Reasons for requesting an interferon gamma release test from internal medicine and rheumatology clinics and evaluation of the results

Alper Sarı, Adem Ertürk, Petek Şarlak Konya
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Abstract

Background/Aim: Tuberculosis is a disease involving many systems, such as the lung, gastrointestinal system, genitourinary system, etc. Detecting this disease in its latency significantly reduces the morbidity and mortality associated with tuberculosis. One of the tests used in latent TB screening is the interferon gamma release test. In rheumatology practices, it is routinely used to screen for latent tuberculosis infections before treatment with biological agents and Janus kinase (JAK) inhibitors, and it can also be used to exclude tuberculosis infection in clinical practice. In our study, we aimed to evaluate the reasons for requesting interferon gamma release tests and the results of this test in patients who requested it. Methods: Patients admitted to internal medicine and rheumatology outpatient clinics were retrospectively screened within the retrospective cohort study. In total, 364 patients who requested interferon gamma release testing were included in the study. Nine patients with unclear test results were excluded. Laboratory results, demographic data, reasons for requesting the interferon gamma release test, and results were evaluated. Results: The interferon gamma release test was requested by 355 patients. Of these, 266 patients (74.9%) asked for latent tuberculosis screening before treatment with biological agents and JAK inhibitors. This was followed by patients with peripheral lymphadenopathy-lung nodules, patients with unexplained elevated acute phase reactants, and patients with constitutional symptoms, respectively. Ten out of 107 patients (9.3%) had an active tuberculosis infection, while six out of ten patients (60%) had pulmonary tuberculosis, and four (40%) had extrapulmonary tuberculosis. Conclusion: The most common reason for requesting the interferon gamma release test in internal medicine and rheumatology clinics was screening for latent tuberculosis before treatment with biologic agents and JAK inhibitors. In internal medicine, it has been observed that this test can also be requested by patients with constitutional symptoms, unexplained elevated acute phase reactants, and a preliminary diagnosis of tuberculosis in order to rule out or strengthen the preliminary diagnosis.
要求内科和风湿病诊所进行干扰素释放试验的原因及结果评估
背景/目的:结核病是一种累及肺、胃肠、泌尿生殖系统等多系统的疾病。在潜伏期发现这种疾病可显著降低与结核病相关的发病率和死亡率。在潜伏性结核筛查中使用的试验之一是干扰素γ释放试验。在风湿病学实践中,在使用生物制剂和Janus激酶(JAK)抑制剂治疗前,常规用于筛查潜伏性结核感染,并且在临床实践中也可用于排除结核感染。在我们的研究中,我们旨在评估要求进行干扰素γ释放试验的原因以及要求进行该试验的患者的结果。方法:在回顾性队列研究中对内科和风湿病门诊收治的患者进行回顾性筛选。总共有364名要求进行干扰素释放测试的患者被纳入研究。排除9例检测结果不明确的患者。对实验室结果、人口统计数据、要求进行干扰素释放试验的原因和结果进行了评估。结果:355例患者要求进行干扰素释放试验。其中,266例(74.9%)患者要求在使用生物制剂和JAK抑制剂治疗前进行潜伏性结核病筛查。其次分别是外周淋巴结病变-肺结节患者、不明原因急性期反应物升高患者和有体质症状的患者。107例患者中有10例(9.3%)有活动性结核感染,10例患者中有6例(60%)有肺结核,4例(40%)有肺外结核。结论:内科和风湿病诊所要求进行干扰素γ释放试验的最常见原因是在使用生物制剂和JAK抑制剂治疗前筛查潜伏性结核病。在内科中,观察到有体质症状、不明原因的急性期反应物升高、初步诊断为结核病的患者也可以要求进行这项检查,以排除或加强初步诊断。
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