TextbookCardiologyBundle Branch Block

Bundle Branch Block

Conduction delay or block in one of the bundle branches causing widened QRS (≥120 ms) with characteristic morphology. LBBB may indicate structural heart disease; RBBB can be a normal variant.

Key Facts

QRS duration ≥120 ms with characteristic morphology distinguishes complete BBB from incomplete (<120 ms) RBBB: RSR' pattern in V1-V2 ('M' shaped), wide slurred S wave in V1, I, V6; may be normal variant in young/healthy individuals LBBB: broad notched R wave in I, aVL, V5-V6 ('M' shaped), deep S wave in V1-V3; usually indicates structural heart disease New LBBB with chest pain should be treated as STEMI equivalent and activate PPCI pathway LBBB makes interpretation of ST segments unreliable — use Sgarbossa criteria for MI diagnosis with LBBB Bifascicular block (RBBB + left anterior or posterior hemiblock): risk of progression to CHB if acute LBBB is associated with increased cardiovascular mortality; RBBB in isolation is generally benign

Overview

Key Facts

Bundle branch block (BBB) occurs when conduction is delayed or blocked in one of the main bundle branches of the His-Purkinje system. This produces a wide QRS complex (≥120 ms) with a characteristic morphology depending on whether the right or left bundle is affected.

Epidemiology

  • RBBB: prevalence ~0.8-2% in the general population; increases with age
  • LBBB: prevalence ~0.5-1%; strongly associated with age and structural heart disease
  • RBBB is more common than LBBB in the general population
  • LBBB prevalence: ~5-10% in patients with heart failure

Aetiology

RBBB:

  • Normal variant (especially in young adults)
  • Right heart strain: PE, cor pulmonale, pulmonary hypertension
  • Ischaemic heart disease
  • Atrial septal defect (ASD)
  • Myocarditis, cardiomyopathy
  • Post-cardiac surgery, right heart catheterisation

LBBB:

  • Hypertensive heart disease
  • Ischaemic heart disease
  • Dilated cardiomyopathy
  • Aortic valve disease (especially aortic stenosis)
  • Degenerative conduction disease
  • Myocarditis
  • Post-TAVI (up to 20-30%)

Pathophysiology

  • Block in one bundle branch causes the ventricle on that side to depolarise late via slow cell-to-cell conduction from the contralateral ventricle
  • This produces a widened QRS with a characteristic 'double-peak' pattern
  • Dyssynchronous ventricular contraction in LBBB can impair cardiac output and contribute to heart failure
  • LBBB can be an indication for cardiac resynchronisation therapy (CRT) in heart failure

Clinical Presentation

RBBB

  • Usually asymptomatic if isolated
  • Wide splitting of S2 (delayed closure of pulmonary valve)
  • May be associated with symptoms of underlying condition (e.g., PE, ASD)

LBBB

  • May be asymptomatic or associated with symptoms of underlying cardiac disease
  • Reversed splitting of S2 (delayed closure of aortic valve)
  • New LBBB with acute chest pain = STEMI equivalent
  • Chronic LBBB may contribute to heart failure via dyssynchrony

Red Flags

  • New LBBB with chest pain: treat as STEMI — activate PPCI pathway
  • New BBB following syncope: risk of intermittent higher-degree block
  • Alternating RBBB and LBBB: indicates bilateral bundle disease, high risk of CHB
  • Bifascicular block with syncope: consider pacemaker

Differential Diagnosis

DiagnosisKey FeaturesInvestigation
Ventricular pre-excitation (WPW)Short PR, delta wave, wide QRSECG
Ventricular paced rhythmPacing spikes, LBBB morphology (RV pacing)Device check
HyperkalaemiaBroad QRS, peaked T wavesU&Es
Ventricular tachycardiaWide complex tachycardia, AV dissociationECG, clinical context
Incomplete BBBQRS 100-119 ms with BBB morphologyECG
Na-channel blocker toxicityWide QRS, history of TCA/flecainide overdoseDrug history, levels

Diagnosis / Investigation

Bedside

  • 12-lead ECG: QRS morphology and width, axis, Sgarbossa criteria if LBBB
  • Comparison with previous ECGs: to determine if BBB is new or old

Bloods

  • Troponin: if new LBBB with symptoms
  • BNP/NT-proBNP: heart failure assessment
  • U&Es: electrolytes
  • D-dimer/CTPA: if PE suspected with RBBB

Imaging

  • Echocardiography: assess LV function, structural heart disease, dyssynchrony
  • Cardiac MRI: if cardiomyopathy or myocarditis suspected

Special Tests

  • Holter monitor: if symptoms suggest intermittent higher-degree block
  • Exercise testing: new BBB during exercise may indicate coronary disease
  • Electrophysiology study: if bifascicular block with syncope to assess HV interval

Management

Non-pharmacological

  • Isolated RBBB in young healthy patient: no treatment needed, reassurance
  • Investigate and treat underlying cause

Pharmacological

  • No specific drug treatment for BBB itself
  • Treat underlying condition: heart failure, ischaemia, hypertension
  • New LBBB with chest pain: full ACS management pathway

Surgical/Interventional

  • CRT (cardiac resynchronisation therapy): indicated for LBBB with QRS ≥150 ms and LVEF ≤35% with heart failure symptoms (NICE TA314)
    • Biventricular pacing resynchronises contraction
    • Landmark trials: COMPANION, CARE-HF, MADIT-CRT
  • Pacemaker: for bifascicular/trifascicular block with syncope or evidence of intermittent CHB
  • ICD ± CRT: if heart failure with reduced EF criteria met

Referral Criteria

  • New LBBB with symptoms: urgent cardiology referral
  • LBBB with heart failure: assess for CRT
  • Bifascicular block with syncope: urgent pacemaker assessment
  • Alternating BBB: urgent pacing consideration

Prognosis

  • Isolated RBBB: benign prognosis, no excess mortality in absence of structural heart disease
  • LBBB: associated with increased cardiovascular mortality (~2-3 fold), largely driven by underlying heart disease
  • New LBBB: ~50% associated with significant cardiac pathology
  • Bifascicular block: annual progression to CHB ~1-4%
  • CRT in LBBB with HF: reduces mortality by ~35% (CARE-HF trial)
  • Post-TAVI LBBB: may need permanent pacemaker in ~10-20%

Other Relevant Information

ECG Patterns Summary

FeatureRBBBLBBB
V1 morphologyRSR' (M-shaped)Deep QS or rS
V6 morphologyDeep slurred SBroad notched R (M-shaped)
QRS duration≥120 ms≥120 ms
AxisOften RADOften LAD
ST/T changesDiscordant in V1-V3Discordant throughout

Sgarbossa Criteria (MI in LBBB)

CriterionPoints
Concordant ST elevation ≥1 mm5
Concordant ST depression ≥1 mm in V1-V33
Discordant ST elevation ≥5 mm2
Score ≥3 suggests MI