Wolff–Parkinson–White syndrome: Difference between revisions

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==Background==
==Background==
*Abbreviation: WPW
*Abbreviation: WPW
*Congenital pre-excitation syndrome
*Presence of an accessory electrical pathway between atria and ventricles predisposing to supraventricular tachycardia
*Associated with certain genetic predispositions, [[Ebstein anomaly]], and [[hypokalemic periodic paralysis]]<ref>https://rarediseases.org/rare-diseases/wolff-parkinson-white-syndrome/</ref> <ref>https://patient.info/doctor/wolff-parkinson-white-syndrome-pro</ref>
===Type A===
*Delta wave and QRS complex predominantly upright in precordial leads <ref>https://patient.info/doctor/wolff-parkinson-white-syndrome-pro</ref>
*Dominant R wave (greater than S amplitude) in V1 may have appearance of right bundle branch block <ref>https://emedicine.medscape.com/article/159222-workup#c8</ref>
===Type B===
*Delta wave and QRS complex predominantly negative in V! and V2
*Delta wave and QRS complex predominantly positive in other precordial leads <ref>https://patient.info/doctor/wolff-parkinson-white-syndrome-pro</ref>
*Appearance of left bundle branch block <ref>https://emedicine.medscape.com/article/159222-workup#c8</ref>


===Orthodromic Type===
===Orthodromic Type===
*More common type occuring ~95% of the time
*Most common variant (~95% of cases)
*Accessory pathway (Kent bundles) is used for retrograde reentry conduction
*Accessory pathway (Kent bundles) allows retrograde reentry conduction
*QRS narrow (delta wave absent)
*QRS narrow (delta wave absent)
**Referred to as 'concealed' accessory pathway <ref>https://emedicine.medscape.com/article/159222-workup#c8</ref>
*May see ST depression, TWI
*May see ST depression, TWI
*Rate 150-250 bpm
*Rate 150-250 bpm
===Antidromic Type===
===Antidromic Type===
*Least common type occuring ~5% of the time
*Least common variant (~5% of cases)
*Accessory pathway used for anterograde conduction
*Accessory pathway used for anterograde conduction
*QRS wide, delta wave present
*QRS wide, delta wave present
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===Atrial Fibrillation and Flutter<ref>Burns E. Wolff-Parkinson-White Syndromes. Life in the Fast Lane. http://lifeinthefastlane.com/ecg-library/pre-excitation-syndromes/.</ref>===
===Atrial Fibrillation and Flutter<ref>Burns E. Wolff-Parkinson-White Syndromes. Life in the Fast Lane. http://lifeinthefastlane.com/ecg-library/pre-excitation-syndromes/.</ref>===
*[[Atrial fibrillation]] in up to 20% of patients with WPW
*[[Atrial fibrillation]] in up to 20% of patients with WPW
**Irregular rhythym, wide QRS complexes
**Irregular rhythm, wide QRS complexes
**Changing QRS complexes in shape and morphology
**Changing QRS complexes in shape and morphology
**Axis remains stable as opposed to polymorphic VT
**Axis remains stable as opposed to polymorphic VT
*[[Atrial flutter]] in ~7% of patients with WPW
*[[Atrial flutter]] in ~7% of patients with WPW
**Similar features to atrial fibrillation with WPW
**Similar features to atrial fibrillation with WPW
**Except regular rhythym
**Except regular rhythm
**Easily mistaken for regular rate VT
**Easily mistaken for monomorphic ventricular tachycardia
**Note that if unclear, always safest to assume VT and treat with shock
*Treatment with AV nodal blocking agents (adenosine, beta-blockers, calcium-channel blockers, amiodarone, digoxin) may incite [[ventricular fibrillation]] or [[ventricular tachycardia]]
*Treatment with AV nodal blocking agents (adenosine, beta-blockers, calcium-channel blockers, amiodarone, digoxin) may incite [[ventricular fibrillation]] or [[ventricular tachycardia]]
*"Manifest WPW" = degeneration into VT or VF
*"Manifest WPW" = degeneration into VT or VF

Revision as of 20:05, 18 March 2019

Background

  • Abbreviation: WPW
  • Congenital pre-excitation syndrome
  • Presence of an accessory electrical pathway between atria and ventricles predisposing to supraventricular tachycardia
  • Associated with certain genetic predispositions, Ebstein anomaly, and hypokalemic periodic paralysis[1] [2]

