4.6 Article

Individualizing Thresholds of Cerebral Perfusion Pressure Using Estimated Limits of Autoregulation

Journal

CRITICAL CARE MEDICINE
Volume 45, Issue 9, Pages 1464-1471

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/CCM.0000000000002575

Keywords

autoregulation; cerebral hemodynamics; cerebral perfusion pressure; intracranial pressure; traumatic brain injury

Funding

  1. Woolf Fisher scholarship
  2. Cambridge Enterprise, Cambridge, United Kingdom
  3. Bill & Melinda Gates Foundation
  4. National Institute of Health Research (NIHR) Research Professorship
  5. Academy of Medical Sciences/Health Foundation Senior Surgical Scientist Fellowship
  6. Ornim Medical
  7. Shire Medical
  8. Neurovive
  9. Calico
  10. NIHR
  11. GlaxoSmithKline
  12. Brainscope
  13. Solvay
  14. NIHR Cambridge Biomedical Centre [RCZB/004]
  15. NIHR Senior Investigator Award [RCZB/014]
  16. MRC [G0600986, G0601025] Funding Source: UKRI
  17. Medical Research Council [G0601025, G0600986] Funding Source: researchfish
  18. National Institute for Health Research [NIHR-RP-R3-12-013, NF-SI-0512-10090] Funding Source: researchfish

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Objectives: In severe traumatic brain injury, cerebral perfusion pressure management based on cerebrovascular pressure reactivity index has the potential to provide a personalized treatment target to improve patient outcomes. So far, the methods have focused on identifying one autoregulation-guided cerebral perfusion pressure target-called cerebral perfusion pressure optimal. We investigated whether a cerebral perfusion pressure autoregulation range-which uses a continuous estimation of the lower and upper cerebral perfusion pressure limits of cerebrovascular pressure autoregulation (assessed with pressure reactivity index)-has prognostic value. Design: Single-center retrospective analysis of prospectively collected data. Setting: The neurocritical care unit at a tertiary academic medical center. Patients: Data from 729 severe traumatic brain injury patients admitted between 1996 and 2016 were used. Treatment was guided by controlling intracranial pressure and cerebral perfusion pressure according to a local protocol. Interventions: None. Methods and Main Results: Cerebral perfusion pressure-pressure reactivity index curves were fitted automatically using a previously published curve-fitting heuristic from the relationship between pressure reactivity index and cerebral perfusion pressure. The cerebral perfusion pressure values at which this U-shaped curve crossed the fixed threshold from intact to impaired pressure reactivity (pressure reactivity index = 0.3) were denoted automatically the lower and upper cerebral perfusion pressure limits of reactivity, respectively. The percentage of time with cerebral perfusion pressure below (% cerebral perfusion pressure < lower limit of reactivity), above (% cerebral perfusion pressure > upper limit of reactivity), or within these reactivity limits (% cerebral perfusion pressure within limits of reactivity) was calculated for each patient and compared across dichotomized Glasgow Outcome Scores. After adjusting for age, initial Glasgow Coma Scale, and mean intracranial pressure, percentage of time with cerebral perfusion pressure less than lower limit of reactivity was associated with unfavorable outcome (odds ratio % cerebral perfusion pressure < lower limit of reactivity, 1.04; 95% CI, 1.02- 1.06; p < 0.001) and mortality (odds ratio, 1.06; 95% CI, 1.04-1.08; p < 0.001). Conclusions: Individualized autoregulation-guided cerebral perfusion pressure management may be a plausible alternative to fixed cerebral perfusion pressure threshold management in severe traumatic brain injury patients. Prospective randomized research will help define which autoregulation-guided method is beneficial, safe, and most practical.

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