Abstract
Several reports showed SARS-CoV-2 rapid antigen tests (RATs) performances among COVID-19 symptomatic subjects in outpatient settings during periods of highest incidence of infections and high rates of hospital admissions, but few data are present for asymptomatic patients. We investigated the role of RATs in an emergency department, as a novel screening tool before admission for COVID-19 asymptomatic patients. A total of 116 patients were screened on admission in a 250-bed community hospital in Morges, Switzerland. RAT detected 2/7 RT-PCR-positive patients and delivered two false-positive results. These data suggest the non-fiability of RATs screening in this clinical scenario.
Keywords: COVID-19 diagnostic testing, emergency ward, health plan implementation, rapid antigen test, SARS-CoV-2
Introduction
The world has been dealing with SARS-CoV-2 pandemic since the first cases of pneumonia of unknown origin described in December 2019 in Wuhan, China [1]. One year later, huge steps have been made in clinical knowledge on this new infectious disease and different types of diagnostic tests have been developed [2]. Reverse transcriptase polymerase chain reaction (RT-PCR), which detects the viral RNA, is now largely considered as the diagnostic gold standard. However, questions remain regarding the optimal clinical use and the indications of antigen tests.
In Switzerland, the first epidemic wave (March-April 2020) forced laboratories to use the maximum of their test capacities. Because of the high flow of patients consulting hospitals' emergency departments, faster diagnostic results were needed for triage, aimed at minimising nosocomial transmissions. Rapid molecular systems detecting viral RNA, such as GeneXpert SARS-CoV-2 PCR test (Cepheid, USA), combined with classic RT-PCR systems, adequately responded to this clinical need, nevertheless with difficulties in reagents supplies.
In October 2020 Switzerland faced a massive second wave, with up to 1800 infections in 14 days/100.000 inhabitants [3], representing one of the world's highest rate at that period. To meet the urgent need for rapid diagnosis immediately followed by quarantine and contact tracing, a key tool for optimal management of epidemics, the Swiss Federal Office of Public Health authorised the use of rapid antigen tests (RATs) in addition to gold-standard RT-PCR [4].
Several reports describe RAT performances, most of them derived from COVID-19 symptomatic subjects in outpatient settings during periods of highest incidence of infections and high rates of hospital admissions [5,6]. To date, more data are needed to clarify the role of RAT as a screening tool among patients admitted to hospital emergency departments, with or without symptoms of COVID-19, during different phases of the epidemic curve. An extensive evaluation was performed in an emergency department of an Italian hospital with Standard Q® COVID-19 Rapid Antigen Test (SD Biosensor, Roche) screening on nasopharyngeal samples from symptomatic and asymptomatic patients [7]. Among patients without COVID-19 symptoms, a sensitivity of 50% and a specificity of 99.6% was reported, with a SARS-CoV-2 prevalence of 6.5%. Another study performed in Germany investigated the use of RAT as a screening tool among symptomatic patients with COVID-19 admitted to the emergency department [8]. In this study, performed with Standard Q® COVID-19 Rapid Antigen Test (SD Biosensor/Roche) on nasopharyngeal samples, sensitivity was 75.3% and specificity 100%, with a COVID-19 prevalence of 32.8%. After the implementation of RAT at the Emergency Department of the Lausanne University Hospital (CHUV) for quick triaging of patients with or without COVID-19 symptoms [9], we applied a combined RAT and RT-PCR nasopharyngeal screening to asymptomatic patients admitted in the emergency department of a 250-bed community hospital (EHC) in Morges, Switzerland.
Materials and methods
Two simultaneous nasopharyngeal swabs were collected to screen asymptomatic adults hospitalised in medical and surgical wards in accordance with a standard procedure of the emergency department of EHC. The first swab was analysed at the bedside using Standard Q® COVID-19 Rapid Antigen Test (SD Biosensor-Republic of Korea/Roche-Switzerland). Patients with a positive RAT were isolated in single rooms waiting for the molecular confirmation, performed on one of the following platforms at the Institute of Microbiology of the Lausanne University Hospital (CHUV): i) Test Cobas 6800® SARS-CoV-2 (Roche, Basel, Switzerland) or ii) automated high-throughput molecular diagnostic platform, using Magnapure RNA-extraction coupled to applied Biosystems 7900 amplification device (Quant Studio 7) and three Hamilton robots (with primers targeting the E- and RdRp-encoding genes) [10]. RAT and RT-PCR results were compared in the frame of the EHC Patients Safety Program. This analysis in the frame of the CHUV Microbiology Laboratory Quality Control Program was approved by the Institutional Ethical Review Board.
