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dc.contributor.authorRodrigues, Pen_US
dc.contributor.authorJoshi, Aen_US
dc.contributor.authorWilliams, Hen_US
dc.contributor.authorWestwood, Men_US
dc.contributor.authorPetersen, SEen_US
dc.contributor.authorZemrak, Fen_US
dc.contributor.authorSchilling, RJen_US
dc.contributor.authorKirkby, Cen_US
dc.contributor.authorWragg, Aen_US
dc.contributor.authorManisty, Cen_US
dc.contributor.authorMohiddin, Sen_US
dc.date.accessioned2017-12-05T09:26:45Z
dc.date.available2017-11-01en_US
dc.date.issued2017-12en_US
dc.date.submitted2017-11-11T16:58:02.969Z
dc.identifier.urihttp://qmro.qmul.ac.uk/xmlui/handle/123456789/29083
dc.description.abstractBACKGROUND: Determining the pathogenesis of sudden cardiac arrest or periarrest without significant coronary artery disease is crucial for management and prognosis. Cardiovascular magnetic resonance (CMR) can detect morphological, functional, or tissue abnormalities, and we sought to evaluate the role of CMR in determining sudden cardiac arrest pathogenesis and prognosis in survivors. METHODS AND RESULTS: We retrospectively reviewed cardiac investigations and clinical outcomes in consecutive survivors of potentially fatal arrhythmias without coronary artery disease admitted to our institutions from 2008 to 2014. After coronary angiography and echocardiography, all underwent CMR and, when indicated, electrophysiology studies. Major adverse cardiac events (MACE), comprising significant nonfatal ventricular arrhythmia or death, was the primary outcome. Of 164 included subjects (65% men; mean age 48 [18-80] years), CMR contributed to the diagnosis in 80 (49%) and was decisive in 50 cases (30%). Dilated cardiomyopathy (n=27), myocarditis or sarcoidosis (n=22), occult myocardial infarction (n=13), and hypertrophic cardiomyopathy (n=9) were most frequent. Arrhythmic causes were found in 14% while no cause was identified in 36%. MACE occurred in 31% of subjects during a median follow-up of 32 months. MACE associated with presence of a CMR diagnosis, extent of late gadolinium enhancement, and left and right ventricular ejection fractions. Right ventricular ejection fraction was an independent predictor of MACE. CONCLUSIONS: CMR identified a likely pathogenesis for sudden cardiac arrest in nearly half of survivors in whom coronary artery disease had been excluded. One in 3 subjects had MACE; risk doubled in those with a CMR diagnosis and some CMR parameters-late gadolinium enhancement, left ventricular ejection fraction, and especially right ventricular ejection fraction-associated with prognosis.en_US
dc.description.sponsorshipCM is supported by the University College London Hospitals National Institute for Health Research (NIHR) Cardiovascular Biomedical Research Centre. SEP acknowledges support from the National Institute for Health Research (NIHR) Cardiovascular Biomedical Research Unit at Barts.en_US
dc.format.extente006709 - ?en_US
dc.languageengen_US
dc.language.isoenen_US
dc.relation.ispartofCirc Cardiovasc Imagingen_US
dc.subjectarrhythmias, cardiacen_US
dc.subjectcoronary artery diseaseen_US
dc.subjectdeath, sudden, cardiacen_US
dc.subjectheart arresten_US
dc.subjectmagnetic resonance imagingen_US
dc.subjectprognosisen_US
dc.subjectAdolescenten_US
dc.subjectAdulten_US
dc.subjectAgeden_US
dc.subjectAged, 80 and overen_US
dc.subjectCoronary Artery Diseaseen_US
dc.subjectDeath, Sudden, Cardiacen_US
dc.subjectFemaleen_US
dc.subjectHearten_US
dc.subjectHumansen_US
dc.subjectMagnetic Resonance Imagingen_US
dc.subjectMaleen_US
dc.subjectMiddle Ageden_US
dc.subjectPrognosisen_US
dc.subjectReproducibility of Resultsen_US
dc.subjectRetrospective Studiesen_US
dc.subjectSurvivorsen_US
dc.subjectYoung Adulten_US
dc.titleDiagnosis and Prognosis in Sudden Cardiac Arrest Survivors Without Coronary Artery Disease: Utility of a Clinical Approach Using Cardiac Magnetic Resonance Imaging.en_US
dc.typeArticle
dc.rights.holder© 2017 American Heart Association, Inc
dc.identifier.doi10.1161/CIRCIMAGING.117.006709en_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/29237609en_US
pubs.issue12en_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
pubs.volume10en_US
dcterms.dateAccepted2017-11-01en_US


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