Evidence map›Paper›PMID 29230691›Full record

ArticleDrug safety2018

Beta-Blocker Use in Pregnancy and Risk of Specific Congenital Anomalies: A European Case-Malformed Control Study.

Jorieke E H Bergman, L Renée Lutke, Rijk O B Gans, Marie-Claude Addor, Ingeborg Barisic, Clara Cavero-Carbonell, Ester Garne, Miriam Gatt, Kari Klungsoyr, Nathalie Lelong and 12 more

Open access · hybridAbstract read
In one paragraph

Article in Drug safety, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
6.2field-weighted citation impact, top 3% of its field
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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 59 citations in OpenAlex.

  1. Guideline
  2. Review
  3. Article
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  8. Review
  9. Atrial fibrillation during pregnancy: a 9-month period with limited options.Herzschrittmachertherapie & Elektrophysiologie · 2021
    Review
  10. Observational
  11. 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

22 authors at 16 institutions in 12 countries.

Jorieke E H BergmanDepartment of Genetics, EUROCAT Northern Netherlands, University of Groningen, University Medical Centre Groningen, P.O. Box 30.001, 9700 RB, Groningen, The Netherlands. j.e.h.van.kammen@umcg.nl.ORCID http://orcid.org/0000-0002-3929-3619
L Renée LutkeDepartment of Genetics, EUROCAT Northern Netherlands, University of Groningen, University Medical Centre Groningen, P.O. Box 30.001, 9700 RB, Groningen, The Netherlands.
Rijk O B GansDepartment of Internal Medicine, University of Groningen, University Medical Centre Groningen, Groningen, The Netherlands.
Marie-Claude AddorDivision of Medical Genetics, CHUV, Lausanne, Switzerland.
Ingeborg BarisicChildren's Hospital Zagreb, Medical School University of Zagreb, Zagreb, Croatia.
Clara Cavero-CarbonellFoundation for the Promotion of Health and Biomedical Research of the Valencian Region, Rare Diseases Research Unit, Valencia, Spain.
Ester GarnePaediatric Department, Hospital Lillebaelt, Kolding, Denmark.
Miriam GattDirectorate for Health Information and Research, Guardamangia, Malta.
Kari KlungsoyrDivision for Health Data and Digitalisation, The Norwegian Institute of Public Health, Bergen, Norway.
Nathalie LelongParis Registry of Congenital Malformations, Obstetrical, Perinatal and Paediatric Epidemiology Research Team, Centre for Biostatistics and Epidemiology, INSERM, UMR 1153, Paris, France.
Catherine LynchDepartment of Public Health, Health Service Executive South East, Kilkenny, Ireland.
Olatz MokoroaPublic Health and Addictions Directorate, Basque Government, Vitoria-Gasteiz, BioDonostia Health Research Institute, Donostia-San Sebastian, Spain.
Vera NelenDepartment of Environment, PIH, Antwerp, Belgium.
Amanda J NevilleIMER Registry (Emilia Romagna Registry of Birth Defects), Centre for Clinical and Epidemiological Research, University of Ferrara, Ferrara, Italy.
Anna PieriniCNR Institute of Clinical Physiology/RTDC Registry (Tuscany Registry of Congenital Defects), Fondazione Toscana "Gabriele Monasterio", Pisa, Italy.
Hanitra RandrianaivoRegistre des Malformations Congenitales de la Reunion, Saint-Pierre, Reunion, France.
Anke RissmannMedical Faculty, Malformation Monitoring Centre, Otto-von-Guericke University, Magdeburg, Saxony-Anhalt, Germany.
David TuckerCongenital Anomaly Register & Information Service for Wales, Public Health Wales, Swansea, UK.
Awi WieselBirth Registry Mainz Model, University Medical Centre of Johannes Gutenberg University, Mainz, Germany.
Helen DolkCentre for Maternal, Foetal and Infant Research, Institute of Nursing and Health Research, Ulster University, Belfast, Northern Ireland, UK.
Maria LoaneCentre for Maternal, Foetal and Infant Research, Institute of Nursing and Health Research, Ulster University, Belfast, Northern Ireland, UK.
Marian K BakkerDepartment of Genetics, EUROCAT Northern Netherlands, University of Groningen, University Medical Centre Groningen, P.O. Box 30.001, 9700 RB, Groningen, The Netherlands.ORCID http://orcid.org/0000-0001-5098-6400
University Medical Center Groningen · NLUniversity of Ulster · GBBasque Government · ESFundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana · ESHealth Service Executive · IEInserm · FRIstituto di Fisiologia Clinica · ITJohannes Gutenberg University Mainz · DELillebaelt Hospital · DKMinistry for Health · MTNorwegian Institute of Public Health · NOOtto-von-Guericke-Universität Magdeburg · DEPeuplements végétaux et bioagresseurs en milieu tropical · REPublic Health Wales · GBUniversity of Ferrara · ITUniversity of Zagreb · HR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe prevalence of chronic hypertension is increasing in pregnant women. Beta-blockers are among the most prevalent anti-hypertensive agents used in early pregnancy.

objectiveThe objective of this study was to investigate whether first-trimester use of beta-blockers increases the risk of specific congenital anomalies in offspring.

methodsA population-based case-malformed control study was conducted in 117,122 registrations of congenital anomalies from 17 European Concerted Action on Congenital Anomalies and Twins (EUROCAT) registries participating in EUROmediCAT with data for all or part of the period between 1995 and 2013. Associations previously reported in the literature (signals) were tested and an exploratory analysis was performed to identify new signals. Odds ratios of exposure to any beta-blocker or to a beta-blocker subgroup were calculated for each signal anomaly compared with two control groups (non-chromosomal, non-signal anomalies and chromosomal anomalies). The exploratory analyses were performed for each non-signal anomaly compared with all the other non-signal anomalies.

resultsThe signals from the literature (congenital heart defects, oral clefts, neural tube defects and hypospadias) were not confirmed. Our exploratory analysis revealed that multi-cystic renal dysplasia had significantly increased odds of occurring after maternal exposure to combined alpha- and beta-blockers (adjusted odds ratio 3.8; 95% confidence interval 1.3-11.0).

conclusionBeta-blocker use in the first trimester of pregnancy was not found to be associated with a higher risk of specific congenital anomalies in the offspring, but a new signal between alpha- and beta-blockers and multi-cystic renal dysplasia was found. Future large epidemiological studies are needed to confirm or refute our findings.

Indexed as

Abnormalities, Drug-InducedAdrenergic beta-AntagonistsAdultAntihypertensive AgentsCase-Control StudiesCongenital AbnormalitiesFemaleHeart Defects, CongenitalHumansOdds RatioPregnancyPregnancy ComplicationsPregnancy Trimester, FirstPrenatal Exposure Delayed EffectsPrevalenceRegistriesAdrenergic beta-AntagonistsAntihypertensive Agents

Identifiers

PMID29230691
PMCPMC5878198
OpenAlexW2772746046

What OpenQuestion holds

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LicenceCC BY-NC
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 OpenQuestion graph.