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Hypertrophic cardiomyopathy and atrial fibrillation: the Cardiomyopathy/Myocarditis Registry of the EURObservational Research Programme of the European Society of Cardiology

Open Heart

Background Hypertrophic cardiomyopathy (HCM) is commonly associated with atrial fibrillation (AF), but its impact on outcomes in real-world practice is uncertain. years) were enrolled in the EURObservational Research Programme (EORP) Cardiomyopathy/Myocarditis Registry. Methods Overall, 1739 adult patients with HCM (40.9%

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Late-gadolinium enhancement predicts appropriate device therapies in non-ischemic recipients of primary prevention implantable cardioverter-defibrillators

HeartRhythm

Better risk stratification is needed to evaluate patients with non-ischemic cardiomyopathy (NICM) for prophylactic implantable cardioverter-defibrillators (ICD). Growing evidence suggests cardiac magnetic resonance imaging (CMR) may be useful in this regard.

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Ventricular Fibrillation, ICD, LBBB, QRS of 210 ms, Positive Smith Modified Sgarbossa Criteria, and Pacemaker-Mediated Tachycardia

Dr. Smith's ECG Blog

He was defibrillated, but they also noticed that he was being internally defibrillated and then found that he had an implantable ICD. He was unidentified and there were no records available After 7 shocks, he was successfully defibrillated and brought to the ED. Bedside US shows extremely poor EF with dilated cardiomyopathy.

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PO-02-115 PREDICTORS OF APPROPRIATE AND INAPPROPRIATE THERAPY WITH PRIMARY PREVENTION IMPLANTABLE CARDIOVERTER DEFIBRILLATORS IN PATIENTS WITH NONISCHEMIC CARDIOMYOPATHY IN A RACIALLY AND ETHNICALLY DIVERSE POPULATION

HeartRhythm

In contrast to primary prevention implantable cardioverter defibrillators (ICD) in ischemic cardiomyopathy, the data supporting ICD placement in patients with non-ischemic cardiomyopathy (NICM) is less robust. Moreover, there is scarce data about risk factors for appropriate and inappropriate therapy in diverse populations.

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Case Report: Four cases of cardiac sarcoidosis in patients with inherited cardiomyopathy—a phenotypic overlap, co-existence of two rare cardiomyopathies or a second-hit disease

Frontiers in Cardiovascular Medicine

Cardiac sarcoidosis (CS), a rare condition characterized by non-caseating granulomas, can manifest with symptoms such as atrioventricular block and ventricular tachycardia (VT), as well as mimic inherited cardiomyopathies. A 58-year-old woman presented with sustained VT with a prior diagnosis of hypertrophic cardiomyopathy (HCM).

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PO-01-015 RATE OF APPROPRIATE AND INAPPROPRIATE THERAPY IN PATIENTS WITH NON-ISCHAEMIC CARDIOMYOPATHY – A COMPARISON BETWEEN PRIMARY AND SECONDARY PREVENTION IMPLANTABLE CARDIOVERTER-DEFIBRILLATOR PATIENTS

HeartRhythm

Implantable cardioverter defibrillators (ICD) have proved their favourable outcomes on survival in selected patients with cardiomyopathy. However, recent studies have questioned the protective role of ICD in non-ischemic cardiomyopathy (NICM) for primary prevention.

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PO-07-069 OUTCOMES OF VENTRICULAR TACHYCARDIA ABLATION IN CHAGASIC CARDIOMYOPATHY

HeartRhythm

Chagasic cardiomyopathy has been associated with high defibrillator shock rates and poor clinical outcomes. The benefits of VT ablation in patients with Chagasic cardiomyopathy have been evaluated in only a few studies. Chagas disease is an endemic condition in Latin America.