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=== | ||
* | *Most common variant (~95% of cases) | ||
*Accessory pathway (Kent bundles) | *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 | *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 | **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 | **Except regular rhythm | ||
**Easily mistaken for | **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
- Arrhythmias:
- Non-arrhythmic cardiac causes:
- Psychiatric causes:
- Drugs and Medications:
- Alcohol
- Caffeine
- Drugs of abuse (e.g. cocaine)
- Medications (e.g. digoxin, theophylline)
- Tobacco
- Misc
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
- Due to loss of normal AV node conduction delay
- Differentiate from premature junctional complex
- 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]
- Patients with chest pain, CHF, electrolyte imbalance, or required cardioversion
- Syncope
- Uncertain diagnosis (wide-complex tachycardia)
- Significant associated structural heart disease (MVP, cardiomyopathy)
- Family history of Sudden cardiac death
- Atrial flutter or atrial fibrillation
See Also
- Paroxysmal supraventricular tachycardia
- Atrial fibrillation (main)
- Atrial fibrillation with RVR
- Tachycardia (narrow)
- Tachycardia (wide)
External Links
References
- ↑ https://rarediseases.org/rare-diseases/wolff-parkinson-white-syndrome/
- ↑ https://patient.info/doctor/wolff-parkinson-white-syndrome-pro
- ↑ https://patient.info/doctor/wolff-parkinson-white-syndrome-pro
- ↑ https://emedicine.medscape.com/article/159222-workup#c8
- ↑ https://patient.info/doctor/wolff-parkinson-white-syndrome-pro
- ↑ https://emedicine.medscape.com/article/159222-workup#c8
- ↑ https://emedicine.medscape.com/article/159222-workup#c8
- ↑ Burns E. Wolff-Parkinson-White Syndromes. Life in the Fast Lane. http://lifeinthefastlane.com/ecg-library/pre-excitation-syndromes/.
- ↑ Ellis CR et al. Wolff-Parkinson-White Syndrome Treatment & Management. eMedicine. Dec 4, 2015. http://emedicine.medscape.com/article/159222-treatment#showall.
