Assessment of the Field Utility of a Rapid Point-of-Care Test for SARS-CoV-2 Antibodies in a Household Cohort

被引:3
|
作者
Churiwal, Mehal [1 ]
Lin, Kelly D. [1 ]
Khan, Salman [2 ]
Chhetri, Srijana [1 ]
Muller, Meredith S. [1 ]
Tompkins, Kathleen [1 ]
Smith, Judy [1 ]
Litel, Christy [1 ]
Whittelsey, Maureen [1 ]
Basham, Christopher [1 ]
Rapp, Tyler [1 ]
Cerami, Carla [1 ,3 ]
Premkumar, Lakshmanane [2 ]
Lin, Jessica T. [1 ]
机构
[1] Univ N Carolina, Inst Global Hlth & Infect Dis, Sch Med, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Dept Microbiol & Immunol, Sch Med, Chapel Hill, NC 27599 USA
[3] London Sch Hyg & Trop Med, MRC Unit Gambia, Fajara, Gambia
来源
基金
美国国家卫生研究院;
关键词
RECEPTOR-BINDING DOMAIN;
D O I
10.4269/ajtmh.21-0592
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Point-of-care (POC) tests to detect SARS-CoV-2 antibodies offer quick assessment of serostatus after natural infection or vaccination. We compared the field performance of the BioMedomics COVID-19 IgM/IgG Rapid Antibody Test against an ELISA in 303 participants enrolled in a SARS-CoV-2 household cohort study. The rapid antibody test was easily implemented with consistent interpretation across 14 users in a variety of field settings. Compared with ELISA, detection of seroconversion lagged by 5 to 10 days. However, it retained a sensitivity of 90% (160/177, 95% confidence interval [CI] 85-94%) and specificity of 100% (43/43, 95% CI 92-100%) for those tested 3 to 5 weeks after symptom onset. Sensitivity was diminished among those with asymptomatic infection (74% [14/19], 95% CI 49-91%) and early in infection (45% [29/64], 95% CI 33-58%). When used appropriately, rapid antibody tests offer a convenient way to detect symptomatic infections during convalescence.
引用
收藏
页码:156 / 159
页数:4
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