Here is a comprehensive guide to 10 Common Heart Diseases with ECG Changes and Images:
10 Common Heart Diseases β ECG Changes & Images
1. π« ST-Elevation Myocardial Infarction (STEMI)
Overview: Acute occlusion of a coronary artery causing transmural myocardial injury. A true cardiac emergency requiring immediate reperfusion.
ECG Changes:
- ST elevation β₯1 mm in β₯2 contiguous leads (β₯2 mm in precordial leads)
- Hyperacute T-waves (tall, peaked) β earliest finding
- Reciprocal ST depression in opposite leads
- Pathological Q-waves develop within hours (irreversible necrosis)
- T-wave inversions in the post-infarct stage
- Localization by leads:
- Anterior (V1βV4): LAD occlusion
- Inferior (II, III, aVF): RCA or circumflex
- Lateral (I, aVL, V5βV6): circumflex artery
ECG Image β Anterior STEMI (LAD occlusion):
Massive anterolateral STEMI: convex ST elevation in V1βV6 and leads I/aVL, with reciprocal ST depression in II/III/aVF. Proximal LAD occlusion.
ECG Image β Inferolateral STEMI:
ST elevation in II, III, aVF and V4βV6 (green circles) with reciprocal depression in I, aVL and V2βV3 (yellow arrows).
2. π Atrial Fibrillation (AF)
Overview: Disorganized electrical activity in the atria producing chaotic depolarization. The most common sustained cardiac arrhythmia worldwide.
ECG Changes:
- Absent P-waves β replaced by fine fibrillatory (f) waves (best seen in V1)
- Irregularly irregular R-R intervals β the hallmark
- Narrow QRS complexes (unless aberrant conduction/WPW)
- Ventricular rate varies widely (slow, controlled, or rapid response)
- Baseline undulation rather than flat isoelectric line
ECG Image:
Classic AF: complete absence of P-waves, fine fibrillatory baseline (visible in V1), narrow QRS with irregular R-R intervals throughout all 12 leads.
3. π Complete (Third-Degree) AV Block
Overview: Complete failure of conduction between atria and ventricles. Atria and ventricles beat independently (AV dissociation).
ECG Changes:
- P-waves and QRS complexes are completely dissociated β no fixed PR interval
- Atrial rate is faster than ventricular rate
- Escape rhythm: narrow QRS (junctional, ~40β60 bpm) or wide QRS (ventricular, ~20β40 bpm)
- Profound bradycardia
- Prolonged QT may occur with ventricular escape rhythm
ECG Image:
Third-degree AV block: P-waves (black arrows in rhythm strip) occur regularly but bear no relationship to the wide QRS escape complexes at ~33 bpm. QTc 560 ms.
4. π« Pulmonary Embolism (PE)
Overview: Acute obstruction of the pulmonary vasculature causes acute right ventricular (RV) pressure overload reflected on the ECG.
ECG Changes:
- Sinus tachycardia β most common finding
- S1Q3T3 pattern (McGinn-White sign): deep S in I, Q-wave in III, T-wave inversion in III
- T-wave inversions V1βV4 β right ventricular strain
- Incomplete or complete RBBB β acute RV dilatation
- Rightward axis deviation
- P pulmonale (peaked P in II) in massive PE
ECG Image:
Acute PE: Sinus tachycardia with classic S1Q3T3 (S-wave lead I, Q-wave lead III, inverted T lead III) and deep T-wave inversions V1βV6 indicating severe RV strain.
5. π₯ Acute Pericarditis
Overview: Inflammation of the pericardial sac causes diffuse epicardial injury, producing widespread ECG changes that evolve through 4 classic stages.
ECG Changes (Stage I β Acute):
- Diffuse concave (saddle-shaped) ST elevation in almost all leads EXCEPT aVR and V1
- PR-segment depression in most leads (highly specific) β aVR shows reciprocal PR elevation
- Spodick's sign: downward sloping TP segment
- No reciprocal ST changes in a typical vascular territory (unlike STEMI)
- ST:T-wave amplitude ratio in V6 >0.25 favors pericarditis
ECG Image:
Acute pericarditis: diffuse concave ST elevation in I, II, III, aVF and V2βV6; PR-segment depression in II, aVF and V4βV6; reciprocal ST depression and PR elevation in aVR.
6. 𧬠Hypertrophic Cardiomyopathy (HCM)
Overview: Genetic (sarcomere protein mutations) disorder causing asymmetric myocardial hypertrophy with myofiber disarray. A leading cause of sudden death in young athletes.
ECG Changes:
- Left ventricular hypertrophy voltage criteria (Sokolow-Lyon: S in V1 + R in V5/V6 >35 mm)
- Deep T-wave inversions β especially in apical HCM (Yamaguchi syndrome): giant negative T-waves in V3βV5
- ST depression with lateral strain pattern
- Absence of septal Q-waves in I, aVL, V5, V6 (due to abnormal septal depolarization)
- Left axis deviation
- Atrial fibrillation common
ECG Image β Apical HCM (Yamaguchi syndrome):
Apical HCM: Normal sinus rhythm with LVH voltage, deep symmetric T-wave inversions across virtually all leads (V2βV6, I, II, aVF). Hallmark of Yamaguchi syndrome.
