Mohd Farid

Mohd Farid
Showing posts with label EKG. Show all posts
Showing posts with label EKG. Show all posts

Saturday, March 14, 2020

You Ask I Find The Answer-ECG Interpretation: Infarction-Injury Part IIIb ST Depression

Infarction

Myocardial Infarction Triad

Injury
(means acute or recent)

ST Depression




The ST segment may become depressed under certain circumstances or conditions. 

During an angina attack, the ST segment may be temporarily depressed.

A subendocardial infarction, an infarct that does not extend through the full thickness of the left ventricular wall, will depress the ST segment.

Positive Stress Test


When a patient with narrowed coronaries exercises, the myocardium demands more blood flow than its arteries can deliver. A stress or exercise test will record depression of the ST segment on EKG when such a patient is exercised.

Digitalis

Digitalis can cause depression of the ST segment, however it has a unique, unforgettable appearance. 


Digitalis causes a gradual downward curve of the ST segment, to give it the appearance of Salvador Dali's mustache. Notice that the lowest portion of the ST segment is depressed below the baseline.

Digitalis produces a unique, gradual downward curve of the ST segment; this is the classical "digitalis effect". 

To identify the classical pattern of digitalis effect, you should observe a lead with no demonstrable S wave. The downward portion of the R wave gradually thickens as it curves down into the ST segment, which is usually depressed. The downward limb of the R wave has a gentle, curving slope that gradually blends into the depressed ST segment. Look for it the next time you have a patient on a digitalis preparation. 

Subendocardial Infarction


Subendocardial infarction causes flat depression of the ST segment; however, any significant ST depression (in leads where the QRS is upright) indicates compromised coronary blood flow until proven otherwise.

Subendocardial infarction (often referred to as subendocardial injury) is identified by flat ST segment depression, which may be either horizontal or down sloping.

Subendocardial infarction, a type of "non Q wave infarction" involves only a small area of myocardium just beneath the endocardial lining.  Classical myocardial infarction is said to be transmural; that is, the full thickness of the left ventricular wall is damaged in the infarcted area. Even though subendocardial infarction involves only a small area of the myocardium, it must be respected as a true MI that requires appropriate care. A subendocardial MI may enlarge or extend and become more life threatening.

Any patient with acute ST depression or elevation, particularly if it persists, should have an immediate, complete workup including cardiac enzymes. 

Credit: Dale Dubin-RapidInterpreatation Of EKG 

You Ask I Find The Answer-ECG Interpretation: Infarction-Injury Part IIIa

Infarction

Myocardial Infarction Triad

Injury
(means acute or recent)


Injury indicates the acuteness of an infarct. Elevation of the ST segment denotes "injury" sometimes called the "current of injury".

The ST segment is that section of baseline between the QRS complex and the T wave. The ST segment contains.

Elevation of the ST segment signifies "injury". The ST segment may be elevated only slightly, or as much as one or more milimeters above the baseline.

ST segment elevation tells us that a myocardial infarction is acute. It is the earliest consistent sign of infarction to record on EKG.

Angina with exertion, "Prinxmetal's angina, can cause transient ST elevation in the absence of an infarction.

ST Elevation

If there is ST elevation, this indicates that the infarction is acute. ST elevation, alone, can indicate an infarction.

Once you have made a diagnosis of infarction, it is important to know whether the infarction just occurred and needs immediate treatment, or if the infarction is old, maybe years old.

The ST segment rises above the baseline with an acute infarction, in fact it is usually the earliest EKG sign of an infarction. With time, the ST segment returns to the baseline. 

If the ST segment is elevated without associated Q waves, this may represent non-Q wave infarction, which is usually a small infarction that may herald an impending larger infarct. Significant ST changes require enzyme studies and close scrutiny.

A ventricular aneurysm (the outward ballooning of the wall of ventricle) can cause persistent ST elevation in most of the chest leads; but in this case, the ST segment does not return to the baseline with time. Pericarditis (next page) produces a unique type of ST segment elevation that may also elevate the T wave off the baseline.

Brugada Syndrome-ST Elevation




RBBB pattern QRS with ST elevation in V1-V3

Can cause sudden cardiac arrest (in absence of coronary obstruction)

Brugada syndrome is a hereditary condition that can cause sudden death in individuals without heart disease. It is characterized by Right Bundle Branch Block with ST elevation in leads V1 to V3. Look for it; this malady is not rare.

Sudden cardiac death (cardiac arrest ) can occur spontaneously in patients with Brugada syndrome.

