Here is a complete, systematic approach to ECG interpretation, based on Harrison's Principles of Internal Medicine (22nd ed.) and Medical Physiology (Boron & Boulpaep).
ECG Interpretation: Complete Systematic Approach
Electrophysiologic Basis
The ECG records depolarization and repolarization of the working atrial and ventricular myocardium. The impulse follows this pathway:
SA node → Atria → AV node → His bundle → Right & Left bundle branches → Purkinje fibers → Ventricular myocardium
The left bundle further divides into the left anterior fascicle and left posterior fascicle.
ECG Paper & Calibration
| Dimension | Small box (1 mm) | Large box (5 mm) |
|---|
| Time (horizontal) | 0.04 s | 0.20 s |
| Voltage (vertical) | 0.1 mV | 0.5 mV |
Standard calibration: 1 mV = 10 mm (10 small boxes tall). Always confirm the calibration pulse at the left margin of each row.
The 14-Step Systematic Checklist
(Per Harrison's 22nd ed. — missing any step is a common source of errors)
Step 1 — Standardization & Technical Features
- Confirm 1 mV calibration pulse is present
- Check lead placement (limb lead reversal is the most common artifact; right arm–left arm reversal inverts lead I and swaps aVR/aVL)
- Look for artifacts: muscle tremor, AC interference, baseline wander
Step 2 — Rhythm
Ask three questions:
- Where is the pacemaker? — P waves before every QRS = sinus origin
- What is the conduction path?
- Is the pacemaker regular and at the correct speed?
Normal sinus rhythm (NSR): Regular P waves, positive in I and II, negative in aVR, each followed by a QRS, rate 60–100 bpm.
| Rhythm clue | Interpretation |
|---|
| No P waves, irregularly irregular | Atrial fibrillation |
| Sawtooth flutter waves ~300/min | Atrial flutter (usually 2:1 or 4:1 block) |
| P waves after QRS | Junctional rhythm |
| Wide QRS, no P, rate 20–40 | Ventricular escape rhythm |
Step 3 — Heart Rate
Method 1 (regular rhythm): Count large boxes between two R waves → Rate = 300 ÷ number of large boxes
| Large boxes (R-R) | Heart rate |
|---|
| 1 | 300 |
| 2 | 150 |
| 3 | 100 |
| 4 | 75 |
| 5 | 60 |
| 6 | 50 |
Method 2 (irregular rhythm): Count QRS complexes in a 6-second strip × 10.
Normal: 60–100 bpm | Bradycardia: <60 | Tachycardia: >100
Step 4 — PR Interval / AV Conduction
- Normal: 0.12–0.20 s (3–5 small boxes)
- Measured from start of P to start of QRS
| Finding | Meaning |
|---|
| PR > 0.20 s (fixed) | 1st-degree AV block |
| PR progressively lengthens → dropped QRS | 2nd-degree block, Mobitz I (Wenckebach) |
| Fixed PR + sudden dropped QRS | 2nd-degree block, Mobitz II |
| No relationship between P and QRS | 3rd-degree (complete) AV block |
| PR < 0.12 s + delta wave | Pre-excitation (WPW) |
Step 5 — QRS Interval
- Normal: < 0.12 s (< 3 small boxes)
- Measured from start to end of QRS
| QRS Duration | Interpretation |
|---|
| < 0.12 s | Normal (narrow complex) |
| 0.12–0.14 s | Incomplete bundle branch block |
| ≥ 0.12 s (≥ 3 boxes) | Complete bundle branch block or ventricular rhythm |
RBBB pattern: rSR' (M-shape) in V1, wide S in I and V6
LBBB pattern: Broad monophasic R in I, aVL, V5–V6; deep QS in V1; ST interpretation unreliable
Step 6 — QT / QTc Interval
- Measured from start of QRS to end of T wave
- Rate-dependent → use corrected QT (QTc)
- Bazett formula: QTc = QT ÷ √(R-R interval in seconds)
- Normal QTc: < 440 ms (men), < 460 ms (women)
| QTc | Clinical significance |
|---|
| > 500 ms | High risk of torsades de pointes |
| Prolonged | Hypokalemia, hypomagnesemia, hypocalcemia, drugs (quinidine, sotalol, haloperidol, erythromycin), congenital LQTS |
| Short QT | Hypercalcemia, digitalis effect |
Step 7 — Mean QRS Axis (Frontal Plane)
Normal axis: −30° to +90°
Quick method using leads I and aVF:
| Lead I | Lead aVF | Axis |
|---|
| Positive | Positive | Normal (0° to +90°) |
| Positive | Negative | Left axis deviation (LAD) |
| Negative | Positive | Right axis deviation (RAD) |
| Negative | Negative | Extreme axis ("no man's land") |
