Abstract

BackgroundImpaired cerebrovascular reactivity after traumatic brain injury (TBI) in adults is emerging as an important prognostic factor, with strong independent association with 6-month outcomes. To date, it is unknown if impaired cerebrovascular reactivity during the acute phase is associated with ongoing impaired continuously measured cerebrovascular reactivity in the long-term, and if such measures are associated with clinical phenotype at those points in time.ObjectiveWe describe a prospective pilot study to assess the use of near-infrared spectroscopy (NIRS) to derive continuous measures of cerebrovascular reactivity during the acute and long-term phases of TBI in adults.MethodsOver 2 years, we will recruit up to 80 adults with moderate/severe TBI admitted to the intensive care unit (ICU) with invasive intracranial pressure (ICP) monitoring. These patients will undergo high-frequency data capture of ICP, arterial blood pressure (ABP), and NIRS for the first 5 days of care. Patients will then have 30 minutes of noninvasive NIRS and ABP monitoring in the clinic at 3, 6, and 12 months post-injury. Outcomes will be assessed via the Glasgow Outcome Scale and Short Form-12 questionnaires. Various relationships between NIRS and ICP-derived cerebrovascular reactivity metrics and associated outcomes will be assessed using biomedical signal processing techniques and both multivariate and time-series statistical methodologies.ResultsStudy recruitment began at the end of February 2020, with data collection ongoing and three patients enrolled at the time of writing. The expected duration of data collection will be from February 2020 to January 2022, as per our local research ethics board approval (B2018:103). Support for this work has been obtained through the National Institutes of Health (NIH) through the National Institute of Neurological Disorders and Stroke (NINDS) (R03NS114335), funded in January 2020.ConclusionsWith the application of NIRS technology for monitoring of patients with TBI, we expect to be able to outline core relationships between noninvasively measured aspects of cerebral physiology and invasive measures, as well as patient outcomes. Documenting these relationships carries the potential to revolutionize the way we monitor patients with TBI, moving to more noninvasive techniques.International Registered Report Identifier (IRRID)DERR1-10.2196/18740

Highlights

  • Continuous measures of cerebrovascular reactivity by near-infrared spectroscopy (NIRS) provide a convenient and noninvasive method of monitoring cerebral autoregulation in adults with traumatic brain injury (TBI) [1,2]. The concept behind these indices is based on the assessment of the correlation between slow-wave[3,4] fluctuations in a measure of pulsatile cerebral blood volume (CBV), such as NIRS regional cerebral oxygen saturation, and a measure of cerebral blood flow driving pressure, such as mean arterial pressure (MAP) or cerebral perfusion pressure (CPP)

  • The first requirement is an in-depth assessment of the time-series relationships between gold standard intracranial pressure (ICP)-derived indices such as pressure reactivity index (PRx) and indices derived from NIRS

  • We will be recruiting adults with moderate/severe TBI admitted to the surgical intensive care unit (SICU) and who require invasive ICP monitoring for clinical purposes based on Brain Trauma Foundation (BTF) guidelines [9]

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Summary

Introduction

Continuous measures of cerebrovascular reactivity by near-infrared spectroscopy (NIRS) provide a convenient and noninvasive method of monitoring cerebral autoregulation in adults with traumatic brain injury (TBI) [1,2] The concept behind these indices is based on the assessment of the correlation between slow-wave (ie, 0.05 Hz to 0.005 Hz)[3,4] fluctuations in a measure of pulsatile cerebral blood volume (CBV), such as NIRS regional cerebral oxygen saturation (rSO2), and a measure of cerebral blood flow driving pressure, such as mean arterial pressure (MAP) or cerebral perfusion pressure (CPP). Impaired cerebrovascular reactivity after traumatic brain injury (TBI) in adults is emerging as an important prognostic factor, with strong independent association with 6-month outcomes To date, it is unknown if impaired cerebrovascular reactivity during the acute phase is associated with ongoing impaired continuously measured cerebrovascular reactivity in the long-term, and if such measures are associated with clinical phenotype at those points in time

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