Evidence map›Paper›PMID 40695096›Full record

ArticleDrug and alcohol dependence2025

Prevalence of congenital heart defects among children with and without diagnosed fetal alcohol spectrum disorders, 2016-2022.

Amanda N Dorsey, Karrie F Downing, Nicholas P Deputy, Mary Kate Weber, Penelope P Howards

Abstract read
In one paragraph

Article in Drug and alcohol dependence, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
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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.

Amanda N DorseyEmory University, Department of Epidemiology, 1518 Clifton Rd NE, Atlanta, GA, USA; National Center on Birth Defects and Developmental Disabilities, CDC, 4770 Buford Hwy, Atlanta, GA, USA; G2S Corporation, Shavano Park, TX, USA. Electronic address: Amanda.dorsey@emory.edu.
Karrie F DowningNational Center on Birth Defects and Developmental Disabilities, CDC, 4770 Buford Hwy, Atlanta, GA, USA. Electronic address: yyx9@cdc.gov.
Nicholas P DeputyNational Center on Birth Defects and Developmental Disabilities, CDC, 4770 Buford Hwy, Atlanta, GA, USA; US Public Health Service Commissioned Corps, Rockville, MD, USA. Electronic address: wwi9@cdc.gov.
Mary Kate WeberNational Center on Birth Defects and Developmental Disabilities, CDC, 4770 Buford Hwy, Atlanta, GA, USA. Electronic address: muw1@cdc.gov.
Penelope P HowardsEmory University, Department of Epidemiology, 1518 Clifton Rd NE, Atlanta, GA, USA. Electronic address: Penelope.howards@emory.edu.

Funding

Intramural CDC HHS CC999999
6 · The paper itself

Abstract

backgroundAlcohol use during pregnancy might be a risk factor for some congenital heart defects (CHDs), but CHD prevalence among children with fetal alcohol spectrum disorders (FASDs) is not well understood. We used two administrative databases to explore CHD prevalence among U.S. children with and without FASDs.

methodsWe limited 2016-2022 Merative™ MarketScan® Multi-State Medicaid and Commercial data to children ≤ 17 years old with ≥ 1 year of continuous enrollment with complete data on mental health and substance use services. CHD prevalence was calculated by FASD status, overall and by age group, using log-binomial prevalence ratios (PRs) and 95 % confidence intervals (CIs). Analyses were repeated after matching on enrollment length, and age and year at the start of enrollment. In the Medicaid sample, we also stratified by demographic characteristics and analyzed severe and non-severe CHD diagnoses separately. Multidimensional bias analysis considered the influence of unmeasured prenatal tobacco exposure.

resultsAmong 8732,345 children in the Medicaid sample, 5.2 % with FASDs and 1.0 % without FASDs had CHDs (matched cohort PR = 3.4 [CI: 2.8, 4.1]). PRs were similar when stratified by sex and race and ethnicity, and when looking at exclusively severe or non-severe CHDs. Among 10,567,765 children in the commercial claims sample, 3.0 % with FASDs and 0.6 % without FASDs had CHDs (matched cohort PR= 4.6 [CI: 3.3, 6.4]).

conclusionCHDs were more common among children with FASDs compared to those without FASDs in two administrative database samples. Increased provider awareness about CHDs as a potential FASD comorbidity may improve timely CHD care.

Indexed as

Fetal Alcohol Spectrum DisordersHeart Defects, CongenitalAdolescentChildChild, PreschoolDatabases, FactualFemaleHumansInfantMaleMedicaidPregnancyPrenatal Exposure Delayed EffectsPrevalenceRisk FactorsUnited StatesComorbidityCongenital heart defectsFetal alcohol spectrum disordersMedicaidSubstance-related disorders

Identifiers

PMID40695096
PMCPMC12330177

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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.