Is lamotrigine safe for an adult with a prior ST‑elevation myocardial infarction who is currently stable?

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Last updated: February 12, 2026View editorial policy

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Lamotrigine Safety in Adults with Prior STEMI

Lamotrigine can be used cautiously in adults with a history of STEMI, but requires careful cardiac monitoring, particularly in patients with pre-existing conduction abnormalities or those taking other sodium channel blockers. The FDA added a warning in 2020 regarding lamotrigine's potential to cause cardiac rhythm and conduction abnormalities based on in vitro data showing Class IB antiarrhythmic effects at therapeutic concentrations 1.

Evidence for Cardiac Safety

The most relevant clinical evidence comes from a 2023 retrospective study in Veterans—a particularly vulnerable cardiac population—which found reassuring safety data 1:

  • No deaths occurred due to cardiac rhythm or conduction causes among 233 patients prescribed lamotrigine 1
  • Only 7.3% of patients who had EKGs showed potential abnormalities (prolonged PR or QTc intervals) that could be related to lamotrigine 1
  • This low incidence occurred despite 87.5% of patients having pre-existing cardiac diagnoses and 47.9% taking concomitant sodium channel blocking medications 1
  • The mean maximum daily dose was 250.8 mg (range 25-800 mg) 1

Key Cardiac Considerations

Conduction abnormalities are the primary concern, not ischemic events 1. The in vitro data suggest lamotrigine may affect cardiac sodium channels, potentially causing:

  • PR interval prolongation 1
  • QTc prolongation 1
  • Wide complex tachycardia in severe overdose (>25 mg/L serum concentration) 2

Clinical Management Algorithm

Before Initiating Lamotrigine:

  • Obtain baseline ECG to document PR interval, QRS duration, and QTc 1
  • Review all concomitant medications for other sodium channel blockers (antiarrhythmics, other anticonvulsants, certain psychotropics) 1
  • Assess cardiac history for pre-existing conduction disease (heart block, bundle branch blocks) 1

During Lamotrigine Treatment:

  • Perform follow-up ECG after reaching therapeutic dose, particularly if symptoms of palpitations, syncope, or presyncope develop 1
  • Monitor for cardiac symptoms including dizziness, syncope, or palpitations that could indicate conduction abnormalities 1
  • Use standard dosing escalation as rapid titration increases risk of adverse effects 1

High-Risk Scenarios Requiring Extra Caution:

  • Concomitant sodium channel blockers: Nearly half of patients in the Veterans study were on additional sodium channel blocking agents without clear harm, but this warrants closer monitoring 1
  • Pre-existing conduction disease: Patients with baseline PR prolongation or bundle branch blocks may be at higher risk 1
  • Elderly patients: The Veterans study population averaged 64.3 years, suggesting reasonable safety in older adults with cardiac disease 1

Post-STEMI Medication Interactions

Your patient with prior STEMI is likely on standard post-MI medications, which are compatible with lamotrigine 3:

  • Beta-blockers: No contraindication; both can be used together 3
  • Aspirin and clopidogrel: No interaction with lamotrigine 3
  • Statins: No interaction 3
  • ACE inhibitors/ARBs: No interaction 3

Critical Pitfall to Avoid

Do not confuse lamotrigine's potential cardiac effects with increased risk of myocardial infarction. The concern is rhythm/conduction disturbances, not coronary ischemia or thrombosis 1, 2. The STEMI history itself does not contraindicate lamotrigine unless there are associated conduction abnormalities 1.

Overdose Considerations

In acute overdose situations (>4 grams ingested), severe cardiac toxicity including wide complex tachycardia and cardiac arrest has been reported 2. However, at therapeutic doses, even in high-risk cardiac patients, serious arrhythmias are rare 1.

Bottom Line for Clinical Practice

Lamotrigine is not contraindicated in patients with prior STEMI who are now stable. Obtain a baseline ECG, monitor for symptoms of conduction abnormalities, and use standard dosing protocols 1. The clinical evidence from vulnerable cardiac populations suggests the theoretical cardiac risks identified in vitro studies do not translate to significant clinical harm at therapeutic doses 1.

References

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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