TY - JOUR
T1 - Novel Noninvasive Method of Cerebrovascular Blood Volume Assessment Using Brain Bioimpedance
AU - Tiba, Mohamad H.
AU - McCracken, Brendan M.
AU - Ansari, Sardar
AU - Belle, Ashwin
AU - Cummings, Brandon C.
AU - Rajajee, Venkatakrishna
AU - Patil, Parag G.
AU - Alam, Hasan B.
AU - Ward, Kevin R.
N1 - Funding Information:
The authors would like to acknowledge and thank the Michigan Center for Integrative Research in Critical Care (MCIRCC) and the Massey Foundation funding program for their support.
Publisher Copyright:
© Copyright 2017, Mary Ann Liebert, Inc.
PY - 2017/11/15
Y1 - 2017/11/15
N2 - Cerebrovascular autoregulation (CAR) is the ability of vessels to modulate their tone in response to changes in pressure. As an auto-protective mechanism, CAR is critical in preventing secondary brain injury post-trauma. Monitoring of changes in cerebral blood volume might be valuable in evaluating CAR and response to various therapies. In this study, we utilized an ocular-brain bioimpedance interface to assess real time changes in cerebral blood volume in response to a number of physiological challenges. We hypothesize that changes in brain bioimpedance (dz) would track changes in cerebral blood volume. Anesthetized animals were instrumented for monitoring of intracranial pressure (ICP), mean arterial blood pressure, cerebral perfusion pressure (CPP) and cerebral blood flow (CBF). Bioimpedance was monitored continuously through electrocardiographic electrodes placed over the eyelids. Interventions such as hyperventilation, vasopressor administration, creation of an epidural hematoma, and systemic hemorrhage were used to manipulate levels of ICP, CPP, and CBF. The dz correlated with changes in ICP, CPP, and CBF (r = -0.72 to -0.88, p < 0.0001). The receiver operating characteristic for dz at different thresholds of CPP and CBF showed high impedance performance with area under the curve between 0.80-1.00 (p < 0.003) and sensitivity and specificity varying between 83%-100% and 70%-100%, respectively. Our preliminary tests show that brain bioimpedance as measured through the ocular-brain interface tracks changes in CPP and CBF with high precision and may prove to be valuable in the future in assessing changes in cerebral blood volume and CAR.
AB - Cerebrovascular autoregulation (CAR) is the ability of vessels to modulate their tone in response to changes in pressure. As an auto-protective mechanism, CAR is critical in preventing secondary brain injury post-trauma. Monitoring of changes in cerebral blood volume might be valuable in evaluating CAR and response to various therapies. In this study, we utilized an ocular-brain bioimpedance interface to assess real time changes in cerebral blood volume in response to a number of physiological challenges. We hypothesize that changes in brain bioimpedance (dz) would track changes in cerebral blood volume. Anesthetized animals were instrumented for monitoring of intracranial pressure (ICP), mean arterial blood pressure, cerebral perfusion pressure (CPP) and cerebral blood flow (CBF). Bioimpedance was monitored continuously through electrocardiographic electrodes placed over the eyelids. Interventions such as hyperventilation, vasopressor administration, creation of an epidural hematoma, and systemic hemorrhage were used to manipulate levels of ICP, CPP, and CBF. The dz correlated with changes in ICP, CPP, and CBF (r = -0.72 to -0.88, p < 0.0001). The receiver operating characteristic for dz at different thresholds of CPP and CBF showed high impedance performance with area under the curve between 0.80-1.00 (p < 0.003) and sensitivity and specificity varying between 83%-100% and 70%-100%, respectively. Our preliminary tests show that brain bioimpedance as measured through the ocular-brain interface tracks changes in CPP and CBF with high precision and may prove to be valuable in the future in assessing changes in cerebral blood volume and CAR.
KW - CBF autoregulation
KW - bioimpedance
KW - blood flow
KW - cerebral blood volume
KW - traumatic brain injury
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U2 - 10.1089/neu.2017.5090
DO - 10.1089/neu.2017.5090
M3 - Article
C2 - 28657491
AN - SCOPUS:85033374509
SN - 0897-7151
VL - 34
SP - 3089
EP - 3096
JO - Central Nervous System Trauma
JF - Central Nervous System Trauma
IS - 22
ER -