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Intravenous immunoglobulin fails to improve ARDS in patients undergoing ECMO therapy
BACKGROUND: Acute respiratory distress syndrome (ARDS) is associated with high mortality rates. ARDS patients suffer from severe hypoxemia, and extracorporeal membrane oxygenation (ECMO) therapy may be necessary to ensure oxygenation. ARDS has various etiologies, including trauma, ischemia-reperfusi...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5827994/ https://www.ncbi.nlm.nih.gov/pubmed/29497534 http://dx.doi.org/10.1186/s40560-018-0278-8 |
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author | Prohaska, Stefanie Schirner, Andrea Bashota, Albina Körner, Andreas Blumenstock, Gunnar Haeberle, Helene A. |
author_facet | Prohaska, Stefanie Schirner, Andrea Bashota, Albina Körner, Andreas Blumenstock, Gunnar Haeberle, Helene A. |
author_sort | Prohaska, Stefanie |
collection | PubMed |
description | BACKGROUND: Acute respiratory distress syndrome (ARDS) is associated with high mortality rates. ARDS patients suffer from severe hypoxemia, and extracorporeal membrane oxygenation (ECMO) therapy may be necessary to ensure oxygenation. ARDS has various etiologies, including trauma, ischemia-reperfusion injury or infections of various origins, and the associated immunological responses may vary. To support the immunological response in this patient collective, we used intravenous IgM immunoglobulin therapy to enhance the likelihood of pulmonary recovery. METHODS: ARDS patients admitted to the intensive care unit (ICU) who were placed on ECMO and treated with (IVIG group; n = 29) or without (control group; n = 28) intravenous IgM-enriched immunoglobulins for 3 days in the initial stages of ARDS were analyzed retrospectively. RESULTS: The baseline characteristics did not differ between the groups, although the IVIG group showed a significantly reduced oxygenation index compared to the control group. We found no differences in the length of ICU stay or ventilation parameters. We did not find a significant difference between the groups for the extent of inflammation or for overall survival. CONCLUSION: We conclude that administration of IgM-enriched immunoglobulins as an additional therapy did not have a beneficial effect in patients with severe ARDS requiring ECMO support. TRIAL REGISTRATION: Clinical Trials: NCT02961166; retrospectively registered. |
format | Online Article Text |
id | pubmed-5827994 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-58279942018-03-01 Intravenous immunoglobulin fails to improve ARDS in patients undergoing ECMO therapy Prohaska, Stefanie Schirner, Andrea Bashota, Albina Körner, Andreas Blumenstock, Gunnar Haeberle, Helene A. J Intensive Care Research BACKGROUND: Acute respiratory distress syndrome (ARDS) is associated with high mortality rates. ARDS patients suffer from severe hypoxemia, and extracorporeal membrane oxygenation (ECMO) therapy may be necessary to ensure oxygenation. ARDS has various etiologies, including trauma, ischemia-reperfusion injury or infections of various origins, and the associated immunological responses may vary. To support the immunological response in this patient collective, we used intravenous IgM immunoglobulin therapy to enhance the likelihood of pulmonary recovery. METHODS: ARDS patients admitted to the intensive care unit (ICU) who were placed on ECMO and treated with (IVIG group; n = 29) or without (control group; n = 28) intravenous IgM-enriched immunoglobulins for 3 days in the initial stages of ARDS were analyzed retrospectively. RESULTS: The baseline characteristics did not differ between the groups, although the IVIG group showed a significantly reduced oxygenation index compared to the control group. We found no differences in the length of ICU stay or ventilation parameters. We did not find a significant difference between the groups for the extent of inflammation or for overall survival. CONCLUSION: We conclude that administration of IgM-enriched immunoglobulins as an additional therapy did not have a beneficial effect in patients with severe ARDS requiring ECMO support. TRIAL REGISTRATION: Clinical Trials: NCT02961166; retrospectively registered. BioMed Central 2018-02-26 /pmc/articles/PMC5827994/ /pubmed/29497534 http://dx.doi.org/10.1186/s40560-018-0278-8 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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 | Research Prohaska, Stefanie Schirner, Andrea Bashota, Albina Körner, Andreas Blumenstock, Gunnar Haeberle, Helene A. Intravenous immunoglobulin fails to improve ARDS in patients undergoing ECMO therapy |
title | Intravenous immunoglobulin fails to improve ARDS in patients undergoing ECMO therapy |
title_full | Intravenous immunoglobulin fails to improve ARDS in patients undergoing ECMO therapy |
title_fullStr | Intravenous immunoglobulin fails to improve ARDS in patients undergoing ECMO therapy |
title_full_unstemmed | Intravenous immunoglobulin fails to improve ARDS in patients undergoing ECMO therapy |
title_short | Intravenous immunoglobulin fails to improve ARDS in patients undergoing ECMO therapy |
title_sort | intravenous immunoglobulin fails to improve ards in patients undergoing ecmo therapy |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5827994/ https://www.ncbi.nlm.nih.gov/pubmed/29497534 http://dx.doi.org/10.1186/s40560-018-0278-8 |
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