Wolff–parkinson–white (Wpw) Syndrome
Basics
Basics
Basics
Description
Description
- Syndrome resulting from the presence of an abnormal (accessory) pathway that bypasses the AV node (Kent bundles) between the atria and ventricles
- Wolff–Parkinson–White (WPW) pattern on the ECG is defined by a short PR interval and a Δ-wave reflecting early conduction (pre-excitation):
- Accessory pathways occur in 0.1–0.3% of the population
- WPW syndrome requires ECG evidence of the accessory pathway and related tachycardia
- Accessory pathways:
- Small bands of tissue that failed to separate during development:
- Left lateral (free wall) accessory pathway: Most common
- The posteroseptal region of the AV groove: Second most common location
- Right free wall
- Anteroseptal
- Conduction in WPW may be antegrade, retrograde, or both
- Orthodromic re-entrant tachycardia is the most common (70%):
- Impulse travels antegrade from the atria down the AV node to the ventricle and then retrograde up the accessory pathway
- This re-entrant tachycardia is a narrow complex rhythm unless a bundle branch block or intraventricular conduction delay is present
- Antidromic is less common (30%):
- Impulse travels antegrade down the accessory pathway and retrograde through the AV node resulting in a wide quasi-random signal (QRS) complex
- Sudden death occurs in 1 per 1,000 patient-years in persons with known ventricular pre-excitation
Etiology
Etiology
- Idiopathic:
- Unknown mechanism in most cases, with familial predisposition
- Rarely inherited as an autosomal dominant trait
- Associated in rare cases with a familial hypertrophic cardiomyopathy
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