Conceptual Overview

Conduction blocks occur when electrical impulses are delayed or completely blocked as they travel through the cardiac conduction system. They can occur at any level - from the AV node to the bundle branches and fascicles.

The cardiac conduction system has a predictable hierarchy:

  • AV node: Connects atrial and ventricular conduction; normally the only electrical bridge between atria and ventricles
  • Bundle of His: Single pathway that emerges from the AV node and penetrates the cardiac skeleton
  • Bundle branches: Right bundle branch (single fascicle) and left bundle branch (divides into anterior and posterior fascicles)
  • Purkinje network: Terminal fibers that deliver impulses to ventricular myocardium

Block at each level produces characteristic ECG patterns and carries different prognostic implications. The key clinical question is always: does this patient need a pacemaker?

Key concept: Blocks within the AV node (supra-Hisian) tend to be more benign because the AV node has rich autonomic innervation and reliable escape rhythms. Blocks below the AV node (infra-Hisian) are more dangerous because the escape pacemakers are slower and less reliable, with a higher risk of asystole.
First-Degree AV Block

First-degree AV block is technically a conduction delay rather than a true block - every atrial impulse still reaches the ventricles, just more slowly than normal.

ECG Characteristics

  • PR interval: Prolonged >0.20 seconds (more than 5 small boxes), but constant and consistent
  • Every P wave is followed by a QRS: 1:1 AV conduction is maintained
  • QRS: Narrow (unless coexisting BBB)
  • Rhythm: Regular

Clinical Significance

  • Often benign - seen in athletes, young healthy individuals, and with increased vagal tone
  • Can be caused by medications (beta-blockers, calcium channel blockers, digoxin, amiodarone)
  • May be associated with inferior MI (AV node ischemia) or myocarditis
  • No specific treatment required in isolation
  • Extreme PR prolongation (>0.30 sec) may cause symptoms due to loss of AV synchrony (atrial contraction against closed AV valves - "pseudo-pacemaker syndrome")
Don't ignore 1st-degree AV block entirely: While isolated 1st-degree block is benign, it can be a harbinger of more advanced block - especially in the setting of acute inferior MI, Lyme disease, or progressive degenerative conduction disease. Follow up with serial ECGs if the clinical context warrants concern.
Second-Degree AV Block - Type I (Wenckebach)

Second-degree Type I (Mobitz I / Wenckebach) block occurs at the level of the AV node. It represents progressive fatigue of AV nodal conduction until a beat is dropped.

ECG Characteristics

  • Progressive PR prolongation: Each successive PR interval gets slightly longer until a P wave is not followed by a QRS (dropped beat)
  • Grouped beating: Repetitive cycles of progressive PR lengthening followed by a dropped QRS
  • RR intervals: Gradually shorten before the dropped beat (the increment of PR prolongation decreases with each cycle)
  • The pause: Contains the dropped P wave; the pause is less than twice the shortest R-R interval in the group
  • QRS: Narrow (block is at the AV node level)

Clinical Significance

  • Usually benign with low risk of progression to complete heart block
  • Block is at the AV node level (supra-Hisian) - reliable escape rhythms exist
  • Common in: athletes, sleep, young healthy patients, inferior MI
  • Drug-related: beta-blockers, calcium channel blockers, digoxin
  • Rarely requires pacing unless symptomatic with hemodynamic compromise
Wenckebach in inferior MI: Very common (up to 15% of inferior MIs). The AV node receives blood supply from the RCA in 85% of patients. This block is typically transient, resolving within days as the ischemia improves. Monitoring is appropriate; temporary pacing is rarely needed.
Second-Degree AV Block - Type II (Mobitz II)

Second-degree Type II (Mobitz II) block occurs below the AV node - at the level of the bundle of His or bundle branches. This is a much more dangerous block with high risk of progression to complete heart block.

