Abstract

BackgroundEpilepsy affects about 1% of the general population. Anti-epileptic drugs (AEDs) prevent or terminate seizures in individuals with epilepsy. Pregnant women with epilepsy may continue taking AEDs. Many of these agents cross the placenta and increase the risk of major congenital malformations, early cognitive and developmental delays, and infant mortality. We aim to evaluate the comparative safety of AEDs approved for chronic use in Canada when administered to pregnant and breastfeeding women and the effects on their infants and children through a systematic review and network meta-analysis.MethodsStudies examining the effects of AEDs administered to pregnant and breastfeeding women regardless of indication (e.g., epilepsy, migraine, pain, psychiatric disorders) on their infants and children will be included. We will include randomized clinical trials (RCTs), quasi-RCTs, non-RCTs, controlled before-after, interrupted time series, cohort, registry, and case-control studies. The main literature search will be executed in MEDLINE, EMBASE, and the Cochrane Central Register of Controlled Trials. We will seek unpublished literature through searches of trial protocol registries and conference abstracts. The literature search results screening, data abstraction, and risk of bias appraisal will be performed by two individuals, independently. Conflicts will be resolved through discussion. The risk of bias of experimental and quasi-experimental studies will be appraised using the Cochrane Effective Practice and Organization of Care Risk-of-Bias tool, methodological quality of observational studies will be appraised using the Newcastle-Ottawa Scale, and quality of reporting of safety outcomes will be conducted using the McMaster Quality Assessment Scale of Harms (McHarm) tool. If feasible and appropriate, we will conduct random effects meta-analysis. Network meta-analysis will be considered for outcomes that fulfill network meta-analysis assumptions.The primary outcome is major congenital malformations (overall and by specific types), while secondary outcomes include fetal loss/miscarriage, minor congenital malformations (overall and by specific types), cognitive development, psychomotor development, small for gestational age, preterm delivery, and neonatal seizures.DiscussionOur systematic review will address safety concerns regarding the use of AEDs during pregnancy and breastfeeding. Our results will be useful to healthcare providers, policy-makers, and women of childbearing age who are taking anti-epileptic medications.Systematic review registrationPROSPERO CRD42014008925.

Highlights

  • Epilepsy affects about 1% of the general population

  • Our systematic review will address safety concerns regarding the use of Anti-epileptic drugs (AEDs) during pregnancy and breastfeeding

  • Our objective is to evaluate the comparative safety of AEDs for infants and children who were exposed in utero or during breastfeeding through a systematic review and network meta-analysis

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Summary

Introduction

Anti-epileptic drugs (AEDs) prevent or terminate seizures in individuals with epilepsy. Epilepsy is the most common chronic neurological condition, affecting 0.6 to 1% of the population [1,2]. Anti-epileptic medications decrease seizures by reducing excitation and enhancing inhibition of neurons [5,6,7]. Many of these medications target different channels, including calcium, sodium, and glutamate, and are broadly classified as first generation agents (e.g., phenobarbitone, phenytoin, carbamazepine, sodium valproate, ethosuximide) and second generation agents (e.g., lamotrigine, levetiracetam, topiramate, gabapentin, vigabatrin, oxcarbazepine, clobazam, clonazepam, zonisamide, lacosamide, rufinamide, primidone) [8]. Due to the broad and varied mechanisms of action, the indications for some of these medications include pain syndromes, psychiatric disorders, and migraine headaches [8]

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