How should I manage severe bradycardia (heart rate 33) in a patient receiving metoprolol?

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 28, 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.

Management of Severe Metoprolol-Induced Bradycardia (Heart Rate 33 bpm)

Stop metoprolol immediately—symptomatic bradycardia with heart rate <50 bpm is an absolute contraindication to continued beta-blocker therapy, and a heart rate of 33 bpm represents life-threatening bradycardia requiring urgent intervention. 1

Immediate Assessment and Stabilization

Check for signs of hemodynamic instability including altered mental status, chest discomfort, acute heart failure, hypotension (systolic BP <100 mmHg), dizziness, lightheadedness, or other signs of shock. 1 Obtain a 12-lead ECG immediately to identify the rhythm, rule out high-grade AV block (second- or third-degree), and assess QRS width. 1 Ensure adequate oxygenation and establish IV access. 1

Measure blood pressure and assess for signs of hypoperfusion such as oliguria, cool extremities, or altered mental status, which indicate severe hemodynamic compromise requiring more aggressive intervention. 1

Pharmacologic Management

Administer atropine 0.5 mg IV every 3-5 minutes (maximum total dose 3 mg) as first-line therapy for acute symptomatic bradycardia while arranging for definitive management. 1 However, recognize that atropine may be less effective in beta-blocker-induced bradycardia compared to vagally-mediated bradycardia. 1

If the patient remains symptomatic or develops cardiac arrest despite atropine, initiate transcutaneous pacing immediately. 1 Do not delay pacing while giving additional atropine doses in patients showing poor perfusion. 1

Advanced Therapies for Refractory Cases

For severe metoprolol toxicity unresponsive to standard measures:

  • High-dose insulin therapy (hyperinsulinemia/euglycemia): Administer 250 units IV bolus followed by continuous infusion, which has been shown to reverse metoprolol-induced cardiac arrest by improving myocardial contractility. 2, 3
  • Intravenous lipid emulsion (ILE): Give 20% lipid emulsion 100 mL bolus followed by 200 mL over 30 minutes, which acts as a lipid extractor to lower serum metoprolol levels. 2, 3
  • Glucagon: Administer 5-10 mg IV bolus (up to 14 mg has been used), though response may be limited. 3
  • Vasopressor support: Epinephrine 0.1 μg/kg/min, norepinephrine 0.5 μg/kg/min, or dobutamine 10 μg/kg/min may be required to maintain perfusion. 3

Critical Warnings About Metoprolol Management

Never abruptly discontinue metoprolol in patients with coronary artery disease without a plan for gradual tapering once stabilized—abrupt withdrawal is associated with a 2.7-fold increased risk of 1-year mortality and can precipitate severe angina, myocardial infarction, and ventricular arrhythmias with up to 50% mortality. 1, 4

Do not restart metoprolol at the original dose after resolution of bradycardia. If beta-blockade is still indicated (e.g., for coronary disease or heart failure), reduce the dose by at least 50% and monitor closely. 1

Evaluation for Contributing Factors

Assess for drug interactions that may have precipitated severe bradycardia:

  • CYP2D6 inhibitors (paroxetine, fluoxetine, bupropion) can increase metoprolol levels 4-6 fold and cause severe bradycardia and AV block. 5
  • Other rate-lowering drugs including digoxin, diltiazem, verapamil, or amiodarone can have additive bradycardic effects. 1
  • Moderate CYP2D6 inhibitors (escitalopram, citalopram, duloxetine) increase metoprolol levels 2-3 fold. 5

Rule out other reversible causes including hypothyroidism, increased intracranial pressure, or infection that may be contributing to bradycardia. 1

Disposition and Monitoring

Admit to an intensive care unit with continuous cardiac monitoring. 1 Monitor heart rate, blood pressure, and rhythm continuously during the acute phase. 1 Watch for signs of worsening heart failure, hypotension, or recurrent bradycardia. 1

Obtain urgent cardiology consultation for consideration of temporary transvenous pacing if transcutaneous pacing is required or if high-grade AV block is present. 1

Long-Term Management Strategy

Once the patient is hemodynamically stable (heart rate >50 bpm, systolic BP >100 mmHg, no symptoms):

  • If beta-blockade remains indicated, restart at 50% of the previous dose (e.g., if on metoprolol tartrate 50 mg twice daily, restart at 25 mg twice daily). 1
  • Monitor heart rate and blood pressure at 1-2 week intervals during dose adjustments. 1
  • Consider switching to metoprolol succinate (extended-release) rather than immediate-release tartrate, as the SR formulation has nearly half the risk of emergent bradycardia compared to IR formulation (12.9 vs 24.1 per 1000 person-years). 6
  • Discontinue or substitute any CYP2D6 inhibiting antidepressants—paroxetine, fluoxetine, and bupropion should not be used with metoprolol; consider switching to sertraline, venlafaxine, mianserin, or mirtazapine which do not significantly inhibit CYP2D6. 5

Common Pitfalls to Avoid

Do not rely solely on atropine in beta-blocker toxicity—it is often insufficient and pacing or advanced therapies may be needed. 1

Do not assume the bradycardia is benign even if blood pressure is maintained—a heart rate of 33 bpm represents severe conduction suppression that can rapidly deteriorate to cardiac arrest. 1

Do not give the full 15 mg IV metoprolol dose if considering IV beta-blockade in the future—this significantly increases hypotension and bradycardia risk. 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.

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.