Gigante, B;
Tamargo, J;
Agewall, S;
Atar, D;
Ten Berg, J;
Campo, G;
Cerbai, E;
Christersson, C;
Dobrev, D;
Ferdinandy, P;
et al.
Gigante, B; Tamargo, J; Agewall, S; Atar, D; Ten Berg, J; Campo, G; Cerbai, E; Christersson, C; Dobrev, D; Ferdinandy, P; Geisler, T; Gorog, DA; Grove, EL; Kaski, JC; Rubboli, A; Wassmann, S; Wallen, H; Rocca, B
(2024)
Update on antithrombotic therapy and body mass. A Clinical consensus Statement of the ESC Working Group on Cardiovascular Pharmacotherapy and the ESC Working Group on Thrombosis.
Eur Heart J Cardiovasc Pharmacother, 10 (7).
pp. 614-645.
ISSN 2055-6845
https://doi.org/10.1093/ehjcvp/pvae064
SGUL Authors: Kaski, Juan Carlos
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Accepted Version
Restricted to Repository staff only until 5 September 2025. Available under License ["licenses_description_publisher" not defined]. Download (3MB) |
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, 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 optimising 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.
Item Type: | Article | ||||||
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Additional Information: | This is a pre-copyedited, author-produced version of an article accepted for publication in European Heart Journal - Cardiovascular Pharmacotherapy following peer review. The version of record Bruna Gigante, Juan Tamargo, Stefan Agewall, Dan Atar, Jurrien ten Berg, Gianluca Campo, Elisabetta Cerbai, Christina Christersson, Dobromir Dobrev, Péter Ferdinandy, Tobias Geisler, Diana A Gorog, Erik L Grove, Juan Carlos Kaski, Andrea Rubboli, Sven Wassmann, Håkan Wallen, Bianca Rocca, Update on antithrombotic therapy and body mass. A Clinical consensus Statement of the ESC Working Group on Cardiovascular Pharmacotherapy and the ESC Working Group on Thrombosis, European Heart Journal - Cardiovascular Pharmacotherapy, 2024;, pvae064 is available online at: https://doi.org/10.1093/ehjcvp/pvae064. | ||||||
Keywords: | Antiplatelet drugs, Antithrombotic drugs, Artificial intelligence drug modelling, BMI, Cardiovascular diseases, Drug variability, Obesity, Obesity classes, Underweight, 1102 Cardiorespiratory Medicine and Haematology, 1115 Pharmacology and Pharmaceutical Sciences | ||||||
Journal or Publication Title: | Eur Heart J Cardiovasc Pharmacother | ||||||
ISSN: | 2055-6845 | ||||||
Language: | eng | ||||||
Dates: |
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Publisher License: | Publisher's own licence | ||||||
PubMed ID: | 39237457 | ||||||
Go to PubMed abstract | |||||||
URI: | https://openaccess.sgul.ac.uk/id/eprint/116897 | ||||||
Publisher's version: | https://doi.org/10.1093/ehjcvp/pvae064 |
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