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The use of double lumen cannula for veno-venous ECMO in trauma patients with ARDS

BACKGROUND: The use of a double lumen cannula for veno-venous extracorporeal membrane oxygenation (v.v. ECMO) offers several advantages such as cannulation with only one cannula, patient comfort and the earlier mobilization and physiotherapy. The cannulation should be performed under visual wire and...

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Autores principales: Gothner, Martin, Buchwald, Dirk, Strauch, Justus T, Schildhauer, Thomas A, Swol, Justyna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4377214/
https://www.ncbi.nlm.nih.gov/pubmed/25886755
http://dx.doi.org/10.1186/s13049-015-0106-2
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author Gothner, Martin
Buchwald, Dirk
Strauch, Justus T
Schildhauer, Thomas A
Swol, Justyna
author_facet Gothner, Martin
Buchwald, Dirk
Strauch, Justus T
Schildhauer, Thomas A
Swol, Justyna
author_sort Gothner, Martin
collection PubMed
description BACKGROUND: The use of a double lumen cannula for veno-venous extracorporeal membrane oxygenation (v.v. ECMO) offers several advantages such as cannulation with only one cannula, patient comfort and the earlier mobilization and physiotherapy. The cannulation should be performed under visual wire and cannula placement into the right atrium, which is associated with risks of malposition and right ventricular perforation. The aim of this patient series is to describe the use of double lumen cannula in trauma patients with posttraumatic ARDS. MATERIAL AND METHODS: Criteria for the v.v ECMO treatment were defined as hypoxaemia (pO2/FiO2 < 200 mmHg, FiO2 0.8-1,0); tidal volume >4-6 ml/kg ideal body weight; mean inspiratory pressure (Pinsp) >32-34 mmHg; respiratory acidosis pH <7.25; and arterial saturation (SaO2) <90%. The analysis included the Injury Severity Score (ISS), the types of injury, time of treatment, complications and outcomes. RESULTS: A total of 24 patients with major trauma were treated for posttraumatic ARDS with v.v. ECMO. The double lumen cannula (Avalon®, Fa. Maquet, Rastatt, Germany) was used in six male patients. The mean ISS was 31 (20–48). The ECMO therapy was started in an average on the third day after trauma. The mean ECMO run time was 7 days ± 5 (6–18), and the hospital stay was in mean of 60 days ± 34 (21–105). CONCLUSION: The use of double lumen cannula for v.v ECMO therapy in trauma patients is a feasible treatment option. No higher risk of bleeding could be found in this case series. A PTT-controlled heparinization is recommended using double lumen cannula. Therefore the use of this cannula type in trauma patients with high risk of bleeding is to discuss controversially.
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spelling pubmed-43772142015-03-30 The use of double lumen cannula for veno-venous ECMO in trauma patients with ARDS Gothner, Martin Buchwald, Dirk Strauch, Justus T Schildhauer, Thomas A Swol, Justyna Scand J Trauma Resusc Emerg Med Original Research BACKGROUND: The use of a double lumen cannula for veno-venous extracorporeal membrane oxygenation (v.v. ECMO) offers several advantages such as cannulation with only one cannula, patient comfort and the earlier mobilization and physiotherapy. The cannulation should be performed under visual wire and cannula placement into the right atrium, which is associated with risks of malposition and right ventricular perforation. The aim of this patient series is to describe the use of double lumen cannula in trauma patients with posttraumatic ARDS. MATERIAL AND METHODS: Criteria for the v.v ECMO treatment were defined as hypoxaemia (pO2/FiO2 < 200 mmHg, FiO2 0.8-1,0); tidal volume >4-6 ml/kg ideal body weight; mean inspiratory pressure (Pinsp) >32-34 mmHg; respiratory acidosis pH <7.25; and arterial saturation (SaO2) <90%. The analysis included the Injury Severity Score (ISS), the types of injury, time of treatment, complications and outcomes. RESULTS: A total of 24 patients with major trauma were treated for posttraumatic ARDS with v.v. ECMO. The double lumen cannula (Avalon®, Fa. Maquet, Rastatt, Germany) was used in six male patients. The mean ISS was 31 (20–48). The ECMO therapy was started in an average on the third day after trauma. The mean ECMO run time was 7 days ± 5 (6–18), and the hospital stay was in mean of 60 days ± 34 (21–105). CONCLUSION: The use of double lumen cannula for v.v ECMO therapy in trauma patients is a feasible treatment option. No higher risk of bleeding could be found in this case series. A PTT-controlled heparinization is recommended using double lumen cannula. Therefore the use of this cannula type in trauma patients with high risk of bleeding is to discuss controversially. BioMed Central 2015-03-28 /pmc/articles/PMC4377214/ /pubmed/25886755 http://dx.doi.org/10.1186/s13049-015-0106-2 Text en © Gothner et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Original Research
Gothner, Martin
Buchwald, Dirk
Strauch, Justus T
Schildhauer, Thomas A
Swol, Justyna
The use of double lumen cannula for veno-venous ECMO in trauma patients with ARDS
title The use of double lumen cannula for veno-venous ECMO in trauma patients with ARDS
title_full The use of double lumen cannula for veno-venous ECMO in trauma patients with ARDS
title_fullStr The use of double lumen cannula for veno-venous ECMO in trauma patients with ARDS
title_full_unstemmed The use of double lumen cannula for veno-venous ECMO in trauma patients with ARDS
title_short The use of double lumen cannula for veno-venous ECMO in trauma patients with ARDS
title_sort use of double lumen cannula for veno-venous ecmo in trauma patients with ards
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4377214/
https://www.ncbi.nlm.nih.gov/pubmed/25886755
http://dx.doi.org/10.1186/s13049-015-0106-2
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