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Interferon-Gamma Release Assay Testing in Children Younger Than 2 Years in a US-Based Health System

医学 静脉切开术 结核菌素 潜伏性肺结核 干扰素γ释放试验 内科学 肺结核 量子化子 干扰素γ 儿科 结核分枝杆菌 细胞因子 病理
作者
James Gaensbauer,Janine Young,Cara Harasaki,Kaylynn Aiona,Robert Belknap,Michelle Haas
出处
期刊:Pediatric Infectious Disease Journal [Ovid Technologies (Wolters Kluwer)]
卷期号:39 (9): 803-807 被引量:12
标识
DOI:10.1097/inf.0000000000002711
摘要

Background: Use of interferon-gamma releasing assays (IGRAs) in children <2 years old may derive many of the same advantages, which have led to preference over tuberculin skin test (TST) in older children, but data are limited. Since 2011, we have tested children <2 years old with Quantiferon-TB Gold/Gold Plus (QFT)) in select clinical scenarios at Denver Health, a health system encompassing a TB clinic, refugee and immigrant screening and primary care. Methods: We identified patients <2 years old tested with QFT between February, 2011 and August, 2019. The primary outcome measure was incident cases of TB among tested patients. Test results and in vitro characteristics were analyzed, as were demographic, epidemiologic and clinical outcomes. Results: We analyzed 116 QFTs ordered in children age 7–23 months. Two were positive, 3 indeterminate, 3 failed/refused phlebotomy and the remainder (93%) were negative. Mitogen tube results were robust. Thirteen patients were TST-positive: 11 were QFT-negative, 1 QFT-positive and 1 failed phlebotomy. Eight patients received some form of TB medication, including 4 QFT-negative patients who were treated for active TB or latent TB infection based on positive TST or clinical findings. Among QFT-negative patients, including 6 TST-positive, not treated for active TB or latent TB infection, no TB disease has been identified over a median follow-up time of 2.96 years. Conclusions: IGRA use was not limited by barriers of phlebotomy, indeterminate result or gamma-interferon production. The risk of missing an infected but IGRA-negative patient can be reduced by treatment of select patients at higher risk. Current recommendations against IGRA use in children <2 years old could be amended to allow careful introduction, particularly among well-appearing BCG-vaccinated patients.
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