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Factor VIIa administration in traumatic brain injury: an AAST-MITC propensity score analysis

BACKGROUND: Recombinant factor VIIa (rFVIIa) has been used off-label as an adjunct in the reversal of warfarin therapy and management of hemorrhage after trauma. Only a handful of these reports are rigorous studies, from which results regarding safety and effectiveness have been mixed. There remains...

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Autores principales: Lombardo, Sarah, Millar, D, Jurkovich, Gregory J, Coimbra, Raul, Nirula, Ram
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5887758/
https://www.ncbi.nlm.nih.gov/pubmed/29766126
http://dx.doi.org/10.1136/tsaco-2017-000134
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author Lombardo, Sarah
Millar, D
Jurkovich, Gregory J
Coimbra, Raul
Nirula, Ram
author_facet Lombardo, Sarah
Millar, D
Jurkovich, Gregory J
Coimbra, Raul
Nirula, Ram
author_sort Lombardo, Sarah
collection PubMed
description BACKGROUND: Recombinant factor VIIa (rFVIIa) has been used off-label as an adjunct in the reversal of warfarin therapy and management of hemorrhage after trauma. Only a handful of these reports are rigorous studies, from which results regarding safety and effectiveness have been mixed. There remains no clear consensus as to the role of rFVIIa in traumatic brain injury (TBI). METHODS: Eleven level 1 trauma centers provided clinical data and head CT scans of patients with a Glasgow Coma Scale (GCS) score of ≤13 and radiographic evidence of TBI. A propensity score (PS) to receive rFVIIa in those surviving ≥2 days was calculated for each patient based on patient demographics, comorbidities, physiology, Injury Severity Score, admission GCS score, and treatment center. Patients receiving rFVIIa within 24 hours of admission were matched to patients who did not receive rFVIIa for outcomes assessment. Subgroup analysis evaluated patients with primary head injury with PS matching. RESULTS: There were 4284 patient observations; 129 received rFVIIa. Groups were comparable after matching. No differences in mortality or morbidity were found. Improvement in GCS score from admission to discharge was less among those receiving rFVIIa (5.5 vs. 2.4; P value 0.001); however, there was no difference in average GCS score at discharge. No significant differences in outcomes were identified in patients with isolated TBI receiving rFVIIa. DISCUSSION: rFVIIa in early management of TBI is not associated with a decreased risk of mortality or morbidity, and may negatively impact recovery and functional status at discharge in the severely injured patient with polytrauma. LEVEL OF EVIDENCE: Level III. STUDY TYPE: Therapeutic/care management.
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spelling pubmed-58877582018-05-14 Factor VIIa administration in traumatic brain injury: an AAST-MITC propensity score analysis Lombardo, Sarah Millar, D Jurkovich, Gregory J Coimbra, Raul Nirula, Ram Trauma Surg Acute Care Open Original Article BACKGROUND: Recombinant factor VIIa (rFVIIa) has been used off-label as an adjunct in the reversal of warfarin therapy and management of hemorrhage after trauma. Only a handful of these reports are rigorous studies, from which results regarding safety and effectiveness have been mixed. There remains no clear consensus as to the role of rFVIIa in traumatic brain injury (TBI). METHODS: Eleven level 1 trauma centers provided clinical data and head CT scans of patients with a Glasgow Coma Scale (GCS) score of ≤13 and radiographic evidence of TBI. A propensity score (PS) to receive rFVIIa in those surviving ≥2 days was calculated for each patient based on patient demographics, comorbidities, physiology, Injury Severity Score, admission GCS score, and treatment center. Patients receiving rFVIIa within 24 hours of admission were matched to patients who did not receive rFVIIa for outcomes assessment. Subgroup analysis evaluated patients with primary head injury with PS matching. RESULTS: There were 4284 patient observations; 129 received rFVIIa. Groups were comparable after matching. No differences in mortality or morbidity were found. Improvement in GCS score from admission to discharge was less among those receiving rFVIIa (5.5 vs. 2.4; P value 0.001); however, there was no difference in average GCS score at discharge. No significant differences in outcomes were identified in patients with isolated TBI receiving rFVIIa. DISCUSSION: rFVIIa in early management of TBI is not associated with a decreased risk of mortality or morbidity, and may negatively impact recovery and functional status at discharge in the severely injured patient with polytrauma. LEVEL OF EVIDENCE: Level III. STUDY TYPE: Therapeutic/care management. BMJ Publishing Group 2018-03-22 /pmc/articles/PMC5887758/ /pubmed/29766126 http://dx.doi.org/10.1136/tsaco-2017-000134 Text en © Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted. This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Original Article
Lombardo, Sarah
Millar, D
Jurkovich, Gregory J
Coimbra, Raul
Nirula, Ram
Factor VIIa administration in traumatic brain injury: an AAST-MITC propensity score analysis
title Factor VIIa administration in traumatic brain injury: an AAST-MITC propensity score analysis
title_full Factor VIIa administration in traumatic brain injury: an AAST-MITC propensity score analysis
title_fullStr Factor VIIa administration in traumatic brain injury: an AAST-MITC propensity score analysis
title_full_unstemmed Factor VIIa administration in traumatic brain injury: an AAST-MITC propensity score analysis
title_short Factor VIIa administration in traumatic brain injury: an AAST-MITC propensity score analysis
title_sort factor viia administration in traumatic brain injury: an aast-mitc propensity score analysis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5887758/
https://www.ncbi.nlm.nih.gov/pubmed/29766126
http://dx.doi.org/10.1136/tsaco-2017-000134
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