Pre-excitation syndrome

Pre-excitation syndrome Microchapters
Overview
Historical Perspective
Classification
Pathophysiology
Differentiating Pre-excitation Syndrome from other Diseases
Epidemiology and Demographics
Risk Factors
Natural History, Complications, and Prognosis
Diagnosis
Treatment
Prevention

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1], Associate Editor-In-Chief: Shivam Singla, M.D.[2]

Overview

Pre-excitation syndrome is a condition where ventricles of the heart depolarize earlier than the normal leading to premature contraction. Normally the atria and the ventricles are isolated electrically and only electrical passage existing in between atria and ventricles is at Atrioventricular Node. In all pre-excitation syndromes, there is also present an additional conducting pathway beside the AV junction. So the electrical impulses pass to the ventricles even before the normal wave of depolarization that is about to conduct through the AV node. This mechanism of depolarization of ventricles through an additional bypass pathway ( Bundle of Kent) much earlier than the usual depolarization pathway (through AV node) is referred to as "Pre- Excitation". The secondary conduction pathways are generally named as Bundle of His.

The typical ECG findings are shortened PR interval and widened QRS interval with a slight slurring in the upstroke region. The clinical syndrome of the above clinical finding of ECG and history of SVT is referred to as Wolff-Parkinson-White syndrome. pre-excitation syndromes are getting more common in the pediatric population as well. The main component is the presence of an additional accessory bypass pathway in the heart through which the impulse conducts faster than than the physiological conduction through AV node, resulting in quick depolarization ofventricles and leads to dangerous arrhythmias. The most common subtype is Wolf-Parkinson -White syndrome. The severe consequences range from arrhythmias, SVT, and sudden cardiac death. The main therapeutic measures for managing the patients are pharmacotherapy and ablation therapy.

Historical Perspective

• WPW syndrome was described in 1930 and named for the John Parkinson, Paul Dudley White, and Louis Wolff.
• They successfully interpreted a series of 11 healthy young patients who had repeated attacks of tachycardia in the presence of short PR interval and bundle branch block pattern on the ECG findings.

• British physiologist "Albert Frank Stanley Kent" (1863 - 1958), first described the lateral branches of AV grove of the monkey heart, which was later named accessory bundle of Kent.

• In 1915, Frank Norman Wilson became the first to describe the condition which would later be referred to as Wolff–Parkinson–White syndrome.

• In 1930, it was first described by Louis Wolff, John Parkinson, and Paul Dudley White.
• They also found the association of WPW with increasing the risk of sudden cardiac death.

Classification

• Pre-excitation syndrome may be classified into sub-types

Type	Conduction pathway	QRS interval	PR interval	Delta wave
Wolff-Parkinson-White syndrome	Bundle of Kent	Wide/long	Usually short	yes
Lown-Ganong-Levine syndrome	"James bundle" (atria to bundle of His)	Normal/Unaffected	Short	no
Mahaim-type	Mahaim fibers	long	normal

• Based on their conduction properties, three types of Accessory pathways are there:
  1. Manifest Accessory Pathways: Conducts more rapidly as compared to AV nodal conduction. Delta waves will commonly be seen on ECG.
  2. Concealed Accessory Pathways: Conducts in the retrograde direction. As its name represents, the changes in ECG will be concealed. No delta waves will be seen.
  3. Latent Accessory Pathways: These are located in the lateral part of the heart as compared to AV node. So the impulses will be delayed in traveling to ventricles through the AV node which is at a much shorter distance as compared to latent fibers that are at the far another end.
     

Pathophysiology

Basics of Pre excitation sydrome

Basic concept of Pathophysiology in pre-excitation syndrome lies in the concept of bypassing the AV node conduction and letting the impulse conduct faster through atria to ventricles via accessory pathways.

These accessory pathways Usually called Bundle of Kent in WPW syndrome, James fiber in LGL syndrome and Mahaim fibers in Mahaim type pre-excitation syndrome. These conducts impulses in forward (not common), backward ( around 15-20%) and in both directions ( Most common type) as well.

