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dc.contributor.authorRussell-Buckland, Joshua
dc.contributor.authorTachtsidis, Ilias
dc.date.accessioned2022-06-09T12:33:31Z
dc.date.available2022-06-09T12:33:31Z
dc.date.issued2020
dc.identifier.urihttps://library.oapen.org/handle/20.500.12657/56698
dc.description.abstractHypoxic ischemic encephalopathy (HIE) is a significant cause of death and neurological disability in newborns. Therapeutic hypothermia at 33.5 °C is one of the most common treatments in HIE and generally improves outcome; however 45–55% of injuries still result in death or severe neurodevelopmental disability. We have developed a systems biology model of cerebral oxygen transport and metabolism to model the impact of hypothermia on the piglet brain (the neonatal preclinical animal model) tissue physiology. This computational model is an extension of the BrainSignals model of the adult brain. The model predicts that during hypothermia there is a 5.1% decrease in cerebral metabolism, 1.1% decrease in blood flow and 2.3% increase in cerebral tissue oxygenation saturation. The model can be used to simulate effects of hypothermia on the brain and to help interpret bedside recordings.en_US
dc.languageEnglishen_US
dc.subject.otherBroadband NIRS, Hypothermia, Systems biologyen_US
dc.titleChapter Developing a Model to Simulate the Effect of Hypothermia on Cerebral Blood Flow and Metabolismen_US
dc.typechapter
oapen.identifier.doi10.1007/978-3-030-34461-0_38en_US
oapen.relation.isPublishedBy6c6992af-b843-4f46-859c-f6e9998e40d5en_US
oapen.relation.isPartOfBookccf57905-ab3b-49f9-b482-fdf984cb3c17en_US
oapen.relation.isFundedByd859fbd3-d884-4090-a0ec-baf821c9abfden_US
oapen.relation.isbn9783030344597en_US
oapen.collectionWellcomeen_US
oapen.pages8en_US
oapen.grant.number104580/Z/14/Z


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