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Phase plane analysis & morphological simulation of intracranial pressure variability for physiological monitoring of acute severe brain injury

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Title
Phase plane analysis & morphological simulation of intracranial pressure variability for physiological monitoring of acute severe brain injury
Name (type = personal)
NamePart (type = family)
Qadri
NamePart (type = given)
Maria J.
NamePart (type = date)
1988-
DisplayForm
Maria J. Qadri
Role
RoleTerm (authority = RULIB)
author
Name (type = personal)
NamePart (type = family)
Craelius
NamePart (type = given)
William
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William Craelius
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Advisory Committee
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chair
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Danish
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Shabbar F
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Shabbar F Danish
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Advisory Committee
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internal member
Name (type = personal)
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Shinbrot
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Troy
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Troy Shinbrot
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Advisory Committee
Role
RoleTerm (authority = RULIB)
internal member
Name (type = personal)
NamePart (type = family)
Wininger
NamePart (type = given)
Michael
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Michael Wininger
Affiliation
Advisory Committee
Role
RoleTerm (authority = RULIB)
outside member
Name (type = corporate)
NamePart
Rutgers University
Role
RoleTerm (authority = RULIB)
degree grantor
Name (type = corporate)
NamePart
School of Graduate Studies
Role
RoleTerm (authority = RULIB)
school
TypeOfResource
Text
Genre (authority = marcgt)
theses
OriginInfo
DateCreated (qualifier = exact)
2018
DateOther (qualifier = exact); (type = degree)
2018-01
CopyrightDate (encoding = w3cdtf); (qualifier = exact)
2018
Place
PlaceTerm (type = code)
xx
Language
LanguageTerm (authority = ISO639-2b); (type = code)
eng
Abstract (type = abstract)
After severe acute brain trauma, cerebrovascular autoregulation (AR) can be impaired, but the performance of this homeostatic mechanism cannot be interrogated directly due to the complexity of the vascular system and existing challenges in assessing cerebrovascular phenomena. When indicated by the severity of brain trauma, clinicians continuously monitor intracranial pressure (ICP) to assess cerebral perfusion as a proxy measure for neural tissue oxygenation. The Monroe-Kellie doctrine states that the sum of the brain tissue, blood in the cerebrovascular bed, and cerebrospinal fluid in the ventricles is held constant within the cranial cavity; the resultant pressure of these volumes within the cranial cavity is ICP which fluctuates during a single cardiac cycle. Where ABP presents two peaks corresponding to systole and diastole, ICP presents three distinct peaks that correspond to cardiac systole (peak 1), cerebrovascular compliance (peak 2), and cardiac diastole (peak 3). Recent research on the morphology of individual intracranial pressure beats indicates the potential to use transient morphological changes in ICP between cardiac cycles in the time domain to gain greater insight into the physiological performance of AR and near-future ICP. In order to highlight fluctuations in ICP behavior between successive cardiac cycles, this dissertation presents a novel method to analyze ICP morphology by transforming this cerebral pressure data from the time-domain to the phase-domain. Since existing mathematical models of the cerebrovascular performance focus on longer time-scale ICP behavior and clinically measured ICP morphology during cardiac cycles is often erratic, this dissertation demonstrates a novel morphological simulation of ICP to test a phase domain metric, the phase area ratio (PAR) in application to ICP monitoring. An additive Gaussian simulation of ICP was developed to specifically examine the behavior of ICP Peak 2 that represents cerebral compliance, which is the component of AR that cannot be assessed directly using other existing physiological measures. This dissertation tests the hypothesis that phase domain analysis of ICP is useful as a forecasting tool for intracranial hypertension (IH) after severe acute brain trauma and post-surgical intervention. To test this hypothesis, 300 simulated ICP cycles and over 1 million clinical ICP cycles from 7 patients were analyzed. The simulated data were analyzed in a linear model that showed an R-squared