The accessory pathways mediate the occurrence of tachyarrhythmia by forming a re-entry circuit and commonly known as AVRT. The direct conduction of impulses from atria to ventricles can also result in the development of tachyarrhythmia's when there is a development of Atrial Fibrillation with RVR

WPW Syndrome

• WPW syndrome is a combination of WPW pattern on ECG + Paroxysmal arrhythmias. The accessory pathways are usually named as Bundle of Kent or AV bypass tracts.

• ECG features of WPW syndrome are
  • Short PR interval <120 ms ( < .12 seconds) with Normal P wave morphology.
  • Widened QRS complex ( >.12 seconds)
  • Delta wave - slurring upstroke of the initial QRS complex due to the early and rapid depolarization of ventricles, the most important criteria for the diagnosis of WPW syndrome.
  • Deflection of T waves opposite to the direction of QRS complexes / Secondary changes in ST-segment and T wave.
  • Types of AVRT varies depending on the direction of the impulse conduction in the re-entry circuit (orthodromic or antidromic). Orthodromic AVRT means the antegrade conduction will be through the AV node and retrograde will be through the accessory pathway - presents with narrow QRS complexes on ECG. Antidromic AVRT means the antegrade conduction will be through the AP and retrograde conduction through AV node - presents with wide complex QRS complexes on ECG. SO, in short, the Orthodromic AVRT preexcitation syndrome will present with narrow complex tachycardia and Antodromic AVRT pre-excitation syndrome will present with wide complex tachycardias.
  • AF with RVR can be diagnosed in patients with WPW by comparing it with the baseline ECG. Means look for comparison between pre-excited QRS complexes on the baseline ECG vs those seen during irregular tachycardia.
  • Mainly categorized into 2 subtypes
    • Type A - Positive delta wave
    • Type B - Negative delta wave

Lown-Ganong-Levine(LGL) Syndrome

• The accessory pathways here are named as James fibers, also known as atrionodal fibers connecting the atrium to the distal AV node. These usually conduct the impulses from atria to the initial portion of the AV node.

• ECG features:
  • PR interval is less than 120ms or .12 seconds with usual normal P wave morphology
  • Normal QRS complex
  • Absence of delta waves
  • Episodic paroxysmal SVT

Mahaim-Type Pre-excitation

• The accessory pathways named as mahaim fibers connect the Atrium, AV node, or bundle of His to the Purkinje fibers or ventricular myocardium.

