Evidence map›Paper›PMID 39680388›Full record

ArticleJAMA pediatrics2025

Adverse Obstetric Outcomes in Pregnancies With Major Fetal Congenital Heart Defects.

Gitte Hedermann, Paula L Hedley, Kasper Gadsbøll, Ida N Thagaard, Lone Krebs, Mona Aarenstrup Karlsen, Cathrine Vedel, Line Rode, Michael Christiansen, Charlotte K Ekelund

Abstract read
In one paragraph

Article in JAMA pediatrics, 2025. 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. Article
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

10 authors.

Gitte HedermannDepartment for Congenital Disorders, Danish National Biobank and Biomarkers, Statens Serum Institut, Copenhagen, Denmark.
Paula L HedleyDepartment for Congenital Disorders, Danish National Biobank and Biomarkers, Statens Serum Institut, Copenhagen, Denmark.
Kasper GadsbøllCenter for Fetal Medicine and Pregnancy, Department of Gynecology, Fertility, and Obstetrics, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.
Ida N ThagaardDepartment for Congenital Disorders, Danish National Biobank and Biomarkers, Statens Serum Institut, Copenhagen, Denmark.
Lone KrebsDepartment of Obstetrics and Gynecology, Copenhagen University Hospital Amager and Hvidovre Hospital, Copenhagen, Denmark.
Mona Aarenstrup KarlsenDepartment of Gynecology, Fertility, and Obstetrics, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.
Cathrine VedelCenter for Fetal Medicine and Pregnancy, Department of Gynecology, Fertility, and Obstetrics, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.
Line RodeCenter for Fetal Medicine and Pregnancy, Department of Gynecology, Fertility, and Obstetrics, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.
Michael ChristiansenDepartment for Congenital Disorders, Danish National Biobank and Biomarkers, Statens Serum Institut, Copenhagen, Denmark.
Charlotte K EkelundCenter for Fetal Medicine and Pregnancy, Department of Gynecology, Fertility, and Obstetrics, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: Understanding the risk profile of obstetric complications in pregnancies with fetal major congenital heart defects (MCHDs) is crucial for obstetric counseling and care. Objective: To investigate the risk of placenta-related adverse obstetric outcomes in pregnancies complicated by fetal MCHDs. Design, Setting, and Participants: This cohort study retrieved data from June 1, 2008, to June 1, 2018, from the Danish Fetal Medicine Database, which includes comprehensive data on more than 95% of all pregnancies in Denmark since the database was instituted in 2008. All singleton pregnancies that resulted in a live-born child after 24 weeks' gestation without chromosomal aberrations were included. A systematic search of the literature was performed in PubMed, Embase, and the Cochrane Library from inception to June 1, 2024, to compile existing knowledge and data on adverse obstetric outcomes among MCHD subtypes. Exposure: Fetal MCHDs including 1 of 11 subtypes. Main Outcomes and Measures: The primary outcome was a composite adverse obstetric outcome defined as preeclampsia, preterm birth, fetal growth restriction, or placental abruption. Secondary outcomes consisted of each adverse obstetric event. Adjusted odds ratios (AORs) were computed using generalized estimating equations adjusted for maternal body mass index, age, smoking, and year of delivery. Meta-analyses were conducted using random-effects models to pool effect sizes for each MCHD subtype and adverse obstetric outcome. Results: A total of 534 170 pregnancies were included in the Danish cohort, including 745 with isolated fetal MCHDs (median [IQR] maternal age, 29.0 [26.0-33.0] years) and 533 425 without MCHDs (median [IQR] maternal age, 30.0 [26.0-33.0] years). Pregnancies with fetal MCHDs exhibited a higher rate of adverse obstetric outcomes at 22.8% compared with 9.0% in pregnancies without fetal MCHDs (AOR, 2.96; 95% CI, 2.49-3.53). Preeclampsia (AOR, 1.83; 95% CI, 1.33-2.51), preterm birth at less than 37 weeks (AOR, 3.84; 95% CI, 3.15-4.71), and fetal growth restriction (AOR, 3.25; 95% CI, 2.42-4.38) occurred significantly more frequently in pregnancies with MCHDs. Except for fetal transposition of the great arteries (AOR, 1.19; 95% CI, 0.66-2.15), all MCHD subtypes carried a greater risk of adverse obstetric outcomes. The meta-analysis included 10 additional studies that supported these results. Conclusions and Relevance: These findings suggest that nearly 1 in 4 women expecting a child with an MCHD, except transposition of the great arteries, may be at high risk of adverse obstetric outcomes.

Indexed as

Heart Defects, CongenitalPregnancy ComplicationsPregnancy OutcomeAdultCohort StudiesDenmarkFemaleFetal Growth RetardationHumansPregnancyPremature Birth

Identifiers

PMID39680388
PMCPMC11791717

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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 Socratic graph.