Wolff-Parkinson-White syndrome natural history
Wolff-Parkinson-White syndrome Microchapters |
Differentiating Wolff-Parkinson-White syndrome from other Diseases |
---|
Diagnosis |
Treatment |
Case Studies |
Wolff-Parkinson-White syndrome natural history On the Web |
Risk calculators and risk factors for Wolff-Parkinson-White syndrome natural history |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Raviteja Guddeti, M.B.B.S. [2]
Please help WikiDoc by adding more content here. It's easy! Click here to learn about editing.
Complications
Complications of Wolff-Parkinson-White syndrome can occur at any age, although some individuals born with an accessory pathway in the heart never experience any health problems associated with the condition.
Possible complications include:
- Complications of surgery
- Reduced blood pressure (caused by continous rapid heart rate)
- Heart failure
- Cardiac arrest
- Side effects of medications
- Ventricular fibrillation: It may rapidly lead to shock, and requires emergency treatment (cardioversion).
- Sudden cardiac death: The younger the age of presentation the more is the risk of sudden cardiac death, because of the more active life style.
Prognosis
Appropriately treated WPW syndrome has an excellent prognosis. Catheter ablation (radiofrequency ablation) cures this disorder in most patients. The success rate for the procedure ranges between 85 - 95%. Success rate varies depending on location of accessory pathway and number of accessory pathways. Successful ablation also prevents future SVT. Asymptomatic patients (Wolf-Parkinson-White pattern) have a very good prognosis.
Factors associated with worse prognosis include:
- A family history of sudden cardiac death
- Significant symptoms of tachyarrhythmias
- Cardiac arrest
Even these patients with worse prognosis regain good prognosis with timely and appropriate treatment using radiofrequecy ablation. Over all risk of death in patients with WPW syndrome reaches 0.15% every year.