第四章:结核感染的诊断

J. Campbell, C. Pease, P. Daley, M. Pai, D. Menzies
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引用次数: 8

摘要

•结核病感染检测的主要目标是确定哪些人患结核病的风险增加,从而可以从结核病预防治疗中受益。•在以下情况下,不建议进行结核病感染检测:〇感染风险低的人,如果感染;〇支持对12岁以上的成人和青少年进行结核病诊断;〇对接触者调查或职业筛查项目之外的个人进行常规大规模筛查;〇监测结核病治疗反应。结核菌素皮肤试验和γ干扰素释放试验都是结核感染诊断可接受的替代方法。在任何需要检测的情况下,这两种检测都可用于结核感染筛查。然而,有偏好和例外:干扰素- γ释放试验是首选的测试,当:〇2岁以上和10岁以下的儿童以前接受过卡介苗(卡介苗)结核病;〇至少10岁的人在婴儿期(1岁以上)后接种卡介苗,或多次接种卡介苗和/或不确定何时接种卡介苗;对于结核菌素皮肤试验的管理和/或读数,没有足够的培训和质量评估与控制,但有进行干扰素释放试验的人员和设施;〇无法或不太可能返回进行结核菌素皮肤试验;结核菌素皮肤试验是禁忌。〇当计划进行系列试验以评估新感染(即转化)的风险时,结核菌素皮肤试验是首选试验。这包括在接触者调查中进行重复检测,或对可能持续接触的卫生保健工作者或其他人群(如惩戒人员或监狱囚犯)进行连续检测。在这些情况下,干扰素释放试验是不可接受的。•在下列情况下,可依次使用两种结核病感染诊断试验:〇如果结核菌素皮肤试验或干扰素- γ释放试验结果均为阴性,则如果感染风险高、结核病进展风险升高、结核病预后不良的风险高和/或患者有可能降低试验敏感性的条件或习惯,则可使用另一种试验来增加敏感性。〇如果最初结核菌素皮肤试验呈阳性,但结核感染的可能性较低,或由于卡介苗导致假阳性结果的风险较高,则可使用干扰素释放试验来增加特异性。•在解释结核病感染诊断测试结果并考虑某人是否有患结核病的风险并可能受益于结核病预防性治疗时,应根据其他因素考虑诊断测试结果,包括该人真正感染的预测试概率、个人患结核病的风险以及测试确定有患结核病风险的人的能力(即:预测价值)。现有的在线工具支持这种解释。
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Chapter 4: Diagnosis of tuberculosis infection
• The primary goal of testing for tuberculosis infection is to identify individuals who are at increased risk for the development of tuberculosis disease and who therefore would benefit from tuberculosis preventive treatment. • Testing for tuberculosis infection is NOT recommended in the following situations: ○ In persons who have a low risk of infection and if infected; ○ To support a tuberculosis disease diagnosis in adults and adolescents >12 years of age; ○ For routine mass screening of individuals outside of contact investigations or occupational screening programs; and ○ For the monitoring of tuberculosis disease treatment response. • Both the tuberculin skin test and interferon-gamma release assay are acceptable alternatives for tuberculosis infection diagnosis. Either test can be used for tuberculosis infection screening in any of the situations in which testing is indicated. However, there are preferences and exceptions: ○ An interferon-gamma release assay is the preferred test when: ○ children over two years of age and less than 10 years of age previously received a Bacille Calmette-Guérin (BCG) vaccine against tuberculosis; ○ persons at least 10 years of age received a BCG vaccine after infancy (older than one year of age), or received a BCG vaccine more than once and/or are uncertain about when they received a BCG vaccine; ○ adequate training and quality assessment and control are NOT available for tuberculin skin test administration and/or reading, but personnel and facilities to perform interferon-gamma release assays are available; ○ a person is unable or unlikely to return to have their tuberculin skin test read; or ○ tuberculin skin testing is contraindicated. ○ The tuberculin skin test is the preferred test when serial testing is planned to assess risk of new infection (ie, conversions). This includes repeat testing in a contact investigation, or serial testing of health care workers or other populations (eg, corrections staff or prison inmates) with potential for ongoing exposure. In these situations, interferon-gamma release assays are not acceptable. • Both tuberculosis infection diagnostic tests may be used sequentially in the following situations: ○ If either the tuberculin skin test or interferon-gamma release assay are negative, the other test may be used to increase sensitivity if the risk for infection is high, the risk for progression to tuberculosis disease is elevated, the risk for a poor outcome from tuberculosis disease is high and/or a person has conditions or habits that may reduce the sensitivity of the test. ○ If the initial tuberculin skin test is positive, but the likelihood of tuberculosis infection is low, or risk of a false positive result due to BCG is high, then an interferon-gamma release assay may be used to increase specificity. • When interpreting a tuberculosis infection diagnostic test result and considering whether someone is at risk of developing tuberculosis disease and would likely benefit from tuberculosis preventive treatment, the diagnostic test result should be considered in light of other factors, including the pretest probability for the person being truly infected, the individual risk of developing tuberculosis disease and the ability of the test to identify persons at risk of tuberculosis disease (ie, predictive value). Online tools exist to support this interpretation.
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来源期刊
CiteScore
1.90
自引率
12.50%
发文量
51
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