Results 161 to 170 of about 73,611 (316)
ABSTRACT Background Pulmonary vein stenosis (PVS) is an uncommon but serious complication of atrial fibrillation (AF) ablation, often misinterpreted as primary pulmonary disease. Timely identification is essential to prevent irreversible injury and to guide appropriate referral for interventional management. Case Presentations Through the discussion of
Cristina Aurigemma +14 more
wiley +1 more source
ABSTRACT Impedance‐guided PulseSelect contact mapping (i‐Pulse) adapts EnSite X Contact Index for a circular multielectrode PFA catheter, enabling real‐time visualization of electrode–tissue contact without fluoroscopy. With ICE guidance, Δimpedance > 5% identified adequate contact, standardized tagging, and guided applications in three atrial ...
Kennosuke Yamashita +5 more
wiley +1 more source
Poland Syndrome With Dextrocardia: A Rare Association Leading to Complex Cardiopulmonary Challenges
ABSTRACT Patients with Poland syndrome, especially those with left‐sided defects accompanied by dextrocardia, may be predisposed to significant respiratory and cardiac complications. This case underscores the importance of early recognition, thorough cardiopulmonary assessment, and proactive planning for airway management and ventilatory support to ...
Sai Kommineni +4 more
wiley +1 more source
ABSTRACT Mitral valve papillary muscle rupture represents a rare yet critical complication of acute myocardial infarction, often leading to severe mitral regurgitation and subsequent pulmonary edema with high mortality. Despite optimal ventilatory support and pharmacological management, patients often exhibit refractory hypoxemia, rendering surgical ...
Zhenjiang Liu
wiley +1 more source
OPERATIVE CORRECTION OF TOTAL LEFT ANOMALOUS PULMONARY VENOUS RETURN WITHOUT ATRIAL SEPTAL DEFECT
Masatake Takagi +5 more
openalex +2 more sources
Echocardiography-based AI for detection and quantification of atrial septal defect [PDF]
Xixiang Lin +16 more
openalex +1 more source
Metabolic Stroke: Atypical Presentation of Succinic Semialdehyde Dehydrogenase Deficiency
ABSTRACT Succinic semialdehyde dehydrogenase (SSADH) deficiency is a rare autosomal recessive neurometabolic disorder caused by biallelic pathogenic variants in ALDH5A1, encoding the mitochondrial enzyme SSADH. This enzyme catalyses the conversion of succinic semialdehyde to succinic acid in the γ‐aminobutyric acid (GABA) degradation pathway.
Sharmila Kiss +10 more
wiley +1 more source

