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ECG Diagnosis: Wolff-Parkinson-White Syndrome
Author(s) -
Joel T. Levis
Publication year - 2010
Publication title -
the permanente journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.445
H-Index - 30
eISSN - 1552-5775
pISSN - 1552-5767
DOI - 10.7812/tpp/09-141
Subject(s) - medicine , white (mutation) , wpw syndrome , accessory pathway , cardiology , bioinformatics , genetics , atrial fibrillation , tachycardia , gene , biology , catheter ablation
Wolff-Parkinson-White Syndrome (WPWS) is defined as the presence of an accessory pathway (AP) and has a predisposition to the development of supraventricular tachydysrhythmias. Conduction over an AP circumvents conduction delay occurring within the atrioventricular node (AVN), which leads to early eccentric activation of the ventricles and fusion complexes.1 If WPWS with atrial fibrillation (AF) is treated by drugs that prolong the AVN refractory period (eg, calcium-channel blockers, beta-blockers, digoxin, adenosine), the rate of conduction through the AP may increase and degenerate to ventricular fibrillation (VF).2 Unstable patients with WPWS and AF should receive immediate electrical cardioversion.3 Stable patients can be chemically cardioverted with IV procainamide. Amiodarone should be used with caution due to its ability to cause ventricular rate acceleration and degeneration into VF.3 Ibutilide is considered an alternative agent, although it has numerous side effects.1 Cardiology or electro-physiology consultation with consideration for radiofrequency mapping and ablation should occur for patients presenting with AF in the setting of WPWS. Figure 1 12-lead ECG in a man, age 33 years, with palpitations, chest discomfort, and shortness of breath Figure 2 12-lead ECG from same patient two days earlier

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