Evidence map›Paper›PMID 41725333›Full record

ArticleActa obstetricia et gynecologica Scandinavica2026

Discrepancy in menstrual and ultrasound-based gestational age is associated with chromosomal aberrations and adverse pregnancy outcomes-Results from a nationwide cohort study.

Simone Hansen, Olav Bjørn Petersen, Ida Vogel, Nina Gros Pedersen, Lars Henning Pedersen, Steffen Ernesto Kristensen, Karin Sundberg, Emilie Thorup, Cathrine Vedel, Kasper Gadsbøll

Abstract read
In one paragraph

Article in Acta obstetricia et gynecologica Scandinavica, 2026. 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.

Simone HansenCenter of Fetal Medicine, Department of Gynecology, Fertility, and Pregnancy, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.ORCID 0009-0004-2059-7710
Olav Bjørn PetersenCenter of Fetal Medicine, Department of Gynecology, Fertility, and Pregnancy, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.ORCID 0000-0001-8517-4082
Ida VogelCenter for Fetal Diagnostics, Aarhus University Hospital, Aarhus, Denmark.ORCID 0000-0002-1125-0393
Nina Gros PedersenDepartment of Obstetrics and Gynecology, Nordsjaellands Hospital, Hilleroed, Denmark.
Lars Henning PedersenDepartment of Clinical Medicine, Aarhus University, Aarhus, Denmark.ORCID 0000-0001-6726-1991
Steffen Ernesto KristensenCenter of Fetal Medicine, Department of Gynecology, Fertility, and Pregnancy, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.ORCID 0000-0003-4633-4738
Karin SundbergCenter of Fetal Medicine, Department of Gynecology, Fertility, and Pregnancy, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.ORCID 0000-0001-5598-5773
Emilie ThorupCenter of Fetal Medicine, Department of Gynecology, Fertility, and Pregnancy, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.ORCID 0000-0001-6546-5544
Cathrine VedelCenter of Fetal Medicine, Department of Gynecology, Fertility, and Pregnancy, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.ORCID 0000-0001-7475-513X
Kasper GadsbøllCenter of Fetal Medicine, Department of Gynecology, Fertility, and Pregnancy, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.ORCID 0000-0002-1331-3503

Funding

Novo Nordisk Fonden NNF23SA0087869Novo Nordisk Fonden NNFSA170030576
6 · The paper itself

Abstract

introductionIn women with a regular cycle, reliable last menstrual period (LMP), and accurate crown-rump length (CRL) estimation, discrepancies in estimated date of delivery (EDD) may indicate impaired fetal growth and increased risk of morbidity. This study examines whether discrepancies between EDD based on LMP (EDD MATERIAL AND

methodsA Danish nationwide register-based cohort study including all singleton pregnancies with both CRL and LMP registered between 2008 and 2018. Exclusion criteria were uncertain LMP, irregular menstrual cycle, EDD discrepancies >±28 days, assisted reproductive technology, and missing outcome data. The cohort was stratified into seven groups according to EDD

resultsA total of 262 329 pregnancies were included; 16% had smaller and 21% had larger CRL than expected from LMP. Negative discrepancies were significantly associated with increased risk of chromosomal aberrations, adverse pregnancy outcomes, and obstetric complications. In the -8 to -14 days group, 1.28% had a chromosomal abnormality (aOR 2.77 [95% CI 2.30-3.31]), and risk remained elevated among pregnancies at low combined first-trimester screening risk (aOR 1.95 [1.55-2.43]). For triploidy and trisomy 18, 91% and 59% of cases, respectively, had discrepancies of <-3 days. In the -8 to -14 days group, adverse pregnancy outcome occurred in 11.0% (aOR 1.49 [1.40-1.59]), and 6.5% had obstetric complications, mainly preeclampsia (aOR 1.19 [1.10-1.29]). Conversely, positive discrepancies were associated with reduced risk of chromosomal abnormalities (aOR 0.67 [0.44-0.96]) and adverse pregnancy outcomes (aOR 0.77 [0.69-0.86]) in the +8 to +14 days group.

conclusionsA smaller than expected CRL was strongly associated with chromosomal aberrations, adverse pregnancy outcomes, and obstetric complications. Incorporating EDD discrepancies into risk algorithms for genetic disease, growth restriction, and preeclampsia may improve prediction and warrants further study.

Indexed as

Chromosome AberrationsCrown-Rump LengthGestational AgePregnancy ComplicationsPregnancy OutcomeUltrasonography, PrenatalAdultCohort StudiesDenmarkFemaleHumansPregnancyRegistrieschromosomal aberrationsfetal growth restrictionfirst trimestergestational agepreeclampsiapregnancy datingpregnancy outcomeprenatal ultrasonography

Identifiers

PMID41725333
PMCPMC13140727

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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.