Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, 2016 BackgroundSupraventricular tachycardia (SVT) is common in complex congenital heart disease (CCHD) patients with single‐ventricle physiology and may cause hemodynamic deterioration.
Shuenn‐Nan Chiu +5 more
doaj +1 more source
Safety and prognostic value of left ventricular endomyocardial biopsy in dilated cardiomyopathy
European Journal of Heart Failure, EarlyView.Safety and prognostic value of left ventricular endomyocardial biopsy in dilated cardiomyopathy. CVF, left ventricular collagen volume fraction; DCM, dilated cardiomyopathy; EMB, endomyocardial biopsy; LV, left ventricular. Aims The need to perform endomyocardial biopsy (EMB) in patients with non‐ischaemic dilated cardiomyopathies (DCM) is debated ...
Elham Kayvanpour +15 more
wiley +1 more source
Narrow QRS Tachycardia with Alternate Wide QRS Beats: What is the Mechanism?
Indian Pacing and Electrophysiology Journal, 2008 A 44-year old lady underwent electrophysiology study for recurrent palpitations and documented narrow QRS regular tachycardia. The baseline ECG showed subtle preexcitation that was easily manifest on atrial pacing.
Kartikeya Bhargava +2 more
doaj
Endless loop tachycardia below the upper tracking rate of a pacemaker: A case report
Journal of Arrhythmia, 2012 An 82-year-old female with a history of hypertrophic cardiomyopathy (HCM), sick sinus syndrome (SSS), and an implanted DDD pacemaker was admitted to our hospital for congestive heart failure caused by rapid atrial fibrillation.
Atsushi Sakamoto +12 more
doaj +1 more source
Circus movement in rabbit atrial muscle as a mechanism of tachycardia. II. The role of nonuniform recovery of excitability in the occurrence of unidirectional block, as studied with multiple microelectrodes. [PDF]
, 1976 Maurits A. Allessie +2 more
openalex +1 more source
Impact of genotype–phenotype associations on prognosis in dilated cardiomyopathy
European Journal of Heart Failure, EarlyView.Prediction of clinical outcomes in genetic dilated cardiomyopathy (DCM). LVEF, left ventricular ejection fraction. Aims Dilated cardiomyopathy (DCM) has a monogenic aetiology in up to 40% of patients. Understanding the spectrum of genotype–phenotype associations in DCM is crucial for risk stratification and personalized treatment.
Sophie L.V.M. Stroeks +27 more
wiley +1 more source
Deep phenotyping of heart failure with preserved ejection fraction through multi‐omics integration
European Journal of Heart Failure, EarlyView.Deep phenotyping of of heart failure with preserved ejection fraction (HFpEF) through multi‐omics integration. AI, artificial intelligence. Aims Heart failure with preserved ejection fraction (HFpEF) has become the predominant form of heart failure and a leading cause of global cardiovascular morbidity and mortality.
Jakob Versnjak +15 more
wiley +1 more source
Symptomatic giant left atrial aneurysm in a child : a rare entity [PDF]
, 2010 Isolated left atrial aneurysms are rare entities in clinical practice. Usually the condition is diagnosed in the second to fourth decades of life. The presence of such lesions in the pediatric age group is scantily described.
Awasthy, Neeraj +4 more
core +1 more source
Demonstration of sustained sinus and atrial re-entry as a mechanism of paroxysmal supraventricular tachycardia. [PDF]
, 1975 Dexi Wu +5 more
openalex +1 more source
European Journal of Heart Failure, EarlyView.Heart failure (HF) and atrial fibrillation (AF) are major global health challenges with rising prevalence and significant morbidity, mortality, and healthcare burden. Despite advances in HF management, AF remains a critical comorbidity that worsens outcomes and requires ad hoc treatment strategies, increasing the risk of non‐adherence and side effects.
Mark Luedde +24 more
wiley +1 more source