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Chapter 3.5 · Section 3: Cardiovascular Management

Arrhythmias

SVT recognition and treatment, AVRT, AVNRT, adenosine protocol, antiarrhythmic drug table, atrial flutter, complete AV block, pacemaker indications, and bedside algorithms for tachyarrhythmia and bradyarrhythmia.
ECG Cardioversion Adenosine Pacemaker Baylor Ed. 33 cross-checked Sept 2026

1. Purpose

Neonatal arrhythmia may first appear as an abnormally fast or slow heart rate detected on a monitor. The best test to confirm and classify the rhythm is a 12-lead ECG.

Heart Rate Calculation
Method 1: Count QRS complexes over 6 seconds × 10
Method 2: HR = 60,000 ÷ R-R interval (ms)

2. First Bedside Question: Stable or Unstable?

Before naming the rhythm, decide whether the baby is stable or unstable.

Assess ImmediatelyConcerning Findings
ActivityLethargy, irritability, decreased responsiveness
BreathingTachypnea, respiratory distress, apnea
FeedingPoor feeding or inability to feed
PerfusionPallor, weak pulses, delayed capillary refill
Blood pressureHypotension or shock
Unstable → Act immediately

Unstable tachyarrhythmia → synchronized cardioversion 0.5–1 J/kg. Do not delay to attempt vagal maneuvers or adenosine.

3. Supraventricular Tachycardia

  • SVT is usually a narrow-complex tachycardia caused by re-entry through an accessory pathway or through the AV node
  • Short SVT episodes may occur in otherwise asymptomatic neonates — but every infant should be assessed promptly for hemodynamic compromise
  • Rate: typically 250–300 bpm with little or no R-R variability
SVT ECG pattern: narrow QRS | rate ≈ 250-300 bpm | regular R-R | P waves often absent or retrograde

4. AVRT (Atrioventricular Re-entrant Tachycardia)

AVRT is the most common neonatal SVT mechanism per the Baylor guideline. The re-entry circuit uses the AV node and an accessory pathway.

TypeBaseline ECG Feature
WPW / overt pre-excitationDelta wave, short PR interval, wide QRS in sinus rhythm
Concealed accessory pathwayBaseline ECG appears normal — pre-excitation not visible in sinus rhythm
WPW Baseline ECG Clues
  • Delta wave (slurred upstroke of QRS)
  • Short PR interval
  • Wide QRS complex (pseudo-bundle branch pattern)

5. AVNRT (AV Nodal Re-entrant Tachycardia)

  • Caused by dual AV nodal pathways — one fast, one slow
  • Regular rhythm; P waves may be hidden within or immediately after the QRS complex
  • Less common than AVRT in neonates
  • Treatment approach is the same as AVRT: vagal maneuver → adenosine → antiarrhythmics

6. Acute SVT Treatment

Clinical StatusTreatment
Unstable SVTSynchronized cardioversion 0.5–1 J/kg — do not delay
Stable SVTTry vagal maneuver first if appropriate
Vagal maneuver failsGive IV adenosine by rapid push using 2-syringe technique
Adenosine failsConsider esmolol, sotalol, procainamide, or amiodarone with cardiology guidance

7. Vagal Maneuvers

Goal: block AV nodal conduction and interrupt the re-entry circuit. Acceptable maneuvers:

  • Gag stimulation with an NG tube
  • Applying an ice bag over the face and ears for 15 seconds (diving reflex)
  • Rectal stimulation
Time limit on vagal maneuvers

In ill neonates, do not continue vagal maneuvers for more than 5 minutes before moving to adenosine or another therapy.

Ocular pressure is contraindicated in neonates

Do not apply ocular pressure as a vagal maneuver in newborns or infants — risk of retinal injury.

8. Adenosine

Adenosine has a very short half-life of ~6–10 seconds. It must be given rapidly through IV access closest to the heart, followed immediately by a rapid normal saline flush (2-syringe technique).

