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Clinical Trials/DRKS00021001
DRKS00021001
Completed
Not Applicable

se of antiepileptic drugs (AED) during pregnancy – an evaluation of treatment patterns based on the German Embryotox database

Pharmakovigilanzzentrum Embryonaltoxikologie Charité-Universitätsmedizin0 sites5,000 target enrollmentMarch 4, 2020
ConditionsG40Epilepsy

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
G40
Sponsor
Pharmakovigilanzzentrum Embryonaltoxikologie Charité-Universitätsmedizin
Enrollment
5000
Status
Completed
Last Updated
last year

Overview

Brief Summary

INTRODUCTION: Epilepsy is a common neurological disease requiring long-term therapy also during pregnancy. Most studies on pregnancy outcomes in women with epilepsy are based on antiseizure medication (ASM) in monotherapy. However, about 20-30% of epilepsy patients require polytherapy and newer ASMs are an option, when seizure control is not achieved with first line ASMs. METHODS: Observational study evaluating the use of newer ASMs with marketing authorization since 2005 reported to the Embryotox Center of Clinical Teratology and Drug Safety in Pregnancy between 2004 and 2019. In addition, course and outcome of lacosamide exposed pregnancies were analysed. RESULTS: Our study confirms the increasing use of newer ASMs also in pregnant women. This is especially true for lacosamide, eslicarbazepine and brivaracetam with rising numbers of exposed pregnancies soon after marketing authorization. Analysis of 55 prospectively and 10 retrospectively ascertained lacosamide exposed pregnancies does not indicate increased risks of major birth defects or spontaneous abortion. However, bradycardia observed in 3 neonates might be related to prenatal lacosamide exposure. CONCLUSION: Available data do not support the assumption of lacosamide being a major teratogen. The increasing use of newer ASMs during pregnancy underscores the need for more studies to guide preconception counselling, especially for lacosamide, eslicarbazepine and brivaracetam.

Registry
who.int
Start Date
March 4, 2020
End Date
TBD
Last Updated
last year
Study Type
Observational
Sex
Female

Investigators

Sponsor
Pharmakovigilanzzentrum Embryonaltoxikologie Charité-Universitätsmedizin

Eligibility Criteria

Inclusion Criteria

  • Enrollment of pregnancies, of which neither the outcome nor pathological results of prenatal diagnostics were known at first contact to the German Embryotox Pharmacovigilance centre. Included are pregnancies with at least one antiepileptic drug exposure at conception in the study period 2000\-2018\.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

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