• ECG findings are usually normal

Differentiating Pre-excitation Syndrome from other Diseases

Arrhythmia	Rhythm	Rate	P wave	PR Interval	QRS Complex	Response to Maneuvers	Epidemiology	Co-existing Conditions
Atrial Fibrillation (AFib)	Irregularly irregular	On a 10-second 12-lead EKG strip, multiply number of QRS complexes by 6	Absent Fibrillatory waves	Absent	Less than 0.12 seconds, consistent, and normal in morphology in the absence of aberrant conduction	Does not break with adenosine or vagal maneuvers	2.7–6.1 million people in the United States have AFib 2% of people younger than age 65 have AFib, while about 9% of people aged 65 years or older have AFib	Elderly Following bypass surgery Mitral valve disease Hyperthyroidism Diabetes Heart failure Ischemic heart disease Chronic kidney disease Heavy alcohol use Left chamber enlargement
Atrial Flutter	Regular or Irregular	75 (4:1 block), 100 (3:1 block) and 150 (2:1 block) beats per minute (bpm), but 150 is more common	Sawtooth pattern of P waves at 250 to 350 bpm Biphasic deflection in V1	Varies depending upon the magnitude of the block, but is short	Less than 0.12 seconds, consistent, and normal in morphology	Conduction may vary in response to drugs and maneuvers dropping the rate from 150 to 100 or to 75 bpm	Incidence: 88 per 100,000 individuals	Elderly Alcohol
Atrioventricular nodal reentry tachycardia (AVNRT)''''	Regular	140-280 bpm	slow-fast AVNRT: Pseudo-S wave in leads II, III, and AVF Pseudo-R' in lead V1. Fast-Slow AVNRT P waves between the QRS and T waves (QRS-P-T complexes) Slow-Slow AVNRT Late P waves after a QRS Often appears as atrial tachycardia. Inverted, superimposed on or buried within the QRS complex (pseudo R prime in V1/pseudo S wave in inferior leads)	Absent (P wave can appear after the QRS complex and before the T wave, and in atypical AVNRT, the P wave can appear just before the QRS complex)	Less than 0.12 seconds, consistent, and normal in morphology in the absence of aberrant conduction QRS alternans may be present	May break with adenosine or vagal maneuvers	60%-70% of all supraventricular tachycardias	Structural heart disease Atrial tachyarrhythmias
Multifocal Atrial Tachycardia	Irregular	Atrial rate is > 100 beats per minute	Varying morphology from at least three different foci Absence of one dominant atrial pacemaker, can be mistaken for atrial fibrillation if the P waves are of low amplitude	Variable PR intervals, RR intervals, and PP intervals	Less than 0.12 seconds, consistent, and normal in morphology	Does not terminate with adenosine or vagal maneuvers	0.05% to 0.32% of electrocardiograms in general hospital admissions	Elderly Chronic obstructive pulmonary disease (COPD)
Paroxysmal Supraventricular Tachycardia	Regular	150 and 240 bpm	Absent Hidden in QRS	Absent	Narrow complexes (< 0.12 s)	Breaks with vagal maneuvers, adenosine, diving reflex, oculocardiac reflex	Prevalence: 0.023 per 100,000	Alcohol Caffeine Nicotine Psychological stress Wolff-Parkinson-White syndrome
Premature Atrial Contractrions (PAC)	Regular except when disturbed by premature beat(s)	80-120 bpm	Upright	> 0.12 second Maybe shorter than that in normal sinus rhythm (NSR) if the origin of PAC is located closer to the AV node Ashman’s Phenomenon: PAC displaying a right bundle branch block pattern	Usually narrow (< 0.12 s)	Breaks with vagal maneuvers, adenosine, diving reflex, oculocardiac reflex		Infants Cardiomyopathy Myocarditis Elderly Coronary artery disease Stroke Increased atrial natriuretic peptide (ANP) Hypercholesterolemia
Wolff-Parkinson-White Syndrome		Regular	Atrial rate is nearly 300 bpm and the ventricular rate is at 150 bpm	With orthodromic conduction due to a bypass tract, the P wave generally follows the QRS complex, whereas in AVNRT, the P wave is generally buried in the QRS complex.	Less than 0.12 seconds	A delta wave and evidence of ventricular pre-excitation if there is conduction to the ventricle via ante-grade conduction down an accessory pathway A delta wave and pre-excitation may not be present because bypass tracts do not conduct ante-grade.	May break in response to procainamide, adenosine, vagal maneuvers	Worldwide prevalence of WPW syndrome is 100 - 300 per 100,000	Ebstein's anomaly Mitral valve prolapse: This cardiac disorder, if present, is associated with left-sided accessory pathways. Hypertrophic cardiomyopathy: This disorder is associated with familial/inherited form of WPW syndrome. Hypokalemic periodic paralysis Pompe disease Tuberous sclerosis
Ventricular Fibrillation (VF)	Irregular	150 to 500 bpm	Absent	Absent	Absent (R on T phenomenon in the setting of ischemia)	Does not break in response to procainamide, adenosine, vagal maneuvers	3-12% cases of acute myocardial infarction (AMI) Out of 356,500 out of hospital cardiac arrests, 23% have VF as initial rhythm	Myocardial ischemia / infarction Cardiomyopathy Channelopathies e.g. Long QT (acquired / congenital) Electrolyte abnormalities (hypokalemia/hyperkalemia, hypomagnesemia) Aortic stenosis Aortic dissection Myocarditis Cardiac tamponade Blunt trauma (Commotio Cordis) Sepsis Hypothermia Pneumothorax Seizures Stroke
Ventricular Tachycardia	Regular	> 100 bpm (150-200 bpm common)	Absent	Absent Initial R wave in V1, initial r > 40 ms in V1/V2, notched S in V1, initial R in aVR, lead II R wave peak time ≥50 ms, no RS in V1-V6, and atrioventricular dissociation	Wide complex, QRS duration > 120 milliseconds	Does not break in response to procainamide, adenosine, vagal maneuvers	5-10% of patients presenting with AMI	Coronary artery disease Aortic stenosis Cardiomyopathy Electrolyte imbalances (e.g., hypokalemia, hypomagnesemia) Inherited channelopathies (e.g., long-QT syndrome) Catecholaminergic polymorphic ventricular tachycardia Arrhythmogenic right ventricular dysplasia Myocardial infarction Torsades de pointes is a form of polymorphic VT that is often associated with a prolonged QT interval

