Results 171 to 180 of about 86,432 (312)

Reel syndrome in a patient with an implantable cardioverter-defibrillator

CorSalud, 2018
The Twiddler syndrome and its variant, the Reel syndrome, are uncommon complications in patients with an implantable cardioverter-defibrillator, but they can cause severe device dysfunction.
Marleny Cruz Cardentey, Jesús A. Castro Hevia, Osmín Castañeda Chirino, Roylán Falcón Rodríguez, Frank López Martínez   +4 more
doaj  

Efficiency of Exclusive Remote Monitoring in Pacemaker Follow‐Up

Pacing and Clinical Electrophysiology, EarlyView.
Markus Sane, Joel Ryynänen, Teemu Malmi, Pekka Raatikainen, Jarkko Karvonen   +4 more
wiley   +1 more source

Resistant to Ablation, Responsive to Hydroquinidine: Precision Medicine Guides Recovery in MEPPC Syndrome Cardiomyopathy

Journal of Arrhythmia, Volume 42, Issue 3, June 2026.
We report a case of MEPPC syndrome presenting with severe dilated cardiomyopathy due to a pathogenic SCN5A p.Arg814Trp variant. Genetic diagnosis enabled precision pharmacotherapy with hydroquinidine, which suppressed multifocal Purkinje‐origin ectopy resistant to catheter ablation and led to marked improvement in left ventricular function.
Jonathan L. Ciofani, Hariharan Raju, Malcolm Anastasius   +2 more
wiley   +1 more source

Canadian implantable defibrillator study (CIDS) : a randomized trial of the implantable cardioverter defibrillator against amiodarone.

Circulation, 2000
S. Connolly, M. Gent, R. Roberts, P. Dorian, Denis Roy, R. Sheldon, L. Mitchell, M. Green, G. Klein, B. O’Brien   +9 more
semanticscholar   +1 more source

Feasibility and Safety on Left Bundle Branch Area Pacing With Standard Stylet‐Driven Lead: ACHIEVE‐SYNC Multicenter Prospective Observational Cohort Study

Journal of Arrhythmia, Volume 42, Issue 3, June 2026.
In the prospective multicenter study, left bundle branch area pacing using stylet‐driven pacing leads demonstrated a high procedural success rate and showed stable lead performance during long‐term follow‐up. ABSTRACT Background Right ventricular pacing increases the risk of dyssynchrony, which raises the need for more physiological pacing strategies ...
Ga‐In Yu, So‐Ryoung Lee, Tae‐Hoon Kim, Min Soo Cho, Daehoon Kim, Hee Tae Yu, Jung‐Myung Lee, Jae‐Sun Uhm, Eue‐Keun Choi, Jun Kim, Boyoung Joung, Hui‐Nam Pak, Moon‐Hyoung Lee   +12 more
wiley   +1 more source

Implantable Cardioverter-Defibrillator for Nonischemic Cardiomyopathy: An Updated Meta-Analysis.

Circulation, 2017
H. Golwala, N. Bajaj, G. Arora, P. Arora
semanticscholar   +1 more source

Twiddler's syndrome in extravascular implantable cardioverter-defibrillator: a case report. [PDF]

Eur Heart J Case Rep
Measom A, Collard R, Chelliah R, Dhutia H, Sze S.   +4 more
europepmc   +1 more source

Cardiovascular Health in Women—Across the Lifespan

Clinical Endocrinology, Volume 104, Issue 6, Page 539-555, June 2026.
ABSTRACT Cardiovascular disease (CVD) remains the leading cause of mortality and morbidity among women worldwide. However, CVD continues to be perceived as a predominantly male issue. CVD in women therefore remains understudied, underrecognized and undertreated.
Jaya Chandrasekhar, Jessica Yao, Simone Gong, Madhuka Wijayarathne, Monique Watts, Swati Mukherjee   +5 more
wiley   +1 more source

Canadian Cardiovascular Society/Canadian Heart Rhythm Society 2016 Implantable Cardioverter-Defibrillator Guidelines.

Canadian Journal of Cardiology, 2017
M. Bennett, R. Parkash, P. Nery, M. Sénéchal, B. Mondésert, D. Birnie, L. Sterns, C. Rinne, D. Exner, F. Philippon, D. Campbell, J. Cox, P. Dorian, V. Essebag, A. Krahn, J. Manlucu, F. Molin, M. Slawnych, M. Talajic   +18 more
semanticscholar   +1 more source

Brugada Syndrome: New Implications for Heterozygous Carriers of the Pathogenic SCN5A c.689T>C(p.Ile230Thr) Variant

American Journal of Medical Genetics Part A, Volume 200, Issue 5, Page 1083-1086, May 2026.
ABSTRACT Pathogenic variants in the SCN5A gene and its subunits have been identified in individuals with Brugada Syndrome. One such SCN5A variant, c.689T>C(p.Ile230Thr), was previously reported as disease‐causing only in homozygous individuals, with heterozygous carriers being unaffected.
Shayla Shojaat, Benjamin Hale, Taylor Warner   +2 more
wiley   +1 more source