Management of Calcium Channel Blocker Overdose
For patients with calcium channel blocker overdose presenting with refractory shock, initiate IV calcium and high-dose insulin euglycemia therapy as first-line treatments, with vasopressors (norepinephrine/epinephrine) for hemodynamic support. 1
Initial Assessment and Stabilization
Immediate Actions
- Establish airway, breathing, and circulation following standard BLS/ACLS protocols 1
- Obtain continuous cardiac monitoring with ECG to identify bradycardia, conduction delays (AV blocks), and dysrhythmias 1, 2
- Secure IV access, preferably central venous access if prolonged therapy is anticipated 1
- Check baseline labs: serum glucose, potassium, ionized calcium, and renal function 1, 2
Decontamination (Asymptomatic Patients)
- Administer activated charcoal for recent ingestions if airway is protected 1, 3
- Consider whole bowel irrigation for sustained-release formulations 3
- Observe immediate-release ingestions for minimum 12 hours; sustained-release preparations require at least 24 hours of monitoring 3
First-Line Pharmacologic Therapy
1. Intravenous Calcium (Class 2a Recommendation)
Administer calcium as the initial antidote for catecholamine-refractory shock 1
- Dosing: 0.3 mEq/kg (0.6 mL/kg of 10% calcium gluconate OR 0.2 mL/kg of 10% calcium chloride) IV over 5-10 minutes 1
- Follow with continuous infusion of 0.3 mEq/kg per hour, titrated to hemodynamic response 1
- Monitor serum ionized calcium levels; avoid severe hypercalcemia (>2× upper limit of normal) 1
- Critical caveat: Do NOT administer calcium if concomitant digoxin toxicity is suspected 3
- Evidence shows variable efficacy in human reports but consistent benefit in animal studies 1
2. High-Dose Insulin Euglycemia Therapy (Class 2a Recommendation)
HIET is reasonable for refractory shock and should be escalated if myocardial dysfunction persists 1, 4
- Initial dosing: 1 U/kg regular insulin bolus with 0.5 g/kg dextrose 1, 4
- Continuous infusion: 0.5-1 U/kg/hr insulin, titrated to clinical effect (can increase incrementally) 1, 4
- Dextrose infusion: 0.5 g/kg/hr, adjusted to maintain glucose 100-250 mg/dL 1
- Monitor glucose every 15 minutes initially during titration phase 1
- Mechanism: Direct positive inotropic effect on myocardial contractility and shifts metabolism to carbohydrate utilization 4, 3
- Requires central venous access for concentrated dextrose solutions (>10%) 1
3. Vasopressors: Norepinephrine and/or Epinephrine
Administer norepinephrine and/or epinephrine as first-line vasopressor support 1
- Use for hemodynamic support in conjunction with calcium and insulin 1
- Dobutamine or epinephrine should be added if cardiogenic shock component is present 1
- Dopamine has shown efficacy in increasing blood pressure in case series 5
4. Potassium Management
Target moderate hypokalemia (2.5-2.8 mEq/L) during HIET 1
- Insulin causes intracellular potassium shift; moderate hypokalemia is expected 1
- Avoid aggressive potassium repletion (animal studies showed asystole with aggressive replacement) 1
Second-Line Therapies (Refractory Cases)
Glucagon (Class 2b Recommendation)
Consider IV glucagon if first-line therapies fail, though evidence is inconsistent 1
- Evidence shows mixed results in both animal and human studies 1
- Some case reports show improvement in bradycardia and hypotension 1
Atropine
Consider atropine for symptomatic bradycardia or conduction disturbances, but expect limited efficacy 1
- Historical data shows only 2 of 8 patients responded positively 5
- More effective for symptomatic bradycardia than for AV nodal blocks 1, 5
Cardiac Pacing (Class 2b Recommendation)
Use temporary pacing for unstable bradycardia or high-grade AV block WITHOUT significant myocardial dysfunction 1
- Pacing addresses rate but not underlying inotropy/vasodilation 1
- Less effective if cardiogenic shock component is dominant 1
Advanced Rescue Therapies
IV Lipid Emulsion Therapy
Administer lipid emulsion for refractory shock or periarrest states 1
- Recommended in 2017 expert consensus for refractory cases 1
- Mechanism: lipid shuttling of drug away from cardiac tissue 1
Venoarterial ECMO (Class 2b Recommendation)
Consider ECMO for refractory shock with significant cardiogenic component or cardiac arrest 1
- Retrospective studies show improved outcomes in drug toxicity-related cardiac arrest 1
- Consensus supports ECMO for reversible causes like CCB toxicity 1
- Should be initiated early if available, before irreversible end-organ damage 1
Intra-Aortic Balloon Pump/Ventricular Assist Devices
Consider mechanical circulatory support for treatment-refractory hypotension 1
- Case reports suggest potential benefit when maximal vasopressor therapy fails 1
Cardiac Arrest Management
If cardiac arrest occurs, follow standard ACLS with addition of:
Special Considerations by CCB Type
Dihydropyridines (amlodipine, nifedipine, nicardipine)
- Predominantly cause peripheral vasodilation 2, 6
- May present with reflex tachycardia rather than bradycardia 2, 6
- At toxic doses, lose receptor specificity and can cause bradycardia 6
Non-Dihydropyridines (verapamil, diltiazem)
- More cardioselective with greater myocardial depression 2, 6
- Verapamil causes AV nodal block more frequently than other CCBs 5
- Higher risk of bradycardia and negative inotropy 6
Common Pitfalls to Avoid
- Do NOT delay insulin therapy: It has direct inotropic effects and should be started early 1, 4
- Do NOT give calcium with digoxin co-ingestion: Risk of severe dysrhythmias 3
- Do NOT aggressively replicate potassium: Target 2.5-2.8 mEq/L during HIET 1
- Do NOT rely on atropine alone: Limited efficacy in CCB toxicity 5
- Do NOT underestimate sustained-release formulations: Require prolonged monitoring (≥24 hours) and consider whole bowel irrigation 3
- Do NOT forget frequent glucose monitoring: Check every 15 minutes initially during HIET 1
Monitoring Parameters Throughout Treatment
- Continuous cardiac telemetry for rhythm and conduction abnormalities 1, 2
- Blood pressure monitoring (arterial line preferred for shock states) 1
- Serum glucose every 15 minutes initially, then hourly once stable 1
- Serum potassium every 1-2 hours during HIET 1
- Ionized calcium levels during calcium infusions 1
- Renal function and urine output 2