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Published on: April 5, 2011
Lamotrigine in idiopathic epilepsy - increased risk of cardiac death?
D Aurlien1, E Taubøll, L Gjerstad
1Department of Neurology, Stavanger University Hospital, Stavanger, Norway. auda@sus.no
Insights
Lamotrigine (LTG) may increase the risk of sudden unexpected death in epilepsy (SUDEP). This study observed four cases in patients on LTG monotherapy, prompting further investigation into this potential link.
Area of Science:
- Cardiology
- Neurology
- Pharmacology
Background:
- Lamotrigine (LTG) is known to inhibit the cardiac rapid delayed rectifier potassium ion current (Ikr).
- Drugs that block Ikr may elevate the risk of cardiac arrhythmias and sudden unexpected death.
Observation:
- Four consecutive cases of sudden unexpected death in epilepsy (SUDEP) were observed between 1995 and 2005.
- All SUDEP cases occurred in non-hospitalized patients receiving LTG monotherapy.
- The affected patients were all females with idiopathic epilepsy.
Findings:
- The observed SUDEP cases raise questions about a potential association with LTG treatment.
- Further research is warranted to determine if LTG contributes to SUDEP risk in specific patient populations.
Implications:
- A systematic study is required to ascertain the relationship between LTG and SUDEP.
- Findings may influence clinical practice regarding LTG prescription, particularly in epilepsy patients with cardiac risk factors.
Objectives:
Lamotrigine (LTG) has recently been shown to inhibit the cardiac rapid delayed rectifier potassium ion current (Ikr). Ikr-blocking drugs may increase the risk of cardiac arrhythmia and sudden unexpected death. With this background, it may be of importance that in our outpatient clinic between August 1, 1995 and August 1, 2005 we registered four consecutive cases of sudden unexpected death in epilepsy (SUDEP) in non-hospitalized patients that were all being treated with LTG in monotherapy. Here we describe and discuss these cases, the relevant literature, and the reasons to question whether these events were as a result of coincidence alone.
Methods:
All the cases were collected consecutively at the outpatient clinic, Department of Neurology, Stavanger University Hospital, Norway. Clinical and pathological data were obtained and the relevant literature reviewed.
Results:
All were females with idiopathic epilepsy.
Conclusions:
A systematic study is needed to reveal whether LTG may increase the risk of SUDEP in certain groups of patients.
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