Abstract
QUESTION One of my female patients has epilepsy and is currently receiving lamotrigine monotherapy. She has recently found that she is 6 weeks pregnant and is concerned about possible side effects of lamotrigine on her fetus. How should I advise her and should I switch to another antiepileptic drug?
ANSWER Lamotrigine (LTG) has not been associated with an increased risk for major malformations in monotherapy in most available studies. Risk of major malformations has been suggested when LTG was taken in doses higher than 200 mg/d and when clefts not caused by any known syndrome have been associated with LTG treatment. Therefore, safety for the fetus cannot yet be proven or rejected, although the drug does not appear to be a major human teratogen.
Epilepsy is the most common neurologic condition in the obstetric population, where women with epilepsy constitute 0.5% of all pregnancies.1,2 The goal of epilepsy treatment is seizure control using antiepileptic drugs (AEDs), despite the fact that the traditional AEDs are known teratogens. Lamotrigine (LTG) is a second-generation AED that is widely used for seizure control in epilepsy as well as in other neurologic and psychiatric disorders. It has been found to be similar in effectiveness to valproic acid.3
Between the years of 1999 and 2003, the use of LTG increased dramatically.4 However, because information on safety of LTG in human pregnancy is still limited, several pregnancy registries have been formed to monitor LTG safety in pregnancy.
Five registries and 1 large prospective study (Table 13–8) recently summarized human studies of LTG. Overall, most of the reported data did not show evidence of increased teratogenic risk, as the rates of major malformations were well within the expected baseline rates. The exception is the North American Antiepileptic Drug Pregnancy Registry,7 which assessed first-trimester LTG monotherapy exposure (n = 564). The prevalence of major malformations found among exposed infants in the first 5 days of life was 2.7% (95% confidence interval [CI], 1.5%–4.3%). Three infants (0.53%) had isolated cleft palates and 2 infants (0.35%) had isolated cleft lips, resulting in a total of 5 infants (0.89%) with oral clefts. This is an apparent higher prevalence of oral clefts than that observed in the control group (0.037%, n = 221 746). In this control group, the prevalence of isolated cleft palate was 0.016% with relative risk (RR) attributed to LTG of 32.8 (95% CI, 10.6–101.3), and the prevalence of isolated cleft lip was 0.021% with RR attributed to LTG of 17.1 (95% CI, 4.3–68.2).7 These results led to the issue of a report by GlaxoSmithKline Inc and Health Canada, warning of potential risks associated with LTG use.9 The good news is that the observed rates of cleft palate and cleft lip were still very low. Hence, while the relative risk might be high, the absolute risk is minimal. This single study will have to be confirmed by other studies, especially because no other existing registry has corroborated it.
Summary of LTG registries findings
Proper seizure control is the primary goal in treating women with epilepsy. Patients should understand the risks associated with uncontrolled seizures as well as the teratogenicity of the anticonvulsive medications in question. The benefits of treatment versus the risk of uncontrolled seizures should be discussed with each patient.
If anticonvulsants cannot be avoided, the most appropriate first-line drug for the seizure type should be used at the lowest effective dose, and monotherapy is preferable to polytherapy. In summary, the present reports do not suggest LTG to be a major human teratogen. Because only 1 study suggests increased risk of oral clefts, the finding must be corroborated before causation can be inferred.
- Copyright© the College of Family Physicians of Canada
