Duration of invasive mechanical ventilation prior to extracorporeal membrane oxygenation is not associated with survival in acute respiratory distress syndrome caused by coronavirus disease 2019.

Acute respiratory distress syndrome COVID-19 Extracorporeal membrane oxygenation Invasive mechanical ventilation

Journal

Annals of intensive care
ISSN: 2110-5820
Titre abrégé: Ann Intensive Care
Pays: Germany
ID NLM: 101562873

Informations de publication

Date de publication:
13 Jan 2022
Historique:
received: 14 10 2021
accepted: 02 01 2022
entrez: 13 1 2022
pubmed: 14 1 2022
medline: 14 1 2022
Statut: epublish

Résumé

Duration of invasive mechanical ventilation (IMV) prior to extracorporeal membrane oxygenation (ECMO) affects outcome in acute respiratory distress syndrome (ARDS). In coronavirus disease 2019 (COVID-19) related ARDS, the role of pre-ECMO IMV duration is unclear. This single-centre, retrospective study included critically ill adults treated with ECMO due to severe COVID-19-related ARDS between 01/2020 and 05/2021. The primary objective was to determine whether duration of IMV prior to ECMO cannulation influenced ICU mortality. During the study period, 101 patients (mean age 56 [SD ± 10] years; 70 [69%] men; median RESP score 2 [IQR 1-4]) were treated with ECMO for COVID-19. Sixty patients (59%) survived to ICU discharge. Median ICU length of stay was 31 [IQR 20.7-51] days, median ECMO duration was 16.4 [IQR 8.7-27.7] days, and median time from intubation to ECMO start was 7.7 [IQR 3.6-12.5] days. Fifty-three (52%) patients had a pre-ECMO IMV duration of > 7 days. Pre-ECMO IMV duration had no effect on survival (p = 0.95). No significant difference in survival was found when patients with a pre-ECMO IMV duration of < 7 days (< 10 days) were compared to ≥ 7 days (≥ 10 days) (p = 0.59 and p = 1.0). The role of prolonged pre-ECMO IMV duration as a contraindication for ECMO in patients with COVID-19-related ARDS should be scrutinised. Evaluation for ECMO should be assessed on an individual and patient-centred basis.

Sections du résumé

BACKGROUND BACKGROUND
Duration of invasive mechanical ventilation (IMV) prior to extracorporeal membrane oxygenation (ECMO) affects outcome in acute respiratory distress syndrome (ARDS). In coronavirus disease 2019 (COVID-19) related ARDS, the role of pre-ECMO IMV duration is unclear. This single-centre, retrospective study included critically ill adults treated with ECMO due to severe COVID-19-related ARDS between 01/2020 and 05/2021. The primary objective was to determine whether duration of IMV prior to ECMO cannulation influenced ICU mortality.
RESULTS RESULTS
During the study period, 101 patients (mean age 56 [SD ± 10] years; 70 [69%] men; median RESP score 2 [IQR 1-4]) were treated with ECMO for COVID-19. Sixty patients (59%) survived to ICU discharge. Median ICU length of stay was 31 [IQR 20.7-51] days, median ECMO duration was 16.4 [IQR 8.7-27.7] days, and median time from intubation to ECMO start was 7.7 [IQR 3.6-12.5] days. Fifty-three (52%) patients had a pre-ECMO IMV duration of > 7 days. Pre-ECMO IMV duration had no effect on survival (p = 0.95). No significant difference in survival was found when patients with a pre-ECMO IMV duration of < 7 days (< 10 days) were compared to ≥ 7 days (≥ 10 days) (p = 0.59 and p = 1.0).
CONCLUSIONS CONCLUSIONS
The role of prolonged pre-ECMO IMV duration as a contraindication for ECMO in patients with COVID-19-related ARDS should be scrutinised. Evaluation for ECMO should be assessed on an individual and patient-centred basis.

