A systematic review of the sensitivity and specificity of lateral flow devices in the detection of SARS-CoV-2

被引:72
作者
Mistry, Dylan A. [1 ]
Wang, Jenny Y. [2 ]
Moeser, Mika-Erik [2 ]
Starkey, Thomas [3 ]
Lee, Lennard Y. W. [1 ,2 ,3 ]
机构
[1] Oxford Univ Hosp, Headley Way, Oxford OX3 9DU, England
[2] Univ Oxford, Oxford, England
[3] Univ Birmingham, Inst Canc & Genom Sci, Birmingham B15 2TT, W Midlands, England
关键词
Coronavirus; COVID-19; SARS-CoV-2; Lateral flow device; Lateral flow test; Viral antigen detection; Rapid antigen detection; Reverse transcriptase polymerase chain reaction; Mass testing; Population testing;
D O I
10.1186/s12879-021-06528-3
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background Lateral flow devices (LFDs) are viral antigen tests for the detection of SARS-CoV-2 that produce a rapid result, are inexpensive and easy to operate. They have been advocated for use by the World Health Organisation to help control outbreaks and break the chain of transmission of COVID-19 infections. There are now several studies assessing their accuracy but as yet no systematic review. Our aims were to assess the sensitivity and specificity of LFDs in a systematic review and summarise the sensitivity and specificity of these tests. Methods A targeted search of Pubmed and Medxriv, using PRISMA principles, was conducted identifying clinical studies assessing the sensitivity and specificity of LFDs as their primary outcome compared to reverse transcriptase polymerase chain reaction (RT-PCR) for the detection of SARS-CoV-2. Based on extracted data sensitivity and specificity was calculated for each study. Data was pooled based on manufacturer of LFD and split based on operator (self-swab or by trained professional) and sensitivity and specificity data were calculated. Results Twenty-four papers were identified involving over 26,000 test results. Sensitivity from individual studies ranged from 37.7% (95% CI 30.6-45.5) to 99.2% (95% CI 95.5-99.9) and specificity from 92.4% (95% CI 87.5-95.5) to 100.0% (95% CI 99.7-100.0). Operation of the test by a trained professional or by the test subject with self-swabbing produced comparable results. Conclusions This systematic review identified that the performance of lateral flow devices is heterogeneous and dependent on the manufacturer. Some perform with high specificity but a great range of sensitivities were shown (38.32-99.19%). Test performance does not appear dependent on the operator. Potentially, LFDs could support the scaling up of mass testing to aid track and trace methodology and break the chain of transmission of COVID-19 with the additional benefit of providing individuals with the results in a much shorter time frame.
引用
收藏
页数:14
相关论文
共 39 条
[1]   Potential Use of Antigen-Based Rapid Test for SARS- CoV-2 in Respiratory Specimens in LowResource Settings in Egypt for Symptomatic Patients and High-Risk Contacts [J].
Abdelrazik, Abeer Mohamed ;
Elshafie, Shahira Morsy ;
Abdelaziz, Hossam M. .
LABORATORY MEDICINE, 2021, 52 (02) :E46-E49
[2]  
Abdulrahman A, 2020, COMP SARS COV 2 NASA, V2020, DOI [11.10.20228973, DOI 10.1101/2020.11.10.20228973], 10.1101/2020.11.10.20228973]
[3]   Field evaluation of a rapid antigen test (Panbio™ COVID-19 Ag Rapid Test Device) for COVID-19 diagnosis in primary healthcare centres [J].
Albert, Eliseo ;
Torres, Ignacio ;
Bueno, Felipe ;
Huntley, Dixie ;
Molla, Estefania ;
Angel Fernandez-Fuentes, Miguel ;
Martinez, Mireia ;
Poujois, Sandrine ;
Forque, Lorena ;
Valdivia, Arantxa ;
Solano de la Asuncion, Carlos ;
Ferrer, Josep ;
Colomina, Javier ;
Navarro, David .
CLINICAL MICROBIOLOGY AND INFECTION, 2021, 27 (03) :472.e7-472.e10
[4]  
Arevalo-Rodriguez I, FALSE NEGATIVE RESUL
[5]  
Berger A, DIAGNOSTIC ACCURACY
[6]   Implementation of rapid SARS-CoV-2 antigenic testing in a laboratory without access to molecular methods: Experiences of a general hospital [J].
Blairon, Laurent ;
Wilmet, Alain ;
Beukinga, Ingrid ;
Tre-Hardy, Marie .
JOURNAL OF CLINICAL VIROLOGY, 2020, 129
[7]  
Bulilete O, EVALUATION PANBIO RA
[8]   Urgent need of rapid tests for SARS CoV-2 antigen detection: Evaluation of the SD-Biosensor antigen test for SARS-CoV-2 [J].
Cerutti, Francesco ;
Burdino, Elisa ;
Milia, Maria Grazia ;
Allice, Tiziano ;
Gregori, Gabriella ;
Bruzzone, Bianca ;
Ghisetti, Valeria .
JOURNAL OF CLINICAL VIROLOGY, 2020, 132
[9]   Rapid SARS-CoV-2 antigen detection assay in comparison with real-time RT-PCR assay for laboratory diagnosis of COVID-19 in Thailand [J].
Chaimayo, Chutikarn ;
Kaewnaphan, Bualan ;
Tanlieng, Nattaya ;
Athipanyasilp, Niracha ;
Sirijatuphat, Rujipas ;
Chayakulkeeree, Methee ;
Angkasekwinai, Nasikarn ;
Sutthent, Ruengpung ;
Puangpunngam, Nattawut ;
Tharmviboonsri, Theerawoot ;
Pongraweewan, Orawan ;
Chuthapisith, Suebwong ;
Sirivatanauksorn, Yongyut ;
Kantakamalakul, Wannee ;
Horthongkham, Navin .
VIROLOGY JOURNAL, 2020, 17 (01)
[10]  
Department of Health and Social Care, 2020, MOR RAP COVID 19 TES