DoseUse
0.1 mg/kg IV rapid pushFirst dose
0.2 mg/kg IV rapid pushSecond dose if no response
Have a code cart available before giving adenosine
  • Potential adverse effects include: atrial or ventricular tachyarrhythmias, asystole, and bronchospasm
  • Warn the family and bedside team before administration — the brief pause can be alarming
2-Syringe Technique

Draw adenosine in one syringe and normal saline flush in another. Connect both to a stopcock at the IV closest to the heart. Push adenosine as fast as possible, then immediately push the flush. Slow administration → drug is metabolized before reaching the AV node → no effect.

9. Long-Term SVT Management

  • Long-term management depends on frequency, severity, and how easily SVT terminates
  • When chronic treatment is needed, beta-blockers (commonly propranolol) are first-line
  • Accessory pathway ablation is generally performed later in childhood rather than in neonates

10. Antiarrhythmic Medication Summary

Medication Main Use Dose (Baylor) Key Caution
Propranolol First-line enteral therapy for uncomplicated neonatal SVT or atrial tachycardia 4 mg/kg/day divided q6h PO Hypoglycemia, hyperkalemia, increased airway resistance (rare but important)
Esmolol IV beta-blocker for recurrent or sustained SVT when rapid onset and short half-life are useful Institution-specific continuous infusion Bradycardia and hypotension
Sotalol Second-line when propranolol fails; can terminate arrhythmia IV PO 120–150 mg/m²/day ÷ q8h; IV 1 mg/kg over 1 hour for active arrhythmia QTc prolongation — daily ECGs during initiation
Flecainide Second-line for SVT and atrial tachycardia PO 120–150 mg/m²/day ÷ q8h Milk affects absorption — give consistently with or without feeds; daily ECGs to monitor QRS duration
Amiodarone Class III antiarrhythmic when beta-blockade fails IV bolus 5 mg/kg over 20–60 min (with pulse); Loading 20 mg/kg/day → Maintenance 5–10 mg/kg/day Hypotension, thyroid toxicity, pulmonary fibrosis, hepatotoxicity, corneal deposits, dermatologic effects, arrhythmias
Ivabradine Reserved for automatic tachycardias (JET, atrial ectopic tachycardia) 0.05 mg/kg q12h PO Bradycardia; no serum level or ECG monitoring marker required

11. Amiodarone Practical Notes

  • IV amiodarone commonly causes hypotension after administration — monitor BP closely during infusion
  • IV amiodarone is incompatible with many solutions, including heparin
  • Use a dedicated IV line for amiodarone — avoid heparinized saline flushes on that line
  • Long-term amiodarone requires monitoring of thyroid function, liver function, chest X-ray, and ophthalmology exams

12. Atrial Flutter

  • Rapid atrial rhythm caused by a macro-reentry circuit in the atria
  • Atrial rate usually >250/min with variable AV conduction and usually narrow QRS
  • ECG: classic sawtooth flutter waves (F waves), most visible in II, III, aVF, V1
  • Associated with CHD in older children — but may occur in structurally normal neonates
  • Most neonatal atrial flutter presents in the first 48 hours of life
Atrial Flutter: sawtooth F-waves | atrial rate ≥250/min | 2:1, 3:1, or variable block | narrow QRS

Treatment

  • Synchronized cardioversion 0.5–1 J/kg is the treatment of choice
  • Transesophageal pacing or IV sotalol may also be considered for conversion
  • In structurally normal hearts, neonatal atrial flutter usually does not recur — long-term medication is usually not needed
Key distinction from SVT

In atrial flutter, adenosine may transiently slow the ventricular rate and reveal sawtooth F-waves, but it will not terminate flutter (unlike AVRT/AVNRT). Cardioversion is definitive.

13. Congenital Complete AV Block

Complete AV block means there is no electrical communication between atria and ventricles.

