Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/29803
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dc.contributor.authorSivathamboo, Shobi-
dc.contributor.authorFriedman, Daniel-
dc.contributor.authorLaze, Juliana-
dc.contributor.authorNightscales, Russell-
dc.contributor.authorChen, Zhibin-
dc.contributor.authorKuhlmann, Levin-
dc.contributor.authorDevore, Sasha-
dc.contributor.authorMacefield, Vaughan-
dc.contributor.authorKwan, Patrick-
dc.contributor.authorD'Souza, Wendyl-
dc.contributor.authorBerkovic, Samuel F-
dc.contributor.authorPerucca, Piero-
dc.contributor.authorO'Brien, Terence J-
dc.contributor.authorDevinsky, Orrin-
dc.date2021-
dc.date.accessioned2022-04-12T04:28:30Z-
dc.date.available2022-04-12T04:28:30Z-
dc.date.issued2021-12-14-
dc.identifier.citationNeurology 2021; 97(24): e2357-e2367en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/29803-
dc.description.abstractWe compared heart rate variability (HRV) in sudden unexpected death in epilepsy (SUDEP) cases and living epilepsy controls. This international, multicenter, retrospective, nested case-control study examined patients admitted for video-EEG monitoring (VEM) between January 1, 2003, and December 31, 2014, and subsequently died of SUDEP. Time domain and frequency domain components were extracted from 5-minute interictal ECG recordings during sleep and wakefulness from SUDEP cases and controls. We identified 31 SUDEP cases and 56 controls. Normalized low-frequency power (LFP) during wakefulness was lower in SUDEP cases (median 42.5, interquartile range [IQR] 32.6-52.6) than epilepsy controls (55.5, IQR 40.7-68.9; p = 0.015, critical value = 0.025). In the multivariable model, normalized LFP was lower in SUDEP cases compared to controls (contrast -11.01, 95% confidence interval [CI] -20.29 to 1.73; p = 0.020, critical value = 0.025). There was a negative correlation between LFP and the latency to SUDEP, where each 1% incremental reduction in normalized LFP conferred a 2.7% decrease in the latency to SUDEP (95% CI 0.95-0.995; p = 0.017, critical value = 0.025). Increased survival duration from VEM to SUDEP was associated with higher normalized high-frequency power (HFP; p = 0.002, critical value = 0.025). The survival model with normalized LFP was associated with SUDEP (c statistic 0.66, 95% CI 0.55-0.77), which nonsignificantly increased with the addition of normalized HFP (c statistic 0.70, 95% CI 0.59-0.81; p = 0.209). Reduced short-term LFP, which is a validated biomarker for sudden death, was associated with SUDEP. Increased HFP was associated with longer survival and may be cardioprotective in SUDEP. HRV quantification may help stratify individual SUDEP risk. This study provides Class III evidence that in patients with epilepsy, some measures of HRV are associated with SUDEP.en
dc.language.isoeng-
dc.titleAssociation of Short-term Heart Rate Variability and Sudden Unexpected Death in Epilepsy.en
dc.typeJournal Articleen
dc.identifier.journaltitleNeurologyen
dc.identifier.affiliationDepartment of Neuroscience, Central Clinical School (S.S., R.N., Z.C., M.B., V.M., P.K., P.P., T.J.O.), Clinical Epidemiology, School of Public Health and Preventive Medicine (Z.C., M.B.),en
dc.identifier.affiliationDepartment of Data Science and AI, Faculty of Information Technology (L.K.), Monash University;en
dc.identifier.affiliationDepartment of Medicine (The Royal Melbourne Hospital) (S.S., R.N., Z.C., M.B., P.K., P.P., T.J.O.), The University of Melbourne;en
dc.identifier.affiliationDepartment of Neurology (S.S., R.N., P.K., P.P., T.J.O.), The Royal Melbourne Hospital;en
dc.identifier.affiliationDepartment of Neurology (S.S., R.N., P.K., P.P., T.J.O.), Alfred Health, Melbourne, Australia;en
dc.identifier.affiliationDepartment of Neurology (D.F., J.L., S.D., O.D.), New York University Grossman School of Medicine, New York;en
dc.identifier.affiliationHuman Autonomic Neurophysiology (V.M.), Baker Heart and Diabetes Institute, Melbourne;en
dc.identifier.affiliationDepartment of Medicine (W.D., M.D.C.B.), St. Vincent's Hospital, The University of Melbourne, Fitzroy;en
dc.identifier.affiliationMedicine (University of Melbourne)en
dc.identifier.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/34649884/en
dc.identifier.doi10.1212/WNL.0000000000012946en
dc.type.contentTexten
dc.identifier.orcid0000-0003-4638-9579en
dc.identifier.orcid0000-0001-9108-207Xen
dc.identifier.orcid0000-0002-1888-6917en
dc.identifier.orcid0000-0003-2554-1850en
dc.identifier.orcid0000-0003-3325-6566en
dc.identifier.orcid0000-0003-4580-841Xen
dc.identifier.orcid0000-0002-7855-7066en
dc.identifier.orcid0000-0003-0044-4632en
dc.identifier.pubmedid34649884-
local.name.researcherBerkovic, Samuel F
item.grantfulltextnone-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.deptMedicine (University of Melbourne)-
crisitem.author.deptEpilepsy Research Centre-
crisitem.author.deptNeurology-
crisitem.author.deptNeurology-
crisitem.author.deptComprehensive Epilepsy Program-
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