Pregnancy with epilepsy: obstetric and neonatal outcome of a controlled study
- PMID: 20036166
- PMCID: PMC2823982
- DOI: 10.1016/j.seizure.2009.11.008
Pregnancy with epilepsy: obstetric and neonatal outcome of a controlled study
Abstract
Purpose: To determine the influence of epilepsy and its treatment on pregnancy and its outcome.
Design: Controlled, observational study.
Setting: National Health Service maternity hospitals in Liverpool and Manchester regions.
Population: 277 women with epilepsy (WWE) and 315 control women.
Methods: WWE were recruited from antenatal clinics. Controls were matched for age and parity but not gestational age. Information was obtained by interview and from clinical records.
Main outcome measures: Obstetric complications, mode of delivery, condition of newborn.
Results: Distribution of epilepsy syndromes was similar to previous surveys. Most WWE (67%) received monotherapy with carbamazepine, sodium valproate or lamotrigine. Half WWE had no seizures during pregnancy but 34% had tonic clonic seizures. Seizure-related injuries were infrequent. Pregnancies with obstetric complications were increased in women with treated epilepsy (WWTE 45%, controls 33%; p=0.01). Most had normal vaginal delivery (WWTE 63%, controls 61%; p=0.65). Low birth weight was not increased (WWTE 6.2%, controls 5.2%; p=0.69). There were more major congenital malformations (MCM) (WWTE 6.6%, controls 2.1%; p=0.02) and fetal/infant deaths (WWTE 2.2%, controls 0.3%; p=0.09). Amongst monotherapies MCM prevalence was highest with valproate (11.3%; p=0.005). Lamotrigine (5.4%; p=0.23) and carbamazepine (3.0%; p=0.65) were closer to controls (2.1%). There was no association between MCM and dose of folic acid pre-conception.
Conclusion: MCM were more prevalent in the babies of WWTE particularly amongst those receiving sodium valproate.
Copyright 2009 British Epilepsy Association. Published by Elsevier Ltd. All rights reserved.
Conflict of interest statement
Statement of conflict of interest
G.A. Baker, R. Bromley, J. Clayton-Smith, U. Kini and G. Mawer have each given expert testimony on fetal anticonvulsant syndrome. G.A.B. has received educational grants from Sanofi Aventis to support this research. The remaining Authors have no conflicts of interest to disclose.
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