4.5 Article

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

Journal

JOURNAL OF NEUROTRAUMA
Volume 38, Issue 20, Pages 2790-2800

Publisher

MARY ANN LIEBERT, INC
DOI: 10.1089/neu.2021.0197

Keywords

cerebral autoregulation; cerebral perfusion; intensive care; optimal cerebral perfusion pressure; precision medicine; traumatic brain injury

Funding

  1. NIHR Cambridge Biomedical Research Centre [BRC-1215-20014]
  2. European Society of Intensive Care (ESICM)
  3. University Maastricht, Maastricht, The Netherlands
  4. Medical Research Council [MR N013433-1]
  5. Gates Cambridge Scholarship
  6. National Institute for Health Research (NIHR), Cambridge Biomedical Research Centre
  7. NIHR Senior Investigator Award
  8. European Union Foundation Program 7 Grant (CENTER-TBI) [602150]
  9. National Institute for Health Research (NIHR): research professorship, Biomedical Research Centre and Global Neurotrauma Research group
  10. Royal College of Surgeons of England
  11. Research Foundation, Flanders (FWO) [1843118N]
  12. KU Leuven [C24/17/072]
  13. Belgian Health Care Knowledge Center [COV201003]

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This study evaluated the feasibility and safety of CA-guided CPP management in TBI patients requiring intracranial pressure monitoring and therapy. The results demonstrate that targeting an individual and dynamic CA-guided CPP is feasible and safe in TBI patients, encouraging further prospective trials powered for clinical outcomes.
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 < 0.001). There were no significant differences between groups for TIL or for other safety end-points. Conclusively, targeting an individual and dynamic CA-guided CPP is feasible and safe in TBIicp patients. This encourages a prospective trial powered for clinical outcomes.

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