Evidence map›Paper›PMID 34488680›Full record

ArticleBMC infectious diseases2021

Antibody seroprevalence and rate of asymptomatic infections with SARS-CoV-2 in Austrian hospital personnel.

Iris Leister, Elisabeth Ponocny-Seliger, Herwig Kollaritsch, Peter Dungel, Barbara Holzer, Johannes Grillari, Heinz Redl, Ivo Ponocny, Claudia Wilfing, Ludwig Aigner and 6 more

Open access · goldAbstract read
In one paragraph

Article in BMC infectious diseases, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 35% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. SARS-CoV-2 herd immunity of the Kyrgyz population in 2021.Medical microbiology and immunology · 2022
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors at 7 institutions in 2 countries.

Iris Leister *ParaMove, SCI Research Unit, BG Trauma Center Murnau, Murnau, Germany, and Paracelsus Medical University, Salzburg, Austria.
Elisabeth Ponocny-Seliger *Institute for Quantitative Methods, Sigmund Freud Private University, Vienna, Austria.
Herwig KollaritschInstitute of Specific Prophylaxis and Tropical Medicine, Medical University of Vienna, Vienna, Austria. dr.herwig.kollaritsch@gmail.com.ORCID http://orcid.org/0000-0001-6393-516X
Peter DungelLudwig-Boltzmann Institute for Experimental and Clinical Traumatology, Vienna, Austria.
Barbara HolzerAustrian Agency for Health and Food Safety, Mödling, Austria.
Johannes GrillariLudwig-Boltzmann Institute for Experimental and Clinical Traumatology, Vienna, Austria.
Heinz RedlLudwig-Boltzmann Institute for Experimental and Clinical Traumatology, Vienna, Austria.
Ivo PonocnyDepartment for Applied Statistics and Economics, Modul University Vienna, Vienna, Austria.
Claudia WilfingLudwig-Boltzmann Institute for Experimental and Clinical Traumatology, Vienna, Austria.
Ludwig AignerParaMove, SCI Research Unit, BG Trauma Center Murnau, Murnau, Germany, and Paracelsus Medical University, Salzburg, Austria.
Markus ExnerLabors.at GmbH, Vienna, Austria.
Michaela StainerLudwig-Boltzmann Institute for Experimental and Clinical Traumatology, Vienna, Austria.
Matthias HacklAustrian Cluster for Tissue Regeneration, Vienna, Austria.
Thomas HausnerLudwig-Boltzmann Institute for Experimental and Clinical Traumatology, Vienna, Austria.
Rainer MittermayrLudwig-Boltzmann Institute for Experimental and Clinical Traumatology, Vienna, Austria.
Wolfgang SchadenLudwig-Boltzmann Institute for Experimental and Clinical Traumatology, Vienna, Austria.
Ludwig Boltzmann Institute for Traumatology, The Research Center in Cooperation with AUVA · ATParacelsus Medical University · ATAustrian Agency for Health and Food Safety · ATAustrian Cluster for Tissue Regeneration · ATMedical University of Vienna · ATMODUL University Vienna · ATSigmund Freud Privatuniversität Wien · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe 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.

methodA 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.

resultsOnly 27 out of 3301 participants (0.82%) had a positive antibody test at any time point during the study confirmed 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 (χ

conclusionsDuring the study period (May 11th-August 3rd) only 0.82% were tested positive for antibodies in our study cohort. The antibody concentration decreases significantly over time with 14.8% (4 out of 27) losing detectable antibodies.

Indexed as

COVID-19SARS-CoV-2Antibodies, ViralAsymptomatic InfectionsAustriaHumansPersonnel, HospitalProspective StudiesSeroepidemiologic StudiesAntibodies, ViralCOVID-19 diagnostic testingSARS-CoV-2Severe acute respiratory syndrome coronavirus 2

Identifiers

PMID34488680
PMCPMC8419821
OpenAlexW3126997522

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.