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Brain Tissue Oxygen and Cerebrovascular Reactivity in Traumatic Brain Injury: A Collaborative European NeuroTrauma Effectiveness Research in Traumatic Brain Injury Exploratory Analysis of Insult Burden

60

Citations

25

References

2020

Year

Abstract

Pressure reactivity index (PRx) and brain tissue oxygen (PbtO<sub>2</sub>) are associated with outcome in traumatic brain injury (TBI). This study explores the relationship between PRx and PbtO<sub>2</sub> in adult moderate/severe TBI. Using the Collaborative European NeuroTrauma Effectiveness Research in Traumatic Brain Injury (CENTER-TBI) high resolution intensive care unit (ICU) sub-study cohort, we evaluated those patients with archived high-frequency digital intraparenchymal intracranial pressure (ICP) and PbtO<sub>2</sub> monitoring data of, a minimum of 6 h in duration, and the presence of a 6 month Glasgow Outcome Scale -Extended (GOSE) score. Digital physiological signals were processed for ICP, PbtO<sub>2</sub>, and PRx, with the % time above/below defined thresholds determined. The duration of ICP, PbtO<sub>2</sub>, and PRx derangements was characterized. Associations with dichotomized 6-month GOSE (alive/dead, and favorable/unfavorable outcome; ≤ 4 = unfavorable), were assessed. A total of 43 patients were included. Severely impaired cerebrovascular reactivity was seen during elevated ICP and low PbtO<sub>2</sub> episodes. However, most of the acute ICU physiological derangements were impaired cerebrovascular reactivity, not ICP elevations or low PbtO<sub>2</sub> episodes. Low PbtO<sub>2</sub> without PRx impairment was rarely seen. % time spent above PRx threshold was associated with mortality at 6 months for thresholds of 0 (area under the curve [AUC] 0.734, <i>p</i> = 0.003), > +0.25 (AUC 0.747, <i>p</i> = 0.002) and > +0.35 (AUC 0.745, <i>p</i> = 0.002). Similar relationships were not seen for % time with ICP >20 mm Hg, and PbtO<sub>2</sub> < 20 mm Hg in this cohort. Extreme impairment in cerebrovascular reactivity is seen during concurrent episodes of elevated ICP and low PbtO<sub>2</sub>. However, the majority of the deranged cerebral physiology seen during the acute ICU phase is impairment in cerebrovascular reactivity, with most impairment occurring in the presence of normal PbtO<sub>2</sub> levels. Measures of cerebrovascular reactivity appear to display the most consistent associations with global outcome in TBI, compared with ICP and PbtO<sub>2</sub>.

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