Type A

  • Delta wave and QRS complex predominantly upright in precordial leads [3]
  • Dominant R wave (greater than S amplitude) in V1 may have appearance of right bundle branch block [4]

Type B

  • Delta wave and QRS complex predominantly negative in V! and V2
  • Delta wave and QRS complex predominantly positive in other precordial leads [5]
  • Appearance of left bundle branch block [6]

Orthodromic Type

  • Most common variant (~95% of cases)
  • Accessory pathway (Kent bundles) allows retrograde reentry conduction
  • QRS narrow (delta wave absent)
    • Referred to as 'concealed' accessory pathway [7]
  • May see ST depression, TWI
  • Rate 150-250 bpm

Antidromic Type

  • Least common variant (~5% of cases)
  • Accessory pathway used for anterograde conduction
  • QRS wide, delta wave present
  • Rate 160-220 bpm, regular

Atrial Fibrillation and Flutter[8]

  • Atrial fibrillation in up to 20% of patients with WPW
    • Irregular rhythm, wide QRS complexes
    • Changing QRS complexes in shape and morphology
    • Axis remains stable as opposed to polymorphic VT
  • Atrial flutter in ~7% of patients with WPW
    • Similar features to atrial fibrillation with WPW
    • Except regular rhythm
    • Easily mistaken for monomorphic ventricular tachycardia
    • Note that if unclear, always safest to assume VT and treat with shock
  • Treatment with AV nodal blocking agents (adenosine, beta-blockers, calcium-channel blockers, amiodarone, digoxin) may incite ventricular fibrillation or ventricular tachycardia
  • "Manifest WPW" = degeneration into VT or VF

Clinical Features

  • Suspect in any patient with ventricular rate >300

Infants

  • Irritability, feeding intolerance
  • CHF
  • Intercurrent febrile illness

Children

  • Chest pain, palpitations
  • Shortness of breath
  • Syncope/near-syncope

Adults

  • Sudden onset "racing heart"

Differential Diagnosis

Palpitations

Evaluation

Workup

Evaluation

Although the ECG and an electrophysiology study are diagnostic, the characteristic features are not always seen on ECG

  • Short PR interval - <0.12sec
  • Delta wave / slurred upstroke
    • Due to early activation of ventricular myocardium
  • QRS duration > 0.10 sec
    • Represents a fusion beat
  • Dominant R wave in V1, Type A WPW
    • Left sided accessory pathway
  • Dominant S wave in V1, Type B WPW
    • Right sided accessory pathway
  • Tall R waves in V1-V3 with T wave inversion
    • Mimic RVH
  • "Negative" delta waves in III and aVF
    • Appear as pseudo-infarct Q waves
    • Mimics prior inferior infarct

Management

Orthodromic

Treat like paroxysmal SVT

  • Unstable
    • Cardioversion (synchronized)
    • Adult: 50-100 J
    • Peds: 0.5-2 J/kg
  • Stable
    • Calcium channel blockers, beta-blockers, procainamide, or adenosine
    • Procainamide safe irrespective of type of pathway conduction

Antidromic

Treat like ventricular tachycardia

  • Synchronized cardioversion
    • Adult: 50-100 J
    • Peds: 0.5-2 J/kg
    • Procainamide: 20-50mg/min IV over 30min (up to 17mg/kg, hypotension, or 50% widening of QRS complex); mainenance 1-4 mg/min
      • Avoid if prolong QT or CHF
    • Amiodarone with 'ABCD' drugs ie adenosine, beta-blockers, calcium-channel blockers, digoxin
  • Wide-complex, irregular (presumed preexcited A-fib)
    • Unsynchronized cardioversion (200J)

Atrial Fibrillation and Atrial Flutter

  • Stable
    • Procainamide 20-50 mg/min until arrhythmia suppressed
    • Synchronized cardioversion, 100 - 200 J
  • Unstable - synchronized cardioversion
    • Consider higher joule dosage and frequency of repeats than for stable
  • Avoid AV nodal blocking agents

Disposition

Discharge

  • Consider if dysrhythmia was easily terminated and can arrange outpatient EP study with possible RF catheter ablation
  • Consider consulting cardiologist regarding outpatient beta-blockers vs. more potent medications (amiodarone, sotalol, flecainide, etc.)

Admit[9]

See Also

External Links

WPW with AFIB

References