ECG Characteristics

  • Constant PR interval: The PR interval does NOT change before the dropped beat (the defining feature that distinguishes it from Wenckebach)
  • Intermittently dropped QRS: P waves march through at a regular rate, but some fail to conduct
  • Conduction ratio: May be 2:1, 3:1, 4:1, or variable
  • QRS: Often wide (reflecting infra-nodal disease) - especially with coexisting BBB pattern
  • No progressive PR prolongation: This is the critical distinguishing feature from Wenckebach

Clinical Significance

  • High risk of progression to complete heart block - often unpredictably and suddenly
  • Block is infra-Hisian; escape rhythms are slow (20-40 bpm), unreliable, and wide-complex
  • Associated with anterior MI (LAD territory affecting the interventricular septum), degenerative conduction disease, and infiltrative cardiomyopathies
  • Almost always requires permanent pacemaker implantation
  • Transcutaneous pacing pads should be applied immediately while arranging definitive pacing
Mobitz II = pacemaker: Any patient with Mobitz Type II block should be evaluated for permanent pacemaker placement. Unlike Wenckebach, this block can progress to complete heart block without warning. Do NOT discharge these patients without cardiology consultation. Atropine is often ineffective and may paradoxically worsen infra-nodal block.
Third-Degree (Complete) Heart Block

Third-degree (complete) AV block represents complete failure of conduction between atria and ventricles. The atria and ventricles beat independently with no relationship between P waves and QRS complexes.

ECG Characteristics

  • AV dissociation: P waves and QRS complexes occur independently - P waves march through at the sinus rate while QRS occurs at the escape rate
  • Regular atrial rate: P-P intervals are constant
  • Regular ventricular rate: R-R intervals are constant, but slower than the atrial rate
  • No consistent PR relationship: PR intervals vary randomly because P waves and QRS complexes are independent
  • Escape rhythm: Junctional (narrow QRS, 40-60 bpm) if block is at AV node; ventricular (wide QRS, 20-40 bpm) if block is infra-nodal

Junctional vs. Ventricular Escape

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Feature Junctional Escape (AV Nodal Block) Ventricular Escape (Infra-Nodal Block)
QRS width Narrow (<0.12 sec) Wide (>0.12 sec)
Escape rate 40-60 bpm 20-40 bpm
Reliability More reliable Less reliable, risk of asystole
Common cause Inferior MI, medications, congenital Anterior MI, degenerative disease
Atropine response May improve Usually ineffective
Prognosis Better, may be transient Worse, usually permanent
Complete heart block emergency management: Apply transcutaneous pacing pads immediately. Atropine (0.5 mg IV, repeat q3-5min, max 3 mg) may work for junctional escape but often fails for ventricular escape. If hemodynamically unstable, initiate transcutaneous pacing; consider dopamine or epinephrine infusion as a bridge to transvenous pacing. All patients with acquired complete heart block need permanent pacemaker evaluation.
Complete heart block in anterior MI: This is ominous. It indicates massive septal necrosis affecting both bundle branches and typically carries high mortality. It requires immediate temporary transvenous pacing and urgent cardiology consultation. In contrast, complete heart block in inferior MI is often transient (mediated by AV nodal ischemia or vagal reflexes) and may resolve within days.
Right Bundle Branch Block (RBBB)

In RBBB, the right bundle branch is blocked and the right ventricle depolarizes late via cell-to-cell spread from the left ventricle. This produces a characteristic wide QRS with terminal right-directed forces.

ECG Criteria

  • QRS duration: ≥0.12 seconds (complete RBBB); 0.10-0.12 seconds (incomplete RBBB)
  • V1-V2: rsR' pattern (M-shaped QRS) - "rabbit ears" with R' taller than r
  • V5-V6, I: Wide, slurred S wave (late right ventricular activation moving away from left-sided leads)
  • Secondary ST-T changes: ST depression and T wave inversion in V1-V3 (expected, not ischemic)

