Switching from Lamotrigine to Oxcarbazepine
For a patient on lamotrigine 600 mg/day, initiate oxcarbazepine at 150 mg at bedtime and increase by 150 mg every 2 days until reaching 900-1200 mg/day, while simultaneously tapering lamotrigine by 100-200 mg every 3-7 days over 2-3 weeks, with mandatory sodium monitoring before starting oxcarbazepine and at 2-4 weeks if risk factors are present. 1, 2
Oxcarbazepine Initiation Strategy
Standard Titration Schedule
- Start oxcarbazepine at 150 mg at bedtime on day 1 1, 2
- Increase by 150 mg every second day until reaching target dose of 900-1200 mg/day in divided doses 1
- Alternative slower approach (preferred by UK experts): 150 mg day one, then 300 mg daily, increased by 300 mg weekly 2
- Target maintenance dose: 900-1200 mg/day in two divided doses 1, 3
- Maximum dose if needed: 2400 mg/day, though higher doses increase adverse events 3
Rapid Titration Option (Use Cautiously)
- Can start with up to 600 mg/day and increase by 600 mg weekly if faster control needed 1
- However, rapid fixed titration to high doses increases risk of nervous system and digestive adverse events 3
Lamotrigine Discontinuation Strategy
Tapering Schedule
- Begin tapering lamotrigine once oxcarbazepine reaches 300-600 mg/day (after 3-7 days of oxcarbazepine initiation)
- Reduce lamotrigine by 100-200 mg every 3-7 days 4
- Total taper duration: approximately 2-3 weeks for the 600 mg dose
- Lamotrigine must be tapered gradually - abrupt discontinuation risks withdrawal seizures and rebound symptoms
Cross-Taper Overlap Period
- Maintain therapeutic overlap for 1-2 weeks minimum
- Both medications will be at partial doses simultaneously during the transition
- The cross-taper should take approximately 3-4 weeks total from start to finish
Critical Monitoring Requirements
Sodium Monitoring (Essential for Oxcarbazepine)
- Check baseline serum sodium before starting oxcarbazepine if: 1, 2
- Patient has renal disease
- Taking diuretics, oral contraceptives, or NSAIDs
- Elderly patients (higher hyponatremia risk) 2
- Any clinical symptoms of hyponatremia (nausea, confusion, headache)
- Recheck sodium at 2-4 weeks and 2-3 months after initiation 1
- Approximately 3% of patients develop hyponatremia (sodium <125 mmol/L) during first months of therapy 1
- Hyponatremia may be more common than trial data suggest, especially in elderly patients 2
Other Safety Monitoring
- No routine CBC, liver function, or renal function monitoring required for oxcarbazepine (unlike carbamazepine) 1, 2
- Monitor for dose-related CNS side effects: dizziness, somnolence, headache, ataxia 3
- Watch for digestive symptoms: nausea, vomiting 3
Important Clinical Considerations
Drug Interactions
- Oxcarbazepine reduces ethinylestradiol and levonorgestrel levels - women on hormonal contraception need additional barrier methods or higher-dose estrogen formulations (≥50 µg) 5, 2
- Oxcarbazepine at 1500 mg/day acts as a weak enzyme inducer, primarily affecting hormonal contraceptives 5
- Minimal cytochrome P450 interactions compared to carbamazepine 6
Rash Considerations
- If patient had carbamazepine rash previously, oxcarbazepine is NOT first choice - cross-reactivity occurs in 25-30% of cases 2
- However, oxcarbazepine does not require HLA-B*15:02 screening (unlike carbamazepine) 4
Dosing Timing
- Administer oxcarbazepine at bedtime initially to minimize dizziness and drowsiness that may interfere with daily activities 4
- Once titrated, divide total daily dose into two administrations 1
Common Pitfalls to Avoid
- Do not switch overnight from lamotrigine to oxcarbazepine - these are different mechanisms requiring gradual cross-taper
- Do not forget sodium monitoring in at-risk patients - asymptomatic hyponatremia is common 2
- Do not taper lamotrigine too quickly - maintain gradual reduction over 2-3 weeks minimum
- Do not use standard hormonal contraception without additional protection during oxcarbazepine therapy 5, 2
- Do not use rapid oxcarbazepine titration unless seizure urgency demands it - slower titration improves tolerability 2, 3