Identifiants

pubmed: 35024972
doi: 10.1186/s13613-022-00980-3
pii: 10.1186/s13613-022-00980-3
pmc: PMC8755897
doi:

Types de publication

Journal Article

Langues

eng

Pagination

6

Informations de copyright

© 2022. The Author(s).

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Auteurs

Martina Hermann (M)

Department of Anaesthesia, Intensive Care Medicine and Pain Medicine, Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria.
Ludwig Boltzmann Institute for Digital Health and Patient Safety, Spitalgasse 23, BT86, 1090, Vienna, Austria.

Daniel Laxar (D)

Ludwig Boltzmann Institute for Digital Health and Patient Safety, Spitalgasse 23, BT86, 1090, Vienna, Austria.

Christoph Krall (C)

Center for Medical Statistics, Informatics and Intelligent Systems, Medical University of Vienna, Spitalgasse 23, BT88, 1090, Vienna, Austria.

Christina Hafner (C)

Department of Anaesthesia, Intensive Care Medicine and Pain Medicine, Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria.
Ludwig Boltzmann Institute for Digital Health and Patient Safety, Spitalgasse 23, BT86, 1090, Vienna, Austria.

Oliver Herzog (O)

Department of Anaesthesia, Intensive Care Medicine and Pain Medicine, Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria.

Oliver Kimberger (O)

Department of Anaesthesia, Intensive Care Medicine and Pain Medicine, Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria.
Ludwig Boltzmann Institute for Digital Health and Patient Safety, Spitalgasse 23, BT86, 1090, Vienna, Austria.

Sebastian Koenig (S)

Department of Anaesthesia, Intensive Care Medicine and Pain Medicine, Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria.

Felix Kraft (F)

Department of Anaesthesia, Intensive Care Medicine and Pain Medicine, Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria.

Mathias Maleczek (M)

Department of Anaesthesia, Intensive Care Medicine and Pain Medicine, Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria.
Ludwig Boltzmann Institute for Digital Health and Patient Safety, Spitalgasse 23, BT86, 1090, Vienna, Austria.

Klaus Markstaller (K)

Department of Anaesthesia, Intensive Care Medicine and Pain Medicine, Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria.

Oliver Robak (O)

Department of Medicine I, Medical University of Vienna, Intensive Care Unit 13i2, Waehringer Guertel 18-20, 1090, Vienna, Austria.

Bernhard Rössler (B)

Department of Anaesthesia, Intensive Care Medicine and Pain Medicine, Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria.

Eva Schaden (E)

Department of Anaesthesia, Intensive Care Medicine and Pain Medicine, Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria.
Ludwig Boltzmann Institute for Digital Health and Patient Safety, Spitalgasse 23, BT86, 1090, Vienna, Austria.

Peter Schellongowski (P)

Department of Medicine I, Medical University of Vienna, Intensive Care Unit 13i2, Waehringer Guertel 18-20, 1090, Vienna, Austria.

Mathias Schneeweiss-Gleixner (M)

Department of Medicine III, Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria.

Thomas Staudinger (T)

Department of Medicine I, Medical University of Vienna, Intensive Care Unit 13i2, Waehringer Guertel 18-20, 1090, Vienna, Austria.

Roman Ullrich (R)

Department of Anaesthesia, Intensive Care Medicine and Pain Medicine, Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria.

Marion Wiegele (M)

Department of Anaesthesia, Intensive Care Medicine and Pain Medicine, Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria.

Harald Willschke (H)

Department of Anaesthesia, Intensive Care Medicine and Pain Medicine, Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria.
Ludwig Boltzmann Institute for Digital Health and Patient Safety, Spitalgasse 23, BT86, 1090, Vienna, Austria.

Christian Zauner (C)

Department of Medicine III, Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria.

Alexander Hermann (A)

Department of Medicine I, Medical University of Vienna, Intensive Care Unit 13i2, Waehringer Guertel 18-20, 1090, Vienna, Austria. alexander.hermann@meduniwien.ac.at.

Classifications MeSH