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Effect of preadmission beta‐blockade on mortality in multiple trauma

BACKGROUND: High levels of circulating catecholamines after multiple trauma have been associated with increased morbidity and mortality. Beta‐adrenergic receptor antagonist (beta‐blocker) therapy has emerged as a potential treatment option, but the effect of preinjury beta‐blockade on trauma‐induced...

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Autores principales: Eriksson, M., von Oelreich, E., Brattström, O., Eriksson, J., Larsson, E., Oldner, A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253788/
https://www.ncbi.nlm.nih.gov/pubmed/30511040
http://dx.doi.org/10.1002/bjs5.83
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author Eriksson, M.
von Oelreich, E.
Brattström, O.
Eriksson, J.
Larsson, E.
Oldner, A.
author_facet Eriksson, M.
von Oelreich, E.
Brattström, O.
Eriksson, J.
Larsson, E.
Oldner, A.
author_sort Eriksson, M.
collection PubMed
description BACKGROUND: High levels of circulating catecholamines after multiple trauma have been associated with increased morbidity and mortality. Beta‐adrenergic receptor antagonist (beta‐blocker) therapy has emerged as a potential treatment option, but the effect of preinjury beta‐blockade on trauma‐induced mortality is unclear. The aim of this study was to assess whether preinjury beta‐blocker therapy is associated with reduced mortality after multiple trauma. METHODS: Severely injured patients, aged at least 50 years, admitted to a level one trauma centre over a 10‐year interval were linked to national and local registries of co‐morbidities, prescription drug use and level of education. The association between preinjury beta‐blocker use and 30‐day mortality was explored using logistic regression analysis. RESULTS: Some 1376 patients were included; 338 (24·6 per cent) were receiving beta‐blockers at the time of trauma. Beta‐blocker users had an increased crude 30‐day mortality rate compared with that for non‐users: 32·8 versus 19·7 per cent respectively (P < 0·001). After adjustment for baseline imbalances and injury‐related factors, there was no association between preinjury beta‐blocker use and mortality (OR 1·09, 95 per cent c.i. 0·70 to 1·70). Separate analyses of individuals with or without severe head injury did not significantly change this association. There was no significant difference in the rate of shock between beta‐blocker users and non‐users. CONCLUSION: Pretrauma beta‐blockade is not associated with 30‐day mortality beyond the effects of age, co‐morbidity and injury severity.
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spelling pubmed-62537882018-12-03 Effect of preadmission beta‐blockade on mortality in multiple trauma Eriksson, M. von Oelreich, E. Brattström, O. Eriksson, J. Larsson, E. Oldner, A. BJS Open Original Articles BACKGROUND: High levels of circulating catecholamines after multiple trauma have been associated with increased morbidity and mortality. Beta‐adrenergic receptor antagonist (beta‐blocker) therapy has emerged as a potential treatment option, but the effect of preinjury beta‐blockade on trauma‐induced mortality is unclear. The aim of this study was to assess whether preinjury beta‐blocker therapy is associated with reduced mortality after multiple trauma. METHODS: Severely injured patients, aged at least 50 years, admitted to a level one trauma centre over a 10‐year interval were linked to national and local registries of co‐morbidities, prescription drug use and level of education. The association between preinjury beta‐blocker use and 30‐day mortality was explored using logistic regression analysis. RESULTS: Some 1376 patients were included; 338 (24·6 per cent) were receiving beta‐blockers at the time of trauma. Beta‐blocker users had an increased crude 30‐day mortality rate compared with that for non‐users: 32·8 versus 19·7 per cent respectively (P < 0·001). After adjustment for baseline imbalances and injury‐related factors, there was no association between preinjury beta‐blocker use and mortality (OR 1·09, 95 per cent c.i. 0·70 to 1·70). Separate analyses of individuals with or without severe head injury did not significantly change this association. There was no significant difference in the rate of shock between beta‐blocker users and non‐users. CONCLUSION: Pretrauma beta‐blockade is not associated with 30‐day mortality beyond the effects of age, co‐morbidity and injury severity. John Wiley & Sons, Ltd 2018-06-23 /pmc/articles/PMC6253788/ /pubmed/30511040 http://dx.doi.org/10.1002/bjs5.83 Text en © 2018 The Authors. BJS Open published by John Wiley & Sons Ltd on behalf of BJS Society Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Articles
Eriksson, M.
von Oelreich, E.
Brattström, O.
Eriksson, J.
Larsson, E.
Oldner, A.
Effect of preadmission beta‐blockade on mortality in multiple trauma
title Effect of preadmission beta‐blockade on mortality in multiple trauma
title_full Effect of preadmission beta‐blockade on mortality in multiple trauma
title_fullStr Effect of preadmission beta‐blockade on mortality in multiple trauma
title_full_unstemmed Effect of preadmission beta‐blockade on mortality in multiple trauma
title_short Effect of preadmission beta‐blockade on mortality in multiple trauma
title_sort effect of preadmission beta‐blockade on mortality in multiple trauma
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253788/
https://www.ncbi.nlm.nih.gov/pubmed/30511040
http://dx.doi.org/10.1002/bjs5.83
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