In Brugada syndrome there is RBBB and ST elevation in leads V1 to V3. The elevated ST segments have a peculiar, peaked downsloping shape, particularly in V1 and V2.

Brugada syndrome is a familial condition caused by dysfunctional cardiac Na+ (sodium) channels. Prophylaxis against the deadly arrhythmias requires ICD implantation in order to immediately treat cardiac arrest (usually ventricular fibrillation). 

This syndrome is responsible for nearly one half of the sudden deaths in healthy young individuals without structural heart disease.

Pericarditis-ST Elevation



With pericarditis, the ST segment is elevated and usually flat or concave. The entire T wave may be elevated off the baseline. 

Pericarditis is inflammation of the membrane (pericardium) that surrounds the heart. Pericarditis may be caused by a virus, bacteria, cancer, or other sources of inflammation, including myocardial infarction.

Pericarditis can elevate the ST segment. It usually produces an elevated ST segment that is flat or slightly concave (middle sags downward). This resolves with time.

Pericarditis seems to elevate the entire T wave off the baseline; that is, the baseline gradually angles back down (often including the P wave) all the way to next QRS.



The characteristics shown in the left illustration are found in lead in which the QRS is usually mainly negative (like the right chest leads). The pattern shown in the right illustration is seen in leads where the QRS is mainly positive (such as the lateral and inferior limb leads). Sometimes PVC's are produced.

You Ask I Find The Answer-ECG Interpretation: Infarction-Ischemia Part II

Infarction

Myocardial Infarction Triad

Ischemia




Ischemia (decreased blood supply) is characterized by inverted T waves.

Ischemia means reduced blood supply (from the coronary arteries); the ischemic area is at the periphery of the infarct.

The characteristic sign of ischemia is the inverted T wave. It may vary from a slightly inverted to a deeply inverted T wave.

Inverted T waves may indicate ischemia in the absence of myocardial infarction. Coronary blood flow can decrease without producing an infarction.

Cardiac ischemia alone can cause chest pain known as angina, which is usually associated with transient T wave inversion.


The typical ischemia T wave is symmetrically inverted.

You should check every EKG that you read for T wave inversion. Since the chest leads are nearest the ventricles, T wave changes are most pronounced in these leads. Always run down V1 to V6 (as well as the limb leads) and check for T wave inversion to see if there is diminished coronary flow.

The T wave of ischemia is both inverted and symmetrical; that is, the right and left sides of the inverted T wave are mirror images.

In adults flat (nonexistent) T waves or minimal T wave inversion may be a normal variant in any of the limb leads (frontal plane). However, any T wave inversion in leads V2 through V6 is considered pathological. Marked T wave inversion in leads V2 and V3 the hallmark of Wellens Syndrome, alerts us to stenosis of the anterior descending coronary. 

Credit: Dale Dubin-RapidInterpreatation Of EKG

Friday, March 13, 2020

You Ask I Find The Answer-ECG Interpretation: Infarction Part I

Infarction

Myocardial Infarction results from the complete occlusion of a coronary artery. The infarcted area of myocardium becomes necrotic (dead), so it cant depolarize or contract. 



Although the heart's chambers are filled with blood, the myocardium's own blood supply is provided exclusively by the coronary arteries. A coronary artery can be gradually narrowed by lipid deposits that become atheromatous plaque beneath the intima lining of the vessel. The intima may eventually rupture, exposing the plaque to the blood within the artery. This initiates the immediate formation of a clot (thrombus). The vessel, already narrowed by the plaque, becomes totally occluded by the thrombus. Instantly the infarcted area of the ventricle (without a blood supply) becomes necrotic. Ventricular foci in the hypoxic area around the infarct become very irritable, this can produce deadly ventricular arrhythmias. 

Myocardial Infarction implies the complete occlussion of a coronary artery, which we can diagnose with the EKG. The electrocardiogram will also tell us which coronary artery or coronary branch is occluded, and it can even reveal any blocks in the ventricular conduction caused by the infarction. By careful interpretation of the EKG, we can also determine if a coronary vessel is narrowed, rendering a decreased blood supply to the heart. Practical livesaving knowledge. 


Myocardial infarction is due to the occlussion of a coronary artery supplying the left ventricle, so an area of the heart is without a blood supply and suffers necrosis.

The terms "myocardial infarction", "coronary occlusion" and "heart attack" refer to the same serious phenomenon. 