Left axis deviation (LAD, more negative than −30°): LBBB, left anterior fascicular block (LAFB), inferior MI, LVH
Right axis deviation (RAD, > +90°): RVH, RBBB, LPFB, lateral MI, Wolff-Parkinson-White, dextrocardia
Step 8 — P Waves
- Normal: Upright in I, II, aVF; inverted in aVR; duration < 0.12 s; amplitude < 2.5 mm
- Right atrial enlargement (P pulmonale): Tall, peaked P > 2.5 mm in II or V1 (positive component)
- Left atrial abnormality (P mitrale): Broad, notched P in limb leads (> 0.12 s); biphasic P in V1 with prominent negative terminal component (> 1 mm × 1 mm)
Step 9 — QRS Voltages
Low voltage: QRS amplitude < 5 mm in all limb leads OR < 10 mm in all precordial leads
→ Causes: pericardial effusion, obesity, COPD/emphysema, hypothyroidism, infiltrative cardiomyopathy
Left ventricular hypertrophy (LVH):
- SV1 + RV5 (or RV6) > 35 mm (Sokolow-Lyon)
- Or R in aVL > 11 mm
- Often accompanied by ST depression + T-wave inversion in lateral leads ("strain pattern")
Right ventricular hypertrophy (RVH):
- R > S in V1 with right axis deviation
- Dominant R in V1 ≥ 7 mm
- ST-T inversion in V1–V3/V4
Step 10 — Precordial R-Wave Progression
- R wave should grow progressively from V1 (small r) to V5–V6 (tall R)
- Transition zone (R = S) normally at V3–V4
- Poor R-wave progression (PRWP): R wave ≤ 3 mm through V1–V3
- Causes: anterior MI, LBBB, LVH, COPD, lead misplacement
Step 11 — Abnormal Q Waves
- Pathological Q waves: Width ≥ 0.04 s (1 small box) AND depth ≥ 25% of the following R wave, in ≥ 2 contiguous leads
- Indicate prior transmural (Q-wave) myocardial infarction
Localization by lead:
| Leads with Q waves | Territory | Artery |
|---|
| V1–V4 | Anterior | LAD |
| I, aVL, V5–V6 | Lateral | LCx |
| II, III, aVF | Inferior | RCA (or LCx) |
| V1–V2 | Posterior (tall R in V1–V2) | RCA/LCx |
(Note: Small q waves in I, aVL, V5, V6 are normal septal q waves)
Step 12 — ST Segments
- Should be isoelectric (on the baseline)
- Measured at the J point (junction of QRS end and ST start)
ST Elevation:
- ≥ 1 mm in ≥ 2 contiguous limb leads OR ≥ 2 mm in ≥ 2 contiguous precordial leads = STEMI until proven otherwise
- Also seen in: acute pericarditis (diffuse, saddle-shaped, PR depression), Brugada syndrome (coved type in V1–V3), LBBB, LVH, early repolarization (concave upward, notched J point)
ST Depression:
- Subendocardial ischemia / NSTEMI
- Digoxin effect (scooped/reverse tick)
- LVH strain
- Reciprocal changes in STEMI
Step 13 — T Waves
- Normally upright in I, II, V3–V6; inverted in aVR; variable in III, aVL, V1
- T-wave inversion: Ischemia, ventricular hypertrophy (strain), bundle branch block, CNS events (massive T-wave inversions in subarachnoid hemorrhage)
- Peaked (hyperacute) T waves: Very early STEMI, hyperkalemia
- Flattened T waves: Ischemia, hypokalemia, hypothyroidism
Step 14 — U Waves
- Small deflection after the T wave, same polarity as T wave
- Best seen in V2–V3
- Prominent U waves: Hypokalemia, bradycardia, drugs (quinidine, amiodarone)
- Inverted U waves: LVH, ischemia
Normal 12-Lead ECG for Reference
Normal 12-lead ECG showing all leads. The calibration pulse (1 mV, 200 ms) is visible at the left of each row. — Medical Physiology (Boron & Boulpaep)
Quick Reference: Normal Values
| Parameter | Normal range |
|---|
| Heart rate | 60–100 bpm |
| PR interval | 0.12–0.20 s |
| QRS duration | < 0.12 s |
| QTc | < 440 ms (men), < 460 ms (women) |
| QRS axis | −30° to +90° |
| P wave duration | < 0.12 s |
| P wave amplitude | < 2.5 mm |
| R-wave transition | V3–V4 |
Key Principle
"Many mistakes in ECG interpretation are errors of omission. Therefore, a systematic approach is essential." — Harrison's Principles of Internal Medicine, 22nd ed.
Always:
- Compare with previous ECGs
- Correlate with the clinical context (age, symptoms, medications)
- Do not rely solely on computer interpretation — always perform your own review
Sources: Harrison's Principles of Internal Medicine 22E (2025, McGraw-Hill); Medical Physiology, Boron & Boulpaep; Ganong's Review of Medical Physiology, 26th ed.