Evidence map›Paper›PMID 33966183›Full record

ArticleDrug safety2021

Signal Detection in EUROmediCAT: Identification and Evaluation of Medication-Congenital Anomaly Associations and Use of VigiBase as a Complementary Source of Reference.

Alana Cavadino, Lovisa Sandberg, Inger Öhman, Tomas Bergvall, Kristina Star, Helen Dolk, Maria Loane, Marie-Claude Addor, Ingeborg Barisic, Clara Cavero-Carbonell and 19 more

Abstract read
PubMed Publisher
In one paragraph

Article in Drug safety, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. In-Depth Genomic Analysis: The New Challenge in Congenital Heart Disease.International journal of molecular sciences · 2024
    Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
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

29 authors.

Alana CavadinoSchool of Population Health, the University of Auckland, Auckland, New Zealand.ORCID 0000-0002-5709-367X
Lovisa SandbergUppsala Monitoring Centre, Uppsala, Sweden.ORCID 0000-0001-6982-5244
Inger ÖhmanUppsala Monitoring Centre, Uppsala, Sweden.ORCID 0000-0001-7784-6272
Tomas BergvallUppsala Monitoring Centre, Uppsala, Sweden.ORCID 0000-0003-4394-3431
Kristina StarUppsala Monitoring Centre, Uppsala, Sweden.ORCID 0000-0002-5384-8609
Helen DolkInstitute of Nursing and Health Research, Ulster University, Newtownabbey, Northern Ireland, UK.
Maria LoaneInstitute of Nursing and Health Research, Ulster University, Newtownabbey, Northern Ireland, UK.ORCID 0000-0002-1206-3637
Marie-Claude AddorDepartment of Woman-Mother-Child, University Hospital Center CHUV, CH 1011, Lausanne, Switzerland.
Ingeborg BarisicChildren's Hospital Zagreb, Centre of Excellence for Reproductive and Regenerative Medicine, Medical School University of Zagreb, Zagreb, Croatia.
Clara Cavero-CarbonellRare Diseases Research Unit, Foundation for the Promotion of Health and Biomedical Research in the Valencian Region, Valencia, Spain.
Ester GarnePaediatric Department, Hospital Lillebaelt, Kolding, Denmark.ORCID 0000-0003-0430-2594
Miriam GattMalta Congenital Anomalies Registry, Directorate for Health Information and Research, Tal-Pietà, Malta.
Babak KhoshnoodParis Registry of Congenital Malformations, Obstetrical, Perinatal and Paediatric Epidemiology Research Team, Centre for Biostatistics and Epidemiology, INSERM, UMR 1153, Paris, France.
Kari KlungsøyrDepartment of Global Public Health and Primary Care, University of Bergen, Bergen, Norway.ORCID 0000-0003-2482-1690
Anna Latos-BielenskaDepartment of Medical Genetics, Poznan University of Medical Sciences, Poznań, Poland.
Nathalie LelongParis Registry of Congenital Malformations, Obstetrical, Perinatal and Paediatric Epidemiology Research Team, Centre for Biostatistics and Epidemiology, INSERM, UMR 1153, Paris, France.
Reneé LutkeDepartment of Genetics, University of Groningen, University Medical Centre Groningen, Groningen, The Netherlands.
Anna Materna-KirylukDepartment of Medical Genetics, Poznan University of Medical Sciences, Poznań, Poland.
Vera NelenDepartment of Environment, PIH, Antwerp, Belgium.
Amanda NevillIMER Registry (Emila Romagna Registry of Birth Defects), Center for Clinical and Epidemiological Research, University of Ferrara, Azienda Ospedaliero, Italy.
Mary O'MahonyDepartment of Public Health, Health Service Executive-South, Cork, Ireland.
Olatz MokoroaBasque Government, Department of Health, Public Health Division of Gipuzkoa, Donostia-San Sebastian, Spain.
Anna PieriniTuscany Registry of Congenital Defects (RTDC), Institute of Clinical Physiology, National Research Council/Fondazione Toscana Gabriele Monasterio, Pisa, Italy.
Hanitra RandrianaivoUnit of congenital malformations, REMACOR- Medical School University of La Réunion St Pierre, Sainte-Clotilde, France.
Anke RissmannMalformation Monitoring Centre Saxony-Anhalt, Medical Faculty Otto-von-Guericke-University, Magdeburg, Germany.ORCID 0000-0002-9437-2790
David TuckerCongenital Anomaly Register and Information Service for Wales, Public Health Wales Knowledge Directorate, Level 3, West Wing Block, Singleton Hospital, Sketty Lane, Swansea, UK.
Awi WieselDepartment of Pediatrics, Birth Registry Mainz Model, University Medical Center of Mainz, Mainz, Germany.
Lyubov YevtushokOMNI-Net Ukraine Birth Defects Program and Rivne Regional Medical Diagnostic Center, Rivne, Ukraine.ORCID 0000-0002-3799-7268
Joan K MorrisPopulation Health Research Institute, St George's, University of London, London, UK. jmorris@sgul.ac.uk.ORCID 0000-0002-7164-612X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionKnowledge on the safety of medication use during pregnancy is often sparse. Pregnant women are generally excluded from clinical trials, and there is a dependence on post-marketing surveillance to identify teratogenic medications.

aimsThis study aimed to identify signals of potentially teratogenic medications using EUROmediCAT registry data on medication exposure in pregnancies with a congenital anomaly, and to investigate the use of VigiBase reports of adverse events of medications in the evaluation of these signals.

methodsSignals of medication-congenital anomaly associations were identified in EUROmediCAT (21,636 congenital anomaly cases with 32,619 medication exposures), then investigated in a subset of VigiBase (45,749 cases and 165,121 exposures), by reviewing statistical reporting patterns and VigiBase case reports. Evidence from the literature and quantitative and qualitative aspects of both datasets were considered before recommending signals as warranting further independent investigation.

resultsEUROmediCAT analysis identified 49 signals of medication-congenital anomaly associations. Incorporating investigation in VigiBase and the literature, these were categorised as follows: four non-specific medications; 11 likely due to maternal disease; 11 well-established teratogens; two reviewed in previous EUROmediCAT studies with limited additional evidence; and 13 with insufficient basis for recommending follow-up. Independent investigations are recommended for eight signals: pregnen (4) derivatives with limb reduction; nitrofuran derivatives with cleft palate and patent ductus arteriosus; salicylic acid and derivatives with atresia or stenosis of other parts of the small intestine and tetralogy of Fallot; carbamazepine with atrioventricular septal defect and severe congenital heart defect; and selective beta-2-adrenoreceptor agonists with posterior urethral valve and/or prune belly.

conclusionEUROmediCAT data should continue to be used for signal detection, accompanied by information from VigiBase and review of the existing literature to prioritise signals for further independent evaluation.

Indexed as

Heart Defects, CongenitalTeratogensFemaleHumansPregnancyPregnancy Trimester, FirstRegistriesTeratogens

Identifiers

What OpenQuestion 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 OpenQuestion graph.