Abstract
Background: The aims of this study are to determine (i) SARS‑CoV‑2 antibody positive employees in Austrian trauma
hospitals and rehabilitation facilities, (ii) number of active virus carriers (symptomatic and asymptomatic) during the
study, (iii) antibody decline in seropositive subjects over a period of around 6 months, (iv) the usefulness of rapid
antibody tests for outpatient screening.
Method: A total of 3301 employees in 11 Austrian trauma hospitals and rehabilitation facilities of the Austrian Social
Insurance for Occupational Risks (AUVA) participated in this open uncontrolled prospective cohort study.
Rapid lateral flow tests, detecting a combination of IgM and IgM against SARS‑CoV‑2), two different types of CLIA
(Diasorin, Roche), RT‑PCR tests and serum neutralization tests (SNTs) were performed. The tests were conducted twice,
with an interval of 42.4±7.7 (Min=30, Max=64) days. Positive participants were re‑tested with CLIA/SNT at a third
time point after 188.0±12.8 days.
Results: Only 27 out of 3301 participants (0.82%) had a positive antibody test at any time point during the study con‑
firmed via neutralization test. Among positively tested participants in either test, 50.4% did not report any symptoms
consistent with common manifestations of COVID‑19 during the study period or within the preceding 6 weeks. In
the group who tested positive during or prior to study inclusion the most common symptoms of an acute viral illness
were rhinitis (21.9%), and loss of taste and olfactory sense (21.9%).
Based on the neutralization test as the true condition, the rapid antibody test performed better on serum than whole
blood as 84.6% instead of 65.4% could be detected correctly. Concerning both CLIA tests overall the Roche test
detected 24 (sensitivity=88.9%) and the Diasorin test 22 positive participants (sensitivity=81.5%).
In participants with a positive SNT result, a significant drop in neutralizing antibody titre from 31.8±22.9 (Md=32.0)
at T1 to 26.1±17.6 (Md=21.3) at T2 to 21.4±13.4 (Md=16.0) at T3 (χ2=23.848, df=2, p < 0.001) was observed
(χ2=23.848, df=2, p < 0.001)—with an average time of 42.4±7.7 days between T1 and T2 and 146.9±13.8 days
between T2 and T3.
Original language | English |
---|---|
Pages (from-to) | 1-14 |
Number of pages | 14 |
Journal | BMC Infectious Diseases |
Volume | 21 |
Issue number | 1:915 |
DOIs | |
Publication status | Published - Sept 2021 |
Keywords
- Severe acute respiratory syndrome coronavirus
- SARS‑CoV‑2
- COVID‑19 diagnostic testing