Initial Management of Symptomatic Bradycardia
For a patient presenting with symptomatic bradycardia, immediately administer atropine 0.5-1 mg IV as first-line therapy, repeating every 3-5 minutes up to a maximum total dose of 3 mg, while simultaneously preparing for transcutaneous pacing if the patient remains unstable. 1, 2, 3
Immediate Assessment and Stabilization
Rapidly determine if bradycardia is causing the symptoms by identifying signs of poor perfusion: altered mental status, ischemic chest discomfort, acute heart failure, hypotension (systolic BP <80-90 mmHg), or shock. 1, 2
Critical Initial Steps (Do Not Delay Treatment)
- Maintain airway patency and assist breathing as necessary 1, 2
- Provide supplemental oxygen if hypoxemic or showing increased work of breathing, as hypoxemia itself causes bradycardia 1, 2
- Establish cardiac monitoring to identify rhythm, blood pressure, and oxygen saturation 1
- Secure IV access for medication administration 1
- Obtain 12-lead ECG if immediately available, but do not delay treatment 1, 2
Identify Reversible Causes While Treating
Common reversible causes requiring immediate attention include: 1
- Medications: Beta-blockers, calcium channel blockers, digoxin, antiarrhythmics 1
- Electrolyte abnormalities: Hyperkalemia, hypokalemia 1
- Acute myocardial infarction, particularly inferior MI 1
- Hypothyroidism, hypothermia, increased intracranial pressure 1
First-Line Pharmacologic Management: Atropine
Administer atropine 0.5-1 mg IV bolus immediately for symptomatic bradycardia. 1, 2, 3
Atropine Dosing Algorithm
- Initial dose: 0.5-1 mg IV push 1, 2, 3
- Repeat every 3-5 minutes as needed 1, 2, 3
- Maximum total dose: 3 mg 1, 2, 3
- Critical warning: Doses <0.5 mg may paradoxically worsen bradycardia and must be avoided 1, 2
When Atropine Is Likely Effective vs. Ineffective
Atropine works best for: 2
- Sinus bradycardia
- AV nodal block (first-degree, Mobitz type I second-degree)
- Sinus arrest
Atropine is likely ineffective for: 2
- Mobitz type II second-degree AV block
- Third-degree AV block with wide QRS complex (infranodal block)
- Post-cardiac transplant patients (may cause paradoxical high-grade AV block) 1, 2
Special Contraindications and Cautions
Avoid atropine in heart transplant patients without evidence of autonomic reinnervation, as it may cause paradoxical high-degree AV block or sinus arrest—use epinephrine instead. 1, 2
Use cautiously in acute myocardial infarction, particularly inferior MI, as increased heart rate may worsen ischemia or increase infarct size. 2
Second-Line Management: When Atropine Fails
Transcutaneous Pacing (TCP)
Initiate TCP immediately in unstable patients who do not respond to atropine (Class IIa recommendation). 1, 2 This is particularly critical when:
- Systolic BP remains <80 mmHg with signs of shock 2
- Patient has Mobitz type II or third-degree AV block with wide QRS 2
- Atropine is contraindicated (transplant patient) 2
TCP serves as a temporizing bridge while preparing for transvenous pacing or permanent pacemaker placement. 2 Note that conscious patients will require sedation/analgesia due to pain from TCP. 2
Chronotropic Infusions
If bradycardia persists despite atropine or TCP is unavailable, initiate IV beta-adrenergic agonist infusion: 1, 2
Dopamine (Preferred for Most Situations)
- Initial dose: 5-10 mcg/kg/min IV infusion 1, 2
- Titrate every 2-5 minutes by 2-5 mcg/kg/min based on heart rate and blood pressure 2
- Maximum dose: 20 mcg/kg/min (higher doses cause excessive vasoconstriction and arrhythmias) 2
- Mechanism: At 5-20 mcg/kg/min provides chronotropic and inotropic effects through beta-1 stimulation 2
Epinephrine (For Severe Hypotension or Transplant Patients)
- Initial dose: 2-10 mcg/min IV infusion (or 0.1-0.5 mcg/kg/min) 1, 2
- Titrate to hemodynamic response 2
- Use when: Severe hypotension with bradycardia, or in heart transplant patients where atropine is contraindicated 2
- Critical warning: Causes more profound vasoconstriction than dopamine; use with extreme caution in acute coronary ischemia 2
Isoproterenol (Alternative Option)
- Dose: 20-60 mcg IV bolus or 1-20 mcg/min infusion 2
- Advantage: Provides chronotropy and inotropy without vasopressor effects 2
- Avoid in familial long QT syndrome—use pacing and beta-blockers instead 2
Special Overdose Situations
For beta-blocker or calcium channel blocker overdose: 1
- Glucagon 3-10 mg IV with infusion of 3-5 mg/hour
For calcium channel blocker overdose specifically: 1
- 10% calcium chloride or 10% calcium gluconate IV
Progression to Definitive Management
Prepare for transvenous pacing if temporary measures (atropine, TCP, chronotropic infusions) are ineffective. 2 In one retrospective study of 518 patients with symptomatic bradycardia, approximately 20% required temporary emergency pacing for initial stabilization, and 50% ultimately required permanent pacemaker implantation. 4, 5
Consider expert consultation for complex cases, particularly when the underlying mechanism remains unclear or when temporary measures fail. 1
Common Pitfalls to Avoid
- Do not give atropine doses <0.5 mg, as this may paradoxically worsen bradycardia 1, 2
- Do not delay TCP while giving additional atropine doses in unstable patients—this can be harmful 2
- Do not exceed atropine total dose of 3 mg, as excessive doses may cause central anticholinergic syndrome (confusion, agitation, hallucinations) 2
- Do not use atropine in heart transplant patients without documented autonomic reinnervation 1, 2
- Do not aggressively increase heart rate in acute MI, as this may worsen ischemia or increase infarct size 2
- Atropine should not delay TCP implementation in patients with poor perfusion 2
Evidence Quality Note
The recommendations for atropine as first-line therapy and TCP for refractory cases are based on ACC/AHA/HRS Class IIa, Level of Evidence B guidelines from 2018. 6 A randomized feasibility trial of 82 patients found identical survival rates (approximately 70%) whether atropine-refractory bradycardia was treated with dopamine or transcutaneous pacing. 2 In a retrospective study of 172 prehospital patients with hemodynamically unstable bradycardia, approximately 50% had either partial or complete response to atropine, with adverse responses being uncommon (2.3%). 7