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Blood transfusion during cardiac surgery is associated with inflammation and coagulation in the lung: a case control study
INTRODUCTION: Blood transfusion is associated with increased morbidity and mortality in cardiac surgery patients, but cause-and-effect relations remain unknown. We hypothesized that blood transfusion is associated with changes in pulmonary and systemic inflammation and coagulation occurring in patie...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3221992/ https://www.ncbi.nlm.nih.gov/pubmed/21314930 http://dx.doi.org/10.1186/cc10032 |
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author | Tuinman, Pieter R Vlaar, Alexander P Cornet, Alexander D Hofstra, Jorrit J Levi, Marcel Meijers, Joost CM Beishuizen, Albertus Schultz, Marcus J Groeneveld, AB Johan Juffermans, Nicole P |
author_facet | Tuinman, Pieter R Vlaar, Alexander P Cornet, Alexander D Hofstra, Jorrit J Levi, Marcel Meijers, Joost CM Beishuizen, Albertus Schultz, Marcus J Groeneveld, AB Johan Juffermans, Nicole P |
author_sort | Tuinman, Pieter R |
collection | PubMed |
description | INTRODUCTION: Blood transfusion is associated with increased morbidity and mortality in cardiac surgery patients, but cause-and-effect relations remain unknown. We hypothesized that blood transfusion is associated with changes in pulmonary and systemic inflammation and coagulation occurring in patients who do not meet the clinical diagnosis of transfusion-related acute lung injury (TRALI). METHODS: We performed a case control study in a mixed medical-surgical intensive care unit of a university hospital in the Netherlands. Cardiac surgery patients (n = 45) were grouped as follows: those who received no transfusion, those who received a restrictive transfusion (one two units of blood) or those who received multiple transfusions (at least five units of blood). Nondirected bronchoalveolar lavage fluid (BALF) and blood were obtained within 3 hours postoperatively. Normal distributed data were analyzed using analysis of variance and Dunnett's post hoc test. Nonparametric data were analyzed using the Kruskal-Wallis and Mann-Whitney U tests. RESULTS: Restrictive transfusion increased BALF levels of interleukin (IL)-1β and D-dimer compared to nontransfused controls (P < 0.05 for all), and IL-1β levels were further enhanced by multiple transfusions (P < 0.01). BALF levels of IL-8, tumor necrosis factor α (TNFα) and thrombin-antithrombin complex (TATc) were increased after multiple transfusions (P < 0.01, P < 0.001 and P < 0.01, respectively) compared to nontransfused controls, but not after restrictive transfusions. Restrictive transfusions were associated with increased pulmonary levels of plasminogen activator inhibitor 1 compared to nontransfused controls with a further increase after multiple transfusions (P < 0.001). Concomitantly, levels of plasminogen activator activity (PAA%) were lower (P < 0.001), indicating impaired fibrinolysis. In the systemic compartment, transfusion was associated with a significant increase in levels of TNFα, TATc and PAA% (P < 0.05). CONCLUSIONS: Transfusion during cardiac surgery is associated with activation of inflammation and coagulation in the pulmonary compartment of patients who do not meet TRALI criteria, an effect that was partly dose-dependent, suggesting transfusion as a mediator of acute lung injury. These pulmonary changes were accompanied by systemic derangement of coagulation. |
format | Online Article Text |
id | pubmed-3221992 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-32219922011-11-22 Blood transfusion during cardiac surgery is associated with inflammation and coagulation in the lung: a case control study Tuinman, Pieter R Vlaar, Alexander P Cornet, Alexander D Hofstra, Jorrit J Levi, Marcel Meijers, Joost CM Beishuizen, Albertus Schultz, Marcus J Groeneveld, AB Johan Juffermans, Nicole P Crit Care Research INTRODUCTION: Blood transfusion is associated with increased morbidity and mortality in cardiac surgery patients, but cause-and-effect relations remain unknown. We hypothesized that blood transfusion is associated with changes in pulmonary and systemic inflammation and coagulation occurring in patients who do not meet the clinical diagnosis of transfusion-related acute lung injury (TRALI). METHODS: We performed a case control study in a mixed medical-surgical intensive care unit of a university hospital in the Netherlands. Cardiac surgery patients (n = 45) were grouped as follows: those who received no transfusion, those who received a restrictive transfusion (one two units of blood) or those who received multiple transfusions (at least five units of blood). Nondirected bronchoalveolar lavage fluid (BALF) and blood were obtained within 3 hours postoperatively. Normal distributed data were analyzed using analysis of variance and Dunnett's post hoc test. Nonparametric data were analyzed using the Kruskal-Wallis and Mann-Whitney U tests. RESULTS: Restrictive transfusion increased BALF levels of interleukin (IL)-1β and D-dimer compared to nontransfused controls (P < 0.05 for all), and IL-1β levels were further enhanced by multiple transfusions (P < 0.01). BALF levels of IL-8, tumor necrosis factor α (TNFα) and thrombin-antithrombin complex (TATc) were increased after multiple transfusions (P < 0.01, P < 0.001 and P < 0.01, respectively) compared to nontransfused controls, but not after restrictive transfusions. Restrictive transfusions were associated with increased pulmonary levels of plasminogen activator inhibitor 1 compared to nontransfused controls with a further increase after multiple transfusions (P < 0.001). Concomitantly, levels of plasminogen activator activity (PAA%) were lower (P < 0.001), indicating impaired fibrinolysis. In the systemic compartment, transfusion was associated with a significant increase in levels of TNFα, TATc and PAA% (P < 0.05). CONCLUSIONS: Transfusion during cardiac surgery is associated with activation of inflammation and coagulation in the pulmonary compartment of patients who do not meet TRALI criteria, an effect that was partly dose-dependent, suggesting transfusion as a mediator of acute lung injury. These pulmonary changes were accompanied by systemic derangement of coagulation. BioMed Central 2011 2011-02-11 /pmc/articles/PMC3221992/ /pubmed/21314930 http://dx.doi.org/10.1186/cc10032 Text en Copyright ©2011 Tuinman et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Tuinman, Pieter R Vlaar, Alexander P Cornet, Alexander D Hofstra, Jorrit J Levi, Marcel Meijers, Joost CM Beishuizen, Albertus Schultz, Marcus J Groeneveld, AB Johan Juffermans, Nicole P Blood transfusion during cardiac surgery is associated with inflammation and coagulation in the lung: a case control study |
title | Blood transfusion during cardiac surgery is associated with inflammation and coagulation in the lung: a case control study |
title_full | Blood transfusion during cardiac surgery is associated with inflammation and coagulation in the lung: a case control study |
title_fullStr | Blood transfusion during cardiac surgery is associated with inflammation and coagulation in the lung: a case control study |
title_full_unstemmed | Blood transfusion during cardiac surgery is associated with inflammation and coagulation in the lung: a case control study |
title_short | Blood transfusion during cardiac surgery is associated with inflammation and coagulation in the lung: a case control study |
title_sort | blood transfusion during cardiac surgery is associated with inflammation and coagulation in the lung: a case control study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3221992/ https://www.ncbi.nlm.nih.gov/pubmed/21314930 http://dx.doi.org/10.1186/cc10032 |
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