What is the recommended treatment for paroxysmal supraventricular tachycardia?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: February 20, 2026View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Treatment of Paroxysmal Supraventricular Tachycardia (PSVT)

For hemodynamically stable PSVT, perform vagal maneuvers first, followed immediately by adenosine 6 mg IV push if unsuccessful; for hemodynamically unstable patients, proceed directly to synchronized cardioversion without attempting vagal maneuvers or medications. 1

Immediate Assessment: Hemodynamic Stability

Determine stability within seconds by assessing for hypotension, altered mental status, shock, chest pain, or acute heart failure. 1, 2

  • Unstable patients: Perform synchronized cardioversion (50-100 J) immediately after sedation—this achieves near-100% termination and pharmacologic therapy must not delay definitive treatment. 1, 2
  • Stable patients: Proceed with the stepwise algorithm below. 1, 3

Step 1: Vagal Maneuvers (First-Line for Stable Patients)

Attempt vagal maneuvers before any medication—they terminate 27-43% of PSVT episodes and carry minimal risk in younger patients. 1, 2, 4

Technique (Patient Must Be Supine)

  • Modified Valsalva maneuver: Patient bears down against a closed glottis for 10-30 seconds, generating ≥30-40 mm Hg intrathoracic pressure—this is the most effective vagal technique. 1, 2
  • Carotid sinus massage: Apply steady pressure over one carotid sinus for 5-10 seconds only after confirming absence of bruit by auscultation. 1, 3
  • Ice-water facial immersion: Apply an ice-cold wet towel to the face to activate the diving reflex. 1, 3

Critical Safety Warning

Never apply pressure to the eyeball—this practice is dangerous and has been abandoned. 1, 2, 3

Age-Related Consideration

Vagal maneuvers are safest in younger patients; in patients >65 years with higher likelihood of coronary or cerebrovascular disease, consider proceeding directly to adenosine to minimize stroke risk from carotid massage. 5

Step 2: Adenosine (First-Line Pharmacologic Agent)

Adenosine terminates 90-95% of AVNRT and 78-96% of AVRT—it is the most effective first-line drug for stable PSVT. 1, 2, 4, 6

Dosing Protocol

  • Initial dose: 6 mg rapid IV push over 1-2 seconds via a large proximal vein (antecubital preferred), followed immediately by 20 mL saline flush. 1, 2
  • Second dose: If no conversion within 1-2 minutes, give 12 mg rapid IV push with flush. 1, 2
  • Third dose: If still no response, give a final 12 mg dose (maximum cumulative dose 30 mg). 2
  • Average time to termination: 30 seconds after an effective dose. 2

Dose Adjustments

  • Reduce to 3 mg in patients taking dipyridamole or carbamazepine, cardiac transplant recipients, or when administering via central venous access. 1, 2
  • Increase dose in patients with significant theophylline, caffeine, or theobromine levels (competitive adenosine antagonists). 1, 2

Absolute Contraindications to Adenosine

  • Asthma or active bronchospasm (risk of severe bronchospasm). 1, 2
  • Second- or third-degree AV block or sick sinus syndrome without pacemaker. 2
  • Pre-excited atrial fibrillation (e.g., Wolff-Parkinson-White)—adenosine may precipitate rapid ventricular response; have defibrillator immediately available if WPW is suspected. 2

Common Transient Side Effects (<60 Seconds)

Flushing, dyspnea, chest discomfort, and transient AV block are common but self-limited. 2, 6

Special Population: Pregnancy

Adenosine is safe and effective during pregnancy. 1, 2

Step 3: Calcium-Channel Blockers (Second-Line)

If adenosine fails or is contraindicated (e.g., asthma), intravenous diltiazem is the preferred alternative, achieving 64-98% conversion. 1, 2, 7, 4

