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. [2] Associate Editor(s)-in-Chief: Shivam Singla, M.D.[3]

Synonyms and keywords: Pre Excitation Syndromes; Lown-Ganong-Levine Syndrome; Pre-Excitation, Mahaim-Type; Wolff-Parkinson-White Syndrome

Overview

Pre-excitation syndrome is a condition in which the ventricles of heart depolarize earlier than expected via some accessory pathway conduction thus, leading to the premature contraction. Normally, atria and ventricles are interconnected with each other via AV node (atrioventricular node). But in all the pre-excitation syndromes, an accessory pathway is present that conducts impulses to ventricles besides the AV node. The accessory pathway passes the electrical impulses to the ventricles before the normal impulse of depolarization passes through the AV node. The phenomenon of depolarizing ventricles through the accessory pathway earlier than the usual depolarization is supposed to happen through the AV node is referred to as "Pre- Excitation". WPW syndrome was described in 1930 and named after John Parkinson, Paul Dudley White, and Louis Wolff. The accessory pathways are named depending upon the regions of atria and ventricles they are connecting such as Bundle of His, Mahaim fibers, and James fibers. The typical ECG findings associated with WPW syndrome are shortened PR interval, widened QRS complex and Delta wave which is a slurring in the upstroke of QRS complex due to preexcitation of ventricles via the accessory pathway. ECG findings along with symptomatic tachyarrhythmias are referred to as Wolff-Parkinson-White syndrome. Although it is more common in the adult, males have an incidence rate of 0.1-0.3 %, WPW can be considered as a congenital anomaly in some cases where it is usually present since the birth and in others, it is considered as a developmental anomaly. Studies have proven its lower prevalence in children aged between 6-13 than those in the age group of 14-15 years of age. Hemodynamically unstable patients should be managed with a direct cardioversion. For the stable patients, medical management should be tried first before going for other acceptable options of catheter ablation or surgical intervention. Although Catheter ablation has widely replaced the surgical option due to its less invasive technique and better outcomes, still in cases where catheter ablation cannot be done or doesn't prove to be effective, the surgical option is worth considering with a curative rate of nearly 100%.

Historical Perspective

• 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, WPW syndrome was first described and named after 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. They also found the association of WPW with increasing the risk of sudden cardiac death.
• British physiologist "Albert Frank Stanley Kent" (1863 - 1958), first described the lateral branches of AV grove of the monkey heart, which were later named as the accessory bundle of Kent.

WPW Syndrome was given its name in 1930 by Wolf, Parkinson, and White. Source: Ecgpedia.org

Classification

• Based on the conduction pathway or fiber subtype, pre-excitation syndrome may be classified into the following 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	No

• 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 are commonly seen in ECG.
2. Concealed Accessory Pathways: Conducts in the retrograde direction. As its name represents, the changes in ECG are concealed and no delta waves are seen.
3. Latent Accessory Pathways: These are located in the lateral part of the heart as compared to AV node. Hence, the impulses are delayed in traveling to the ventricles through the AV node which is at a much shorter distance as compared to the latent fibers located at the farther end.

Pathophysiology

Normal electrical conduction pathway of heart

• Normally, the electrical activity of the heart starts from SA node.
• The impulse generation usually happens in the right atrium near the entrance of superior vena cava and it travels from SA node to the AV node.
• The AV node modulates the rate and number of impulses to be conducted to the ventricles. It also modulates the speed of transmission from atria to ventricles which represents the PR interval on ECG.
• From the AV node, an electrical impulse is transmitted to the bundle of His, to left and right branches extending to the ventricular myocardium.

Pre-excitation pathway

• WPW is another word for pre-excitation of the ventricle through the accessory pathway instead of going through the usual pathway of AV node which usually slows down the speed of conduction of impulses transmitting to ventricles.
• The accessory pathway creates a channel directly to conduct the impulses to ventricles resulting in premature excitation.
• In "Type A Pre-excitation" accessory pathway lies between Left atria ventricles and in Type B pre-excitation fibers carry impulses between right atria and ventricles.
• 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 is a combination of WPW pattern on ECG + Paroxysmal arrhythmias.
• The accessory pathways are usually named as Bundle of Kent or AV bypass tracts.
• 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.
• The accessory pathways named as Mahaim fibers connect the Atrium, AV node, or bundle of His to the Purkinje fibers or ventricular myocardium.

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 the 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 it is regarded as a developmental anomaly. Studies proved it's 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 development of atrial fibrillation or sudden cardiac death include:
  • Pilots
  • Male gender
  • Athletes
  • Policemen
  • Steelworkers
  • Firemen
  • Past history of syncope
  • Age (peak ages for the development of atrial fibrillation include 30 years and 50 years)

Natural History, Complications, and Prognosis

Natural History

• There are a lot of studies being done in the past to describe the natural history or disease course of pre-excitation syndrome. But data from a recent study- "Long term natural history of patients with WPW treated with or without catheter ablation" showed promising results in explaining the reduced long-term mortality rates in WPW patients who are matched for age and gender. Also explained the lower mortality rates in catheter ablated patients as compared to non ablated ones. Although the patients can die with sudden cardiac death but the rate of this scenaio is very less and not commonly observed.

