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Outcomes of patients with acute respiratory failure on veno-venous extracorporeal membrane oxygenation requiring additional circulatory support by veno-venoarterial extracorporeal membrane oxygenation.
Erlebach, Rolf; Wild, Lennart C; Seeliger, Benjamin; Rath, Ann-Kathrin; Andermatt, Rea; Hofmaenner, Daniel A; Schewe, Jens-Christian; Ganter, Christoph C; Müller, Mattia; Putensen, Christian; Natanov, Ruslan; Kühn, Christian; Bauersachs, Johann; Welte, Tobias; Hoeper, Marius M; Wendel-Garcia, Pedro D; David, Sascha; Bode, Christian; Stahl, Klaus.
  • Erlebach R; Institute of Intensive Care Medicine, University Hospital Zurich, Zurich, Switzerland.
  • Wild LC; Department of Anaesthesiology and Intensive Care Medicine, University Hospital Bonn, Bonn, Germany.
  • Seeliger B; Department of Respiratory Medicine and German Centre of Lung Research (DZL), Hannover Medical School, Hanover, Germany.
  • Rath AK; Department of Gastroenterology, Hepatology and Endocrinology, Hannover Medical School, Hanover, Germany.
  • Andermatt R; Institute of Intensive Care Medicine, University Hospital Zurich, Zurich, Switzerland.
  • Hofmaenner DA; Institute of Intensive Care Medicine, University Hospital Zurich, Zurich, Switzerland.
  • Schewe JC; Department of Anaesthesiology and Intensive Care Medicine, University Hospital Bonn, Bonn, Germany.
  • Ganter CC; Institute of Intensive Care Medicine, University Hospital Zurich, Zurich, Switzerland.
  • Müller M; Institute of Intensive Care Medicine, University Hospital Zurich, Zurich, Switzerland.
  • Putensen C; Department of Anaesthesiology and Intensive Care Medicine, University Hospital Bonn, Bonn, Germany.
  • Natanov R; Department of Cardiothoracic, Transplant and Vascular Surgery, Hannover Medical School, Hanover, Germany.
  • Kühn C; Department of Cardiothoracic, Transplant and Vascular Surgery, Hannover Medical School, Hanover, Germany.
  • Bauersachs J; German Research Foundation (DFG), Clinical Research Group (KFO 311): "(Pre)terminal Heart and Lung Failure: Unloading and Repair", Germany.
  • Welte T; German Research Foundation (DFG), Clinical Research Group (KFO 311): "(Pre)terminal Heart and Lung Failure: Unloading and Repair", Germany.
  • Hoeper MM; Department of Cardiology and Angiology, Hannover Medical School, Hanover, Germany.
  • Wendel-Garcia PD; Department of Respiratory Medicine and German Centre of Lung Research (DZL), Hannover Medical School, Hanover, Germany.
  • David S; German Research Foundation (DFG), Clinical Research Group (KFO 311): "(Pre)terminal Heart and Lung Failure: Unloading and Repair", Germany.
  • Bode C; Department of Respiratory Medicine and German Centre of Lung Research (DZL), Hannover Medical School, Hanover, Germany.
  • Stahl K; German Research Foundation (DFG), Clinical Research Group (KFO 311): "(Pre)terminal Heart and Lung Failure: Unloading and Repair", Germany.
Front Med (Lausanne) ; 9: 1000084, 2022.
Article in English | MEDLINE | ID: covidwho-2240539
ABSTRACT

Objective:

Veno-venous (V-V) extracorporeal membrane oxygenation (ECMO) is increasingly used to support patients with severe acute respiratory distress syndrome (ARDS). In case of additional cardio-circulatory failure, some experienced centers upgrade the V-V ECMO with an additional arterial return cannula (termed V-VA ECMO). Here we analyzed short- and long-term outcome together with potential predictors of mortality.

Design:

Multicenter, retrospective analysis between January 2008 and September 2021.

Setting:

Three tertiary care ECMO centers in Germany (Hannover, Bonn) and Switzerland (Zurich). Patients Seventy-three V-V ECMO patients with ARDS and additional acute cardio-circulatory deterioration required an upgrade to V-VA ECMO were included in this study. Measurements and main

results:

Fifty-three patients required an upgrade from V-V to V-VA and 20 patients were directly triple cannulated. Median (Interquartile Range) age was 49 (28-57) years and SOFA score was 14 (12-17) at V-VA ECMO upgrade. Vasoactive-inotropic score decreased from 53 (12-123) at V-VA ECMO upgrade to 9 (3-37) after 24 h of V-VA ECMO support. Weaning from V-VA and V-V ECMO was successful in 47 (64%) and 40 (55%) patients, respectively. Duration of ECMO support was 12 (6-22) days and ICU length of stay was 32 (16-46) days. Overall ICU mortality was 48% and hospital mortality 51%. Two additional patients died after hospital discharge while the remaining patients survived up to two years (with six patients being lost to follow-up). The vast majority of patients was free from higher degree persistent organ dysfunction at follow-up. A SOFA score > 14 and higher lactate concentrations at the day of V-VA upgrade were independent predictors of mortality in the multivariate regression analysis.

Conclusion:

In this analysis, the use of V-VA ECMO in patients with ARDS and concomitant cardiocirculatory failure was associated with a hospital survival of about 50%, and most of these patients survived up to 2 years. A SOFA score > 14 and elevated lactate levels at the day of V-VA upgrade predict unfavorable outcome.
Keywords

Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Observational study / Prognostic study Language: English Journal: Front Med (Lausanne) Year: 2022 Document Type: Article Affiliation country: Fmed.2022.1000084

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Observational study / Prognostic study Language: English Journal: Front Med (Lausanne) Year: 2022 Document Type: Article Affiliation country: Fmed.2022.1000084