The heart derives its own blood supply from the coronary arteries, so when a coronary artery or one of its major branches is occluded, an area of the myocardium is without blood supply. 

The infarcted (necrotic) area is primarily in the left ventricle; deadly arrhythmias may result.

We understand that the coronary arteries also supply the right ventricle, so there is often some involvement of the right ventricle,. But since most of the critical problems originate in left ventricular infarcts, myocardial infarction is usually conceptualized in term of the left ventricle. 


Commonly, the thick left ventricle that suffers myocardial infarction

The left ventricle is the thickest chamber of the heart; so if the coronary arteries are narrowed, the left ventricle (which uses the greatest blood supply) is the first to suffer from an obstructed coronary artery.

Blood is pumped to all parts of the body by the powerful, thick, left ventricle.

When we describe infarcts by location, we are speaking of an area within the left ventricle. Coronary arteries to the left ventricle usually send smaller branches  to other regions of the heart, so an infarction of the left ventricle can include a small portion of another chamber.


The necrotic infarcted area of the ventricle (that has no blood supply) is electrically dead and cannot depolarize.

Infarctions usually involve an area of the wall of the left ventricle.

An area of infarction cannot be depolarized because the cells there are without s blood supply, so they are necrotic (functionally dead).

This necrotic infarcted area produces an electrical void, while the rest of the heart (with an adequate blood supply) functions as usual. The infarcted region does not depolarize, so it does not contract, thereby impairing the muscular function of the left ventricle. Also, hypoxic ventricular foci nearby are often the source of serious ventricular arrhythmias. 


The myocardial infarction triad is "ischemia", "injury" and "necrosis", but any of the three may occur alone.

Necrosis (death) of a ventricular region produces dead mayocardial cells that cannot depolarize.

The myocardial infarction triad is the basis for recognizing and diagnosing a myocardial infarction.

The word hypoxia means decreased oxygen; in the heart, it is usually caused by ischemia, which literally means reduced blood supply (diminished blood flow).

"Ischemia", "injury" and "necrosis" need not all be present at once in order to establish the diagnosis of myocardial infarction. Routine EKG interpretation requires checking these infarction criteria.

Credit: Dale Dubin-RapidInterpreatation Of EKG 

Sunday, August 13, 2017

Basic ECG Part III-P Wave & PR Interval

Basic ECG Part III
P Wave & PR Interval

Credit To Dr Rayney Azmi Bin Ali

++Characteristics Of The Normal Sinus P Wave++

Morphology

Smooth contour
Monophasic in lead II
Biphasic in V1

Axis

Normal P wave axis is between 0° and +75°
P waves should be upright in leads I and II, inverted in aVR
Duration

*< 120 ms

Amplitude

*< 2.5 mm in the limb leads,
*< 1.5 mm in the precordial leads

Atrial abnormalities are most easily seen in the inferior leads (II, III and aVF) and lead V1, as the P waves are most prominent in these leads.

The Atrial Waveform-Relationship To The P Wave

*Atrial depolarisation proceeds sequentially from right to left, with the right atrium activated before the left atrium.
*The right and left atrial waveforms summate to form the P wave.
*The first 1/3 of the P wave corresponds to right atrial activation, the final 1/3 corresponds to left atrial activation; the middle 1/3 is a combination of the two.
*In most leads (e.g. lead II), the right and left atrial waveforms move in the same direction, forming a monophasic P wave.
*However, in lead V1 the right and left atrial waveforms move in opposite directions. This produces a biphasic P wave with the initial positive deflection corresponding to right atrial activation and the subsequent negative deflection denoting left atrial activation.
*This separation of right and left atrial electrical forces in lead V1 means that abnormalities affecting each individual atrial waveform can be discerned in this lead. Elsewhere, the overall shape of the P wave is used to infer the atrial abnormality.



First Degree AV Block Vs Second Degree Mobitz Type I (Wenckebach)

++First Degree AV Block++

*PR interval > 200ms (five small squares)
*‘Marked’ first degree block if PR interval > 300ms

Causes of First Degree AV Block

*Increased vagal tone
*Athletic training
*Inferior MI
*Mitral valve surgery
*Myocarditis (e.g. Lyme disease)
*Electrolyte disturbances (e.g. Hyperkalaemia)
*AV nodal blocking drugs (beta-blockers, calcium channel blockers, digoxin, amiodarone)
*May be a normal variant

++Second Degree Mobitz Type I (Wenckebach)++

Definition Of Wenckebach Phenomenon:

*Progressive prolongation of the PR interval culminating in a non-conducted P wave.
*The PR interval is longest immediately before the dropped beat.
*The PR interval is shortest immediately after the dropped beat.