Clinical Significance

  • Isolated RBBB: Can be a normal variant, particularly in young healthy individuals
  • New RBBB: May indicate acute right ventricular strain (PE, RV infarction), anterior MI, or myocarditis
  • Chronic RBBB: Seen with right ventricular hypertrophy, ASD, chronic lung disease
  • RBBB does NOT obscure STEMI diagnosis: ST elevation in the setting of RBBB is interpretable (unlike LBBB)
Memory aid - "WiLLiaM MaRRoW":
WiLLiaM = In LBBB: W pattern in V1, M pattern in V6
MaRRoW = In RBBB: M pattern in V1, W pattern in V6
This refers to the QRS morphology in the key leads for distinguishing BBBs.
Left Bundle Branch Block (LBBB)

In LBBB, the left bundle branch is blocked and the left ventricle depolarizes late via right-to-left septal activation. This produces a wide QRS with prolonged left-directed forces and profoundly alters the ECG baseline, making ischemia difficult to diagnose.

ECG Criteria

  • QRS duration: ≥0.12 seconds
  • V1: Broad, deep QS or rS pattern (W-shaped)
  • V5-V6, I, aVL: Tall, broad, monophasic R wave (M-shaped) - often notched or slurred
  • No septal Q waves: In V5-V6, I (because septal activation is reversed)
  • Appropriate discordance: ST-T changes opposite to QRS direction (expected - this is NOT ischemia)

Clinical Significance

  • LBBB is almost always pathologic - unlike RBBB, it is rarely a normal variant
  • Common causes: Hypertensive heart disease, coronary artery disease, cardiomyopathy, aortic valve disease, degenerative conduction disease
  • New LBBB with chest pain: Historically treated as STEMI equivalent; current guidelines emphasize using the Sgarbossa criteria to identify MI in the setting of LBBB

Sgarbossa Criteria (Diagnosing MI with LBBB)

  • Concordant ST elevation ≥1 mm in any lead with a positive QRS (5 points) - most specific
  • Concordant ST depression ≥1 mm in V1-V3 (3 points) - posterior MI equivalent
  • Excessive discordant ST elevation: ST elevation ≥1 mm AND ratio of ST elevation to S wave depth >0.25 (Modified Sgarbossa / Smith criteria) - 2 points
  • Score ≥3 suggests acute MI in the setting of LBBB
LBBB and STEMI diagnosis: Do NOT assume all LBBB patients with chest pain are having a STEMI. Use modified Sgarbossa criteria to identify concordant ST changes that indicate true ischemia. "New LBBB = STEMI" is an oversimplification that has been revised in current guidelines. However, new LBBB with ischemic symptoms should still prompt urgent cardiology consultation and serial ECGs.
The most specific Sgarbossa criterion: Concordant ST elevation (ST segment moves in the SAME direction as the QRS) is ~96% specific for MI. In LBBB, normal repolarization should be discordant (opposite to QRS). When ST changes move in the same direction as the QRS, something is forcing them to overcome the expected discordance - that something is acute ischemia.
Fascicular Blocks (Hemiblocks)

The left bundle branch divides into two fascicles: the left anterior fascicle (thin, with single blood supply) and the left posterior fascicle (thick, with dual blood supply). Block of one fascicle produces axis deviation without significant QRS widening.

Left Anterior Fascicular Block (LAFB)

  • Axis: Left axis deviation (−45° to −90°)
  • QRS duration: Normal or slightly prolonged (<0.12 sec)
  • Lead pattern: Small q in I, aVL with tall R; small r in II, III, aVF with deep S
  • Clinical significance: Common, often benign. The anterior fascicle is thin with a single blood supply (LAD), making it vulnerable
  • Most common fascicular block

Left Posterior Fascicular Block (LPFB)

  • Axis: Right axis deviation (>+90°)
  • QRS duration: Normal or slightly prolonged (<0.12 sec)
  • Lead pattern: Small r in I, aVL with deep S; small q in II, III, aVF with tall R
  • Clinical significance: Much less common because the posterior fascicle is thick with dual blood supply (LAD + RCA). When present, usually indicates more severe conduction disease
  • Diagnosis of exclusion: Must rule out RVH, PE, lateral MI, and other causes of right axis deviation before diagnosing LPFB

