Resuscitation after cardiac arrest (CA) entails significant risk of coma or disorders of consciousness resulting in poor neurological outcome. There is an acute need to monitor the brain function during and after resuscitation to optimize intervention and improve outcome. Our previous studies developed electrophysiological markers of post-CA brain injury, including quantitative EEG (qEEG) and quantitative evoked potentials (qEP), and their relationship to outcome and neurological deficits. Further, we demonstrated benefits of therapeutic hypothermia using these objective means. We discovered quantitative methods to track neurological injury from CA and patterns of electrical rhythms associated following resuscitation, such as burst suppression, and utilized these novel tools to demonstrate electrophysiological recovery and enhanced neurological outcome assisted by therapeutic hypothermia. The central hypothesis for this renewal is that recovery of cortical function has both cortical and subcortical origins and arousal from coma and recovery can be facilitated through hypothermic protection and pharmacological stimulation of both cortical and subcortical structures, and guided using quantitative electrophysiological markers.
The specific aims are: 1) To discover clinically relevant, quantitative cortical electrophysiological markers o arousal from coma. 2) To discover changes in cortical-subcortical neurological signals and their coupling after resuscitation. 3) To establish the neuroprotective effects of therapeutic hypothermia assessed through restoration of cortical electrophysiological function and cortical-subcortical network connectivity. 4) To promote arousal from coma through pharmacologic intervention by Orexin-A infusion and resulting stimulation of cortical-subcortical network connectivity. 5) To translate this research into an objective feedback system and optimization of delivery of titrated therapeutic hypothermia for neuroprotection and pharmacological arousal by Orexin-A infusion. CA results in hundreds of thousands of deaths each year and, even for survivors, the outcome remains dismal. Our multi-faceted approach will result in mechanistic understanding of arousal, means of monitoring cortical function, and treatments to accelerate recovery of cortical function. Starting with direct multi-unit recordings of cortical and subcorticl components of the arousal system, we will provide mechanistic understanding of arousal and successful restoration after resuscitation. Further, our qEEG and qEP based monitoring approaches will result in clinically relevant, translatable monitoring of interventions, both hypothermia and pharmacological. Our research will thus result in a comprehensive development of real-time neurophysiologic monitoring technology to optimize treatment options. Upon validation, the proposed quantitative, neuroelectrophysiology-guided optimization of TH/Orexin-A delivery should be applicable to monitoring patients and guiding clinical management.

Public Health Relevance

The proposed project is motivated by critical care needs of patients after cardiac arrest (CA) who survivors after CA and suffer from disorders of consciousness and coma that is ultimately a major contributor to poor outcome. We aim to study the problem of global ischemic brain injury and develop monitoring technologies for neuro-electrophysiologic markers of coma and arousal after CA. The goal is to develop quantitative measures of injury and uncover the cortical-subcortical network mechanisms so as to optimize the interventions with induced hypothermia and/or pharmacological infusion by using objective quantitative measures.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
2R01HL071568-11A1
Application #
8759183
Study Section
(NOIT)
Program Officer
Desvigne-Nickens, Patrice
Project Start
2002-07-01
Project End
2018-05-31
Budget Start
2014-08-01
Budget End
2015-05-31
Support Year
11
Fiscal Year
2014
Total Cost
Indirect Cost
Name
Johns Hopkins University
Department
Biomedical Engineering
Type
Schools of Medicine
DUNS #
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Greenwald, Elliot; Masters, Matthew R; Thakor, Nitish V (2016) Implantable neurotechnologies: bidirectional neural interfaces--applications and VLSI circuit implementations. Med Biol Eng Comput 54:1-17
Stupple, Aaron; Geocadin, Romergryko G; Celi, Leo Anthony (2016) Conversation prior to resuscitation: The new CPR. Resuscitation 99:e3
Sun, Yu; Thakor, Nitish (2016) Photoplethysmography Revisited: From Contact to Noncontact, From Point to Imaging. IEEE Trans Biomed Eng 63:463-77
Manno, Edward M; Freeman, William D; Livesay, Sarah et al. (2016) Expertise Matters. Crit Care Med 44:e1147-e1148
Ng, Kian Ann; Greenwald, Elliot; Xu, Yong Ping et al. (2016) Implantable neurotechnologies: a review of integrated circuit neural amplifiers. Med Biol Eng Comput 54:45-62
Greenwald, Elliot; So, Ernest; Wang, Qihong et al. (2016) A Bidirectional Neural Interface IC With Chopper Stabilized BioADC Array and Charge Balanced Stimulator. IEEE Trans Biomed Circuits Syst :
Greenwald, Elliot; Masters, Matthew R; Thakor, Nitish V (2016) Erratum to: Implantable neurotechnologies: bidirectional neural interfaces--applications and VLSI circuit implementations. Med Biol Eng Comput 54:19-22
Vipin, Ashwati; Kortelainen, Jukka; Al-Nashash, Hasan et al. (2015) Prolonged Local Hypothermia Has No Long-Term Adverse Effect on the Spinal Cord. Ther Hypothermia Temp Manag 5:152-62
Sandroni, Claudio; Geocadin, Romergryko G (2015) Neurological prognostication after cardiac arrest. Curr Opin Crit Care 21:209-14
Callaway, Clifton W; Donnino, Michael W; Fink, Ericka L et al. (2015) Part 8: Post-Cardiac Arrest Care: 2015 American Heart Association Guidelines Update for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care. Circulation 132:S465-82

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