What is the recommended dosage and administration of Diltiazem (Tab Dilzem) for a patient with Supraventricular Tachycardia (SVT)?

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Diltiazem for Supraventricular Tachycardia

For acute SVT termination in hemodynamically stable patients, give diltiazem 0.25 mg/kg (15-20 mg for average adult) IV over 2 minutes, followed by a second dose of 0.35 mg/kg (20-25 mg) after 15 minutes if needed. 1, 2

Acute Management Protocol

Initial Dosing

  • First bolus: 0.25 mg/kg (approximately 15-20 mg for average 70 kg patient) administered IV over 2 minutes 1, 2
  • Second bolus: If inadequate response after 15 minutes, give 0.35 mg/kg (approximately 20-25 mg) IV over 2 minutes 1, 2
  • Success rate: Diltiazem terminates SVT in 64-98% of hemodynamically stable patients 1
  • Time to conversion: Median 2-3 minutes after infusion initiation 3, 4

Continuous Infusion (for rate control)

  • Initial rate: 10 mg/hour after successful bolus conversion 1, 2
  • Titration: May increase by 5 mg/hour increments up to maximum 15 mg/hour 1, 2
  • Duration: Maximum 24 hours (longer durations not studied) 2
  • Some patients maintain response at 5 mg/hour 2

Oral Therapy for Ongoing Management

For patients declining catheter ablation or requiring chronic suppression, oral diltiazem is a Class I recommendation. 1

  • Starting dose: 120 mg daily 5
  • Maximum dose: 480 mg daily (proven effective in randomized trials) 5
  • Diltiazem is well-tolerated and effective as an alternative to ablation for long-term AVNRT management 1

Critical Safety Considerations

Absolute Contraindications

Do not give diltiazem if any of the following are present: 1, 5

  • Wide-complex tachycardia (unless proven supraventricular origin) - risk of hemodynamic collapse if ventricular tachycardia 1
  • Pre-excited atrial fibrillation/flutter (WPW syndrome with AF) - may accelerate ventricular rate and cause ventricular fibrillation 1, 5
  • Systolic heart failure or severe LV dysfunction - negative inotropic effects worsen cardiac output 1, 5
  • Hypotension - diltiazem causes further blood pressure reduction 5
  • AV block greater than first degree (without pacemaker) 5

Common Adverse Effects

  • Hypotension: Most frequent side effect, occurring in approximately 6-11% of patients 5, 3
  • Slow infusion over 20 minutes may reduce hypotension risk 1
  • Bradycardia: Monitor for excessive rate slowing, especially with concurrent beta-blocker use 1

Clinical Pearls

When to Use Diltiazem

  • Second-line agent after adenosine fails or when adenosine is contraindicated 1, 5
  • Preferred over beta-blockers for acute SVT termination - diltiazem more effective than esmolol in head-to-head comparison 1, 6
  • Useful for recurrent SVT after adenosine conversion due to longer duration of action 1
  • Particularly effective when AV node is part of reentrant circuit (AVNRT, orthodromic AVRT) 4

Drug Interactions

Avoid sequential administration with beta-blockers - the longer half-life of both agents causes overlapping effects and risk of profound bradycardia 1

Mechanism

Diltiazem works by slowing AV nodal conduction and increasing AV nodal refractoriness, terminating reentrant tachycardias dependent on the AV node 5, 4

Efficacy by SVT Type

  • AVNRT: 100% conversion rate in studies 4
  • AVRT (orthodromic): 81-84% conversion rate 3, 4
  • Atrial fibrillation/flutter: Effective for rate control but lower conversion rates 7

If Diltiazem Fails

  • First bolus ineffective: The second bolus (0.35 mg/kg) succeeds in most non-responders 6
  • Both boluses fail: Proceed to synchronized cardioversion in stable patients 1
  • Consider alternative diagnosis (pre-excited AF, ventricular tachycardia) 1

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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