Epidemiology and Demographics

• WPW is commonly found with an incidence of around 0.1-3.0 per thousand population
• More common in the male population as compared to females.
• Familial studies are done to found its association proved that around .55% more commonly found in first degree relatives.
• More common in young and healthy individuals and as the age advances the prevalence of disease decreases because of loss of pre-excitation.
• WPW can be considered as a congenital anomaly in some cases where it is usually present since birth and in others and in others it is regarded as a developmental anomaly. Studies proved its lower prevalence in children aged between 6-13 than those in the age group of 14-15 years of age.
  

Risk Factors

High-risk population for sudden cardiac death in Wolff-Parkinson-White syndrome include:

• Policemen
• Athletes
• Firemen
• Pilots
• Steelworkers

Risk factors for the development of atrial fibrillation in WPW syndrome include:

• Male gender
• Age (peak ages for the development of atrial fibrillation include 30 years and 50 years)
• Past history of syncope

Natural History, Complications and Prognosis

Complications

• Most common complications studied in patients having accessory pathway conduction are Arrhythmias and Sudden cardiac death
  • Tachyarrhythmias:
    • If there is a development of atrial fibrillation or flutter then there is fast conduction across the tracts leads to an increased risk of dangerous ventricular arrhythmias.
    • AV nodal blocking agents may also be the factor responsible for the increased conduction through accessory pathways causing life-threatening ventricular arrhythmias or hemodynamic instability resulting and with a worse prognosis.
  • Sudden cardiac death:
    • Sudden cardiac death as a complication in patients with AP conduction is more common in a young male with age less than 35, history of arrhythmias in the past, anatomical location of accessory pathway- that is the septal location of the accessory pathway, having multiple accessory pathways.
    • The studies proved the risk of sudden cardiac death related to the pre-excitation syndrome is around 1.5% in childhood with the highest risk in the first two decades of life.

Prognosis

• Prognosis is usually very good till the time patient is getting managed and treated appropriately. Catheter ablation showed promising results in the curative treatment of patients suffering from this disorder.
• Sudden cardiac death is rarely seen in patients with this syndrome but when it happens it is most commonly related to arrhythmias.
• The most common misconception about the prognosis of WPW syndrome is related to symptoms of the patient but the most important determinant of prognosis is dependent on the electrophysiologic properties of the accessory pathways
• The conduction through accessory pathways usually decreases with age. This is due to fibrotic changes that happen with time.

Diagnosis

AVRT ( Orthodromic and Antidromic)

WPW Syndrome

• WPW syndrome is a combination of WPW pattern on ECG + Paroxysmal arrhythmias. The accessory pathways are usually named as Bundle of Kent or AV bypass tracts.