Complete AV Block: P waves completely dissociated from QRS | atrial rate ~120-150 bpm | ventricular rate ~50-80 bpm
FeatureDetail
Atrial rateUsually 120–150 bpm
Ventricular escape rateUsually 50–80 bpm
Most common causeMaternal autoimmune disease (anti-Ro/SSA, anti-La/SSB antibodies) — lupus or Sjögren syndrome
Associated structural CHDHeterotaxy syndrome, congenitally corrected TGA (ccTGA)
Important mimicLong QT syndrome — measure QTc whenever AV block is suspected

Management

  • Some infants are asymptomatic with an adequate escape rhythm — observe
  • Temporary heart rate support: isoproterenol infusion or epinephrine
  • Emergency transcutaneous pacing if acutely unstable
  • Permanent pacemaker is definitive therapy for clinically significant complete AV block
Measure QTc — long QT syndrome can mimic complete AV block

2:1 AV block in long QT syndrome may resemble complete heart block on the monitor. Obtain a 12-lead ECG and measure QTc before concluding the rhythm is congenital complete AV block.

14. Pacemaker Implantation

  • Permanent pacemaker decisions should follow pediatric pacing guidelines with cardiology/electrophysiology involvement
  • In neonates: epicardial pacemaker placement through sternotomy is the usual approach (transvenous leads are too large)
  • Neonates often need to weigh ~3 kg before implantation can be considered

Postoperative Concerns

  • Infection or bleeding in the pacemaker pocket
  • Cardiac strangulation from leads as the heart grows
  • Pacemaker malfunction or lead dislodgment

Pacing Modes

ModeDescription
VVI — Single-chamber ventricularPaces and senses ventricle; inhibited by intrinsic ventricular activity; does NOT preserve AV synchrony
DDD — Dual-chamberPaces and senses both atrium and ventricle; allows AV synchrony and better heart-rate response

15. NASPE/NBG Pacemaker Code

Code LetterMeaning
AAtrium
VVentricle
DDual (atrium + ventricle)
ONone
TTriggered response to sensing
IInhibited response to sensing
RRate response (when used as 4th letter)
Reading the code

The 3-letter code reads: Chamber Paced – Chamber Sensed – Response to Sensing. Example: VVI = ventricle paced, ventricle sensed, inhibited by intrinsic beat. DDD = dual paced, dual sensed, dual response (triggered or inhibited).

16. Bedside Algorithm — Tachyarrhythmia

Neonatal Tachyarrhythmia — Bedside Approach
STEP 1 — Confirm rhythm with ECG (12-lead preferred)
↓
STEP 2 — Assess stability: perfusion, pulses, respiratory status, feeding, pallor, activity
↓
STEP 3a — UNSTABLE narrow-complex tachycardia → Synchronized cardioversion 0.5–1 J/kg immediately
↓
STEP 3b — STABLE SVT → attempt vagal maneuver (ice/face, gag, rectal) for up to 5 minutes
↓
STEP 4 — Vagal maneuver fails → rapid IV adenosine 0.1 mg/kg (2-syringe technique); second dose 0.2 mg/kg if no response
↓
STEP 5 — Adenosine fails → involve cardiology; consider esmolol, sotalol, procainamide, or amiodarone
↓
STEP 6 — Recurrent SVT → choose long-term therapy based on frequency, severity, and ease of termination (propranolol first-line)

17. Bedside Algorithm — Bradyarrhythmia

Neonatal Bradyarrhythmia — Bedside Approach
STEP 1 — Confirm rhythm with ECG; look for AV dissociation
↓
STEP 2 — Measure QTc — long QT syndrome can mimic complete AV block
↓
STEP 3 — Assess perfusion, feeding, respiratory status, BP, lactate, activity
↓
STEP 4 — Evaluate maternal autoimmune disease history (anti-Ro/SSA, anti-La/SSB); screen for associated CHD
↓
STEP 5 — If unstable → temporary support: isoproterenol infusion, epinephrine, or emergency transcutaneous pacing
↓
STEP 6 — Consult cardiology/electrophysiology early for pacemaker planning when complete AV block is clinically significant

