Results 41 to 50 of about 3,843,249 (204)

Emergency treatment of Wolff-Parkinson-White syndrome

, 2011
This article describes the aetiology of Wolff-Parkinson-White syndrome and discusses the benefits and disadvantages of some of the available cardioversion medications with which it can be ...
Brace, Samantha J., Brace, Samantha
core   +1 more source

The coexistence of Wolff-Parkinson-White syndrome (WPW) and atrioventricular nodal reentrant tachycardia (AVNRT)

Turkish Journal of Emergency Medicine, 2018
Atrioventricular nodal reentrant tachycardia (AVNRT) is the most common type of reentrant paroxysmal supraventricular tachycardia that occurs in the presence of dual AV nodal physiology.
Ali Elitok, Gökhan Aksan, Mehmet Rasih Sonsöz, Mehmet Tezcan, Özgür Çevrim   +4 more
doaj   +1 more source

Left ventricular noncompactation and pre-excitation: an unusual finding in adults

Clinical and Biomedical Research, 2017
Left ventricular noncompaction (LVNC) is a rare form of cardiomyopathy characterized by prominent left ventricular (LV) trabeculae, deep intertrabecular recesses, and the thin compacted layer.
Diego Chemello, Fernando Pivatto Júnior
doaj   +2 more sources

Utility of unipolar recordings for complex Wolff–Parkinson–White ablation

Indian Pacing and Electrophysiology Journal, 2015
Radiofrequency ablation has been shown to be a safe and effective treatment strategy for the management of symptomatic patients with Wolff–Parkinson–White syndrome. It is supported by a success rate of 95% and a recurrence rate of less than 5%.
Ponnusamy Shunmuga Sundaram, Jasbir Sra
doaj   +1 more source

Wolff-Parkinson-White Syndrome

AACN Advanced Critical Care
Chhabra L, Goyal A, Benham MD.
europepmc   +3 more sources

Diagnostic Accuracy of 12‐Lead ECG Algorithms for Accessory Pathway Localization in WPW: A Meta‐Analysis

Pacing and Clinical Electrophysiology, EarlyView.
ABSTRACT Background In Wolff–Parkinson–White (WPW) syndrome, accurate localization of accessory pathways before catheter ablation can improve procedural planning and efficiency. Several 12‐lead electrocardiographic (ECG) algorithms have been proposed, but their diagnostic performance has not been consistently established.
Elsayed S. Moubarak, Ahmed Farid Gadelmawla, Almothana Manasrah, Anas Mansour, Mohamed S. Elgendy, Omar Elkoumi, Husam Abu Suilik, Suhaib El Khatib, Naser Albekaen, Ahmed Moustafa, Rania Samir, Islam Saboukh, Nadica Trajkovska, Angeliki Darma, Vanessa Sciacca, Thomas Fink, Moneeb Khalaph, Christian Sohns, Philipp Sommer, Hassan El‐Shirbiny   +19 more
wiley   +1 more source

Epidemiological profile of Wolff-Parkinson-White syndrome in a general population younger than 50 years of age in an era of radiofrequency catheter ablation

, 2017
Background: The prevalence of Wolff-Parkinson-White (WPW) syndrome varies between 0.68 and 1.7/1000. The epidemiological profile may be modified after the introduction of transcatheter interventions.
Lu, Chun-Wei;Wu, Mei-Hwan;Chen, Hui-Chi;Kao, Feng-Yu;Huang, San-Kuei, 盧俊維;吳美環   +1 more
core   +1 more source

Anaesthetic Techniques for Cardiac Ablation—A Scoping Review

Acta Anaesthesiologica Scandinavica, Volume 70, Issue 9, October 2026.
ABSTRACT Background Cardiac arrhythmias, particularly atrial fibrillation, have rising prevalence and represent a growing global health burden. Catheter ablation is a commonly used treatment demanding sedation or anaesthesia for comfort, stability and safety. Anaesthetic techniques vary globally, and the optimal strategy has yet to be determined.
Mathilde Bang Fredensborg, Anne Færgemand Præstegaard, Sebastian Bach Fiege, Ann M. Møller   +3 more
wiley   +1 more source

Socioeconomic Status, Race, and Ethnicity in Management of Pediatric Supraventricular Tachycardia

Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
Background An electrophysiology study (EPS) with ablation is often the preferred approach to management of supraventricular tachycardia (SVT) and/or preexcitation (Wolff‐Parkinson‐White syndrome) in children and adolescents.
Karina Javalkar, Lynn A. Sleeper, Jane Newburger, Audrey Dionne   +3 more
doaj   +1 more source

Expanding the Phenotype of TUFM ‐Related Combined Oxidative Phosphorylation Deficiency 4

American Journal of Medical Genetics Part A, Volume 200, Issue 8, Page 1884-1889, August 2026.
ABSTRACT Combined oxidative phosphorylation deficiency 4 (COXPD4) is a rare mitochondrial condition caused by biallelic deleterious variants in the nuclear‐encoded gene TUFM. To date, most individuals with COXPD4 have presented with encephalopathy, hypotonia, and abnormal brain imaging. Many of the reported individuals died in infancy. We aim to expand
Noémie Villeneuve‐Cloutier, Jodi Warman‐Chardon, Danielle K. Bourque   +2 more
wiley   +1 more source