Abstract

Purpose: Reported antibiotic use in coronavirus disease 2019 (COVID-19) is far higher than the actual rate of reported bacterial co- and superinfection. A better understanding of antibiotic therapy in COVID-19 is necessary. Methods: 6457 SARS-CoV-2-infected cases, documented from March 18, 2020, until February 16, 2021, in the LEOSS cohort were analyzed. As primary endpoint, the correlation between any antibiotic treatment and all-cause mortality/progression to the next more advanced phase of disease was calculated for adult patients in the complicated phase of disease and procalcitonin (PCT) ≤ 0.5 ng/ml. The analysis took the confounders gender, age, and comorbidities into account. Results: Three thousand, six hundred twenty-seven cases matched all inclusion criteria for analyses. For the primary endpoint, antibiotic treatment was not correlated with lower all-cause mortality or progression to the next more advanced (critical) phase (n = 996) (both p > 0.05). For the secondary endpoints, patients in the uncomplicated phase (n = 1195), regardless of PCT level, had no lower all-cause mortality and did not progress less to the next more advanced (complicated) phase when treated with antibiotics (p > 0.05). Patients in the complicated phase with PCT > 0.5 ng/ml and antibiotic treatment (n = 286) had a significantly increased all-cause mortality (p = 0.029) but no significantly different probability of progression to the critical phase (p > 0.05). Conclusion: In this cohort, antibiotics in SARS-CoV-2-infected patients were not associated with positive effects on all-cause mortality or disease progression. Additional studies are needed. Advice of local antibiotic stewardship- (ABS-) teams and local educational campaigns should be sought to improve rational antibiotic use in COVID-19 patients.

Original languageEnglish
JournalInfection
Volume50
Issue number2
Pages (from-to)423-436
Number of pages14
ISSN0300-8126
DOIs
Publication statusPublished - 04.2022

Funding

The LEOSS registry was supported by the German Centre for Infection Research (DZIF) and the Willy Robert Pitzer Foundation. We express our gratitude to all study teams that supported the LEOSS study. The following study teams contributed at least five per thousand to the analyses of this study: Klinikum Passau (Martina Haselberger), Technische Universität München (Christoph D. Spinner), Universitätsklinikum Jena (Maria Madeleine Ruethrich), Universitätsklinikum Düsseldorf (Bjoern-Erik Jensen), Klinikum Dortmund gGmbH (Martin Hower), Universitätsklinikum Schleswig-Holstein—Lübeck (Jan Rupp), Universitätsklinikum Augsburg (Christoph Roemmele), Universitätsklinikum Frankfurt (Maria Vehreschild), Städtisches Klinikum Karlsruhe (Christian Degenhardt), Klinikum Ingolstadt (Stefan Borgmann), Universitätsklinikum Regensburg (Frank Hanses), Katholisches Klinikum Bochum (St. Josef-Hospital) Ruhr-Universität Bochum (Kerstin Hellwig), Kliniken Maria Hilf GmbH Mönchengladbach (Jürgen vom Dahl), Universitätsklinikum Essen (Sebastian Dolff), Klinikum Bremen-Mitte (Christiane Piepel), Klinikum Braunschweig (Jan Kielstein), Universitätsklinikum Tübingen (Siri Göpel), Evangelisches Stadtkrankenhaus Saarbrücken (Marc Neufang), Malteser Krankenhaus St. Franziskus Hospital Flensburg (Milena Milovanovic), Johannes Wesling Klinikum Minden, Ruhr-Universität Bochum (Kai Wille), Robert-Bosch-Krankenhaus Stuttgart (Katja Rothfuss), Klinikum Leverkusen (Lukas Eberwein), Kreuznacher Diakonie Hunsrück (Wolfgang Rimili), Marien Hospital Herne, Ruhr-Universität Bochum (Timm Westhoff), Oberlausitz Kliniken (Maximilian Worm), Medizinische Hochschule Hannover (Gernot Beutel), Universitätsklinikum Köln (Norma Jung), Elblandklinikum Riesa (Joerg Schubert), Klinikum Fulda (Philipp Markart), Sophien- und Hufeland Klinikum Weimar (Jessica Rueddel), Elisabeth-Krankenhaus Essen (Ingo Voigt), Universitätsklinikum des Saarlandes (Homburg) (Robert Bals), Tropenklinik Paul-Lechler Krankenhaus Tübingen (Claudia Raichle) The infrastructure group of the LEOSS study: Jörg Janne Vehreschild (Goethe-Universität Frankfurt), Carolin E. M. Jakob (Universitätsklinikum Köln), Lisa Pilgram (Goethe-Universität Frankfurt), Melanie Stecher (Universitätsklinikum Köln), Maximilian Schons (Universitätsklinikum Köln), Susana Nunes de Miranda (Universitätsklinikum Köln), Nick Schulze (Universitätsklinikum Köln), Sandra Fuhrmann (Universitätsklinikum Köln), Clara Brünn (Universitätsklinikum Köln), Annika Claßen (Universitätsklinikum Köln), Bernd Franke (Universitätsklinikum Köln), Fabian Praßer (Charité, Universitätsmedizin Berlin) und Martin Lablans (Universitätsklinikum Mannheim). The LEOSS registry was supported by the German Centre for Infection Research (DZIF) and the Willy Robert Pitzer Foundation. Open Access funding enabled and organized by Projekt DEAL. This analysis received no financial support. LEOSS was financially supported by the Willy Robert Pitzer Foundation and the German Centre for Infection Research (DZIF).

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Research Areas and Centers

  • Academic Focus: Center for Infection and Inflammation Research (ZIEL)

DFG Research Classification Scheme

  • 2.21-03 Medical Microbiology and Mycology, Hygiene, Molecular Infection Biology
  • 2.22-31 Clinical Infectiology and Tropical Medicine

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