Other Features Of Second Degree Mobitz Type I

*The P-P interval remains relatively constant.
*The greatest increase in PR interval duration is typically between the first and second beats of the cycle.
*The R-R interval progressively shortens with each beat of the cycle.
*The Wenckebach pattern tends to repeat in P:QRS groups with ratios of 3:2, 4:3 or 5:4.

Mechanism 

*Mobitz I is usually due to reversible conduction lock at the level of the AV node.
*Malfunctioning AV node cells tend to progressively fatigue until they fail to conduct an impulse.
*This is different to cells of the His-Purkinje system which tend to fail suddenly and unexpectedly (i.e. producing a Mobitz II block).

Causes of Wenckebach Phenomenon

*Drugs: beta-blockers, calcium channel blockers, digoxin, amiodarone
*Increased vagal tone (e.g. athletes)
*Inferior MI
*Myocarditis
*Following cardiac surgery (mitral valve repair, Tetralogy of Fallot repair)

Clinical Significance of AV Block: Second Degree, Mobitz I

*Mobitz I is usually a benign rhythm, causing minimal haemodynamic disturbance and with low risk of progression to third degree heart block.
*Asymptomatic patients do not require treatment.
*Symptomatic patients usually respond to atropine.
*Permanent pacing is rarely required.

++Second Degree Mobitz Type II++

AV Block: 2nd degree, Mobitz II Overview

*Intermittent non-conducted P waves without progressive prolongation of the PR interval (compare this to Mobitz I).
*The PR interval in the conducted beats remains constant.
*The P waves ‘march through’ at a constant rate.
*The RR interval surrounding the dropped beats is an exact multiple of the preceding RR interval (e.g. double the preceding RR interval for a single dropped beat, treble for two dropped beats, etc)

Mechanism

*Mobitz II is usually due to failure of conduction at the level of the His-Purkinje system (i.e. below the AV node).
*While Mobitz I is usually due to a functional suppression of AV conduction (e.g. due to drugs, reversible ischaemia), Mobitz II is more likely to be due to structural damage to the conducting system (e.g. infarction, fibrosis, necrosis).
*Patients typically have a pre-existing LBBB or bifascicular block, and the 2nd degree AV block is produced by intermittent failure of the remaining fascicle (“bilateral bundle-branch block”).
*In around 75% of cases, the conduction block is located distal to the Bundle of His, producing broad QRS complexes.
*In the remaining 25% of cases, the conduction block is located within the His Bundle itself, producing narrow QRS complexes.
*Unlike Mobitz I, which is produced by progressive fatigue of the AV nodal cells, Mobitz II is an “all or nothing” phenomenon whereby the His-Purkinje cells suddenly and unexpectedly fail to conduct a supraventricular impulse.
*There may be no pattern to the conduction blockade, or alternatively there may be a fixed relationship between the P waves and QRS complexes, e.g. 2:1 block, 3:1 block.

Causes of Mobitz II

*Anterior MI (due to septal infarction with necrosis of the bundle branches).
*Idiopathic fibrosis of the conducting system (Lenegre’s or Lev’s disease).
*Cardiac surgery (especially surgery occurring close to the septum, e.g. mitral valve repair)
*Inflammatory conditions (rheumatic fever, myocarditis, Lyme disease).
*Autoimmune (SLE, systemic sclerosis).
*Infiltrative myocardial disease (amyloidosis, haemochromatosis, sarcoidosis).
*Hyperkalaemia.
*Drugs: beta-blockers, calcium channel blockers, digoxin, amiodarone.

Clinical Significance

*Mobitz II is much more likely than Mobitz I to be associated with haemodynamic compromise, severe bradycardia and progression to 3rd degree heart block.
*Onset of haemodynamic instability may be sudden and unexpected, causing syncope (Stokes-Adams attacks) or sudden cardiac death.
*The risk of asystole is around 35% per year.
*Mobitz II mandates immediate admission for cardiac monitoring, backup temporary pacing and ultimately insertion of a permanent pacemaker.




Second Degree AV Block Vs SVT

++AV Block:Second Degree, “Fixed Ratio” Blocks++

Fixed Ratio AV blocks

*Second degree heart block with a fixed ratio of P waves: QRS complexes (e.g. 2:1, 3:1, 4:1).
*Fixed ratio blocks can be the result of either Mobitz I or Mobitz II conduction.

