Evidence mapPaperPMID 39237457Full record

SynthesisEuropean heart journal. Cardiovascular pharmacotherapy2024

Update on antithrombotic therapy and body mass: a clinical consensus statement of the European Society of Cardiology Working Group on Cardiovascular Pharmacotherapy and the European Society of Cardiology Working Group on Thrombosis.

Bruna Gigante, Juan Tamargo, Stefan Agewall, Dan Atar, Jurrien Ten Berg, Gianluca Campo, Elisabetta Cerbai, Christina Christersson, Dobromir Dobrev, Péter Ferdinandy and 8 more

Abstract readSystematic ReviewConsensus Statement
In one paragraph

Synthesis in European heart journal. Cardiovascular pharmacotherapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Additional Stroke Risk Factors Beyond the CHAJournal of clinical medicine · 2026
    Article
  5. Review
  6. When more is worse: aspirin backfires in anticoagulated post-PCI patients.European heart journal. Cardiovascular pharmacotherapy · 2025
    Article
  7. Review
  8. Antiplatelet treatment in different clinical settings.European heart journal. Cardiovascular pharmacotherapy · 2025
    Article
  9. Article
  10. Antiplatelet Therapy in Heart Disease.Reviews in cardiovascular medicine · 2025
    Review
  11. 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

18 authors.

Bruna GiganteDivision of Cardiovascular Medicine, Department of Medicine, Karolinska Institutet, 17177 Stockholm, Sweden.ORCID 0000-0003-4508-7990
Juan TamargoDepartment of Pharmacology and Toxicology, School of Medicine, Universidad Complutense, de Madrid, Instituto de Investigación Sanitaria Gregorio Marañón, CIBERCV, 28040 Madrid, Spain.ORCID 0000-0002-7979-7758
Stefan AgewallDivision of Clinical Science, Danderyds Hospital, Karolinska Institutet,  18288 Stockholm, Sweden.ORCID 0000-0002-6942-6312
Dan AtarInstitute of Clinical Sciences, University of Oslo, NO-0318 Oslo, Norway.ORCID 0000-0003-1513-8793
Jurrien Ten BergSt Antonius Hospital, Koekoekslaan 1, 3435 CM Nieuwegein, the Netherlands.
Gianluca CampoAzienda Ospedaliero Universitaria di Ferrara, Via Aldo Moro 8, Cona, FE 44124, Italy.ORCID 0000-0002-5150-188X
Elisabetta CerbaiDepartment of Neurofarba, University of Florence, Viale G. Pieraccini 6, 50139  Florence, Italy.ORCID 0000-0001-7839-1361
Christina ChristerssonCardiology, Department of Medical Sciences, Uppsala University, 753 09 Uppsala, Sweden.ORCID 0000-0001-9116-8084
Dobromir DobrevInstitute of Pharmacology, University Duisburg-Essen, 45141 Essen, Germany.ORCID 0000-0002-4612-117X
Péter FerdinandyDepartment of Pharmacology and Pharmacotherapy, Semmelweis University, Budapest 1089, Hungary.ORCID 0000-0002-6424-6806
Tobias GeislerDepartment of Cardiology and Angiology, University Hospital, 72076 Tübingen, Germany.
Diana A GorogFaculty of Medicine, National Heart and Lung Institute, Imperial College, Dovehouse Street, London SW3 6LY, UK.ORCID 0000-0002-9286-1451
Erik L GroveDepartment of Cardiology, Aarhus University Hospital, Palle Juul-Jensens Boulevard 99, 8200 Aarhus, Denmark.ORCID 0000-0002-1466-0865
Juan Carlos KaskiMolecular and Clinical Sciences Research Institute, St George's University of London, Cranmer Terrace, London SW17 0RE, UK.
Andrea RubboliDepartment of Emergency, Internal Medicine, and Cardiology, Division of Cardiology, S. Maria delle Croci Hospital, Viale Randi 5, 48121 Ravenna, Italy.ORCID 0000-0001-8657-6235
Sven WassmannCardiology Pasing, Munich, and Faculty of Medicine, University of the Saarland, 66421 Homburg/Saar, Germany.
Håkan WallenDepartment of Cardiology, Danderyds Hospital, 18288 Stockholm, Sweden.ORCID 0000-0003-2617-8328
Bianca RoccaDepartment of Neurofarba, University of Florence, Viale G. Pieraccini 6, 50139  Florence, Italy.ORCID 0000-0001-8304-6423

Funding

Abbott VascularAbbVieAstraZenecaBayerBoehringer IngelheimBristol-Myers SquibbDaiichi Sankyo CompanyMedtronicPfizerSMTZonMw
6 · The paper itself

Abstract

Obesity and underweight are a growing health problem worldwide and a challenge for clinicians concerning antithrombotic therapy, due to the associated risks of thrombosis and/or bleeding. This clinical consensus statement updates a previous one published in 2018, by reviewing the most recent evidence on antithrombotic drugs based on body size categories according to the World Health Organization classification. The document focuses mostly on individuals at the extremes of body weight, i.e. underweight and moderate-to-morbid obesity, who require antithrombotic drugs, according to current guidelines, for the treatment or prevention of cardiovascular diseases or venous thromboembolism. Managing antithrombotic therapy or thromboprophylaxis in these individuals is challenging, due to profound changes in body composition, metabolism and organ function, and altered drug pharmacokinetics and pharmacodynamics, as well as weak or no evidence from clinical trials. The document also includes artificial intelligence simulations derived from in silico pharmacokinetic/pharmacodynamic models, which can mimic the pharmacokinetic changes and help identify optimal regimens of antithrombotic drugs for severely underweight or severely obese individuals. Further, bariatric surgery in morbidly obese subjects is frequently performed worldwide. Bariatric surgery causes specific and additional changes in metabolism and gastrointestinal anatomy, depending on the type of the procedure, which can also impact the pharmacokinetics of antithrombotic drugs and their management. Based on existing literature, the document provides consensus statements on optimizing antithrombotic drug management for underweight and all classes of obese patients, while highlighting the current gaps in knowledge in these complex clinical settings, which require personalized medicine and precision pharmacology.

Indexed as

Fibrinolytic AgentsBariatric SurgeryBody Mass IndexCardiologyHemorrhageHumansObesityRisk AssessmentRisk FactorsThinnessThrombosisTreatment OutcomeFibrinolytic AgentsAntiplatelet drugsAntithrombotic drugsArtificial intelligence drug modellingBMICardiovascular diseasesDrug variabilityObesityObesity classesUnderweight

Identifiers

PMID39237457
PMCPMC12635471

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.