Coronavirus disease 2019 (COVID-19) is currently threatening global health. Evidence from various countries indicates that healthcare workers (HCWs) are at increased risk for COVID-19.Reference Adams and Walls1,Reference Chirico, Nucera and Magnavita2 Many previous studies have focused on the molecular testing of symptomatic HCWs, ignoring the fact that a significant proportion of infected people might not exhibit any symptoms and that false-negative PCR results are not uncommon.Reference Mizumoto, Kagaya, Zarebski and Chowell3,Reference Woloshin, Patel and Kesselheim4 Although available serologic tests have somewhat uncertain performance characteristics, assessment of antibodies to severe acute respiratory virus-2 (SARS-CoV-2) provides a better estimate of the true prevalence and has therefore been recommended by leading healthcare experts.Reference Weinstein, Freedberg, Hyle and Paltiel5
The aims of this prospective cohort study were to assess seropositivity for SARS-CoV-2, to identify risk exposures, and to describe the spectrum of COVID-19 symptoms among hospital workers.
Methods
Participants and setting
Between March 19 and April 3, 2020, hospital workers (≥16 years) from 2 tertiary-care hospitals (Cantonal Hospital St Gallen and the Children’s Hospital of Eastern Switzerland) were invited to participate. COVID-19 cases in this region peaked between March 23 and March 30 (53 cases per 100,000 population per week). Hospital admissions were highest in the second week of April.
Serology testing
Participants’ sera were analyzed for SARS-CoV-2 antibodies using 3 different tests: a lateral flow immunochromatographic assay (LFIA, Sugentech, Yuseong-gu, Daejeon, Republic of Korea), a chemiluminescence microparticle immunoassay (CMIA, Abbott Diagnostics, Lake Bluff, IL), and an electro-chemiluminescence immunoassay (ECLIA, Roche Diagnostics, Basel, Switzerland). Participants with a positive signal in any test provided a second sample 4 weeks later (all tests performed again). True seropositivity was assumed in cases of positive IgG in LFIA and either CMIA or ECLIA (at the same time). This procedure corresponds to an orthogonal testing algorithm in which an independent second test confirms the positive result of the first test (https://www.cdc.gov/coronavirus/2019-ncov/lab/resources/antibody-tests-guidelines.html). Samples with positive IgG in LFIA only were additionally tested with a chemiluminescence immunoassay (CLIA) directed at the spike proteins S1/S2 (DiaSorin, Italy). PCR was not routinely performed.
Online questionnaire
Participants filled in a web-based questionnaire asking about respiratory and general symptoms and COVID-19 exposures (3 weeks prior to baseline testing). The intensity of patient contact was stratified as follows: HCWs caring for confirmed COVID-19 patients; HCWs exposed to patients without known COVID-19; and others.
Statistical analysis
Participants with positive or negative serology were compared. The Fisher exact test was used for dichotomous variables; the Mann-Whitney U test was used for continuous variables. The positive predictive value (PPV) was calculated for LFIA using the true positives as numerator and all positive test results as denominator (baseline and follow-up results were pooled). Analyses were performed with R version 3.6.3 software (R Foundation for Statistical Computing, Vienna, Austria). The Ethical Commission of Eastern Switzerland approved the study (no. 2020-00502).
Results
We included 1,012 hospital workers with a median age of 38.3 years (range, 16.9–64.8); 761 (75%) were women. Most were nurses (n = 398, 39%) or physicians (n = 268, 27%) (Table 1).
Baseline Characteristics of Study Participants
Note. HCW, healthcare worker.
a Wilcoxon rank sum test or the Fisher exact test.
b One participant answer not available.
At the baseline, 58 of 1,012 participants (5.7%) showed a positive signal in at least 1 test. In the LFIA, 13 participants had IgG (8 confirmed by ECLIA/CMIA) and 45 had IgM only. At follow-up, 2 participants showed a positive LFIA (IgG) and ECLIA/CMIA result in addition to the 8 samples confirmed at baseline, resulting in 10 of 1,012 true seropositives (1.0%) and 48 of 1,012 false seropositives (4.7%) (Fig. 1). Also, 5 participants had isolated LFIA IgG at baseline and follow-up and remained negative with anti-S1/S2 CLIA (DiaSorin). Overall, the PPV of the LFIA was 64% (18 true positive of 28 positive results) for IgG and 13% (12 true positive of 96 positive results) for IgM. ECLIA and CMIA results were consistent except for 1 participant (ECLIA negative and CMIA positive).
Results from baseline serology testing (n = 1,012) and from 4-week follow-up (n = 58). Cases with discrepant results between baseline and follow-up are highlighted with arrows.
