Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/32755
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dc.contributor.authorFan, Feiven-
dc.contributor.authorBeare, Richard-
dc.contributor.authorTakagi, Michael-
dc.contributor.authorAnderson, Nicholas-
dc.contributor.authorBressan, Silvia-
dc.contributor.authorClarke, Cathriona J-
dc.contributor.authorDavis, Gavin A-
dc.contributor.authorDunne, Kevin-
dc.contributor.authorFabiano, Fabian-
dc.contributor.authorHearps, Stephen J C-
dc.contributor.authorIgnjatovic, Vera-
dc.contributor.authorParkin, Georgia-
dc.contributor.authorRausa, Vanessa C-
dc.contributor.authorSeal, Marc-
dc.contributor.authorShapiro, Jesse S-
dc.contributor.authorBabl, Franz E-
dc.contributor.authorAnderson, Vicki-
dc.date2023-
dc.date.accessioned2023-04-26T05:24:23Z-
dc.date.available2023-04-26T05:24:23Z-
dc.date.issued2023-07-01-
dc.identifier.citationJournal of Neurosurgery. Pediatrics 2023; 32(1)en_US
dc.identifier.issn1933-0715-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/32755-
dc.description.abstractPersisting postconcussive symptoms (pPCS), particularly headache, can significantly disrupt children's recovery and functioning. However, the underlying pathophysiology of these symptoms remains unclear. The goal in this study was to determine whether pPCS are related to cerebral blood flow (CBF) at 2 weeks postconcussion. The authors also investigated whether variations in CBF can explain the increased risk of acute posttraumatic headache (PTH) in female children following concussion. As part of a prospective, longitudinal study, the authors recruited children 5-18 years old who were admitted to the emergency department of a tertiary pediatric hospital with a concussion sustained within 48 hours of admission. Participants underwent pseudocontinuous arterial spin labeling MRI at 2 weeks postconcussion to quantify global mean gray and white matter perfusion (in ml/100 g/min). Conventional frequentist analysis and Bayesian analysis were performed. Comparison of recovered (n = 26) and symptomatic (n = 12) groups (mean age 13.15 years, SD 2.69 years; 28 male) found no differences in mean global gray and white matter perfusion at 2 weeks postconcussion (Bayes factors > 3). Although female sex was identified as a risk factor for PTH with migraine features (p = 0.003), there was no difference in CBF between female children with and without PTH. Global CBF was not associated with pPCS and female PTH at 2 weeks after pediatric concussion. These findings provide evidence against the use of CBF measured by arterial spin labeling as an acute biomarker for pediatric concussion recovery.en_US
dc.language.isoeng-
dc.subjectBayesian analysisen_US
dc.subjectarterial spin labelingen_US
dc.subjectcerebral blood flowen_US
dc.subjectpediatric concussionen_US
dc.subjectpersisting postconcussive symptomsen_US
dc.subjectposttraumatic headacheen_US
dc.subjecttraumaen_US
dc.subjecttraumatic brain injuryen_US
dc.titleCerebral blood flow in children with persisting postconcussive symptoms and posttraumatic headache at 2 weeks postconcussion.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleJournal of Neurosurgery. Pediatricsen_US
dc.identifier.affiliationMurdoch Children's Research Institute, Melbourne, Victoria.en_US
dc.identifier.affiliationMelbourne School of Psychological Sciences, University of Melbourne, Victoria.en_US
dc.identifier.affiliationDepartment of Women's and Children's Health, University of Padova, Italy.en_US
dc.identifier.affiliationNeurosurgeryen_US
dc.identifier.affiliationDepartment of Pediatrics, University of Melbourne, Victoria.en_US
dc.identifier.affiliationDepartment of Rehabilitation Medicine, Royal Children's Hospital, Melbourne, Victoria, Australia.en_US
dc.identifier.affiliationInstitute for Clinical and Translational Research, Johns Hopkins All Children's, St. Petersburg, Florida.en_US
dc.identifier.affiliationSchool of Psychology, Deakin University, Geelong, Victoria.en_US
dc.identifier.affiliationPsychology Service, Royal Children's Hospital, Melbourne, Victoria, Australia.en_US
dc.identifier.doi10.3171/2023.3.PEDS2339en_US
dc.type.contentTexten_US
dc.identifier.pubmedid37086163-
dc.description.startpage1-
dc.description.endpage8-
local.name.researcherDavis, Gavin A
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
crisitem.author.deptNeurosurgery-
crisitem.author.deptThe Florey Institute of Neuroscience and Mental Health-
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