Results 31 to 40 of about 8,451,399 (181)

Novel genes for QTc interval. How much heritability is explained, and how much is left to find? [PDF]

open access: yes, 2010
The corrected QT (QTc) interval is a complex quantitative trait, believed to be influenced by several genetic and environmental factors. It is a strong prognostic indicator of cardiovascular mortality in patients with and without cardiac disease.
Spector, Timothy D.   +9 more
core   +1 more source

Acquired long QT interval in athletes [PDF]

open access: yes, 2022
Long QT syndrome (LQTS) is a common disorder that leads to dramatic patient outcomes, chief among which is sudden cardiac death. This review provides detailed data on the diagnosis, prevalence, classification, etiology.
A. S. Yunisova, A. V. Smolensky
core   +1 more source

CLINICAL SIGNIFICANCE OF DRUGINDUCED INTERVALS QT AND QTC PROLONGATION

open access: yesРациональная фармакотерапия в кардиологии, 2015
Interval QT prolongation is a predictor of the life-threatening cardiac arrhythmias — polymorphic ventricular tachycardia (torsade de pointes). Long QT syndrome may be congenital or acquired.
N. V. Furman, S. S. Shmatova
doaj   +3 more sources

Torsades de pointes during laparoscopic adrenalectomy of a pheochromocytoma: a case report

open access: yesJournal of Medical Case Reports, 2011
Introduction Torsades de pointes is a rare but potentially lethal arrhythmia. The amount of literature available on Torsades de pointes occurring in patients with pheochromocytoma is limited, and we found no literature describing this dysrhythmia in a ...
Wiesfeld Ans CP   +4 more
doaj   +1 more source

Prevalence of Long QT Syndrome in Children with Congenital Sensory-Neural Deafness

open access: yesJournal of Ardabil University of Medical Sciences, 2021
Background & objectives: Long QT syndrome (LQTS), congenital or acquired disorder, is characterized by a prolonged QT interval associated with syncope attacks and sudden death.
Ahmad Jamei Khosroshahi   +4 more
doaj  

Defying the Odds of Sudden Cardiac Death in Hypertrophic Cardiomyopathy

open access: yesJACC: Case Reports, 2020
We report an unusual case of a patient with hypertrophic obstructive cardiomyopathy, anomalous aortic origin of a coronary artery, obesity hypoventilation syndrome, and acquired long QT syndrome who was able to defy the odds of sudden cardiac death in ...
Ara H. Rostomian, MD, MPH, MBA   +2 more
doaj   +1 more source

Prolonged QT Interval in Cirrhosis: Twisting Time?

open access: yesGut and Liver, 2022
Approximately 30% to 70% of patients with cirrhosis have QT interval prolongation. In patients without cirrhosis, QT prolongation is associated with an increased risk of ventricular arrhythmias, such as torsade de pointes (TdP).
William Lee   +3 more
doaj   +1 more source

Human Engineered Heart Tissues Reproduce Trigger‐ and Substrate‐Driven Mechanisms of Ventricular Tachycardia

open access: yesAdvanced Science, EarlyView.
Engineered heart tissues (EHTs) derived from human iPSCs replicate mechanisms of ventricular tachycardia at the tissue level. Acquired Long‐QT conditions cause early afterdepolarizations, wavebreak, and transient rotors; in contrast, focal cryoinjury forms a stable substrate that supports ongoing reentry.
Matthew Fiedler   +4 more
wiley   +1 more source

Long QT syndrome ECG analysis

open access: yes, 2019
Automated analysis of ECGs obtained from patients with long QT ...
Andrew Li (411246)   +11 more
core   +2 more sources

QT interval prolongation in Takotsubo syndrome: a frightening feature with no major prognostic impact

open access: yesMonaldi Archives for Chest Disease, 2023
Despite the frequent and often severe repolarization abnormalities seen in Takotsubo syndrome (TTS), the underlying mechanism of life-threatening arrhythmias is incompletely understood, and the risk remains uncertain. TTS is considered a potential cause
Ana Isabel Pinho   +8 more
doaj   +1 more source

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