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dc.contributor.authorWhitaker, Jen_US
dc.contributor.authorNeji, Ren_US
dc.contributor.authorKim, Sen_US
dc.contributor.authorConnolly, Aen_US
dc.contributor.authorAubriot, Ten_US
dc.contributor.authorCalvo, JJen_US
dc.contributor.authorKarim, Ren_US
dc.contributor.authorRoney, CHen_US
dc.contributor.authorMurfin, Ben_US
dc.contributor.authorRichardson, Cen_US
dc.contributor.authorMorgan, Sen_US
dc.contributor.authorIsmail, TFen_US
dc.contributor.authorHarrison, Jen_US
dc.contributor.authorde Vos, Jen_US
dc.contributor.authorAalders, MCGen_US
dc.contributor.authorWilliams, SEen_US
dc.contributor.authorMukherjee, Ren_US
dc.contributor.authorO'Neill, Len_US
dc.contributor.authorChubb, Hen_US
dc.contributor.authorTschabrunn, Cen_US
dc.contributor.authorAnter, Een_US
dc.contributor.authorCamporota, Len_US
dc.contributor.authorNiederer, Sen_US
dc.contributor.authorRoujol, Sen_US
dc.contributor.authorBishop, MJen_US
dc.contributor.authorWright, Men_US
dc.contributor.authorSilberbauer, Jen_US
dc.contributor.authorRazavi, Ren_US
dc.contributor.authorO'Neill, Men_US
dc.date.accessioned2022-05-17T10:42:06Z
dc.date.available2021-09-20en_US
dc.date.issued2021en_US
dc.identifier.issn2297-055Xen_US
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/78450
dc.description.abstractBackground: The majority of data regarding tissue substrate for post myocardial infarction (MI) VT has been collected during hemodynamically tolerated VT, which may be distinct from the substrate responsible for VT with hemodynamic compromise (VT-HC). This study aimed to characterize tissue at diastolic locations of VT-HC in a porcine model. Methods: Late Gadolinium Enhancement (LGE) cardiovascular magnetic resonance (CMR) imaging was performed in eight pigs with healed antero-septal infarcts. Seven pigs underwent electrophysiology study with venous arterial-extra corporeal membrane oxygenation (VA-ECMO) support. Tissue thickness, scar and heterogeneous tissue (HT) transmurality were calculated at the location of the diastolic electrograms of mapped VT-HC. Results: Diastolic locations had median scar transmurality of 33.1% and a median HT transmurality 7.6%. Diastolic activation was found within areas of non-transmural scar in 80.1% of cases. Tissue activated during the diastolic component of VT circuits was thinner than healthy tissue (median thickness: 5.5 mm vs. 8.2 mm healthy tissue, p < 0.0001) and closer to HT (median distance diastolic tissue: 2.8 mm vs. 11.4 mm healthy tissue, p < 0.0001). Non-scarred regions with diastolic activation were closer to steep gradients in thickness than non-scarred locations with normal EGMs (diastolic locations distance = 1.19 mm vs. 9.67 mm for non-diastolic locations, p < 0.0001). Sites activated late in diastole were closest to steep gradients in tissue thickness. Conclusions: Non-transmural scar, mildly decreased tissue thickness, and steep gradients in tissue thickness represent the structural characteristics of the diastolic component of reentrant circuits in VT-HC in this porcine model and could form the basis for imaging criteria to define ablation targets in future trials.en_US
dc.format.extent744779 - ?en_US
dc.languageengen_US
dc.relation.ispartofFront Cardiovasc Meden_US
dc.rightsCreative Commons Attribution License
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.subjectcardiovascular magnetic resonanceen_US
dc.subjectlate gadolinium enhancementen_US
dc.subjectmechanical circulatory supporten_US
dc.subjectvenous-arterial extra corporeal membrane oxygenation (VA-ECMO)en_US
dc.subjectventricular tachycardiaen_US
dc.titleLate Gadolinium Enhancement Cardiovascular Magnetic Resonance Assessment of Substrate for Ventricular Tachycardia With Hemodynamic Compromise.en_US
dc.typeArticle
dc.rights.holder© 2021 Whitaker, Neji, Kim, Connolly, Aubriot, Calvo, Karim, Roney, Murfin, Richardson, Morgan, Ismail, Harrison, de Vos, Aalders, Williams, Mukherjee, O'Neill, Chubb, Tschabrunn, Anter, Camporota, Niederer, Roujol, Bishop, Wright, Silberbauer, Razavi and O'Neill.
dc.identifier.doi10.3389/fcvm.2021.744779en_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/34765656en_US
pubs.notesNot knownen_US
pubs.publication-statusPublished onlineen_US
pubs.volume8en_US
dcterms.dateAccepted2021-09-20en_US
rioxxterms.funderDefault funderen_US
rioxxterms.identifier.projectDefault projecten_US


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