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低发病地区结核接触者中 QuantiFERON®-TB gold in-tube 检测的观察性研究。

Observational study of QuantiFERON®-TB gold in-tube assay in tuberculosis contacts in a low incidence area.

机构信息

Service de pneumologie, CHU de Caen, Caen, France.

出版信息

PLoS One. 2012;7(8):e43520. doi: 10.1371/journal.pone.0043520. Epub 2012 Aug 24.

Abstract

BACKGROUND

QuantiFERON®-TB Gold in-Tube (QFT) assay is a recently developed test to assess latent tuberculosis infection in contagious tuberculosis (TB) contact subjects. To assess the QFT assay in recently exposed contacts of active tuberculosis patients in a French area with low TB incidence but high Bacille Calmette-Guerin coverage, and evaluate progression rates to TB disease.

METHODOLOGY/PRINCIPAL FINDINGS: Between January 2007 and December 2009, 687 contacts of culture-confirmed tuberculosis cases underwent the QFT assay, with tuberculin skin test (TST) in 473, and a 34 months mean follow-up. Of 687 contacts, 148 were QFT positive, while 526 were negative and 13 indeterminate. QFT was positive in 35% of individuals with TST ≥ 10 mm, 47.5% with TST ≥ 15 mm or phlyctenular, but in 21% of cases in which two-step TST (M0 and M3) remained negative. Conversely, QFT was negative in 69% of cases with two-step TST showing conversion from negative to positive. All indeterminate QFT were associated with TST induration <10 mm in diameter. For 29 QFT-positive subjects, no chemoprophylaxis was given due to medical contraindications. Of the remaining 119 QFT-positive contacts, 97 accepted chemoprophylaxis (81.5%), and 79 (81.4%) completed the treatment. Two contacts progressed to TB disease: one subject was QFT positive and had declined chemoprophylaxis, while the other one was QFT negative. QFT positive predictive value for progression to TB was 1.96% (1/51) with a 99.8% (525/526) negative predictive value.

CONCLUSIONS/SIGNIFICANCE: Our results confirm the safety of the QFT-based strategy for assessing the TB chemoprophylaxis indication, as only one contact developed TB disease out of 526 QFT-negative subjects.

摘要

背景

QuantiFERON®-TB Gold in-Tube(QFT)检测是一种最近开发的检测方法,用于评估传染性肺结核(TB)接触者中的潜伏性结核感染。在法国一个结核发病率低但卡介苗覆盖率高的地区,评估 QFT 检测在活动性肺结核患者近期接触者中的作用,并评估其发展为结核病的比率。

方法/主要发现:2007 年 1 月至 2009 年 12 月,687 例培养确诊结核病病例的接触者接受了 QFT 检测,其中 473 例接受了结核菌素皮肤试验(TST),平均随访 34 个月。687 名接触者中,148 名 QFT 阳性,526 名 QFT 阴性,13 名 QFT 不确定。TST≥10mm 者中,35%的 QFT 阳性,TST≥15mm 或出现疱疹者中,47.5%的 QFT 阳性,但两步 TST(M0 和 M3)持续阴性者中,21%的 QFT 阳性。相反,两步 TST 由阴性转为阳性者中,69%的 QFT 阴性。所有不确定的 QFT 均与 TST 硬结直径<10mm 有关。由于医学禁忌,29 例 QFT 阳性患者中,未给予化学预防。在其余 119 例 QFT 阳性接触者中,97 例接受了化学预防(81.5%),其中 79 例(81.4%)完成了治疗。2 例接触者发展为结核病:1 例 QFT 阳性且拒绝化学预防,另 1 例 QFT 阴性。QFT 阳性预测值为 1.96%(51/2598),阴性预测值为 99.8%(526/526)。

结论/意义:我们的结果证实了基于 QFT 的策略在评估结核化学预防指征方面的安全性,因为在 526 例 QFT 阴性接触者中,只有 1 例发展为结核病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0a2/3427381/06dbbc70158d/pone.0043520.g001.jpg

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