Mobitz I or II?

*It is not always possible to determine the type of conduction disturbance producing a fixed ratio block, although clues may be present.
*Mobitz I conduction is more likely to produce narrow QRS complexes, as the block is located at the level of the AV node. This type of fixed ratio block tends to improve with atropine and has an overall more benign prognosis.
*Mobitz II conduction typically produces broad QRS complexes, as it usually occurs in the context of pre-existing LBBB or bifascicular block. This type of fixed ratio block tends to worsen with atropine and is more likely to progress to 3rd degree heart block or asystole.
*However, this distinction is not infallible. In approximately 25% of cases of Mobitz II, the block is located in the Bundle of His, producing a narrow QRS complex. Furthermore, Mobitz I may occur in the presence of a pre-existing bundle branch block or interventricular conduction delay, producing a broad QRS complex.
*The only way to be certain is to observe the patient for a period of time (e.g. watch the cardiac monitor, print a long rhythm strip, take serial ECGs) and observe what happens to the PR intervals. Often, periods of 2:1 or 3:1 block will be interspersed with more characteristic Wenckebach sequences or runs of Mobitz II.

++High Grade AV Block++

High Grade AV Block Definition

*Second degree heart block with a P:QRS ratio of 3:1 or higher, producing an extremely slow ventricular rate.
*Unlike 3rd degree heart block there is still some relationship between the P waves and the QRS complexes.
*High-grade AV block may result from either Mobitz I or Mobitz II AV block.


++AV Block: Third Degree (Complete Heart Block)++



Complete Heart Block (CHB) Overview

*In complete heart block, there is complete absence of AV conduction – none of the supraventricular impulses are conducted to the ventricles.
*Perfusing rhythm is maintained by a junctional or ventricular escape rhythm. Alternatively, the patient may suffer ventricular standstill leading to syncope (if self-terminating) or sudden cardiac death (if prolonged).
*Typically the patient will have severe bradycardia with independent atrial and ventricular rates.

Mechanism

*Complete heart block is essentially the end point of either Mobitz I or Mobitz II AV block.
*It may be due to progressive fatigue of AV nodal cells as per Mobitz I (e.g. secondary to increased vagal tone in the acute phase of an inferior MI).
*Alternatively, it may be due to sudden onset of complete conduction failure throughout the His-Purkinje system, as per Mobitz II (e.g. secondary to septal infarction in acute anterior MI).
*The former is more likely to respond to atropine and has a better overall prognosis.

Causes Of Complete Heart Block

The causes are the same as for Mobitz I and Mobitz II second degree heart block. The most important aetiologies are:

*Inferior myocardial infarction
*AV-nodal blocking drugs (e.g. calcium-channel blockers, beta-blockers, digoxin)
*Idiopathic degeneration of the conducting system (Lenegre’s or Lev’s disease)

Clinical Significance

*Patients with third degree heart block are at high risk of ventricular standstill and sudden cardiac death.
*They require urgent admission for cardiac monitoring, backup temporary pacing and usually insertion of a permanent pacemaker.

Complete Heart Block Should Not Be Confused With

*High grade AV block: A type of severe second degree heart block with a very slow ventricular rate but still some evidence of occasional AV conduction.

*AV dissociation: This term indicates only the occurrence of independent atrial and ventricular contractions and may be caused by entities other than complete heart block (e.g. “interference-dissociation” due to the presence of a ventricular rhythm such as AIVR or VT).



PAC Vs Junctional Rhythm

Inverted P Wave

*P-wave inversion in the inferior leads indicates a non-sinus origin of the P waves.
*When the PR interval is < 120 ms, the origin is in the AV junction (e.g. accelerated junctional rhythm).
*When the PR interval is ≥ 120 ms, the origin is within the atria (e.g. ectopic atrial rhythm).

Multiple P Wave Morphologies

*The presence of multiple P wave morphologies indicates multiple ectopic pacemakers within the atria and/or AV junction.
*If ≥ 3 different P wave morphologies are seen, then multifocal atrial rhythm is diagnosed.
*If ≥ 3 different P wave morphologies are seen and the rate is ≥ 100, then multifocal atrial tachycardia (MAT) is diagnosed.

