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COVID-19 Induced Acute Respiratory Distress Syndrome-A Multicenter Observational Study.
Herrmann, Johannes; Adam, Elisabeth Hannah; Notz, Quirin; Helmer, Philipp; Sonntagbauer, Michael; Ungemach-Papenberg, Peter; Sanns, Andreas; Zausig, York; Steinfeldt, Thorsten; Torje, Iuliu; Schmid, Benedikt; Schlesinger, Tobias; Rolfes, Caroline; Reyher, Christian; Kredel, Markus; Stumpner, Jan; Brack, Alexander; Wurmb, Thomas; Gill-Schuster, Daniel; Kranke, Peter; Weismann, Dirk; Klinker, Hartwig; Heuschmann, Peter; Rücker, Viktoria; Frantz, Stefan; Ertl, Georg; Muellenbach, Ralf Michael; Mutlak, Haitham; Meybohm, Patrick; Zacharowski, Kai; Lotz, Christopher.
  • Herrmann J; Department of Anesthesiology and Critical Care, University Hospital Würzburg, Julius-Maximilians-University Würzburg, Würzburg, Germany.
  • Adam EH; Department of Anesthesiology, Intensive Care Medicine and Pain Therapy, University Hospital Frankfurt, Goethe-University, Frankfurt, Germany.
  • Notz Q; Department of Anesthesiology and Critical Care, University Hospital Würzburg, Julius-Maximilians-University Würzburg, Würzburg, Germany.
  • Helmer P; Department of Anesthesiology, Intensive Care Medicine and Pain Therapy, University Hospital Frankfurt, Goethe-University, Frankfurt, Germany.
  • Sonntagbauer M; Department of Anesthesiology, Intensive Care Medicine and Pain Therapy, University Hospital Frankfurt, Goethe-University, Frankfurt, Germany.
  • Ungemach-Papenberg P; Department of Anesthesiology and Critical Care, Klinikum Aschaffenburg-Alzenau, Aschaffenburg, Germany.
  • Sanns A; Department of Anesthesiology and Critical Care, Klinikum Aschaffenburg-Alzenau, Aschaffenburg, Germany.
  • Zausig Y; Department of Anesthesiology and Critical Care, Klinikum Aschaffenburg-Alzenau, Aschaffenburg, Germany.
  • Steinfeldt T; Department of Anesthesiology and Critical Care, Diakoneo Diak Klinikum Schwabisch Hall, Schwabisch-Hall, Germany.
  • Torje I; Department of Critical Care, Emergency Medicine and Anesthesiology, ARDS/ECMO-Centre, Campus Kassel of the University of Southampton, Southampton, Germany.
  • Schmid B; Department of Anesthesiology and Critical Care, University Hospital Würzburg, Julius-Maximilians-University Würzburg, Würzburg, Germany.
  • Schlesinger T; Department of Anesthesiology and Critical Care, University Hospital Würzburg, Julius-Maximilians-University Würzburg, Würzburg, Germany.
  • Rolfes C; Department of Critical Care, Emergency Medicine and Anesthesiology, ARDS/ECMO-Centre, Campus Kassel of the University of Southampton, Southampton, Germany.
  • Reyher C; Department of Critical Care, Emergency Medicine and Anesthesiology, ARDS/ECMO-Centre, Campus Kassel of the University of Southampton, Southampton, Germany.
  • Kredel M; Department of Anesthesiology and Critical Care, University Hospital Würzburg, Julius-Maximilians-University Würzburg, Würzburg, Germany.
  • Stumpner J; Department of Anesthesiology and Critical Care, University Hospital Würzburg, Julius-Maximilians-University Würzburg, Würzburg, Germany.
  • Brack A; Department of Anesthesiology and Critical Care, University Hospital Würzburg, Julius-Maximilians-University Würzburg, Würzburg, Germany.
  • Wurmb T; Department of Anesthesiology and Critical Care, University Hospital Würzburg, Julius-Maximilians-University Würzburg, Würzburg, Germany.
  • Gill-Schuster D; Department of Anesthesiology and Critical Care, Sana-Klinikum Offenbach GmbH, Offenbach, Germany.
  • Kranke P; Department of Anesthesiology and Critical Care, University Hospital Würzburg, Julius-Maximilians-University Würzburg, Würzburg, Germany.
  • Weismann D; Department of Internal Medicine I, University Hospital Würzburg, Würzburg, Germany.
  • Klinker H; Department of Internal Medicine II, University Hospital Würzburg, Würzburg, Germany.
  • Heuschmann P; Institute for Clinical Epidemiology and Biometry, Julius-Maximilians-University, Würzburg, Germany.
  • Rücker V; Clinical Trial Center, University Hospital Würzburg, Julius-Maximilians-University, Würzburg, Germany.
  • Frantz S; Institute for Clinical Epidemiology and Biometry, Julius-Maximilians-University, Würzburg, Germany.
  • Ertl G; Department of Internal Medicine I, University Hospital Würzburg, Würzburg, Germany.
  • Muellenbach RM; Department of Internal Medicine I, University Hospital Würzburg, Würzburg, Germany.
  • Mutlak H; Department of Critical Care, Emergency Medicine and Anesthesiology, ARDS/ECMO-Centre, Campus Kassel of the University of Southampton, Southampton, Germany.
  • Meybohm P; Department of Anesthesiology and Critical Care, Sana-Klinikum Offenbach GmbH, Offenbach, Germany.
  • Zacharowski K; Department of Anesthesiology and Critical Care, University Hospital Würzburg, Julius-Maximilians-University Würzburg, Würzburg, Germany.
  • Lotz C; Department of Anesthesiology, Intensive Care Medicine and Pain Therapy, University Hospital Frankfurt, Goethe-University, Frankfurt, Germany.
Front Med (Lausanne) ; 7: 599533, 2020.
Article in English | MEDLINE | ID: covidwho-1005805
ABSTRACT

Background:

Proportions of patients dying from the coronavirus disease-19 (COVID-19) vary between different countries. We report the characteristics; clinical course and outcome of patients requiring intensive care due to COVID-19 induced acute respiratory distress syndrome (ARDS).

Methods:

This is a retrospective, observational multicentre study in five German secondary or tertiary care hospitals. All patients consecutively admitted to the intensive care unit (ICU) in any of the participating hospitals between March 12 and May 4, 2020 with a COVID-19 induced ARDS were included.

Results:

A total of 106 ICU patients were treated for COVID-19 induced ARDS, whereas severe ARDS was present in the majority of cases. Survival of ICU treatment was 65.0%. Median duration of ICU treatment was 11 days; median duration of mechanical ventilation was 9 days. The majority of ICU treated patients (75.5%) did not receive any antiviral or anti-inflammatory therapies. Venovenous (vv) ECMO was utilized in 16.3%. ICU triage with population-level decision making was not necessary at any time. Univariate analysis associated older age, diabetes mellitus or a higher SOFA score on admission with non-survival during ICU stay.

Conclusions:

A high level of care adhering to standard ARDS treatments lead to a good outcome in critically ill COVID-19 patients.
Keywords

Full text: Available Collection: International databases Database: MEDLINE Type of study: Observational study / Prognostic study Language: English Journal: Front Med (Lausanne) Year: 2020 Document Type: Article Affiliation country: Fmed.2020.599533

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Observational study / Prognostic study Language: English Journal: Front Med (Lausanne) Year: 2020 Document Type: Article Affiliation country: Fmed.2020.599533