Bifascicular and Trifascicular Block

  • Bifascicular block: RBBB + LAFB (most common combination) or RBBB + LPFB
  • Trifascicular block: Bifascicular block + 1st-degree AV block (suggests disease in the remaining fascicle but does NOT guarantee it)
  • Clinical significance: Bifascicular block with syncope or alternating BBB patterns should prompt evaluation for permanent pacing
Bifascicular block + syncope = EP study: A patient with RBBB + LAFB (or LPFB) who presents with syncope has significant risk of intermittent complete heart block. Measure the HV interval during electrophysiology study - if ≥70 ms or if infra-Hisian block is provoked, a permanent pacemaker is indicated.
Quick Reference
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Block Type Key ECG Finding Pacemaker Needed?
1st-degree AV PR >0.20 sec, all P waves conducted No (unless extreme PR with symptoms)
2nd-degree Type I Progressive PR prolongation → dropped QRS Rarely (if symptomatic)
2nd-degree Type II Constant PR → suddenly dropped QRS Yes - high progression risk
3rd-degree (complete) AV dissociation; P waves and QRS independent Yes (almost always)
RBBB rsR' in V1; wide S in I, V6 No (isolated)
LBBB Broad R in I, V6; QS in V1 No (isolated)
LAFB Left axis deviation (−45° to −90°) No
LPFB Right axis deviation (exclusion diagnosis) No (isolated)
Bifascicular + syncope RBBB + LAFB/LPFB with symptoms Likely - needs EP study
Clinical Pearls
"Wenckebach = in the node, Mobitz II = below the node": This anatomic distinction drives everything. AV nodal blocks (Wenckebach) are relatively benign with reliable escape rhythms. Infra-nodal blocks (Mobitz II) are dangerous because escape pacemakers are slow, unreliable, and the block can progress suddenly to asystole.
"2:1 block = the diagnostic dilemma": With 2:1 conduction, you can't tell if the PR is progressively prolonging (Wenckebach) or constant (Mobitz II) because you only see one conducted beat at a time. Look at QRS width: narrow QRS favors Wenckebach; wide QRS favors Mobitz II. Atropine may help differentiate (improves Wenckebach, often worsens Mobitz II).
"WiLLiaM MaRRoW": LBBB = W in V1, M in V6. RBBB = M in V1, W in V6. This simple mnemonic immediately tells you which bundle branch block you're looking at.
"Atropine can be dangerous": In infra-nodal block (Mobitz II, complete heart block with wide escape), atropine increases sinus rate but DOESN'T improve conduction below the AV node. The faster sinus rate may suppress the ventricular escape rhythm, potentially causing asystole. Use transcutaneous pacing instead.
New LBBB ≠ automatic cath lab: While historically "new LBBB + chest pain = STEMI," current ACC/AHA guidelines no longer recommend using new LBBB alone as a STEMI equivalent. Apply Sgarbossa/modified Sgarbossa criteria to identify concordant ST changes. However, new LBBB with ongoing ischemic symptoms and hemodynamic instability should still prompt urgent evaluation.
Lyme disease and heart block: In endemic areas, consider Lyme disease in young patients with new AV block (especially fluctuating or high-grade). Lyme carditis can cause any degree of AV block, often with rapid progression and resolution. IV ceftriaxone is the treatment, and temporary pacing is sometimes needed. A permanent pacemaker is almost never required.
References
  1. Kusumoto FM, Schoenfeld MH, Barrett C, et al. 2018 ACC/AHA/HRS Guideline on the Evaluation and Management of Patients With Bradycardia and Cardiac Conduction Delay. Circulation. 2019;140(13):e382-e482.
  2. Smith SW, Dodd KW, Henry TD, et al. Diagnosis of ST-Elevation Myocardial Infarction in the Presence of Left Bundle Branch Block With the ST-Elevation to S-Wave Ratio in a Modified Sgarbossa Rule. Ann Emerg Med. 2012;60(6):766-776.
  3. Khan, M. G. (2007). Rapid ECG Interpretation. Humana.
  4. Wang, K. (2012). Atlas of Electrocardiography. JP Medical Ltd.
  5. ECG Library - LITFL - Life in the Fast Lane. https://litfl.com/ecg-library/
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