ECG Image β HCM Variants (Composite):
Composite showing HCM variants: Panel A = concentric hypertrophy (high R-wave voltage), B = septal hypertrophy, C = apical (giant T-wave inversions 12 mm in V5), each correlated with cardiac MRI.
7. β‘ Wolff-Parkinson-White (WPW) Syndrome
Overview: Presence of an accessory bypass tract (Bundle of Kent) that pre-excites the ventricle, bypassing the AV node. Can cause life-threatening tachyarrhythmias.
ECG Changes:
- Short PR interval (<120 ms) β AV node bypassed
- Delta wave β slurred initial upstroke of QRS (pre-excitation)
- Widened QRS (>120 ms) β fusion of normal and accessory conduction
- Secondary ST-T changes β discordant to QRS
- Accessory pathway location estimated by delta wave polarity:
- Negative delta in inferior leads (II, III, aVF) β posteroseptal pathway
- Positive in V1 β left-sided pathway
ECG Image:
Classic WPW: Short PR interval, prominent delta waves in leads II and III (red arrows), widened QRS, consistent with an anteroseptal accessory pathway. Risk of sudden death via AF with rapid ventricular conduction.
8. π₯ Ventricular Tachycardia (VT)
Overview: Rapid rhythm originating below the bundle of His, often in the context of structural heart disease (post-MI scar, cardiomyopathy). A potentially fatal arrhythmia.
ECG Changes:
- Wide QRS complexes (β₯120 ms), regular, rate 100β250 bpm
- AV dissociation β P-waves unrelated to QRS (if visible)
- Fusion beats and capture beats (pathognomonic)
- Concordance in precordial leads (all positive or all negative)
- NW ("no man's land") axis β extreme right axis deviation
- Brugada criteria (RBBB-type) or Josephson's sign (notching near S-wave nadir)
ECG Image:
Monomorphic VT: High-rate, wide-complex rhythm with positive concordance across precordial leads V1βV6. No visible P-waves. Superior axis. Associated with structural heart disease.
9. 𧬠Brugada Syndrome
Overview: Inherited sodium channelopathy (SCN5A mutation) causing a distinctive ECG pattern and increased risk of ventricular fibrillation and sudden cardiac death, particularly in young men during sleep/rest.
ECG Changes:
- Type 1 (Diagnostic) β "Coved" pattern in V1βV2 (or V1βV3 with high precordial placement):
- J-point elevation β₯2 mm
- Convex (downward) ST segment
- Negative (inverted) T-wave
- Type 2 & 3 are "saddle-back" patterns (not diagnostic alone)
- Features may be dynamic β unmasked by fever, sodium channel blockers, autonomic changes
- Arrhythmias: polymorphic VT, ventricular fibrillation
ECG Image:
Type 1 Brugada pattern: Classic "coved" morphology in V1βV2 β J-point elevation with downsloping convex ST segment terminating in inverted T-wave. Diagnostic hallmark of Brugada syndrome.
10. π Long QT Syndrome (LQTS)
Overview: Inherited or acquired disorder of ventricular repolarization causing QT prolongation and risk of Torsades de Pointes (TdP) β a polymorphic VT that can degenerate to ventricular fibrillation.
ECG Changes:
- Prolonged QTc: β₯450 ms (men), β₯460 ms (women); β₯500 ms = high risk
- Abnormal T-wave morphology by subtype:
- LQT1: broad-based, smooth T-wave
- LQT2: bifid/notched T-wave (most visible)
- LQT3: long flat ST segment with late-peaked T-wave
- T-wave alternans β beat-to-beat T-wave variation; marker of high instability
- Torsades de Pointes: polymorphic VT with "twisting" QRS complexes around isoelectric line
- Triggered by "R-on-T" phenomenon, bradycardia, or pause (short-long-short sequence)
ECG Image β Prolonged QT with Torsades de Pointes:
Severe LQTS: Marked QT prolongation with R-on-T PVC triggering Torsades de Pointes β the classic "twisting" polymorphic VT. Life-threatening arrhythmia requiring urgent management.
Quick Reference Summary Table
| # | Disease | Key ECG Finding | Emergency? |
|---|
| 1 | STEMI | ST elevation + reciprocal depression | β
Yes |
| 2 | Atrial Fibrillation | No P-waves, irregularly irregular | β οΈ Sometimes |
| 3 | Complete AV Block | AV dissociation, escape rhythm, bradycardia | β
Yes |
| 4 | Pulmonary Embolism | S1Q3T3, RV strain, sinus tachycardia | β
Yes |
| 5 | Acute Pericarditis | Saddle-shaped ST elevation, PR depression | β οΈ Urgent |
| 6 | HCM | LVH, giant T-wave inversions (apical) | β οΈ Monitor |
| 7 | WPW Syndrome | Short PR, delta waves, wide QRS | β
Risk |
| 8 | Ventricular Tachycardia | Wide complex, AV dissociation, rate >100 | β
Yes |
| 9 | Brugada Syndrome | Coved ST elevation V1βV2 | β
Risk |
| 10 | Long QT Syndrome | Prolonged QTc, T-wave alternans, TdP | β
Yes |
Key ECG Principle: Always interpret ECGs in full clinical context. Many patterns overlap β the combination of rate, rhythm, axis, interval measurements, and morphology together with the clinical picture guides diagnosis and management.