What medications can be used to lower heart rate (hr) in patients with tachycardia?

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Medications for Lowering Heart Rate in Tachycardia

Beta blockers are the first-line medications for lowering heart rate in patients with tachycardia, with metoprolol being particularly effective for rate control in various tachyarrhythmias. 1

First-Line Medications

Beta Blockers

  • Most effective drug class for rate control, achieving heart rate endpoints in 70% of patients compared to 54% with calcium channel blockers 1
  • Reduce heart rate by blocking catecholamine effects, reducing AV node conduction 1
  • Options include:
    • Metoprolol: 25-100 mg BID (immediate release) or 50-400 mg daily (extended release) 1
    • Atenolol: 25-100 mg daily 1
    • Esmolol: For IV administration in acute settings (500 mcg/kg IV bolus, then 50-300 mcg/kg/min) 1
    • Propranolol: 80-240 mg daily in divided doses 1
  • Contraindications: Asthma, obstructive airway disease, decompensated heart failure, pre-excited atrial fibrillation/flutter 1

Non-dihydropyridine Calcium Channel Blockers

  • Commonly used for tachycardia treatment with improved quality of life and exercise tolerance 1
  • Slow AV node conduction and increase AV node refractoriness 1
  • Options include:
    • Diltiazem: Initial dose 15-20 mg IV over 2 minutes; maintenance 120-360 mg daily orally 1
    • Verapamil: Initial dose 2.5-5 mg IV over 2 minutes; maintenance 120-360 mg daily orally 1
  • Contraindicated in decompensated heart failure, pre-excited AF/flutter, or rhythms consistent with VT 1

Second-Line Medications

Digoxin

  • Useful for rate control in patients with heart failure or LV dysfunction 1
  • Dosing: 0.125-0.375 mg daily orally 1
  • Limitations:
    • Delayed onset of action (60+ minutes) with peak effect up to 6 hours 1
    • Less effective during high sympathetic tone states 1
    • Not effective for exercise-induced tachycardia 1

Amiodarone

  • Consider when other measures are unsuccessful or contraindicated 1
  • Multichannel blocker with additional beta-blocking properties 1
  • Dosing: 150 mg IV over 10 minutes, followed by 1 mg/min infusion for 6 hours, then 0.5 mg/min 1
  • Oral dosing: 800 mg daily for 1 week, 600 mg daily for 1 week, 400 mg daily for 4-6 weeks, then 200 mg daily maintenance 1
  • Side effects include bradycardia, hypotension, pulmonary toxicity, thyroid dysfunction 1

Ivabradine

  • Novel agent that selectively inhibits the I(f) current in the sinoatrial node 2
  • Particularly useful for inappropriate sinus tachycardia 1
  • Dosing: 2.5-7.5 mg twice daily 1
  • Can be combined with beta blockers for enhanced rate control 1
  • Side effects include phosphenes (visual brightness) in about 3% of patients 1

Special Considerations

  • For acute rate control in unstable patients, IV medications or electrical cardioversion may be required 1
  • In pre-excited atrial fibrillation, avoid digoxin, non-dihydropyridine calcium channel blockers, and amiodarone as they may increase ventricular response 1
  • For specific tachyarrhythmias:
    • Atrial fibrillation/flutter: Beta blockers or calcium channel blockers are first-line 1
    • SVT: Adenosine (6 mg IV rapid push, may repeat with 12 mg) for acute termination 1
    • Inappropriate sinus tachycardia: Beta blockers or ivabradine 1

Monitoring and Titration

  • Assess heart rate control both at rest and during activity 1
  • Beta blockers should be titrated to the highest tolerated dose regardless of baseline heart rate 3
  • Target heart rate reduction rather than specific medication dose 4
  • Monitor for side effects such as hypotension, bradycardia, and heart failure exacerbation 1

Common Pitfalls

  • Underdosing of beta blockers is common in clinical practice - most patients receive less than half the recommended target dose 5
  • Limited up-titration occurs in the first 60-90 days after hospital discharge 5
  • Combination therapy may be needed for refractory tachycardia, but monitor closely for excessive bradycardia 1
  • Avoid non-dihydropyridine calcium channel blockers in patients with decompensated heart failure 1

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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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