CFP
HOME HELP CONTACT US FEEDBACK SUBSCRIPTIONS CURRENT ISSUE PAST ISSUES SEARCH
QUICK SEARCH:   [advanced]


     

Can Fam Physician
Vol. 53, No. 6, June 2007, pp.1007 - 1009
Copyright © 2007 by The College of Family Physicians of Canada
This Article
Right arrow Abstract Freely available
Right arrow Résumé
Right arrow Full Text (PDF)
Right arrow Rapid Responses: Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when Rapid Responses are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Shor, S.
Right arrow Articles by Nulman, I.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Shor, S.
Right arrow Articles by Nulman, I.

Current Practice

Teratogenicity of lamotrigine

Sarit Shor, Gideon Koren, MD FRCPC and Irena Nulman, MD
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.


View this table:
[in this window]
[in a new window]

  		Table 1 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.


   References
TOP
 References
 

  1. Yerby MS. Pregnancy and epilepsy. Epilepsia 1991;32(Suppl_6):S51-9.[Medline]
  2. Dansky LV, Andermann E, Andermann F. Marriage and fertility in epileptic patients. Epilepsia 1980;21(3):261-71.[Medline]
  3. Morrow J, Russell A, Guthrie E, Parsons L, Robertson I, Waddell R, et al. Malformation risks of antiepileptic drugs in pregnancy: a prospective study from the UK Epilepsy and Pregnancy Register. J Neurol Neurosurg Psychiatry 2006;77(2):193-8.[Abstract/Free Full Text]
  4. Vajda FJ, Hitchcock A, Graham J, Solinas C, O’Brien TJ, Lander CM, et al. Foetal malformations and seizure control: 52 months data of the Australian Pregnancy Registry. Eur J of Neurol 2006;13(6):645-54.
  5. GlaxoSmithKline. The lamotrigine pregnancy registry [Interim Report]. Wilmington, NC: Kendle International Inc; 2007.
  6. Wide K, Winbladh B, Kallen B. Major malformations in infants exposed to antiepileptic drugs in utero, with emphasis on carbamazepine and valproic acid: a nation-wide, population-based register study. Acta Paediatr 2004;93(2):174-6.[Medline]
  7. Holmes LB, Wyszynski DF, Baldwin EJ, Habecker E, Glassman LH, Smith CR. Increased risk for non-syndromic cleft palate among infants exposed to lamotrigine during pregnancy [Abstract]. Birth Defects Res A Clin Mol Teratol 2006;76(5):318.
  8. Meador KJ, Baker GA, Finnell RH, Kalayjian LA, Liporace JD, Loring DW, et al. In utero antiepileptic drug exposure: fetal death and malformations. Neurology 2006;67(3):407-12.[Abstract/Free Full Text]
  9. Dillon JA. Health Canada endorsed important safety information on LAMICTAL® (lamotrigine) tablets [Report]. Mississauga, Ont: GlaxoSmithKline; 2006;(August 1). Available from: http://www.gsk.ca/en/health_info/LAMICTAL_DHCPL_ENG_FNL.pdf. Accessed 2007 Mar 7.




This Article
Right arrow Abstract Freely available
Right arrow Résumé
Right arrow Full Text (PDF)
Right arrow Rapid Responses: Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when Rapid Responses are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Shor, S.
Right arrow Articles by Nulman, I.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Shor, S.
Right arrow Articles by Nulman, I.

HOME HELP CONTACT US FEEDBACK SUBSCRIPTIONS CURRENT ISSUE PAST ISSUES SEARCH