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A 76-year-old female visited the emergency department with complaining of dizziness and syncope. She had a history of paroxysmal atrial fibrillation (AF) and had been prescribed flecainide 50 mg and apixaban 5 mg 12-hourly in another hospital 1 day before the presentation. Upon admission, her electrocardiogram showed profound bradycardia and extremely long sinus arrest, which required temporary cardiac pacing. Within 24 hours, her intrinsic rhythm was restored, and the temporary pacemaker was removed. Transthoracic and transesophageal echocardiography revealed no structural heart disease or thrombus in the left atrial appendage. Cardiac computed tomography showed no coronary artery stenosis, but a pulmonary thrombus in the right pulmonary artery. She underwent an electrophysiology study, and four pulmonary vein (PV) isolations were attempted to treat the paroxysmal AF. A bidirectional PV conduction block was acquired in all PVs despite spontaneous dissociation of PV potential in the right PV. Programmed stimulation following ablation resulted in sinus node dysfunction. After the procedure, the patient did not complain of dizziness and syncope for 72 hours of telemetry monitoring. She was discharged with anticoagulant and did not show any further symptoms for 6 months. Flecainide acetate is a class Ic antiarrhythmics, and its clinical efficacy has been confirmed in several clinical trials. However, it can unmask sinus node dysfunction in asymptomatic patients with paroxysmal AF. Clinicians should screen candidates for sinus nodal diseases when prescribing flecainide.
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http://dx.doi.org/10.12793/tcp.2022.30.e19 | DOI Listing |
Medicine (Baltimore)
September 2025
Department of Intensive Care Unit, The Eighth Clinical Medical College of Guangzhou University of Chinese Medicine, Foshan Hospital of Traditional Chinese Medicine, Foshan City, Guangdong Province, China.
Rationale: Mental and behavioral abnormalities are difficult neurological conditions, and the site of the lesion may involve the basal ganglia. Its etiology is varied and requires a detailed differential diagnosis.
Patient Concerns: An 81-year-old woman had a history of "cerebral infarction" for 5 years.
JACC Case Rep
September 2025
Cardiology Department, CHU Clermont-Ferrand, Clermont-Ferrand, France; Université Clermont Auvergne, CHU Clermont-Ferrand, CNRS, SIGMA Clermont, Institut Pascal, Clermont-Ferrand, France.
Background: Cardiac syncope due to sinus arrest may result from either a vasovagal cardioinhibitory mechanism or an intrinsic sinus node dysfunction.
Case Summary: A 67-year-old woman with a recently diagnosed right hilar mass presented with new-onset episodes of syncope associated with sinus arrest. Resting electrocardiogram was normal, and no electrolyte abnormalities were identified.
Cureus
August 2025
Emergency Medicine Department, Charleston Area Medical Center, Charleston, USA.
Sudden cardiac death (SCD) in young individuals raises serious concern, prompting physicians to explore multiple etiologies. Coronary artery anomalies are rare congenital heart defects, affecting a small percentage of the population, and are a known cause of SCD in young individuals. We present a case of sudden cardiac arrest in a 36-year-old male athlete with an anomalous left main coronary artery (ALCA) arising from the right coronary sinus, a rare anomaly that has been associated with SCD in young athletes during intense exertion.
View Article and Find Full Text PDFCirc Arrhythm Electrophysiol
August 2025
Assistance Publique-Hôpitaux de Marseille, Centre Hospitalier Universitaire La Timone, Service de Cardiologie, France (B.M., J.-C.D.).
Background: Bradyarrhythmia is a common and potentially serious cause of syncope, often difficult to detect due to its intermittent nature. Traditional ECG monitoring methods either provide low diagnostic accuracy or delay diagnosis, increasing the risk of recurrence. We hypothesized that a deep learning-enabled, 24-hour, single-lead ECG could detect past episodes of bradyarrhythmia.
View Article and Find Full Text PDFCureus
July 2025
Acute Medicine, Northwick Park Hospital, London North West University Healthcare NHS Foundation Trust, London, GBR.
Long QT syndrome (LQTS) is a rare cardiac electrophysiological disorder that predisposes individuals to life-threatening arrhythmias such as torsades de pointes and ventricular fibrillation (VF). It may be congenital or acquired, with many cases triggered by specific medications or electrolyte disturbances. However, presentations in elderly individuals without prior cardiac history or drug exposure are exceedingly rare.
View Article and Find Full Text PDF