Journal
JOURNAL OF NEUROTRAUMA
Volume 37, Issue 13, Pages 1556-1565Publisher
MARY ANN LIEBERT, INC
DOI: 10.1089/neu.2019.6814
Keywords
cerebral autoregulation; intracranial hemorrhage; traumatic brain injury
Funding
- Hannelore Kohl Stiftung (Germany)
- OneMind (USA)
- Integra LifeSciences Corporation (USA)
- Cambridge Commonwealth Trust
- National Institutes of Health (NIH) through the National Institute for Neurological Diseases and Stroke (NINDS)
- National Institutes of Health (NIH) through the National Institute for Biomedical Imaging and Bioengineering (NIBIB)
- University of Manitoba Thorlakson Chair in Surgical Research Establishment Fund
- University of Manitoba VPRI Research Investment Fund (RIF)
- Winnipeg Health Sciences Centre Foundation
- University of Manitoba Rudy Falk Clinician-Scientist Professorship
- Academy of Medical Sciences/The Health Foundation Clinician Scientist Fellowship
- National Institute for Health Research (NIHR)
- NIHR Research Professorship
- NIHR Senior Investigator Award
- MRC [G0601025] Funding Source: UKRI
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Failure of cerebral autoregulation has been linked to unfavorable outcome after traumatic brain injury (TBI). Preliminary evidence from a small, retrospective, single-center analysis suggests that autoregulatory dysfunction may be associated with traumatic lesion expansion, particularly for pericontusional edema. The goal of this study was to further explore these associations using prospective, multi-center data from the Collaborative European Neurotrauma Effectiveness Research in TBI (CENTER-TBI) and to further explore the relationship between autoregulatory failure, lesion progression, and patient outcome. A total of 88 subjects from the CENTER-TBI High Resolution ICU Sub-Study cohort were included. All patients had an admission computed tomography (CT) scan and early repeat scan available, as well as high-frequency neurophysiological recordings covering the between-scan interval. Using a novel, semiautomated approach at lesion segmentation, we calculated absolute changes in volume of contusion core, pericontusional edema, and extra-axial hemorrhage between the imaging studies. We then evaluated associations between cerebrovascular reactivity metrics and radiological lesion progression using mixed-model regression. Analyses were adjusted for baseline covariates and non-neurophysiological factors associated with lesion growth using multi-variate methods. Impairment in cerebrovascular reactivity was significantly associated with progression of pericontusional edema and, to a lesser degree, intraparenchymal hemorrhage. In contrast, there were no significant associations with extra-axial hemorrhage. The strongest relationships were observed between RAC-based metrics and edema formation. Pulse amplitude index showed weaker, but consistent, associations with contusion growth. Cerebrovascular reactivity metrics remained strongly associated with lesion progression after taking into account contributions from non-neurophysiological factors and mean cerebral perfusion pressure. Total hemorrhagic core and edema volumes on repeat CT were significantly larger in patients who were deceased at 6 months, and the amount of edema was greater in patients with an unfavourable outcome (Glasgow Outcome Scale-Extended 1-4). Our study suggests associations between autoregulatory failure, traumatic edema progression, and poor outcome. This is in keeping with findings from a single-center retrospective analysis, providing multi-center prospective data to support those results.
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