Results
From 04/12/2020 to 04/01/2021, we consecutively screened 116 asymptomatic patients. 63 (54.3%) females and 53 (45.7%) males were tested, with a median age of 46.7 years [IQR 35.3-69.6] (population characteristics are described in Table 1).
Table 1.
Subjects characteristics | Patients without CoVID-19 symptoms (n = 116) |
|
---|---|---|
SARS-CoV-2-positive RAT (n = 4) | SARS-CoV-2-negative RAT (n = 112) | |
Gender | ||
Female | 2 (50%) | 61 (54.5%) |
Male | 2 (50%) | 51 (45.5%) |
Age | ||
Median [IQR], years | 41.9 [30.7-61.2] | 46.7 [35.3-69.6] |
SARS-CoV-2 RT-PCR result | ||
Negative | 2 (50%)a | 107 (95.5%) |
Positive | 2 (50%) | 5 (4.5%) |
Viral load | ||
Median [IQR], cp/ml | 1.8e+08 [1.8e+08 - 1.8e+08]b | 1.9e+04 [6.2e+03 - 8e+05] |
RAT, rapid diagnostic testing; RT-PCR, reverse transcriptase polymerase chain reaction; IQR, interquartile range; Cp/ml, viral copies per millilitre.
Among 4 positive RAT results, 2 were false-positive results, not confirmed by RT-PCR. In this setting, RAT detected less than one third (2/7, 28.6%) of asymptomatic hospitalised patients, who resulted positive by RT-PCR.
One of 7 RT-PCR-positive patients (also tested positive with RAT) had a iral load at the limit of detection, that was not quantifiable.
As compared with RT-PCR, RAT detected two out of seven SARS-CoV-2 positive patients and delivered two false-positive results, exhibiting a sensitivity of 28.6%, a specificity of 98.2% and a positive predictive value of only 50%. The prevalence of SARS-CoV-2 carriage of 6% in accordance with RT-PCR results was significantly underestimated by RAT to 1.7%.
Discussion
RATs are an attractive option for COVID-19 diagnostics due to low costs, rapidity and point-of-care solutions. However, they show a gap in analytical sensitivity as compared with the gold-standard RT-PCR, the detection of the viral load being reduced by a factor 1.000 to 10.000.
In Switzerland, RATs are authorised for immediate COVID-19 diagnosis in outpatients with symptoms lasting less than 4 days and early cohorting in-patients due to high numbers of hospitalisations, when pre-test probability is above 20% [4]. This second condition was recommended because in settings with disease prevalence above 20%, the diagnostic performance gap might be partially compensated by the diagnostic speed, allowing prompt isolation of highly contagious patients, thus reducing the risk of nosocomial transmission.
Turcato et al interestingly investigated the global clinical benefit derived from RAT screening against symptom-based screening in the emergency department with a decision curve analysis (DCA), reporting a considerable net benefit even in settings with SARS-CoV-2 prevalence lower than 15% [7]. DCA is a useful, fast and easy alternative to a full decision analysis for giving a global overlook of benefits. Nevertheless, being only based on the reasonable range of threshold probabilities, DCA might have simplified some assumptions (e.g.: symptoms evaluation performed with the support of imaging/inflammatory parameters/clinical scores versus simple symptoms evaluation for initial triaging purposes) and more complex decision analyses might be needed before ultimately applying changes to screening strategy recommendations.
On the other hand, the data gathered so far showed a clinically relevant difference between RAT diagnostic performances in symptomatic and asymptomatic patients, with significantly lower sensitivity in the absence of symptoms. Hence, adopting an RAT-based screening strategy in patients without symptoms of COVID-19 might miss a significant number of asymptomatic SARS-CoV-2 carriers. This increases the risk of nosocomial transmission from patients with false-negative RAT results. Moreover, false-positive RAT results likely raise the hazard of hospital-acquired COVID-19, if the patient is cohorted with SARS-CoV-2 RT-PCR-positive patients.
These RATs limitations represent key issues for patients' safety in the hospital arguing against the use of RAT screening among asymptomatic patients admitted via the emergency department.