Diltiazem Dosing

  • 15-20 mg (≈0.25 mg/kg) IV over 2 minutes; clinical effect typically within 3-5 minutes. 1, 2, 7
  • A slower infusion over up to 20 minutes reduces hypotension risk. 2

Verapamil Alternative

  • 2.5-5 mg IV over 2 minutes; effect within 3-5 minutes. 1, 2

Absolute Contraindications to Calcium-Channel Blockers

Do NOT administer diltiazem or verapamil if any of the following are present: 1, 2, 3, 7

  1. Ventricular tachycardia cannot be excluded (may cause hemodynamic collapse)
  2. Pre-excited atrial fibrillation (e.g., WPW)—may precipitate ventricular fibrillation
  3. Suspected systolic heart failure or severe LV dysfunction (negative inotropic effects)
  4. Hemodynamic instability

Step 4: Intravenous Beta-Blockers (Third-Line)

Beta-blockers are reasonable alternatives with excellent safety profiles, though slightly less effective than calcium-channel blockers. 1, 2

Metoprolol Dosing

  • 2.5-5 mg IV every 2-5 minutes; maximum cumulative dose 15 mg over 10-15 minutes. 1, 2

Esmolol Alternative

Useful for short-term rate control, particularly when concurrent hypertension is present. 1, 2

Caution

Use carefully in severe COPD; never combine IV calcium-channel blockers with IV beta-blockers due to synergistic hypotension and bradycardia. 2

Step 5: Synchronized Cardioversion (Last Resort for Stable Patients)

If all pharmacologic options fail or are contraindicated, synchronized cardioversion achieves 80-100% termination with appropriate sedation. 1, 2, 3

Post-Conversion Management

Immediate Monitoring

Maintain continuous ECG monitoring because premature atrial or ventricular complexes commonly trigger recurrent PSVT within seconds to minutes. 2

Management of Immediate Recurrence

  • Administer a longer-acting AV-nodal blocker (oral diltiazem, verapamil, or beta-blocker) to prevent reinitiation. 1, 2
  • Consider "pill-in-the-pocket" therapy for patient self-management of future episodes. 2

Long-Term Prevention

Catheter ablation is first-line therapy for preventing recurrent PSVT, with single-procedure success rates of 94.3-98.5% and superior cost-effectiveness compared to chronic pharmacotherapy. 2, 3, 4

  • Oral beta-blockers, diltiazem, or verapamil are reasonable alternatives for patients who decline or are not candidates for ablation. 1, 3
  • Flecainide or propafenone may be considered in patients without structural heart disease who are not ablation candidates. 3

Patient Education

Teach vagal maneuver techniques (modified Valsalva, ice-water facial immersion) for self-termination of future episodes. 2, 3

Special Scenario: Pre-Excited Atrial Fibrillation (Wolff-Parkinson-White)

If PSVT converts to atrial fibrillation with pre-excitation (wide, irregular QRS): 1, 2, 3

  • Avoid adenosine, diltiazem, verapamil, beta-blockers, and digoxin—these enhance accessory-pathway conduction and may precipitate ventricular fibrillation.
  • Unstable: Immediate synchronized cardioversion.
  • Stable: IV procainamide or ibutilide to slow accessory-pathway conduction.

Critical Pitfalls to Avoid

  • Do not delay cardioversion in unstable patients to attempt drug therapy. 1, 2
  • Do not give calcium-channel blockers when VT or pre-excited AF cannot be excluded. 1, 2, 3
  • Do not use adenosine in asthma due to severe bronchospasm risk. 1, 2
  • Do not apply eyeball pressure during vagal maneuvers. 1, 2, 3
  • Do not combine IV calcium-channel blockers with IV beta-blockers. 2
  • Obtain a 12-lead ECG during tachycardia to exclude VT and identify pre-excitation before administering AV-nodal blockers. 1, 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

Supraventricular Tachycardia Treatment Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Adenosine and the treatment of supraventricular tachycardia.

The American journal of medicine, 1992

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.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.