Read a Paediatric ECG

Paediatric ECG interpretation becomes significantly easier once the clinician understands one key physiological principle:

The neonatal heart is right ventricular dominant. The mature heart is left ventricular dominant.

Most normal paediatric ECG findings are explained by this transition.

During fetal life:

  • pulmonary vascular resistance is high
  • the right ventricle performs most of the cardiac work
  • right ventricular muscle mass exceeds left ventricular mass

After birth:

  • pulmonary vascular resistance falls
  • pulmonary blood flow increases
  • left ventricular workload progressively increases
  • the ECG gradually shifts toward the adult pattern

This physiological transition explains why:

  • right axis deviation is normal in neonates
  • dominant R waves in V1 are normal in infancy
  • juvenile T-wave inversion occurs in children

Understanding the physiology prevents overcalling normal findings as pathology.


When Should a Paediatric ECG Be Performed?

Clinical Scenario Important Diagnoses Syncope Long QT syndrome, WPW, heart block Exertional collapse Hypertrophic cardiomyopathy, catecholaminergic VT Chest pain Myocarditis, pericarditis Palpitations Supraventricular tachycardia Cyanosis Congenital heart disease Seizure-like episodes Arrhythmia masquerading as seizure Electrolyte disturbance Hyperkalaemia, hypocalcaemia Drug overdose QT prolongation Family history of sudden death Inherited channelopathy


A Safe Systematic Approach

Interpret every paediatric ECG in the same sequence:

  1. Calibration and technical quality
  2. Heart rate
  3. Rhythm
  4. Axis
  5. P waves
  6. PR interval
  7. QRS complex
  8. QTc
  9. ST segments and T waves

A fixed sequence reduces missed pathology.


Step 1 — Calibration and Technical Quality

Always confirm:

  • correct patient
  • exact age
  • paper speed
  • amplitude calibration

Standard calibration:

  • 25 mm/sec
  • 10 mm/mV

Movement artefact is extremely common in children and may imitate arrhythmia.

Incorrect lead placement is another common cause of misinterpretation.

Before diagnosing pathology:

Confirm the ECG is technically adequate.


Step 2 — Heart Rate

Children normally have faster heart rates than adults. Age Normal Heart Rate Neonate 100–180 bpm Infant 100–160 bpm Toddler 90–150 bpm School-age child 70–120 bpm Adolescent 60–100 bpm

Heart rate can be estimated rapidly by:

300 divided by the number of large squares between R waves.


Important Clinical Distinction

Sinus tachycardia:

  • gradual onset
  • variable rate
  • identifiable P waves
  • associated with fever, dehydration, pain

Supraventricular tachycardia:

  • abrupt onset
  • fixed rapid rate
  • often absent P waves
  • usually >220 bpm in infants

Any infant with a heart rate above 220 bpm should be assumed to have SVT until proven otherwise.


Step 3 — Rhythm

First determine whether sinus rhythm is present.

Features of sinus rhythm:

  • P wave before every QRS
  • consistent PR interval
  • upright P waves in leads I and aVF

Sinus Arrhythmia

Sinus arrhythmia is normal in children.

Heart rate:

  • increases during inspiration
  • decreases during expiration

This reflects normal vagal tone and should not be mistaken for pathological irregular rhythm.


Step 4 — Axis

Normal Neonatal Axis

Right axis deviation is physiological in neonates because of right ventricular dominance. Age Group Expected Axis Neonate Right axis deviation Infant Gradual normalization Child Normal axis Adolescent Adult pattern


When Axis Becomes Abnormal

Persistent right axis deviation beyond infancy may suggest:

  • pulmonary hypertension
  • atrial septal defect
  • right ventricular hypertrophy

Left axis deviation in a neonate should raise concern for:

  • atrioventricular septal defect
  • congenital heart disease

Extreme axis deviation at any age requires further investigation.


Step 5 — P Waves

Normal P-wave duration:

  • less than 0.09 seconds in children

Tall peaked P waves

Suggest:

  • right atrial enlargement

Broad bifid P waves

Suggest:

  • left atrial enlargement

Absent P waves

Consider:

  • junctional rhythm
  • atrial fibrillation
  • SVT

Atrial fibrillation is uncommon in children and usually implies underlying pathology.


Step 6 — PR Interval

The PR interval reflects conduction from atria to ventricles. Age Normal PR Interval Infant 0.08–0.15 sec Child 0.10–0.17 sec Adolescent 0.12–0.20 sec


Prolonged PR Interval

Consider:

  • first-degree heart block
  • myocarditis
  • beta-blockers
  • digoxin toxicity

Short PR Interval with Delta Wave

Classic for Wolff-Parkinson-White syndrome.

Features:

  • short PR interval
  • slurred QRS upstroke
  • widened QRS complex

WPW predisposes to re-entry tachyarrhythmias and sudden cardiac death.

All confirmed WPW should be referred to paediatric cardiology.