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 the severity of symptoms in a patient but the most important determinant of prognosis is the dependence 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

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 (<0.12 seconds) with Normal P wave morphology.
  • Widened QRS complex (>0.12 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

WPW ECG changes with significant 1) Delta wave 2) PR interval shortening 3) Wide QRS complexes. [1]

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 maybe asymptomatic, however, the individuals commonly experience the following symptoms:
  • Palpitations
  • Dizziness or lightheadedness
  • Shortness of breath
  • Chest pain
  • Fatigue
  • Anxiety
  • Fainting
  • Difficulty breathing

Treatment

Medical Treatment

• HEMODYNAMICALY UNSTABLE PATIENT -- DIRECT SYNCHRONIZED CARDIOVERSION, BIPHASIC ( INITIAL 100 J, LATER ON- 200J OR 360J).
• HEMODYNAMICALLY STABLE PATIENTS -- THE FOLLOWING ALGORITHM CAN BE FOLLOWED

GENERAL PROTOCOL

General protocol includes the following:

• Antiarrhythmic drug
  • Helps in slowing the accessory pathway conduction and thus plays a major role in the acute events.
• AV Nodal blocking agents should NOT be used
  • As they aggravate WPW by increasing the conduction through the accessory pathway.
• Address the underlying cause triggering dysrhythmias which includes
  • Coronary artery disease
  • Cardiomyopathy
  • Electrolyte derangement
  • Anemia
  • Thyroid disease

IN CASE OF ACUTE AVRT/AVNRT

• Treated by blocking the AV nodal conduction
  • Help in blocking the pathways responsible for causing dysrhythmias through the involvement of the AV node (AVRT/AVNRT).
  • Vagal Maneuvers - Valsalva maneuver, immersing the face in cold water or ice water, carotid sinus massage
  • IV Adenosine- very short half-life and commonly used in dose around 6-12 mg
  • IV Verapamil- this is a calcium channel blocker and commonly used as 5-10 mg.

ATRIAL FLUTTER/FIBRILLATION

• If wide complex tachycardia is present:
  • Use IV Amiodarone or Procainamaide

RADIOFREQUENCY ABLATION

• This modality has replaced drug therapy and other surgical treatment options by showing promising results. Best results are studied these days when it is used in conjunction with cryoblation (commonly used for septal Accessory pathways and for accessory pathways near small coronary arteries).
• This technique is used widely with best results in:
  • Patients with AVRT showing symptoms of dysrhythmias
  • Patients with impaired functional daily activities having no symptoms with ventricular pre-excitation
  • Patients with WPW and family history of sudden cardiac death in first or second-degree relatives.
  • Patients with AVRT OR A.FIB with RVR
  • Patients with h/o Pre-excited A.FIB
• Patients who are not willing to undergo radiofrequency ablation can be managed on medical management with the use of Anti-arrhythmic. Though its role in the prevention of future episodes of arrhythmias is limited still this is the most commonly used modality of choice.

Class 3 Antiarrhythmics and class IC drugs are used with AV nodal blocking agents in patients with a history of atrial flutter or A.Fib. Sotalol and Flecainide would be the safe options to use in pregnancy.

Surgical management

• Surgical management includes the following options:
  • ENDOCARDIAL SURGICAL APPROACH
  • EPICARDIAL SURGICAL APPROACH
  • Due to the continuing advancement in medical science, Radiofrequency catheter ablation is widely used as a preferred treatment option.
  • Role of the surgical approach nowadays is limited to:
    • Patients who are undergoing cardiac surgery due to other causes.
    • Patients in whom catheter ablation is tried but failed in the past.
    • Patients with multiple areas or foci generating the impulses usually requires a surgical approach for best outcomes.

Prevention

• The most common preventive measures used against WPW are radiofrequency catheter ablation.
  • This helps in preventing future attacks by doing the ablation of accessory pathways with a success rate of >95%.
• Although the success rate for the surgical approach is 100% still the catheter ablation is preferred as it is less invasive and associated with lower complication rates.
• Surgical success and best prognostic outcomes nowadays are only seen in patients who are having heart surgeries done for other causes such as cardiac Bypass grafting or for valvular repair.
• General measures that help in preventing the episodes like Valsalva maneuvers should be taught to the patient so that tachycardia can be relieved during an acute episode.
• Although medicines/Antiarrhythmic can help prevent recurrent episodes this is only preferred in patients who are not the candidates for catheter ablation or surgical approach.