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美国医护人员大规模常规筛查中应用 QuantiFERON-TB Gold 检测的挑战。

Challenges with QuantiFERON-TB Gold assay for large-scale, routine screening of U.S. healthcare workers.

机构信息

1 Department of Medicine and.

出版信息

Am J Respir Crit Care Med. 2013 Oct 15;188(8):1005-10. doi: 10.1164/rccm.201305-0831OC.

Abstract

RATIONALE

North American occupational health programs that switched from the tuberculin skin test (TST) to IFN-γ release assays for latent tuberculosis screening are reporting challenges with interpretation of serial testing results in healthcare workers (HCWs). However, limited data exist on the reproducibility of serial IFN-γ release assay results in low-risk HCWs.

OBJECTIVES

To evaluate the short-term reproducibility of QuantiFERON-TB Gold In-Tube (QFT) in a large cohort of HCWs and to define a QFT cutoff yielding a conversion rate equivalent to historical TST rates.

METHODS

We retrospectively evaluated the QFT results from HCWs with two or more QFT tests performed between June 2008 and July 2010 at an academic institution. Outcome measures were proportions of reproducibility, quantitative results, and conversion rates with alternate QFT cutoffs.

MEASUREMENTS AND MAIN RESULTS

A total of 9,153 HCWs with two or more QFT tests were included in the analysis. Of 8,227 individuals with a negative result, 4.4% (n = 361) converted their QFT result over 2 years. A total of 261 (72.3%) of the HCWs with conversions underwent repeat short-term testing after the first positive result with 64.8% reverting (n = 169). An IFN-γ cutoff of 5.3 IU/ml or higher (manufacturer's cutoff is ≥0.35 IU/ml) yielded a conversion rate of 0.4%, equal to our institution's historical TST conversion rate.

CONCLUSIONS

The manufacturer's definition of QFT conversion results in an inflated conversion rate that is incompatible with our low-risk setting. A significantly higher QFT cutoff value is needed to match the historical TST conversion rate. Nonreproducible conversions in most converters suggested false-positive results.

摘要

背景

北美职业健康计划在对潜伏性结核病筛查中已将结核菌素皮肤试验(TST)转换为干扰素-γ释放试验(IGRA),但目前正在报告医护人员(HCW)对连续检测结果的解读存在挑战。然而,低风险 HCW 中连续 IGRA 结果的可重复性数据有限。

目的

评估大样本量 HCW 中 QuantiFERON-TB Gold In-Tube(QFT)的短期可重复性,并定义 QFT 截止值,以获得与历史 TST 率相当的转化率。

方法

我们回顾性评估了 2008 年 6 月至 2010 年 7 月期间在一所学术机构中进行了两次或更多次 QFT 检测的 HCW 的 QFT 结果。主要观察指标为重复性、定量结果和不同 QFT 截止值的转化率。

测量和主要结果

共有 9153 名 HCW 进行了两次或更多次 QFT 检测,其中 8227 名(90.5%)的结果为阴性。在这组人群中,4.4%(n=361)在 2 年内 QFT 结果转为阳性。在首次阳性结果后,共有 261 名(72.3%)HCW 进行了短期重复检测,其中 64.8%(n=169)结果转为阴性。IGF-γ截止值为 5.3 IU/ml 或更高(制造商的截止值为≥0.35 IU/ml),转化率为 0.4%,与本机构的历史 TST 转化率相当。

结论

制造商对 QFT 转换的定义导致转化率过高,与我们的低风险环境不兼容。需要更高的 QFT 截止值来匹配历史 TST 转化率。大多数转化者的不可重复性转化提示可能存在假阳性结果。

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