Outcome of children born to epileptic mothers treated with carbamazepine during pregnancy.
Department of Anatomy and Cell Biology, Jerusalem Institute of Child Development, Hebrew University Hadassah Medical School and Ministry of Health, Israel.
AIM: The purpose of the study was to assess whether there was an increased rate of congenital anomalies or significant developmental delay in infants of women with epilepsy who had been treated with carbamazepine during pregnancy. METHODS: 47 children were studied, aged 6 months-6 years, who were born to 37 epileptic mothers on carbamazepine monotherapy (group A). All children had a complete physical and neurodevelopmental assessment by a developmental paediatrician, and 41 a complete psychological evaluation. They were compared with 47 children of similar socioeconomic status (group B). RESULTS: Six of the 47 children in group A had typical facial features of 'carbamazepine syndrome'. The average cognitive score of children in group A was significantly lower than in group B. This was mainly because all six children with carbamazepine syndrome had a development quotient or intelligence quotient below 90. There were no differences between the two groups in physical growth or in the rate of major anomalies. Two children in group A had cleft palate but in each case this was found in a parent as well. CONCLUSIONS: In utero exposure to carbamazepine may result in 'carbamazepine syndrome' characterised by facial dysmorphic features and mild mental retardation. Prevalence of carbamazepine syndrome does not seem to be related to the dose of carbamazepine or the presence of maternal convulsions. It may depend upon heredofamilial factors that have yet to be defined. One possible factor is decreased activity of the enzyme epoxide hydrolase with resulting increased concentrations of carbamazepine epoxide which may be teratogenic.
This article has been cited by other articles:
-
Kini, U, Adab, N, Vinten, J, Fryer, A, Clayton-Smith, J, on behalf of the Liverpool and Manchester Neurodev,
(2006). Dysmorphic features: an important clue to the diagnosis and severity of fetal anticonvulsant syndromes. Arch. Dis. Child. Fetal Neonatal Ed.
91: F90-F95
[Abstract] [Full Text] -
Vinten, J., Adab, N., Kini, U., Gorry, J., Gregg, J., Baker, G. A., for the Liverpool and Manchester Neurodevelopment,
(2005). Neuropsychological effects of exposure to anticonvulsant medication in utero. Neurology
64: 949-954
[Abstract] [Full Text] -
(2005). Antiepileptics, pregnancy and the child. DTB
43: 13-16
[Abstract] [Full Text] -
Adab, N, Kini, U, Vinten, J, Ayres, J, Baker, G, Clayton-Smith, J, Coyle, H, Fryer, A, Gorry, J, Gregg, J, Mawer, G, Nicolaides, P, Pickering, L, Tunnicliffe, L, Chadwick, D W
(2004). The longer term outcome of children born to mothers with epilepsy. J. Neurol. Neurosurg. Psychiatry
75: 1575-1583
[Abstract] [Full Text] -
Costa, L. G., Steardo, L., Cuomo, V.
(2004). Structural Effects and Neurofunctional Sequelae of Developmental Exposure to Psychotherapeutic Drugs: Experimental and Clinical Aspects. Pharmacol. Rev.
56: 103-147
[Abstract] [Full Text] -
Gaily, E., Kantola-Sorsa, E., Hiilesmaa, V., Isoaho, M., Matila, R., Kotila, M., Nylund, T., Bardy, A., Kaaja, E., Granstrom, M. -L.
(2004). Normal intelligence in children with prenatal exposure to carbamazepine. Neurology
62: 28-32
[Abstract] [Full Text] -
Pennell, P. B.
(2003). The importance of monotherapy in pregnancy. Neurology
60: S31-38
[Abstract] [Full Text] -
Dean, J C S, Hailey, H, Moore, S J, Lloyd, D J, Turnpenny, P D, Little, J
(2002). Long term health and neurodevelopment in children exposed to antiepileptic drugs before birth. J. Med. Genet.
39: 251-259
[Abstract] [Full Text] -
Diav-Citrin, O., Shechtman, S., Arnon, J., Ornoy, A.
(2001). Is carbamazepine teratogenic?: A prospective controlled study of 210 pregnancies. Neurology
57: 321-324
[Abstract] [Full Text] -
Holmes, L. B., Harvey, E. A., Coull, B. A., Huntington, K. B., Khoshbin, S., Hayes, A. M., Ryan, L. M.
(2001). The Teratogenicity of Anticonvulsant Drugs. NEJM
344: 1132-1138
[Abstract] [Full Text] -
Adab, N, Jacoby, A, Smith, D, Chadwick, D
(2001). Additional educational needs in children born to mothers with epilepsy. J. Neurol. Neurosurg. Psychiatry
70: 15-21
[Abstract] [Full Text] -
Moore, S J, Turnpenny, P, Quinn, A, Glover, S, Lloyd, D J, Montgomery, T, Dean, J C S
(2000). A clinical study of 57 children with fetal anticonvulsant syndromes. J. Med. Genet.
37: 489-497
[Abstract] [Full Text] -
Rosser, E. M, Wilson, L. C
(1999). Drugs for epilepsy have teratogenic risks. BMJ
318: 1289a-1289
[Full Text] -
Parman, T., Chen, G., Wells, P. G.
(1998). Free Radical Intermediates of Phenytoin and Related Teratogens. PROSTAGLANDIN H SYNTHASE-CATALYZED BIOACTIVATION, ELECTRON PARAMAGNETIC RESONANCE SPECTROMETRY, AND PHOTOCHEMICAL PRODUCT ANALYSIS. J. Biol. Chem.
273: 25079-25088
[Abstract] [Full Text]
Register for free content
The full back archive is now available for all BMJ Journals. Institutional subscribers may access the entire archive as part of their subscription. Personal subscribers will also have access to all content when logged in. Non-subscribers who register have free access to all articles published before 2006 right back to volume 1 issue 1. Register here to access the free archive of all BMJ Journals.
Don't forget to sign up for content alerts so you keep up to date with all the articles as they are published.