18. Common Mistakes

MistakeBetter Action
Treating monitor heart rate without ECG confirmation Obtain ECG — it is the preferred method for rhythm diagnosis; monitor alone is insufficient
Continuing vagal maneuvers too long in an ill neonate Do not continue vagal maneuvers beyond 5 minutes before escalating to adenosine
Giving adenosine slowly Use rapid IV push with immediate flush through access closest to the heart; slow delivery is ineffective
Giving adenosine without emergency readiness Have code cart available — asystole, bronchospasm, and tachyarrhythmias can occur
Starting sotalol without QTc monitoring Obtain daily ECGs during initiation because sotalol can prolong QTc and cause Torsades de Pointes
Giving flecainide inconsistently with feeds Give consistently with or without feeds — milk impairs absorption and inconsistent timing causes variable drug levels
Forgetting complete AV block mimics Measure QTc — long QT syndrome can present with 2:1 AV block resembling complete heart block
Assuming atrial flutter always requires chronic medication In structurally normal hearts, neonatal atrial flutter usually does not recur — long-term medication is usually not needed

19. Parent Explanation

What to Tell Families

"An arrhythmia means the baby's heartbeat is too fast, too slow, or irregular. The ECG — a painless test that reads the heart's electrical activity — tells us exactly what rhythm is present and guides treatment."


"If the baby is unstable, we treat right away with a controlled electrical shock to reset the heart rhythm, or with a pacemaker if the rate is too slow."


"If the baby is stable, we may first try safe bedside maneuvers — like briefly applying ice to the face — or a rapid medicine called adenosine, which works for just a few seconds but is enough to stop the abnormal rhythm."


"Some babies need longer-term medicine or a pacemaker, depending on the type of rhythm and how well the baby tolerates episodes. Most neonatal SVT responds well to treatment, and many babies eventually outgrow it."

Key Takeaways — Chapter 3.5

  • Confirm all arrhythmias with ECG — monitor rate alone is not enough
  • Assess stability first: unstable tachyarrhythmia → synchronized cardioversion 0.5–1 J/kg immediately
  • AVRT (most common) vs. AVNRT (less common) — both cause narrow-complex SVT at 250–300 bpm
  • WPW: delta wave + short PR + wide QRS in sinus rhythm
  • Stable SVT: vagal maneuver (≤5 min) → adenosine 0.1 mg/kg (then 0.2 mg/kg) by 2-syringe rapid push
  • Have code cart at bedside before giving adenosine — asystole and bronchospasm can occur
  • Long-term SVT: propranolol first-line; sotalol/flecainide second-line (daily ECGs during initiation)
  • Flecainide: give consistently with/without feeds — milk affects absorption
  • Amiodarone: use dedicated line; incompatible with heparin; watch for hypotension during infusion
  • Atrial flutter: cardioversion 0.5–1 J/kg; adenosine slows rate but does not terminate; usually no long-term meds in normal hearts
  • Complete AV block: measure QTc first — long QT can mimic; maternal anti-Ro/SSA/La/SSB; check for heterotaxy and ccTGA
  • Pacemaker: epicardial in neonates (~3 kg); VVI = no AV synchrony; DDD = dual-chamber with AV synchrony

References

  • Baylor College of Medicine — Guidelines for Acute Care of the Neonate, current edition: Chapter 3.5
  • Brugada J, et al. Management of pediatric arrhythmias. Circulation. 2019
  • Lapage MJ, Bradley DJ. Supraventricular tachycardia in children. Pediatr Ann. 2019
  • Perry JC, Garson A Jr. Supraventricular tachycardia due to Wolff-Parkinson-White syndrome in children: early disappearance and late recurrence. J Am Coll Cardiol. 1990
  • Villain E. Indications for pacing in patients with congenital heart disease. Pacing Clin Electrophysiol. 2008
  • Baruteau AE, et al. Congenital and childhood atrioventricular blocks. Eur J Pediatr. 2016
  • Moodley S, et al. Neonatal atrial flutter: a case series and literature review. Pediatr Cardiol. 2011
  • Manolis AS, et al. Amiodarone in cardiac arrhythmias: review of efficacy and safety. Curr Med Res Opin. 2020