Step 7 — QRS Complex

Normal QRS duration in young children:

  • less than 0.08 seconds

Narrow QRS

Usually supraventricular origin.

Wide QRS

Consider:

  • bundle branch block
  • ventricular rhythm
  • hyperkalaemia
  • pre-excitation syndromes

Important Neonatal QRS Findings

The following are normal in neonates:

  • dominant R wave in V1
  • right ventricular voltages
  • rightward axis

These findings are physiological before approximately 6 months of age.


Right Ventricular Hypertrophy

Consider RVH if:

  • dominant R wave in V1 persists beyond infancy
  • upright T wave persists in V1 after infancy
  • qR pattern appears in V1

Common causes:

  • pulmonary hypertension
  • congenital heart disease

Left Ventricular Hypertrophy

Consider LVH if:

  • tall R waves in V5–V6
  • deep S waves in V1–V2
  • associated ST-T abnormalities

In older children:

Always consider hypertrophic cardiomyopathy.


Step 8 — QTc

QTc assessment is one of the most important components of paediatric ECG interpretation.

Prolonged QTc may lead to:

  • Torsades de Pointes
  • ventricular fibrillation
  • sudden cardiac death

QTc Interpretation

QTc Interpretation <0.44 sec Normal 0.44–0.46 sec Borderline 0.46–0.50 sec Prolonged >0.50 sec High risk

QTc should ideally be measured in:

  • lead II
  • alternatively V5 if unclear

Avoid V2 and V3 because U waves may falsely prolong the QT interval.


Causes of QT Prolongation

Important causes include:

  • congenital long QT syndrome
  • hypocalcaemia
  • hypomagnesaemia
  • myocarditis
  • head injury

Common QT-Prolonging Medications

Drug Group Examples Antiemetics Ondansetron, metoclopramide Macrolides Erythromycin, azithromycin Antifungals Fluconazole Antipsychotics Haloperidol Antidepressants SSRIs, tricyclics Antiarrhythmics Amiodarone, sotalol

Always review QTc before prescribing QT-prolonging medications.


Step 9 — ST Segments and T Waves

Juvenile T-Wave Pattern

T-wave inversion in V1–V3 is frequently normal in children and may persist into adolescence.

This normal juvenile pattern is commonly overcalled as pathology.


Significant ST-T Abnormalities

Diffuse ST elevation:

  • myocarditis
  • pericarditis

Tall peaked T waves:

  • hyperkalaemia

Dynamic ECG changes:

  • always clinically significant

Hyperkalaemia ECG Progression

Memorise the sequence:

  1. Tall peaked T waves
  2. PR prolongation
  3. QRS widening
  4. Sine-wave appearance
  5. Cardiac arrest

Hyperkalaemia is immediately life-threatening.


Important Emergency ECG Patterns

Supraventricular Tachycardia

Typical findings:

  • narrow complex tachycardia
  • 220–300 bpm in infants
  • absent or retrograde P waves
  • abrupt onset and termination

Wolff-Parkinson-White Syndrome

Typical findings:

  • short PR interval
  • delta wave
  • widened QRS

WPW can precipitate sudden cardiac death if atrial fibrillation occurs.


Complete Heart Block

Findings:

  • P waves independent of QRS complexes
  • atria and ventricles beat separately
  • slow ventricular escape rhythm

Important causes:

  • neonatal lupus
  • congenital heart disease
  • myocarditis
  • postoperative complications

Long QT Syndrome

Suspect in:

  • exercise-induced syncope
  • emotional-trigger syncope
  • family history of sudden death
  • recurrent unexplained seizures
  • prolonged QTc on repeated ECGs

Management includes:

  • avoiding QT-prolonging medications
  • beta-blockers
  • cardiology referral
  • family screening

Common Diagnostic Pitfalls

Pitfall Reality Right axis deviation in neonate called abnormal Usually physiological Dominant R in V1 labelled RVH in neonate Often normal Juvenile T-wave inversion called ischaemia Commonly physiological Sinus arrhythmia diagnosed as pathology Normal vagal tone Subtle delta wave missed Always assess PR interval carefully SVT mistaken for sinus tachycardia SVT has abrupt onset and fixed rate


Red Flags Requiring Urgent Cardiology Review

  • QTc >0.50 sec
  • Delta wave with syncope
  • Complete heart block
  • Exertional syncope
  • LVH in a young athlete
  • Family history of sudden death
  • Sustained tachyarrhythmia
  • Dynamic ST changes

Final Clinical Advice

Do not memorise paediatric ECG patterns blindly.

Interpret the ECG through physiology.

Most normal paediatric ECG findings reflect:

  • postnatal circulatory adaptation
  • developmental physiology
  • changing ventricular dominance with age

The ECG should never be interpreted in isolation.

Always correlate with:

  • symptoms
  • examination findings
  • family history
  • haemodynamic status
  • previous ECGs

© stethal.wordpress.com | For educational purposes. Always refer to local guidelines and senior clinicians for clinical decision-making.

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