• ECG features of WPW syndrome are
  • Short PR interval <120 ms ( < .12 seconds) with Normal P wave morphology.
  • Widened QRS complex ( >.12 seconds)
  • Delta wave - slurring upstroke of the initial QRS complex due to the early and rapid depolarization of ventricles, the most important criteria for the diagnosis of WPW syndrome.
  • Deflection of T waves opposite to the direction of QRS complexes / Secondary changes in ST-segment and T wave.
  • Types of AVRT varies depending on the direction of the impulse conduction in the re-entry circuit (orthodromic or antidromic). Orthodromic AVRT means the antegrade conduction will be through the AV node and retrograde will be through the accessory pathway - presents with narrow QRS complexes on ECG. Antidromic AVRT means the antegrade conduction will be through the AP and retrograde conduction through AV node - presents with wide complex QRS complexes on ECG. SO, in short, the Orthodromic AVRT preexcitation syndrome will present with narrow complex tachycardia and Antidromic AVRT pre-excitation syndrome will present with wide complex tachycardia.
  • AF with RVR can be diagnosed in patients with WPW by comparing it with the baseline ECG. Means look for comparison between pre-excited QRS complexes on the baseline ECG vs those seen during irregular tachycardia.
  • Mainly categorized into 2 subtypes
    • Type A - Positive delta wave
    • Type B - Negative delta wave

Lown-Ganong-Levine(LGL) Syndrome

• The accessory pathways here are named as James fibers, also known as atrionodal fibers connecting the atrium to the distal AV node. These usually conduct the impulses from atria to the initial portion of the AV node.

• ECG features:
  • PR interval is less than 120ms or .12 seconds with usual normal P wave morphology
  • Normal QRS complex
  • Absence of delta waves
  • Episodic paroxysmal SVT

Mahaim-Type Pre-excitation

• The accessory pathways named as Mahaim fibers connect the Atrium, AV node, or bundle of His to the Purkinje fibers or ventricular myocardium.

• ECG findings are usually normal

History and Symptoms

People with Pre- Excitation syndromes may be asymptomatic, however, the individuals commonly experience following symptoms:

• Palpitations
• Dizziness or lightheadedness.
• Shortness of breath.
• Chest pain
• Fatigue.
• Anxiety.
• Fainting
• Difficulty breathing

Treatment

Medical Treatment

Orthodromic AVRT

• Hemodynamically Unstable patients (Low BP, Altered mental state, pulmonary edema)- Synchronized DC Cardioversion.
• Hemodynamically stable- Vagal maneuvers, Adenosine, CCB, and DC cardioversion as a last resort only if the patient not responding to medical therapy.

Antidromic AVRT

• Hemodynamically unstable patients:- Urgent synchronized DC cardioversion.
• Hemodynamically stable patients:- Amiodarone, procainamide, or ibutilide.

AF with WPW

• Hemodynamically unstable patients: Urgent synchronized DC cardioversion
• Hemodynamically stable patients:- Procainamide or ibutilide.
• Caution: Adenosine, CCB, Beta-blockers enhances conduction via accessory pathway resulting in worsening & possible degeneration into VT or VF

Surgery

• Surgery is the mainstay of therapy for [disease name].
• [Surgical procedure] in conjunction with [chemotherapy/radiation] is the most common approach to the treatment of [disease name].
• [Surgical procedure] can only be performed for patients with [disease stage] [disease name].

Prevention

For preventing the recurrence of episodes major options available are

• Radio frequency ablation
  • Ablation of accessory pathway tracts
  • cures 95% of the time
• Surgery.
  • Success rate for surgical ablation is around 100 percent along with lower complication rates. Radiofrequency ablation is a less invasive option and preferred over surgery.
  • Surgery can be considered if a patient is undergoing cardiac surgery for other reasons such as CABG or other heart valve surgery.
• Medications
  • Although Medications can prevent recurrent episodes of tachycardia they are only used on patients who are not the candidates for ablation or surgery.
  • These patients must be taught to perform Valsalva maneuvers that can relieve tachycardia during the episodes.