P Pulmonale

Right Atrial Enlargement-Lead II

*In right atrial enlargement, right atrial depolarisation lasts longer than normal and its waveform extends to the end of left atrial depolarisation.
*Although the amplitude of the right atrial depolarisation current remains unchanged, its peak now falls on top of that of the left atrial depolarisation wave.
*The combination of these two waveforms produces a P waves that is taller than normal (> 2.5 mm), although the width remains unchanged (< 120 ms).

Right Atrial Enlargement-Lead V1


*Right atrial enlargement causes increased height (> 1.5mm) in V1 of the initial positive deflection of the P wave.

P Mitrale

Left Atrial Enlargement-Lead II

*In left atrial enlargement, left atrial depolarisation lasts longer than normal but its amplitude remains unchanged.
*Therefore, the height of the resultant P wave remains within normal limits but its duration is longer than 120 ms.
*A notch (broken line) near its peak may or may not be present (“P mitrale”).

Left Atrial Enlargement-Lead V1


Left atrial enlargement causes widening (> 40ms wide) and deepening (> 1mm deep) in V1 of the terminal negative portion of the P wave.



Biatrial Enlargement

*Biatrial enlargement is diagnosed when criteria for both right and left atrial enlargement are present on the same ECG.
*The spectrum of P-wave changes in leads II and V1 with right, left and bi-atrial enlargement is summarised in the following diagram.
*Common P Wave Abnormalities.

Common P Wave Abnormalities

*P mitrale (bifid P waves), seen with left atrial enlargement.
*P pulmonale (peaked P waves), seen with right atrial enlargement.
*P wave inversion, seen with ectopic atrial and junctional rhythms.
*Variable P wave morphology, seen in multifocal atrial rhythms.




Wolff-Parkinson-White Syndrome Pre Excitation Atrial Fibrillation

Wolff-Parkinson-White Syndrome With Delta Wave

++PR Interval++

*The PR interval is the time from the onset of the P wave to the start of the QRS complex.
*It reflects conduction through the AV node.
*The normal PR interval is between 120 – 200 ms duration (three to five small squares).
*If the PR interval is > 200 ms, first degree heart block is said to be present.
*PR interval < 120 ms suggests pre-excitation (the presence of an accessory pathway between the atria and ventricles) or AV nodal (junctional) rhythm.
*Type Of AV Block has been describe above.

Short PR interval (<120ms)

A short PR interval is seen with:
*Preexcitation syndromes.
*AV nodal (junctional) rhythm.

Wolff-Parkinson-White (WPW) And Lown-Ganong-Levine (LGL) Syndromes.

*These involve the presence of an accessory pathway connecting the atria and ventricles.
*The accessory pathway conducts impulses faster than normal, producing a short PR interval.
*The accessory pathway also acts as an anatomical re-entry circuit, making patients susceptible to re-entry tachyarrhythmias.
*Patients present with episodes of paroxsymal supraventricular tachycardia (SVT), specifically atrioventricular re-entry tachycardia (AVRT), and characteristic features on the resting 12-lead ECG.

Wolff-Parkinson-White Syndrome

*The characteristic features of Wolff-Parkinson-White syndrome are a short PR interval, broad QRS and a slurred upstroke to the QRS complex, the delta wave.
*Short PR (<120ms), broad QRS and delta waves in WPW syndrome

Wolff -Parkinson- White Syndrome Cases Usually

*ECG pattern depends on where the accessory pathway inserts.
Classically:
*Short PR interval <120 msecs.
*QRS > 100msecs.
*Delta wave-slurred upstroke at beginning of QRS.
Different insertions:
*Normal QRS if pathway inserts into infranodal conduction tissue just below AV node
*Grossly wide and abnormal QRS if pathway inserts into non-conduction tissue.

Key Management Points For WPW

*A heart rate ≥ 200 should make you think of a pre-excitation syndrome.
*Narrow complex SVT is treated identically to non-WPW SVT.
*Don’t try and be clever with drugs in broad complex tachycardias and WPW.
*Using AV nodal blockers in WPW and AF can result in 1:1 conduction to the ventricles.
*This is also know as Ventricular Fibrillation.
*Just shut-up + DC cardiovert them.

Lown-Ganong-Levine Syndrome

*The features of LGL syndrome are a very short PR interval with normal P waves and QRS complexes and absent delta waves.
*Short PR interval with normal QRS complexes in LGL syndrome

AV Nodal (Junctional) Rhythm

*Junctional rhythms are narrow complex, regular rhythms arising from the AV node.
*P waves are either absent or abnormal (e.g. inverted) with a short PR interval (retrograde P waves).