Nonischemic dilated cardiomyopathy prognosis
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The natural history and prognosis of cardiomyopathies varies depending on the underlying aetiology of the disorder.17 Cardiomyopathies can be broadly characterised into five key sub-groups, all of which may benefit from the use of CMRI: Dilated cardiomyopathy (DCM): DCM is reportedly the most common phenotype of cardiomyopathy. It is defined as left ventricular dilatation and systolic ...
SEVERITY OF MITRAL REGURGITATION – POOR PROGNOSTIC …
DILATED NONISCHEMIC CARDIOMYOPATHY . Raluca Ianula1, Mădălina Daşoveanu1, Eduard Ovricenco1, Anca Popa1, Cătălina Andrei1, Anca Mihăilescu2, Crina Sinescu1 . 1Cardiology Clinic, Bagdasar-Arseni Emergency Clinic Hospital, Bucharest. 2Cardiolgy Clinic, Colţea Clinic Hospital . Summary. The purpose of this paper is to detect predicting factors of uneventful survival in patients …
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Nonischemic dilated cardiomyopathy (DCM) is a common heart disease, associated with high risk of progressive heart failure, arrhythmia and sudden cardiac death. In a large proportion of patient, DCM has a genetic etiology and a familial transmission. Compared to other cardiomyopathies, such as hypertrophic cardiomyopathy, a large number of mutant genes and alleles have been associated with DCM ...
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The Heart Failure Origin & Ontology Task (HOOT) Project – Using Ontology Development to Categorize and Analyze Clinical Data with Nonischemic Dilated Cardiomyopathy. AMIA Summit on Translational Bioinformatics, March 12-15, 2008, San Francisco, CA.
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Chronic coronary heart disease Heart failure Congenital heart disease Neurological disorders Structurally normal hearts Sudden infant death syndrome Cardiomyopathies Dilated cardiomyopathy Hypertrophic cardiomyopathy Arrhythmogenic right ventricular cardiomyopathy bpm = beats per minutes; LBBB = left bundle-branch block; ms = milliseconds; s = seconds; VT = ventricular tachycardia.
[DOC File]Myocardial Fibrosis in Brugada Syndrome Demonstrated by ...
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Brugada syndrome; Cardiac magnetic resonance; Cardiomyopathy; Late gadolinium enhancement; Arrhythmogenic right ventricular cardiomyopathy Introduction. The Brugada syndrome (BrS) is an inherited arrhythmia syndrome characterised by ST-segment elevation in the right precordial ECG leads. It is associated with ventricular fibrillation (VF) and sudden cardiac death (SCD) in the absence of …
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A total of 314 new cases of cardiomyopathy were reported during the 10-year study period: 184 cases of DCM (58.6%), 80 cases of HCM (25.5%), 42 cases of unclassified cardiomyopathy (13.4%), and 8 cases of restrictive cardiomyopathy (2.5%). Of 42 children with unclassified cardiomyopathy, 29 had LVNC (9.2% of all cases), 9 had cardiac hypertrophy with initially impaired systolic function, 2 had ...
[DOCX File]The Role Of Cardiovascular Magnetic Resonance Imaging In ...
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Cardiomyopathy . Cardio-oncology. Prognosis . Introduction. Heart failure (HF) can be defined haemodynamically as any abnormality of cardiac structure or function resulting in a failure to deliver oxygen at a rate adequate for tissue requirements, despite normal filling pressures – or only at the expense of increased . filling pressures [1](Ponikowski et al., 2016). Around half of HF ...
[DOC File]Michele Emdin, MD, PhD
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Late gadolinium enhancement as a predictor of functional recovery, need for defibrillator implantation and prognosis in non-ischemic dilated cardiomyopathy. Barison A, Aimo A, Ortalda A, Todiere G, Grigoratos C, Passino C, Camici PG, Aquaro GD, Emdin M. Int J Cardiol. 2018 Jan 1;250:195-200. doi: 10.1016/j.ijcard.2017.10.043. Epub 2017 Oct 19 ...
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Dilated cardiomyopathy (DCM) is defined as ‘left ventricular or biventricular systolic dysfunction and dilatation that is not explained by abnormal loading conditions or coronary artery disease.’ (1) It is recognised to be a spectrum of clinical states rather than a single entity; the prevalence of DCM is 1 in 2500 with an incidence of 7 in 100,000. (2) (Image 1) Image 1. The DCM disease ...
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