Transparency declaration
We have no specific conflict of interest related to the present work. However, please note that the corresponding author of this article, Prof Gilbert Greub, is co-funder of a start-up called “JeuPRO” that is distributing the games Krobs and MyKrobs, which are two games on microbes.
Funding
No dedicated external funding. This work was part of the measures taken by the hospital to prevent SARS-CoV-2 transmission between hospitalized subjects by systematically screening all patients with antigen tests and RT-PCR.
Editor: Michel Drancourt
References
- 1.WHO. Rolling updates on coronavirus disease (COVID-19) WHO.int2020 [updated July 30, 2020; cited 2020 March 11]. Speaking at the COVID-19 media briefing, the WHO Director-General said:; “WHO has been assessing this outbreak around the clock and we are deeply concerned both by the alarming levels of spread and severity, and by the alarming levels of inaction.We have therefore made the assessment that COVID-19 can be characterised as a pandemicPandemic is not a word to use lightly or carelessly. It is a word that, if misused, can cause unreasonable fear, or unjustified acceptance that the fight is over, leading to unnecessary suffering and death. Describing the situation as a pandemic does not change WHO's assessment of the threat posed by this virus. It doesn't change what WHO is doing, and it doesn't change what countries should do.We have never before seen a pandemic sparked by a coronavirus. This is the first pandemic caused by a coronavirus.And we have never before seen a pandemic that can be controlled, at the same time.”]. Available from: https://www.who.int/emergencies/diseases/novel-coronavirus-2019/events-as-they-happen.
- 2.Caruana G., Croxatto A., Coste A.T., Opota O., Lamoth F., Jaton K. Diagnostic strategies for SARS-CoV-2 infection and interpretation of microbiological results. Clin Microbiol Infect. 2020 Sep;26:1178–1182. doi: 10.1016/j.cmi.2020.06.019. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.ECDC COVID-19 situation update worldwide, as of week 2 2021. https://covid19-country-overviews.ecdc.europa.eu/ updated January 2021. Available from:
- 4.FOPH Coronavirus : Tests. https://www.bag.admin.ch/bag/en/home/krankheiten/ausbrueche-epidemien-pandemien/aktuelle-ausbrueche-epidemien/novel-cov/testen.html updated December 2020; cited 2020 2 November Available from:
- 5.Schwob J.-M., Miauton A., Petrovic D., Perdrix J., Senn N., Jaton K. Title: antigen rapid tests, nasopharyngeal PCR and saliva PCR to detect SARS-CoV-2: a prospective comparative clinical trial. medXriv. 2020 doi: 10.1371/journal.pone.0282150. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Fenollar F., Bouam A., Ballouche M., Fuster L., Prudent E., Colson P. Evaluation of the Panbio Covid-19 rapid antigen detection test device for the screening of patients with Covid-19. J Clin Microbiol. 2020 doi: 10.1128/JCM.02589-20. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Turcato G., Zaboli A., Pfeifer N., Ciccariello L., Sibilio S., Tezza G. Clinical application of a rapid antigen test for the detection of SARS-CoV-2 infection in symptomatic and asymptomatic patients evaluated in the emergency department: a preliminary report. J Infect. 2020 doi: 10.1016/j.jinf.2020.12.012. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Möckel M., Corman V.M., Stegemann M.S., Hofmann J., Stein A., Jones T.C. 2021. SARS-CoV-2 Antigen Rapid Immunoassay for Diagnosis of COVID-19 in the Emergency Department. Biomarkers : biochemical indicators of exposure, response, and susceptibility to chemicals; pp. 1–13. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Caruana G., Croxatto A., Kampouri E., Kritikos A., Opota O., Foerster M. Implementing SARS-CoV-2 Rapid antigen testing in the Emergency wArd of a Swiss university hospital: the INCREASE study. Microorganisms. 2021 Apr 10;9:798. doi: 10.3390/microorganisms9040798. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Opota O., Brouillet R., Greub G., Jaton K. Comparison of SARS-CoV-2 RT-PCR on a high-throughput molecular diagnostic platform and the cobas SARS-CoV-2 test for the diagnostic of COVID-19 on various clinical samples. Pathog Dis. 2020;78(8) doi: 10.1093/femspd/ftaa061. [DOI] [PMC free article] [PubMed] [Google Scholar]