam Cmiel, Lucyna Mastalerz, Krzysztof Sladek, Ewa Nizankowska-Mogilnicka
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引用次数: 19

摘要

背景:本研究的目的是利用QuantiFERON-TB金管(QFT-GIT)试验和结核菌素皮肤试验(TST)评估克拉科夫危险人群中潜伏性结核感染(LTBI)的患病率;我们还试图评估4-5年随访期间进展为活动性疾病的比率。方法:对来自无家可归者、密切接触者、定期接触者、长期护理机构(ltcf)居民和低风险组的785名受试者进行QFT-GIT测试,701名受试者进行TST测试。结果:在无家可归者、密切接触者、周期性接触者、长期接触者和低危人群中,QFT-GIT阳性率分别为36.7%、27.2%、27.0%、21.1%和23.7%,TST阳性率分别为55.8%、47.4%、47.6%、43.2%和47.9%。在63名无家可归者中,5名在248人/年的随访中发展为活动性结核病(发病率(IR) 20 / 1000人/年,95%置信区间(CI) 8.4-48.5);148名密切接触者中,5人在740人/年的随访中出现活动性结核病(IR 7, 95% CI 2.8-16.2);在145名定期接触者中,2名在580人/年的随访中发展为活动性结核病(IR 4, 95% CI 0.9-13.8)。在QFT-GIT阳性受试者中,每1000人的IR (95% CI)为无家可归者30(9.0-86.1),密切接触者18(5.7-54.7),周期性接触者13(3.2-51.3)。在波兰,没有政策规定为QFT或TST呈阳性的人提供LTBI治疗;因此,对未经治疗的受试者的疾病进展率进行了分析。结论:在研究风险组中,QFT-GIT和TST阳性的发生率较高。在无家可归者和密切接触者群体中,活动性结核病的最佳预测指标是QFT-GIT阳性和TST阳性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparison of IGRA tests and TST in the diagnosis of latent tuberculosis infection and predicting tuberculosis in risk groups in Krakow, Poland.

Background: The objective of this study was to assess the prevalence of latent tuberculosis infection (LTBI) in risk groups in Krakow, using the QuantiFERON-TB Gold In-Tube (QFT-GIT) test and the tuberculin skin test (TST); we also sought to assess the rate of progression to active disease over 4-5 y of follow-up.

Methods: QFT-GIT tests were performed on 785 subjects and the TST on 701 subjects from the risk groups of homeless persons, close contacts, periodic contacts, and residents of long-term care facilities (LTCFs), and subjects from a low risk group.

Results: In homeless persons, close contacts, periodic contacts, LTCF residents, and low risk persons, a positive QFT-GIT was found in 36.7%, 27.2%, 27.0%, 21.1%, and 23.7% of subjects, respectively, while a positive TST was found in 55.8%, 47.4%, 47.6%, 43.2%, and 47.9%, respectively. Of 63 homeless subjects, 5 developed active TB over 248 person-y of follow-up (incidence rate (IR) 20 per 1000 person-y, 95% confidence interval (CI) 8.4-48.5); of 148 close contacts, 5 developed active TB over 740 person-y of follow-up (IR 7, 95% CI 2.8-16.2); of 145 periodic contacts, 2 developed active TB over 580 person-y of follow-up (IR 4, 95% CI 0.9-13.8). The IR per 1000 person-y (95% CI) among subjects with a positive QFT-GIT was 30 (9.0-86.1) for homeless subjects, 18 (5.7-54.7) for close contacts, and 13 (3.2-51.3) for periodic contacts. In Poland there is no policy for the provision of LTBI treatment to people with a positive QFT or TST; therefore, the estimated rates of disease progression were analysed amongst untreated subjects.

Conclusions: The prevalence of positive QFT-GIT and TST was high in the study risk groups. The best predictor of active TB in the homeless and close contacts groups was a positive QFT-GIT together with a positive TST.

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