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Comparative Risk of Major Congenital Malformations With Antiseizure Medication Combinations vs Valproate Monotherapy in Pregnancy

拉莫三嗪 左乙拉西坦 唑尼沙胺 托吡酯 医学 怀孕 癫痫 药物流行病学 儿科 人口 内科学 药理学 精神科 生物 遗传学 环境卫生 药方
作者
Jack Cohen,Silje Alvestad,Elizabeth A. Suarez,Andrea L. Schaffer,Randi Selmer,Alys Havard,Brian T. Bateman,Carolyn E. Cesta,Helga Zoëga,Ingvild Odsbu,Krista F. Huybrechts,Lars Jøran Kjerpeseth,Loreen Straub,Maarit K. Leinonen,Marte‐Helene Bjørk,Mette Nørgaard,Mika Gissler,Sinna Pilgaard Ulrichsen,Sonia Hernández–Dı́az,Torbjörn Tomson,Kari Furu
出处
期刊:Neurology [Ovid Technologies (Wolters Kluwer)]
卷期号:102 (2)
标识
DOI:10.1212/wnl.0000000000207996
摘要

Background and ObjectivesValproate should be avoided in pregnancy, but it is the most effective drug for generalized epilepsies. Alternative treatment may require combinations of other drugs. Our objectives were to describe first trimester use of antiseizure medication (ASM) combinations that are relevant alternatives to valproate and determine whether specific combinations were associated with a lower risk of major congenital malformations (MCM) compared with valproate monotherapy.MethodsWe conducted a population-based cohort study using linked national registers from Denmark, Finland, Iceland, Norway, and Sweden and administrative health care data from the United States and New South Wales, Australia. We described first trimester use of ASM combinations among pregnant people with epilepsy from 2000 to 2020. We compared the risk of MCM after first trimester exposure to ASM combinations vs valproate monotherapy and low-dose valproate plus lamotrigine or levetiracetam vs high-dose valproate (≥1,000 mg/d). We used log-binomial regression with propensity score weights to calculate adjusted risk ratios (aRRs) and 95% CIs for each dataset. Results were pooled using fixed-effects meta-analysis.ResultsAmong 50,905 pregnancies in people with epilepsy identified from 7.8 million total pregnancies, 788 used lamotrigine and levetiracetam, 291 used lamotrigine and topiramate, 208 used levetiracetam and topiramate, 80 used lamotrigine and zonisamide, and 91 used levetiracetam and zonisamide. After excluding pregnancies with use of other ASMs, known teratogens, or a child diagnosed with MCM of infectious or genetic cause, we compared 587 exposed to lamotrigine-levetiracetam duotherapy and 186 exposed to lamotrigine-topiramate duotherapy with 1959 exposed to valproate monotherapy. Pooled aRRs were 0.41 (95% CI 0.24–0.69) and 1.26 (0.71–2.23), respectively. Duotherapy combinations containing low-dose valproate were infrequent, and comparisons with high-dose valproate monotherapy were inconclusive but suggested a lower risk for combination therapy. Other combinations were too rare for comparative safety analyses.DiscussionLamotrigine-levetiracetam duotherapy in first trimester was associated with a 60% lower risk of MCM than valproate monotherapy, while lamotrigine-topiramate was not associated with a reduced risk. Duotherapy with lamotrigine and levetiracetam may be favored to treat epilepsy in people with childbearing potential compared with valproate regarding MCM, but whether this combination is as effective as valproate remains to be determined.Classification of EvidenceThis study provides Class II evidence that in people with epilepsy treated in the first trimester of pregnancy, the risk of major congenital malformations is lower with lamotrigine-levetiracetam duotherapy than with valproate alone, but similar with lamotrigine-topiramate.
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