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Targeting Autoregulation-Guided Cerebral Perfusion Pressure after Traumatic Brain Injury (COGiTATE): A Feasibility Randomized Controlled Clinical Trial

Authors :
Iwan C. C. van der Horst
Peter Smielewski
Jeanette Tas
Bart Depreitere
Ari Ercole
Ruud C van Kaam
Analisa L Liberti
Marcel J. H. Aries
Sander M. J. van Kuijk
David K. Menon
Peter J. Hutchinson
Marek Czosnyka
Geert Meyfroidt
Cornelia W. E. Hoedemaekers
Erta Beqiri
Roel H. L. Haeren
Joseph Donnelly
Intensive Care
MUMC+: MA Arts Assistenten IC (9)
RS: MHeNs - R3 - Neuroscience
MUMC+: MA Med Staf Spec Neurochirurgie (9)
MUMC+: MA AIOS Neurochirurgie (9)
Neurochirurgie
MUMC+: MA Intensive Care (3)
MUMC+: MA Medische Staf IC (9)
RS: Carim - V04 Surgical intervention
MUMC+: KIO Kemta (9)
Epidemiologie
RS: CAPHRI - R2 - Creating Value-Based Health Care
RS: MHeNs - R1 - Cognitive Neuropsychiatry and Clinical Neuroscience
Hutchinson, Peter [0000-0002-2796-1835]
Smielewski, Peter [0000-0001-5096-3938]
Ercole, Ari [0000-0001-8350-8093]
Apollo - University of Cambridge Repository
Source :
Journal of Neurotrauma, 38(20), 2790-2800. Mary Ann Liebert Inc., Journal of Neurotrauma, 38, 20, pp. 2790-2800, Journal of Neurotrauma, 38, 2790-2800
Publication Year :
2021
Publisher :
Mary Ann Liebert Inc, 2021.

Abstract

Managing traumatic brain injury (TBI) patients with a cerebral perfusion pressure (CPP) near to the cerebral autoregulation (CA)-guided "optimal" CPP (CPPopt) value is associated with improved outcome and might be useful to individualize care, but has never been prospectively evaluated. This study evaluated the feasibility and safety of CA-guided CPP management in TBI patients requiring intracranial pressure monitoring and therapy (TBIicp patients). The CPPopt Guided Therapy: Assessment of Target Effectiveness (COGiTATE) parallel two-arm feasibility trial took place in four tertiary centers. TBIicp patients were randomized to either the Brain Trauma Foundation (BTF) guideline CPP target range (control group) or to the individualized CA-guided CPP targets (intervention group). CPP targets were guided by six times daily software-based alerts for up to 5 days. The primary feasibility end-point was the percentage of time with CPP concordant (±5 mm Hg) with the set CPP targets. The main secondary safety end-point was an increase in therapeutic intensity level (TIL) between the control and intervention group. Twenty-eight patients were randomized to the control and 32 patients to the intervention group. CPP in the intervention group was in the target range for 46.5% (interquartile range, 41.2-58) of the monitored time, significantly higher than the feasibility target specified in the published protocol (36%; p

Details

ISSN :
08977151
Database :
OpenAIRE
Journal :
Journal of Neurotrauma, 38(20), 2790-2800. Mary Ann Liebert Inc., Journal of Neurotrauma, 38, 20, pp. 2790-2800, Journal of Neurotrauma, 38, 2790-2800
Accession number :
edsair.doi.dedup.....068a8bf0c84cb3251a3e113c930e0dea
Full Text :
https://doi.org/10.17863/cam.72267