Point-of-Care C-Reactive Protein Testing to Facilitate Implementation of Isoniazid Preventive Therapy for People Living With HIV

被引:23
作者
Yoon, Christina [1 ]
Davis, J. Lucian [1 ,2 ]
Huang, Laurence [1 ,3 ]
Muzoora, Conrad [4 ]
Byakwaga, Helen [4 ,5 ]
Scibetta, Colin [6 ]
Bangsberg, David R. [4 ,7 ,8 ]
Nahid, Payam [1 ]
Semitala, Fred C. [9 ]
Hunt, Peter W. [3 ]
Martin, Jeffrey N. [5 ]
Cattamanchi, Adithya [1 ,2 ]
机构
[1] Univ Calif San Francisco, San Francisco Gen Hosp, Div Pulm & Crit Care Med, Dept Med, San Francisco, CA USA
[2] Univ Calif San Francisco, San Francisco Gen Hosp, Curry Int TB Ctr, San Francisco, CA USA
[3] Univ Calif San Francisco, San Francisco Gen Hosp, Div HIV AIDS, Dept Med, San Francisco, CA USA
[4] Mbarara Univ Sci & Technol, Dept Med, Mbarara, Uganda
[5] Univ Calif San Francisco, Dept Epidemiol & Biostat, San Francisco, CA 94143 USA
[6] Univ Calif San Francisco, Dept Internal Med, San Francisco, CA 94143 USA
[7] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Ctr Global Hlth, Boston, MA USA
[8] Ragon Inst Massachusetts Gen Hosp Massachusetts I, Boston, MA USA
[9] Makerere Univ, Dept Med, Kampala, Uganda
基金
美国国家卫生研究院;
关键词
tuberculosis; HIV; isoniazid preventive therapy; WHO symptom screen; C-reactive protein; TB screening; ANTIRETROVIRAL THERAPY; PULMONARY TUBERCULOSIS; PROGNOSTIC VALUE; FOOD INSECURITY; PROCALCITONIN; INDIVIDUALS;
D O I
10.1097/QAI.0000000000000085
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Symptom-based tuberculosis screening identifies less than one-third of eligible HIV-infected patients as candidates for isoniazid preventive therapy (IPT). We evaluated whether testing for C-reactive protein (CRP) improves patient selection for IPT. Methods: We measured CRP levels (normal <10 mg/L) using a point-of-care (POC) assay on stored serum samples from HIV-infected Ugandan adults initiating antiretroviral therapy. We assessed diagnostic accuracy in reference to baseline tuberculosis status adjudicated by an expert committee and calculated net reclassification improvement to quantify the incremental discriminatory benefit of POC-CRP in determining IPT eligibility compared to the World Health Organization (WHO) symptom screen. Results: Of 201 patients (median CD4 cell count, 137 cells/mL; interquartile range, 83-206), 5 (2.5%) had tuberculosis. Compared to the WHO symptom screen, POC-CRP had similar sensitivity (100% vs. 80%, P = 0.30) but greater specificity (21% vs. 87%, P < 0.0001) for tuberculosis. If based on the WHO symptom screen, no patients with tuberculosis but only 42 of 196 patients without tuberculosis would have been considered IPT eligible. If POC-CRP were used instead, 1 patient with tuberculosis (reclassification of cases, -20%; P = 0.32) and 129 patients without tuberculosis (reclassification of noncases, +66%; P < 0.001) would have been reclassified as IPT eligible, a net reclassification improvement of 46% (P = 0.03). In addition, POC-CRP testing would have reduced the proportion of patients without active tuberculosis requiring confirmatory tuberculosis testing (87% vs. 21%, P < 0.0001). Conclusions: POC-CRP testing increased more than 4-fold the proportion of HIV-infected adults immediately identified as IPT eligible and decreased the proportion of patients requiring referral for further tuberculosis diagnostic testing. POC-CRP testing could substantially improve implementation of tuberculosis screening guidelines.
引用
收藏
页码:551 / 556
页数:6
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