Seropositive participants more frequently reported fever or feverishness and limb or muscle pain than seronegative participants. Respiratory symptoms were reported by 73% of seropositive and 54% of seronegative participants (P = .36). Similar differences were detected between participants with true-positive and false-positive serology results (Supplementary Figs. S1 and S2). Of the 10 seropositive patients, 2 (20%) denied any symptoms.
All positive participants worked in adult care (P = .77); 2 of 20 (10%) reported unprotected contact with confirmed COVID-19 cases outside work and household versus 30 of 972 (3%) among seronegative workers (P = .04). The intensity of patient contact was not associated with seropositivity (P = .20), although all seropositive participants reported some form of patient contact. Among those with patient contact, HCWs who wear masks were less likely to test positive (2 of 370, 0.5%) than those who did not wear masks (8 of 642, 1.2%) (P = .009) (Table 1).
Discussion
In this prospective hospital worker cohort, 1% had SARS-CoV-2 antibodies detected at baseline. The high proportion of false-positive LFIA results (particularly IgM) underscores the low PPV of these tests when prevalence is low. Fever or feverishness and muscle or limb pain were most useful in discriminating patients with positive and negative serologies. The strengths of the study are the use of 3 different tests and our analysis of a followup sample in case of a positive signal at baseline.
Given the COVID-19 peak in the region around collection of baseline samples, and considering a latency between infection and IgG detection of 2–3 weeks, these data represent an early phase of the local epidemic. This explains the low positivity rate and the low PPV of 64% (IgG) and 13% (IgM) for the LFIA. Data suggest cross reactions between endemic coronaviruses and SARSCoV-2, particularly for assays targeting the nucleocapsid protein.Reference Sethuraman, Jeremiah and Ryo6 However, despite being directed against nucleocapsid, the CMIA and ECLIA used in this study have previously demonstrated excellent specificity (>99%) and acceptable sensitivities (93.9 and 87.7%, respectively).Reference Mahase7 The concordant results between CMIA and ECLIA, as well as between CMIA/ECLIA and CLIA (directed at S1/S2 proteins), further strengthen our confidence in the specificity of the tests. Regarding sensitivity, recent evidence shows that a humoral immune response is mounted less frequently in patients with mild COVID-19.Reference Cervia, Nilsson and Zurbuchen8 Indeed, the reported sensitivities of the CMIA and ECLIA are 93.9 and 87%, which might have underestimated our seroprevalence.Reference Mahase7 Notably, LFIA screening identified 2 patients by positive IgM but negative CMIA and ECLIA at baseline, who eventually had IgG seroconversion in all tests. This finding is in line with data from the Infectious Diseases Society of America (IDSA) guideline on SARS-CoV serology testing showing a lower sensitivity of CMIA IgG compared to LFIA IgM early after infection.Reference Hanson, Caliendo and Arias9
Although limited by the small case number, constitutional symptoms were more useful than respiratory symptoms in discriminating between seropositive and seronegative participants. Although COVID-19 may be a mild illness, it appears that illness caused by other respiratory viruses were more likely to cause isolated respiratory symptoms without constitutional symptoms than COVID-19. Furthermore, 20% of SARS-CoV-2–positive patients denied any symptoms, which is in line with current estimates.Reference Mizumoto, Kagaya, Zarebski and Chowell3
Serologically positive participants more likely reported exposure to COVID-19 cases outside work, whereas the intensity of patient contact did not differ compared to seronegative participants. Despite being compatible with data showing no increased seroprevalence of HCWs working in high-risk settings,Reference Steensels, Oris and Coninx10 these results should be interpreted with caution. Because of the early time point of baseline collection in relation to the local epidemic, providers might have had too little exposure to hospitalized COVID-19 patients to detect an exposure effect. The apparent protective effect of masks may reflect a reduction in undetected, unprotected exposure to other HCW or patients, or be an epi-phenomenon associated with adherence to other preventive practices.
In conclusion, seroprevalence was 1% at baseline in this prospective HCW cohort from Switzerland. Using 3 different tests, we challenge the usefulness of serology tests with limited specificity when prevalence is low. A prospective analysis of cohort data will allow us to better study the spectrum of symptoms and risk exposures associated with COVID-19.
Supplementary material
To view supplementary material for this article, please visit https://doi.org/10.1017/ice.2020.1244
Acknowledgments
Financial support
The study was funded by the Swiss National Sciences Foundation and the Federal Office of Public Health. PK is financially supported by an Ambizione grant of the Swiss National Sciences Foundation.
Conflicts of interest
All authors report no conflicts of interest relevant to this article.
Open access
