4.4 Article

Association between cerebrovascular reactivity in adult traumatic brain injury and improvement in patient outcome over time: an exploratory analysis

Journal

ACTA NEUROCHIRURGICA
Volume 164, Issue 12, Pages 3107-3118

Publisher

SPRINGER WIEN
DOI: 10.1007/s00701-022-05366-9

Keywords

Autoregulation; Cerebrovascular reactivity; Outcome transition; Traumatic brain injury; TBI

Funding

  1. University of Manitoba BSc in Medicine program
  2. Richard Hoeschen Memorial Award
  3. University of Manitoba-Department of Surgery GFT Research Grant
  4. University of Manitoba Office of Research Services (ORS)-University Research Grant Program (URGP)
  5. University of Manitoba Biomedical Engineering Fellowship Program
  6. Edward R. Toporeck Graduate Fellowship in Engineering
  7. University of Manitoba Clinician Investigator Program
  8. University of Manitoba Dean's Fellowship
  9. Manitoba Medical Services Foundation Research and Education Fellowship
  10. R. Samuel McLaughlin Research Fellowship
  11. UMGSA Scholarship at the University of Manitoba
  12. NSERC [RGPIN-2022-03621]
  13. University of Manitoba Graduate Enhancement of Tri-Agency Stipend (GETS) program
  14. Centre on Aging at the University of Manitoba
  15. Manitoba Public Insurance (MPI) Professorship in Neuroscience
  16. MPI TBI Research Operating Fund
  17. Health Sciences Centre Foundation Winnipeg
  18. Natural Sciences and Engineering Research Council of Canada (NSERC) [RGPIN-2022-03621, ALLRP-576386-22, DGECR2022-00260]
  19. Canada Foundation for Innovation (CFI) [38583]
  20. Research Manitoba [3906]
  21. University of Manitoba VPRI Research Investment Fund (RIF)

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Impaired cerebrovascular reactivity during the acute phase of TBI is associated with failure to clinically improve over time, highlighting the importance of cerebrovascular reactivity monitoring in the recovery process of moderate/severe TBI.
Background Impaired cerebrovascular reactivity following moderate/severe traumatic brain injury (TBI) has emerged as a key potential driver of morbidity and mortality. However, the major contributions to the literature so far have been solely focused on single point measures of long-term outcome. Therefore, it remains unknown whether cerebrovascular reactivity impairment, during the acute phase of TBI, is associated with failure to improve in outcome across time. Methods Cerebrovascular reactivity was measured using three intracranial pressure-based surrogate metrics. For each patient, % time spent above various literature-defined thresholds was calculated. Patients were dichotomized based on outcome transition into Improved vs Not Improved between 1 and 3 months, 3 and 6 months, and 1 and 6 months, based on the Glasgow Outcome Scale-Extended (GOSE). Univariate and multivariable logistic regression analyses were performed, adjusting for the International Mission for Prognosis and Analysis of Clinical Trials (IMPACT) variables. Results Seventy-eight patients from the Winnipeg Acute TBI Database were included in this study. On univariate logistic regression analysis, higher % time with cerebrovascular reactivity metrics above clinically defined thresholds was associated with a lack of clinical improvement between 1 and 3 months and 1 and 6 months post injury (p < 0.05). These relationships held true on multivariable logistic regression analysis. Conclusion Our study demonstrates that impaired cerebrovascular reactivity, during the acute phase of TBI, is associated with failure to improve clinically over time. These preliminary findings highlight the significance that cerebrovascular reactivity monitoring carries in outcome recovery association in moderate/severe TBI.

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