Evidence map›Paper›PMID 39976348›Full record

ArticleBirth defects research2025

Prenatal Opioid Use Disorder and the Risk of Congenital Anomalies in Offspring: A Population-Based Study.

Kaylee Ramage, Jennifer Yee, Sebastian Srugo, Julian Little, Shiliang Liu

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Article in Birth defects research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

5 authors.

Kaylee RamageDepartment of Community Health Sciences, University of Calgary, Calgary, Canada.
Jennifer YeeCentre for Surveillance and Applied Research, Public Health Agency of Canada, Ottawa, Canada.
Sebastian SrugoCentre for Surveillance and Applied Research, Public Health Agency of Canada, Ottawa, Canada.
Julian LittleSchool of Epidemiology and Public Health, University of Ottawa, Ottawa, Canada.
Shiliang LiuCentre for Surveillance and Applied Research, Public Health Agency of Canada, Ottawa, Canada.ORCID 0000-0002-4496-0279

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo examine whether prenatal opioid use disorder (OUD) diagnosis is associated with the risk of congenital anomalies (CAs) in offspring.

methodsWe conducted a population-based study of mother-newborn dyads comprising. 4143 761 births delivered in Canada from 2006 to 2021. We used robust Poisson regression to examine the association between prenatal OUD diagnosis and risk of non-chromosomal CAs, adjusted for maternal age, parity, multiple gestation, co-morbidities (including mental health disorders, chronic illnesses and other substance use disorders), and infant sex.

resultsWe identified a total of 21, 638 births to persons who were diagnosed with prenatal OUD and 65, 992 (159.3 per 10,000) newborns with CAs. The overall risk of CAs was 2.3 times higher in infants born to birthing persons with a diagnosis of OUD (95% CI 2.2, 2.5). Compared to those without OUD diagnoses, births to persons with a diagnosis of OUD had a higher risk of specific types of congenital microcephaly (aRR 5.2, 95% CI 4.1, 6.6), cleft palate (RR 4.8, 95% CI 3.7, 6.1), pulmonary valve atresia with intact ventricular septum (aRR 2.7, 95% CI 1.1, 6.7), and atrial septal defect (aRR 3.1, 95% CI 2.8, 3.5), among others. In particular, infants born to those with an OUD diagnosis had a 1.8 (95% CI 1.4, 2.3)-fold increased risk of having severe congenital heart disease.

conclusionOur findings suggest an association between prenatal OUD diagnosis and certain CAs in the offspring. Future research is necessary to better understand the role of socio-demographic factors on these associations.

Indexed as

Congenital AbnormalitiesOpioid-Related DisordersPregnancy ComplicationsPrenatal Exposure Delayed EffectsAdultCanadaFemaleHumansInfant, NewbornMalePregnancyRisk Factorsbirth defectscongenital anomalycongenital heart diseasecongenital microcephalyopioid use

Identifiers

PMID39976348
PMCPMC11841020

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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.