Yoon Christina, Semitala Fred C, Atuhumuza Elly, Katende Jane, Mwebe Sandra, Asege Lucy, Armstrong Derek T, Andama Alfred O, Dowdy David W, Davis J Luke, Huang Laurence, Kamya Moses, Cattamanchi Adithya
Department of Medicine, Division of Pulmonary and Critical Care Medicine, University of California, San Francisco, Zuckerberg San Francisco General Hospital, San Francisco, CA, USA.
Department of Medicine, Makerere University College of Health Sciences, Kampala, Uganda; Makerere University Joint AIDS Program, Kampala, Uganda.
Lancet Infect Dis. 2017 Dec;17(12):1285-1292. doi: 10.1016/S1473-3099(17)30488-7. Epub 2017 Aug 25.
Symptom-based screening for tuberculosis is recommended for all people living with HIV. This recommendation results in unnecessary Xpert MTB/RIF testing in many individuals living in tuberculosis-endemic areas and thus poor implementation of intensified case finding and tuberculosis preventive therapy. Novel approaches to tuberculosis screening are needed to help achieve global targets for tuberculosis elimination. We assessed the performance of C-reactive protein (CRP) measured with a point-of-care assay as a screening tool for active pulmonary tuberculosis.
For this prospective study, we enrolled adults (aged ≥18 years) living with HIV with CD4 cell count less than or equal to 350 cells per μL who were initiating antiretroviral therapy (ART) from two HIV/AIDS clinics in Uganda. CRP concentrations were measured at study entry with a point-of-care assay using whole blood obtained by fingerprick (concentration ≥10 mg/L defined as screen positive for tuberculosis). Sputum samples were collected for Xpert MTB/RIF testing and culture. We calculated the sensitivity and specificity of point-of-care CRP and WHO symptom-based screening in reference to culture results. We repeated the sensitivity analysis with Xpert MTB/RIF as the reference standard.
Between July 8, 2013, and Dec 15, 2015, 1237 HIV-infected adults were enrolled and underwent point-of-care CRP testing. 60 (5%) patients with incomplete or contaminated cultures were excluded from the analysis. Of the remaining 1177 patients (median CD4 count 165 cells per μL [IQR 75-271]), 163 (14%) had culture-confirmed tuberculosis. Point-of-care CRP testing had 89% sensitivity (145 of 163, 95% CI 83-93) and 72% specificity (731 of 1014, 95% CI 69-75) for culture-confirmed tuberculosis. Compared with WHO symptom-based screening, point-of-care CRP testing had lower sensitivity (difference -7%, 95% CI -12 to -2; p=0·002) but substantially higher specificity (difference 58%, 95% CI 55 to 61; p<0·0001). When Xpert MTB/RIF results were used as the reference standard, sensitivity of point-of-care CRP and WHO symptom-based screening were similar (94% [79 of 84] vs 99% [83 of 84], respectively; difference -5%, 95% CI -12 to 2; p=0·10).
The performance characteristics of CRP support its use as a tuberculosis screening test for people living with HIV with CD4 count less than or equal to 350 cells per μL who are initiating ART. HIV/AIDS programmes should consider point-of-care CRP-based tuberculosis screening to improve the efficiency of intensified case finding and increase uptake of tuberculosis preventive therapy.
National Institutes of Health; President's Emergency Plan for AIDS Relief; University of California, San Francisco, Nina Ireland Program for Lung Health.
建议对所有艾滋病毒感染者进行基于症状的结核病筛查。这一建议导致许多生活在结核病流行地区的人接受了不必要的Xpert MTB/RIF检测,从而导致强化病例发现和结核病预防性治疗的实施效果不佳。需要新的结核病筛查方法来帮助实现全球消除结核病的目标。我们评估了即时检测法测定的C反应蛋白(CRP)作为活动性肺结核筛查工具的性能。
在这项前瞻性研究中,我们招募了年龄≥18岁、CD4细胞计数小于或等于每微升350个细胞且开始接受抗逆转录病毒治疗(ART)的艾滋病毒感染者,这些感染者来自乌干达的两家艾滋病毒/艾滋病诊所。在研究开始时,使用即时检测法通过手指采血获得的全血测量CRP浓度(浓度≥10mg/L定义为结核病筛查阳性)。收集痰液样本进行Xpert MTB/RIF检测和培养。我们根据培养结果计算了即时检测CRP和世界卫生组织基于症状筛查的敏感性和特异性。我们以Xpert MTB/RIF作为参考标准重复了敏感性分析。
在2013年7月8日至2015年12月15日期间,招募了1237名艾滋病毒感染成人并进行了即时检测CRP检测。60名(5%)培养结果不完整或受污染的患者被排除在分析之外。在其余1177名患者(CD4计数中位数为每微升165个细胞[四分位间距75 - 271])中,163名(14%)有培养确诊的结核病。即时检测CRP对培养确诊的结核病的敏感性为89%(163例中的145例,95%置信区间83 - 93),特异性为72%(1014例中的731例,95%置信区间69 - 75)。与世界卫生组织基于症状的筛查相比,即时检测CRP的敏感性较低(差异 - 7%,95%置信区间 - 12至 - 2;p = 0.002),但特异性显著更高(差异58%,95%置信区间55至61;p < 0.0001)。当以Xpert MTB/RIF结果作为参考标准时,即时检测CRP和世界卫生组织基于症状筛查的敏感性相似(分别为94%[84例中的79例]和99%[84例中的83例];差异 - 5%,95%置信区间 - 12至2;p = 0.10)。
CRP的性能特征支持将其用作对开始接受ART且CD4计数小于或等于每微升350个细胞的艾滋病毒感染者的结核病筛查试验。艾滋病毒/艾滋病项目应考虑基于即时检测CRP的结核病筛查,以提高强化病例发现的效率并增加结核病预防性治疗的接受率。
美国国立卫生研究院;总统艾滋病紧急救援计划;加利福尼亚大学旧金山分校,尼娜·爱尔兰肺部健康项目。