value of no more than 0.76 for PAR and peak 2 amplitude, and the model showed a 0.93 R-squared value or higher between mICP and peak 2 behavior. The Spearman’s correlation presented weak positive correlations between PAR and ICP ranging from 0.4 for the 1-hr time span to -0.1 for the 0.1-hr time span in time segments preceding intracranial hypertension (preIH). Overall in the clinical data examination, PAR was successfully able to differentiate between time periods of intracranial normotension and preIH time periods ranging from 1 to 0.1 hours using a Kolmogorov-Smirnov test for 67.9% of time periods tested in the seven patients. PAR performed with a lower area under the curve (0.53) than the time domain metric, Sample Entropy (SE) (0.71), when tested as a threshold classifier using receiver operator characteristic analysis for all time points in the exemplar patient. When analyzing all patient data, the area under the curve for PAR came out to 0.43 for a 1-hr window. A confusion matrix analysis of all patient data that yielded similar results as the receiver operator curve analysis. Using a logistic regression approach for prediction measurement, the results showed that PAR adds value to the performance of the model, where a longer amount of prior information yields better predictions for shorter times into the future. When PAR was used in conjunction with other metrics in a classifier, PAR-based metrics were more valuable that PAR itself. Overall PAR is a parameter that (1) requires less data for calculation than existing metrics, (2) has a bounded range between 0 to 1, and (3) does not have discontinuities like comparable complexity metrics. Ultimately, this work shows that PAR contributes unique information to existing multi-parameter prediction algorithms to forecast IH.
Subject (authority = RUETD)
Topic
Biomedical Engineering
Subject (authority = ETD-LCSH)
Topic
Brain--Wounds and injuries
RelatedItem (type = host)
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Title
Rutgers University Electronic Theses and Dissertations
Identifier (type = RULIB)
ETD
Identifier
ETD_8541
PhysicalDescription
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electronic resource
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application/pdf
InternetMediaType
text/xml
Note
Supplementary File: Matlab + R Files
Extent
1 online resource (xvii, 104 p. : ill.)
Note (type = degree)
Ph.D.
Note (type = bibliography)
Includes bibliographical references
Note (type = statement of responsibility)
by Maria J. Qadri
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TitleInfo
Title
School of Graduate Studies Electronic Theses and Dissertations
Identifier (type = local)
rucore10001600001
Location
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NjNbRU
Identifier (type = doi)
doi:10.7282/T36T0QWK
Genre (authority = ExL-Esploro)
ETD doctoral
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Rights

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The author owns the copyright to this work.
RightsHolder (type = personal)
Name
FamilyName
Qadri
GivenName
Maria
MiddleName
J.
Role
Copyright Holder
RightsEvent
Type
Permission or license
DateTime (encoding = w3cdtf); (qualifier = exact); (point = start)
2017-11-21 20:08:14
AssociatedEntity
Name
Maria Qadri
Role
Copyright holder
Affiliation
Rutgers University. School of Graduate Studies
AssociatedObject
Type
License
Name
Author Agreement License
Detail
I hereby grant to the Rutgers University Libraries and to my school the non-exclusive right to archive, reproduce and distribute my thesis or dissertation, in whole or in part, and/or my abstract, in whole or in part, in and from an electronic format, subject to the release date subsequently stipulated in this submittal form and approved by my school. I represent and stipulate that the thesis or dissertation and its abstract are my original work, that they do not infringe or violate any rights of others, and that I make these grants as the sole owner of the rights to my thesis or dissertation and its abstract. I represent that I have obtained written permissions, when necessary, from the owner(s) of each third party copyrighted matter to be included in my thesis or dissertation and will supply copies of such upon request by my school. I acknowledge that RU ETD and my school will not distribute my thesis or dissertation or its abstract if, in their reasonable judgment, they believe all such rights have not been secured. I acknowledge that I retain ownership rights to the copyright of my work. I also retain the right to use all or part of this thesis or dissertation in future works, such as articles or books.
Copyright
Status
Copyright protected
Availability
Status
Open
Reason
Permission or license
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