Evidence map›Paper›PMID 38720955›Full record

ArticleNeurology. Clinical practice2024

Specific Birth Defects Following Antiseizure Medications Used By Pregnant Women With Epilepsy.

Kelsey K Wiggs, Martin E Rickert, Patrick D Quinn, Brian M D'Onofrio, A Sara Öberg

Abstract read
In one paragraph

Article in Neurology. Clinical practice, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Kelsey K WiggsDivision of Behavioral Medicine and Clinical Psychology (KKW), Cincinnati Children's Hospital, Cincinnati, OH; Department of Psychological and Brain Sciences (KKW, MER, BMDO); Department of Applied Health Science (PDQ), School of Public Health, Indiana University-Bloomington, IN; Department of Medical Epidemiology and Biostatistics (BMDO, ASO), Karolinska Institutet, Stockholm, Sweden; and Department of Epidemiology (ASO), T.H. Chan School of Public Health, Harvard, Boston.ORCID https://orcid.org/0000-0002-8013-7925
Martin E RickertDivision of Behavioral Medicine and Clinical Psychology (KKW), Cincinnati Children's Hospital, Cincinnati, OH; Department of Psychological and Brain Sciences (KKW, MER, BMDO); Department of Applied Health Science (PDQ), School of Public Health, Indiana University-Bloomington, IN; Department of Medical Epidemiology and Biostatistics (BMDO, ASO), Karolinska Institutet, Stockholm, Sweden; and Department of Epidemiology (ASO), T.H. Chan School of Public Health, Harvard, Boston.ORCID https://orcid.org/0000-0002-7010-7300
Patrick D QuinnDivision of Behavioral Medicine and Clinical Psychology (KKW), Cincinnati Children's Hospital, Cincinnati, OH; Department of Psychological and Brain Sciences (KKW, MER, BMDO); Department of Applied Health Science (PDQ), School of Public Health, Indiana University-Bloomington, IN; Department of Medical Epidemiology and Biostatistics (BMDO, ASO), Karolinska Institutet, Stockholm, Sweden; and Department of Epidemiology (ASO), T.H. Chan School of Public Health, Harvard, Boston.ORCID https://orcid.org/0000-0002-6770-8762
Brian M D'OnofrioDivision of Behavioral Medicine and Clinical Psychology (KKW), Cincinnati Children's Hospital, Cincinnati, OH; Department of Psychological and Brain Sciences (KKW, MER, BMDO); Department of Applied Health Science (PDQ), School of Public Health, Indiana University-Bloomington, IN; Department of Medical Epidemiology and Biostatistics (BMDO, ASO), Karolinska Institutet, Stockholm, Sweden; and Department of Epidemiology (ASO), T.H. Chan School of Public Health, Harvard, Boston.ORCID https://orcid.org/0000-0002-5248-7434
A Sara ÖbergDivision of Behavioral Medicine and Clinical Psychology (KKW), Cincinnati Children's Hospital, Cincinnati, OH; Department of Psychological and Brain Sciences (KKW, MER, BMDO); Department of Applied Health Science (PDQ), School of Public Health, Indiana University-Bloomington, IN; Department of Medical Epidemiology and Biostatistics (BMDO, ASO), Karolinska Institutet, Stockholm, Sweden; and Department of Epidemiology (ASO), T.H. Chan School of Public Health, Harvard, Boston.ORCID https://orcid.org/0000-0001-6638-1895

Funding

Maternal use of prescribed opioid analgesics and risk of adverse offspring outcomesR01DA048042 · NIDA · TRUSTEES OF INDIANA UNIVERSITY · PI D'ONOFRIO, BRIAN M, OBERG, ANNA SARA · 2019 to 2021
$1.2M
NIDA NIH HHS R01 DA048042
6 · The paper itself

Abstract

Background and Objectives: Previous research has been limited in the comprehensive study of associations between the use of individual antiseizure medications (ASMs) in pregnancy and specific groups of birth defects, and systematic reviews and meta-analyses on the topic are limited by pooled samples and study designs. This study investigated birth defects related to ASM use in pregnancy in children born to women with epilepsy in Sweden over 20 years. Methods: We used data from Swedish national registers to follow a cohort of 17,996 children born to women diagnosed with epilepsy any time before conception in Sweden from 1996 to 2016, following them through 2017. We examined maternal-reported use of the 4 most commonly reported ASMs: lamotrigine (n = 2,148, 11.9%), carbamazepine (n = 1,940, 10.8%), valproic acid (n = 1,043, 5.80%), and levetiracetam (n = 587, 3.26%). We identified birth defects using diagnoses recorded at the time of discharge from the hospital and inpatient and outpatient diagnoses recorded in the first year of life. Models were estimated in a stepped fashion: unadjusted, adjusted for covariates, among a subcohort born to women diagnosed 10 years before conception (n = 14,586), and restricted to monotherapy. Results: Valproic acid use in pregnancy had the strongest and most widespread associations with birth defects in children, with carbamazepine also having links to several birth defects, including respiratory system and genital organ defects. Lamotrigine use in pregnancy was associated with cleft lip/palate and chromosomal abnormalities. Levetiracetam was most often used with other ASMs and preliminarily associated with many birth defects. Discussion: Our findings support avoidance of valproic acid use in pregnancy whenever possible. Lamotrigine and carbamazepine may be safer alternatives. However, these medications were also associated with certain birth defects, including some not reported previously. We are among the first to examine the possible effects of levetiracetam use in pregnancy, though more research is needed to investigate this further.

Identifiers

PMID38720955
PMCPMC11073867

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.