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Stokes-Adams syndrome, a rarely reported disease
Camilo Andrés Rincón Romero1, Sebastián Forero Amézquita2, Julio César Velasco Castro1
1Research Department, Hospital Regional de la Orinoquía, Yopal, Colombia.
The Journal of Medicine Access
|February 28, 2025
Summary
Stokes-Adams syndrome, a rare cause of syncope and seizures due to decreased cardiac output, requires prompt diagnosis. Pacemaker implantation effectively treated a patient with this condition, preventing recurrence.
Area of Science:
- Cardiology
- Neurology
Background:
- Stokes-Adams syndrome is a rare condition characterized by transient loss of consciousness and potential seizures, stemming from reduced cardiac output and subsequent cerebral hypoxia.
- Common causes include high-degree atrioventricular block, paroxysmal ventricular arrest, and pulseless ventricular tachycardia, often necessitating cardiac interventions.
Observation:
- A case study of a 78-year-old male patient presenting with Stokes-Adams syndrome secondary to 2:1 atrioventricular block was analyzed.
- The patient experienced syncopal and convulsive episodes attributed to the cardiac conduction abnormality.
Findings:
- Definitive pacemaker implantation was performed on the patient.
- Following pacemaker implantation, the patient experienced no recurrence of syncopal or convulsive episodes, indicating successful management.
Implications:
- Recognizing Stokes-Adams syndrome as a potential cause of syncope or seizures is crucial for timely diagnosis and intervention.
- Early identification through clinical history and paraclinical tests can prevent sudden death, a significant risk associated with this condition.
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