What is the appropriate dose of Diltiazem (diltiazem) for an adult patient with a history of cardiovascular disease and rapid ventricular response?

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Last updated: January 22, 2026View editorial policy

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Diltiazem Dosing for Rapid Ventricular Response (RVR)

For acute RVR in atrial fibrillation, administer an initial IV bolus of 0.25 mg/kg (approximately 15-20 mg for average adults) over 2 minutes, though lower doses of 0.13-0.2 mg/kg may be equally effective with reduced hypotension risk. 1, 2

Acute IV Management

Initial Bolus Dosing

  • Standard dose: 0.25 mg/kg IV over 2 minutes (approximately 15-20 mg for average adult) 1, 3
  • Alternative low-dose approach: 0.13-0.2 mg/kg may achieve similar rate control with significantly lower hypotension rates (18% vs 35% with standard dosing) 2
  • Recent evidence demonstrates that doses ≥0.13 mg/kg achieve heart rate <100 bpm in mean time of 169 minutes compared to 318 minutes with lower doses 4

Second Bolus (if needed)

  • If inadequate response after 15 minutes, administer 0.35 mg/kg (approximately 25 mg) over 2 minutes 1

Continuous Infusion

  • Start at 5-15 mg/hour after bolus for sustained rate control 5
  • Median effective infusion rate is 10 mg/hour 5
  • Continue infusion for 6-20 hours until transitioning to oral therapy 5

Transition to Oral Therapy

Timing and Dosing

  • Administer first oral dose while patient remains on IV infusion 5
  • Discontinue IV infusion 4 hours after first oral dose 5
  • Oral dosing: Extended-release formulations 180-360 mg once daily 6, 5
  • Median effective oral dose is 300 mg/day 5
  • 77% of patients maintain rate control during transition from IV to oral therapy 5

Long-term Maintenance

  • Usual maintenance range: 120-360 mg daily of extended-release formulation 7, 6
  • For chronic rate control in atrial fibrillation, doses of 240-360 mg daily are typically required 6

Critical Contraindications

Absolute contraindications include: 6, 1

  • Second or third-degree AV block without functioning pacemaker
  • Sick sinus syndrome without pacemaker
  • Wolff-Parkinson-White syndrome with atrial fibrillation/flutter (risk of accelerated conduction down accessory pathway)
  • Decompensated systolic heart failure or severe LV dysfunction
  • Cardiogenic shock
  • Hypotension (SBP <90 mmHg)

Important Safety Considerations

Drug Interactions

  • Avoid routine combination with beta-blockers due to increased risk of profound bradycardia, AV block, and heart failure 7, 6
  • Diltiazem is a moderate CYP3A4 inhibitor: doses >120 mg/day significantly increase bleeding risk when combined with apixaban or rivaroxaban (HR 1.29 for serious bleeding) 8
  • Consider dose reduction of apixaban/rivaroxaban or use metoprolol as alternative rate-control agent in anticoagulated patients 8

Monitoring Requirements

  • Blood pressure and heart rate before and after each bolus 6
  • Continuous cardiac monitoring during IV administration 1
  • ECG monitoring in patients with conduction system disease 6
  • Have resuscitation equipment immediately available 1

Common Adverse Effects

  • Hypotension is most common (18-42% depending on dose), especially with IV administration 2, 4
  • Bradycardia occurs but rarely requires discontinuation 4
  • Peripheral edema with chronic oral therapy (dose-related, more common in women) 7

Clinical Pearls

  • Lower initial doses (0.13-0.2 mg/kg) reduce hypotension risk without sacrificing efficacy in most patients 2, 4
  • Diltiazem works by slowing AV nodal conduction and increasing refractoriness 1
  • In hemodynamically unstable patients, synchronized cardioversion is preferred over medication 1
  • For patients with pre-existing ventricular dysfunction, consider alternative agents as diltiazem may worsen heart failure 6, 1
  • Asymptomatic low blood pressure (e.g., 115/60 mmHg) does not require dose adjustment when heart rate control is the primary goal 6

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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