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Journal Article

Citation

Armstead WM, Vavilala MS. J. Neurotrauma 2019; ePub(ePub): ePub.

Affiliation

Harborview Medical Center, 21618, Harborview Injury Prevention Research Center, Seattle, Washington, United States ; vavilala@uw.edu.

Copyright

(Copyright © 2019, Mary Ann Liebert Publishers)

DOI

10.1089/neu.2018.6119

PMID

30834818

Abstract

Recent clinical trials in traumatic brain injury (TBI) have failed to demonstrate therapeutic effects even when there appears to be good evidence for efficacy in one or more appropriate preclinical models. While existing animal models mimic the injury, difficulties in translating promising therapeutics are exacerbated by the lack of alignment of discrete measures of the underlying injury pathology between the animal models and human subjects. To address this mismatch, we have incorporated reverse translation of bedside experience to inform preclinical studies in a large animal (pig) model of TBI that mirror practical clinical assessments. Cerebral autoregulation is impaired after TBI, contributing to poor outcome. Cerebral Perfusion Pressure (CPP) is often normalized by use of vasoactive agents to increase mean arterial pressure (MAP) and thereby limit impairment of cerebral autoregulation and neurological deficits. However, vasoactive agents clinically used to elevate MAP to increase CPP after TBI, such as phenylephrine, dopamine, norepinephrine, and epinephrine, have not sufficiently been compared regarding effect on CPP, autoregulation, and survival after TBI, and clinically, current vasoactive agent use is variable. The cerebral effects of these clinically commonly used vasoactive agents are not known. This review will emphasize pediatric work and will describe bidirectional translational studies using a more human like animal model of TBI to identify better therapeutic strategies to improve outcome post injury. These studies additionally investigated the mechanism(s) involved in improvement of outcome in the setting of TBI.


Language: en

Keywords

ANIMAL STUDIES; CBF autoregulation; MODELS OF INJURY; PEDIATRIC BRAIN INJURY

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