Results 211 to 220 of about 53,129 (300)

NKX2-5 Mutation and ICD Implantation in a Pregnant AV Block Patient. [PDF]

open access: yesJACC Case Rep
Alhmouz MM   +7 more
europepmc   +1 more source

Outcomes of Focused Double Extrastimuli Mapping and Ablation in Ventricular Tachycardia

open access: yesJournal of Cardiovascular Electrophysiology, Volume 37, Issue 1, Page 137-148, January 2026.
ABSTRACT Background Conventional substrate mapping for scar‐related ventricular tachycardia (VT) often fails to fully delineate critical arrhythmogenic components. Functional mapping strategies using extrastimuli have shown promise but are limited by procedural complexity.
Surachat Jaroonpipatkul   +6 more
wiley   +1 more source

Effects of Intraoperative Ventilation Strategies on Ventilation Inhomogeneity and Inflammatory Response in Pediatric Cardiac Surgery—A Randomized Pilot Study

open access: yesPediatric Anesthesia, Volume 36, Issue 1, Page 88-99, January 2026.
ABSTRACT Background Respiratory arrest during cardiopulmonary bypass (CPB) in pediatric cardiac surgery risks lung dysfunction including derecruitment, atelectasis, and inflammation. Continuous positive airway pressure (CPAP) and lung‐protective ventilation (LPV) during aortic cross‐clamping show inconsistent results in mitigating these risks.
Charlotte Billstein   +7 more
wiley   +1 more source

Mid-Term Functional Recovery after Surgical Correction of ALCAPA: A 16-Year Single-Center Experience. [PDF]

open access: yesAnn Thorac Cardiovasc Surg
Beyter MB   +7 more
europepmc   +1 more source

Heart block in repair of ventricular septal defect: Reply

open access: yesThe Journal of Thoracic and Cardiovascular Surgery, 1974
openaire   +1 more source

Hope in Miniature: The First Case of Implantation of a “Tiny Pacemaker” in Italy as a Successful Treatment for Congenital Atrioventricular Block in a Low Birth Weight Child

open access: yesCase Reports in Cardiology, Volume 2026, Issue 1, 2026.
Congenital complete atrioventricular block (CAVB) is a rare cardiac condition occurring in approximately one in 15,000 to one in 22,000 live births. Maternal autoimmune diseases, with anti‐ssA (Ro) and anti‐ssB (La) antibodies implicated in 56%–90% of cases, are primary causes.
Ferrari Paola   +5 more
wiley   +1 more source

Syndromic Congenital Heart Disease Diagnosed in Adulthood: A Reminder of the Phenotypic Variability of Alagille Syndrome

open access: yesCase Reports in Cardiology, Volume 2026, Issue 1, 2026.
Alagille syndrome is a rare multisystemic genetic condition most commonly associated with neonatal liver disease. Variable expressivity is a defining feature of Alagille syndrome, resulting in a broad spectrum of phenotypic variation among individuals who meet the diagnostic criteria. We present an atypical case of cardiac‐predominant Alagille syndrome
Matthew K. Campbell   +4 more
wiley   +1 more source

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