What is the recommended acute adenosine dosing for a hemodynamically stable patient with supraventricular tachycardia, including weight‑based adjustments and contraindications?

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Adenosine Dosing for Acute Supraventricular Tachycardia

For hemodynamically stable patients with SVT, administer adenosine 6 mg as a rapid IV push over 1–2 seconds through a proximal vein, followed immediately by a 20 mL saline flush; if no conversion occurs within 1–2 minutes, give 12 mg IV push, and repeat 12 mg once more if needed (maximum cumulative dose 30 mg). 1, 2, 3

Standard Dosing Protocol

  • First dose: 6 mg rapid IV bolus administered over 1–2 seconds, followed immediately by 20 mL saline flush 1, 2, 3
  • Second dose: 12 mg rapid IV bolus if no conversion within 1–2 minutes 1, 2, 3
  • Third dose: 12 mg rapid IV bolus may be repeated once more if still no response 1, 2, 3
  • Maximum cumulative dose: 30 mg total (6 mg + 12 mg + 12 mg) 2, 3

The 6 mg initial dose successfully converts 70–80% of PSVT cases involving AVNRT or AVRT, with overall conversion rates of 90–95% for AVNRT and 78–96% for AVRT across all doses. 2, 3

Critical Administration Technique

  • Use the most proximal IV access available (antecubital preferred over distal sites) to ensure rapid delivery to central circulation before the drug is metabolized 2, 3
  • Administer as a rapid bolus over 1–2 seconds, not a slow push—adenosine's half-life is less than 10 seconds, requiring immediate delivery 1, 2, 3
  • Follow immediately with 20 mL saline flush to propel the medication into central circulation 1, 2, 3
  • Maintain continuous ECG monitoring during administration to document conversion or aid diagnostic evaluation 2, 3

Weight-Based Adjustments and Special Populations

Reduced Initial Dose (3 mg)

Reduce the initial dose to 3 mg in the following situations: 2, 3

  • Patients taking dipyridamole (potentiates adenosine effect) 1, 2
  • Patients taking carbamazepine (potentiates adenosine effect) 2, 3
  • Cardiac transplant recipients (denervated hearts are hypersensitive) 2, 3
  • Administration via central venous access (bypasses peripheral degradation) 2, 3

Increased Dose Requirements

Larger doses may be required for patients with significant blood levels of: 1, 2, 3

  • Theophylline (competitive antagonist at adenosine receptors) 1, 2, 3
  • Caffeine (competitive antagonist) 1, 2, 3
  • Theobromine (competitive antagonist) 2, 3

Single bolus doses of 18 mg have been reported as safe in clinical practice, particularly in patients with impaired venous return or those taking methylxanthines. 2, 4

Absolute Contraindications

  • Asthma or active bronchospasm—adenosine can precipitate severe bronchospasm and is absolutely contraindicated 1, 2, 3
  • Second- or third-degree AV block or sick sinus syndrome without a pacemaker 1, 2
  • Pre-excited atrial fibrillation (e.g., Wolff-Parkinson-White syndrome)—adenosine may initiate atrial fibrillation with rapid ventricular rates, potentially triggering ventricular fibrillation 1, 2

A defibrillator must be readily available when administering adenosine, particularly in patients where WPW syndrome is a consideration. 2, 3

Expected Response and Timing

  • Average time to termination: approximately 30 seconds after an effective dose 2
  • If no effect within 1–2 minutes, the dose is considered insufficient and the next higher dose should be administered 1, 2, 3
  • Early recurrence of tachycardia occurs in up to one-third of patients due to adenosine's ultra-short half-life 5

Common Side Effects

Most side effects are transient and self-limited (lasting less than 60 seconds) due to adenosine's very short half-life: 1, 2

  • Flushing (most common) 1, 2
  • Dyspnea 1, 2
  • Chest discomfort or pain 1, 2
  • Transient AV block 1
  • Premature ventricular contractions 1

Management After Adenosine Administration

If Conversion Occurs

  • Monitor continuously for recurrence—premature complexes post-conversion commonly trigger recurrent SVT episodes 2
  • If immediate recurrence occurs, consider a longer-acting AV nodal blocking agent (diltiazem or β-blocker) to prevent reinitiation 1, 2

If Adenosine Fails to Convert

  • Adenosine may unmask underlying atrial flutter or atrial tachycardia by transiently slowing AV conduction, even when it doesn't terminate the arrhythmia—this diagnostic effect guides subsequent therapy 2, 3
  • For stable patients: administer a longer-acting AV nodal blocker—IV diltiazem 15–20 mg over 2 minutes (64–98% conversion rate) or IV metoprolol 2.5–5 mg every 2–5 minutes (maximum 15 mg) 1, 2
  • For unstable patients: proceed immediately to synchronized cardioversion 1, 2

Critical Safety Warnings

Do NOT administer verapamil or diltiazem (alternative agents) if any of the following are present: 2

  • Ventricular tachycardia cannot be excluded
  • Pre-excited atrial fibrillation (WPW syndrome)
  • Suspected systolic heart failure
  • Hemodynamic instability

Pregnancy Considerations

  • Adenosine is safe and effective during pregnancy and is the preferred pharmacologic agent after vagal maneuvers 2, 3
  • If the patient becomes hemodynamically unstable, electrical cardioversion is indicated 2

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Adenosine Administration for Supraventricular Tachycardia

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Adenosine Dosing for Supraventricular Tachycardia

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

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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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