How do I read an electrocardiogram (EKG)?

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How to Read an EKG: A Systematic Approach

Begin by verifying the technical quality of the recording—check for proper calibration (10 mm/mV gain, 25 mm/s paper speed), adequate electrode contact, and absence of significant artifact—because technical errors are the most common source of misinterpretation. 1, 2

Step 1: Verify Technical Quality and Calibration

Before interpreting any waveforms, confirm the recording meets technical standards:

  • Check the calibration pulse is present and shows 10 mm height (representing 1 mV) at standard 25 mm/s paper speed 3
  • Assess baseline stability and look for electrical interference, muscle artifact, or baseline wander that could distort measurements 2, 4
  • Verify proper electrode placement, as precordial lead misplacement of just 2 cm can cause significant diagnostic errors, and fewer than two-thirds of placements are within 1.25 inches of intended landmarks 3
  • Confirm the paper speed, because at 25 mm/s each small box (1 mm) = 0.04 seconds and each large box (5 mm) = 0.20 seconds 1, 3

Common pitfall: Lead misplacement, particularly transposition of V1 and V2, can mimic anteroseptal infarction by reversing R-wave progression 3. Always verify lead placement if the tracing appears inconsistent with clinical presentation.

Step 2: Calculate Heart Rate

Use one of two methods depending on rhythm regularity:

  • For regular rhythms: Count the number of large boxes (5 mm) between consecutive R waves and divide 300 by this number 2
  • For irregular rhythms: Count QRS complexes in a 6-second strip (30 large boxes) and multiply by 10 2
  • Normal range: 60-100 beats per minute in adults; <60 = bradycardia, >100 = tachycardia 2

Note that sinus bradycardia ≥30 bpm is a normal variant in athletes 2.

Step 3: Identify the Rhythm

Systematically assess rhythm characteristics:

  • Look for P waves before each QRS complex with consistent morphology 2
  • Measure PR interval (normal: 120-200 ms or 3-5 small boxes) to assess AV conduction 2
  • Assess rhythm regularity: completely irregular rhythm suggests atrial fibrillation; occasional premature beats or pauses may indicate ectopy 2
  • Confirm sinus rhythm requires: P wave before each QRS, consistent PR interval, upright P in lead II, and rate 60-100 bpm 2

Step 4: Measure Intervals and Assess Conduction

Measure key intervals using the earliest onset and latest offset across multiple simultaneously recorded leads:

  • PR interval: 120-200 ms (3-5 small boxes); prolonged PR suggests first-degree AV block 2
  • QRS duration: <120 ms (3 small boxes); ≥120 ms indicates bundle branch block or ventricular conduction delay 2
  • QT interval: Measure from earliest QRS onset to latest T-wave end, preferably in leads II, V5, or V6 2, 3
    • Correct for heart rate using Bazett's formula: QTc = QT ÷ √RR (both in seconds) 2, 3
    • Normal QTc: <450 ms in men, <460 ms in women 2

Critical pitfall: Paper speed affects QT measurement—at 50 mm/s each box = 0.02 seconds, not 0.04 seconds. Always verify paper speed before calculating intervals 3, 5. QT measurements are also affected by amplifier gain, with measurements 8 ms longer for each doubling of gain 5.

Step 5: Determine Electrical Axis

Use leads I and aVF to quickly determine axis:

  • Normal axis (-30° to +90°): Positive QRS in both lead I and aVF 2
  • Left axis deviation (-30° to -90°): Positive in lead I, negative in aVF 2
  • Right axis deviation (+90° to +180°): Negative in lead I, positive in aVF 2
  • Extreme axis deviation (+180° to -90°): Negative in both leads I and aVF 2

Step 6: Assess for Chamber Enlargement

Examine voltage criteria and morphologic patterns:

  • Left ventricular hypertrophy: S wave in V1 + R wave in V5 or V6 >35 mm (3.5 mV) using Sokolow-Lyon criteria 2
    • Note: Voltage criteria decline with age and vary by population; sensitivity is only 11.2% in hypertensive patients 2
  • Atrial enlargement: Look for broad, notched P waves (left atrial) or tall, peaked P waves (right atrial) 2

Important caveat: QRS voltage criteria are affected by body habitus, age, and recording gain. A doubling of amplifier gain increases measured voltage by approximately 8 mm 5.

Step 7: Evaluate for Ischemia, Injury, and Infarction

Systematically examine ST segments, T waves, and Q waves:

  • ST elevation: ≥1 mm (0.1 mV) in limb leads or ≥1.5-2 mm in precordial leads suggests acute injury 2
  • ST depression: Horizontal or downsloping depression ≥0.5 mm may indicate ischemia 2
  • T-wave abnormalities: Inversion, hyperacute appearance, or flattening may indicate ischemia or evolving infarction 2
  • Pathological Q waves: Duration >40 ms (1 small box) or depth >25% of R-wave amplitude suggests prior myocardial infarction 2
  • Localize findings to determine affected coronary territory (anterior, inferior, lateral, posterior) 2

Critical distinction: Early repolarization (benign variant common in athletes) shows J-point elevation with upward-concave ST segments, whereas acute injury shows convex ST elevation 2.

Step 8: Recognize High-Risk Patterns

Identify potentially life-threatening conditions:

  • Brugada pattern: Coved ST-segment elevation in V1-V2 with downsloping morphology indicates risk of ventricular arrhythmia 2
  • Wolff-Parkinson-White: Shortened PR interval (<120 ms) with delta wave indicates accessory pathway 2
  • Hypertrophic cardiomyopathy: Deep Q waves, markedly inverted T waves, and unusually high voltage 2
  • Prolonged QTc: >500 ms significantly increases risk of torsades de pointes 2

Step 9: Consider Clinical Context

Never interpret the EKG in isolation—the same finding has different implications depending on symptoms and clinical presentation. 1, 2

  • Patients with known coronary disease, cardiomyopathy, hypertension, or diabetes require explicit consideration of these conditions when interpreting findings 2
  • Age-specific variants must be recognized: T-wave inversions in V1-V3 are normal in children >1 month old 2
  • In neonates, normal axis ranges 55-200° at birth, decreasing to ≤160° by 1 month 2

Step 10: Verify Computer Interpretation

Computer-generated interpretations are prone to frequent errors and must never be accepted without physician review. 1, 2

  • Computer programs correctly classify only 91.3% of EKGs compared to 96.0% for cardiologists 1
  • Computer interpretation is an adjunct, not a substitute, and all reports require physician overreading 1
  • Physicians' own accuracy varies widely—median 54% pre-training and 67% post-training across all levels 6

Critical Pitfalls to Avoid

  • Electrode misplacement is the most common technical error and can create false diagnoses 3
  • Inadequate high-frequency response (<150 Hz in adults, <250 Hz in children) systematically underestimates QRS amplitude and smooths Q waves, potentially missing infarction 1, 3
  • Torso electrode placement (Mason-Likar) for monitoring cannot be used interchangeably with standard limb lead placement for diagnostic interpretation 1
  • Failure to compare with prior EKGs misses important interval changes 1
  • Over-reliance on voltage criteria alone without considering clinical context leads to diagnostic errors 2
  • Ignoring paper speed and gain settings causes systematic measurement errors—QT measurements differ by 11 ms between 100 and 50 mm/s, and by 16 ms between 50 and 25 mm/s 5

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

EKG Interpretation Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

ECG Calibration and Technical Standards

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Reducing Interference in Electrocardiograms

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Research

Errors in manual measurement of QT intervals.

British heart journal, 1994

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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