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Garcia, Cholson Banjo E.

 Conduction disturbance

 Originate from:

◦ sinus node

◦ AV node

◦ bundle branch

 Sinoatrial Block

 Atrioventricular Block

 Bundle Branch Block

 Fascicular Block

 Impaired conduction from the SA node to the

atria

 No depolarization of the atria

 Absence of PQRST complex

 Etiology

◦ Increased vagal tone

◦ Inferior wall MI

◦ Age related degeneration

◦ Drugs (digoxin, beta blockers, ccb, class IA-

antiarrythmic)

◦ Hyperkalemia

◦ myocarditis

 RR interval: irregular (creating a pause, atria is

blocked so it never depolarized

 PP interval surrounding the pause is commonly

multiple of the previous PP interval

 1st degree AV block

 2nd degree AV block, Type 1 (Mobitz or

Wenkebach)

 2nd degree AV block, Type 2 (Mobitz II)

 3rd degree AV block (CHB)

 Prolonged conduction between the atria and

the ventricles

 Partial block within the AV node

 Prolongation of the PR interval and

preservation of the underlying rhythm

• Etiology

– Drugs

– Increased vagal tone

– Hyperkalemia

– MI (inferior wall)

– Myocarditis

– Degeneration of conducting pathways assoc. with

aging

– Idiopathic cause

 PR interval: > 0.20 seconds

 Length of PR interval is constant

 P wave is followed by a QRS complex

 Mobitz type I or Wenckebach

 Intermittent conduction between the atria and

ventricle

 Found with the AV node

• Etiology

– Digitalis

– Escessive vagal tone

– MI (inferior wall)

– Ischemic heart disease

– Myocarditis

– Normal variant

 Progressive lengthening of the PR interval

until a QRS complex is dropped; P wave

appears on time, but no QRS follows

 RR interval: irregular owing to drop beats

causing the QRS complex to appear clustered

together (narrow)

 “Grouped Beating”

 PP: constant

 Mobitz type II

 Intermittent and sudden loss of conduction

between atria and the ventricles

 Found below the bundle of his

 Can proceed to complete heart block

 Ventricular rate tends to be slower and

cardiac output diminishes

• Etiology

– Acute Myocardial Infarction (anterior wall)

– Drugs (digitalis, beta blocker, ccb)

– Degeneration of electrical conduction system

(assoc. with aging)

 PR interval: constant or fixed

 QRS: wider than normal because of associated

conduction block in ventricles

 Conduction ratio varies (1:1, 2:1; 3:1)

 PP: regular

 RR: irregular

 Complete heart block

 Complete absence of conduction between

atria and ventricles

• Etiology

– Drug toxicity (digoxin, beta blocker, ccb)

– Excessive vagal tone

– Acute MI

– Age-related Degeneration of electrical conduction

system

– Myocarditis

– Endocarditis

– Cardiac Surgery

– Congenital origin

 Atrial and ventricular rates are different

 No relationship between P waves and the QRS

complex

 P waves appear but no QRS

 PP and RR interval: constant

 Look for 3 ECG patterns

1. Look for the RR interval. Regular or irregular?

2. Look at the P wave. Is there one or more P wave

for every QRS

3. Look at the PR interval. Stay the same or change?

 If REGULAR (1st degree or 3rd degree)

◦ Only 1 P wave for every QRS

◦ PR interval stay the same

 1st degree

◦ more than 1 P wave

◦ PR interval changes

 3rd degree

 IRREGULAR ( 2nd degree)

◦ PR interval change: 2nd degree AV block, TYPE I

◦ PR interval stay the same: 2nd degree AV Block, TYPE

II

 Defect in the intraventricular conduction

 Supravetricular impulse: from the unblocked

branch depolarizes one ventricle

 Blocked branch: impluse spread slowly

through the ventricular muscle resulting in

abnormal depolarization

 Hallmark: abnormal wide QRS complex

 Conduction Delay in the right bundle branch

• Etiology

– RVH

– Right ventricular strain

– ASD

– Wolf parkinson -white

– Coronary artery disease

– Myocarditis

– Cardiac contusion

– Idiopathic cause

 QRS complex: 0.12 or more in width

 QRS is wide and positive assumes in lead V1

 rSR: leads V1 and V2

 Wide or Deep I, avL V5 and V6

 Down slopping of ST segment V1 and V2

• Etiology

– LVH

– Cardiomyopathy

– HPN

– Wolf parkinson -white

– Coronary artery disease

– Myocarditis

 QRS complex: 0.12 or more in width

 QRS is negative V1 and V2

 rSR (rabbit ear) in I, avL, V5, V6

 Wide or deep S V1 and V2

 Down slopping of ST segment I, avL, V5, V6

Right Bundle Branch Block Left Bundle Branch Block



QRS wide and QRS wide and

predominantly positive V1 predominantly negative

V1

rSR in lead V1 rSR in lead V6



Deep S in lead V6 Deep S in lead V1



Late intrinsicoid Late intrinsicoid

deflection in lead V1 deflection in lead V6

 Hemiblocks

 Disturbed conduction in either the anterior or

posterior division, or fasicle, of the left

bundle branch

 Delay in the conduction through the anterior

fascicle of the LBB

 Anterior fascicle long thin and has a single

blood supply, making it vulnerable to block

• Etiology

– Coronary artery disease

– MI

– Congenital Heart disease

– Cardiac surgery

– Aging process

– Normal variant

 QRS: prolonged (0.08-0.11)

 Left axis deviation QRS axis (-45 and -90)

 Small q wave and a tall R wave in lead I and

avL

 Small r wave and deep S wave in lead II, III

and avF

 Delay in the conduction through the posterior

fascicle of the LBB

 Posterior: short, thick and has double blood

supply

 Appearance implies large amount of

Myocardial injury has occurred

• Etiology

– Coronary artery disease

– MI

– Congenital Heart disease

– Cardiac surgery

 QRS: prolonged (0.08-0.11)

 Right axis deviation QRS axis (+90 and

+180)

 Small q wave and a tall R wave in lead II, III

and avF

 Small r wave and deep S wave in lead I and

avL

LAFB LPFB

LAD RAD

qR in lead I qR in lead III

rS in lead III rS in lead I



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