Antithrombotic therapy in diabetes: which, when, and for how long?

Author:

Ajjan Ramzi A1ORCID,Kietsiriroje Noppadol12ORCID,Badimon Lina345ORCID,Vilahur Gemma34,Gorog Diana A67ORCID,Angiolillo Dominick J8,Russell David A19ORCID,Rocca Bianca10ORCID,Storey Robert F11

Affiliation:

1. The LIGHT Laboratories, Leeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds, Leeds LS2 7JT, UK

2. Endocrinology and Metabolism Unit, Internal Medicine Department, Faculty of Medicine, Prince of Songkla University, Songkhla 90110, Thailand

3. Cardiovascular Program ICCC, Research Institute Hospital de la Santa Creu i Sant Pau, IIB-Sant Pau, Sant Antoni M. Claret 167, 08025 Barcelona, Spain

4. Centro de Investigación Biomédica en Red Cardiovascular (CIBERCV), Instituto de Salud Carlos III, Sant Antoni M. Claret 167, 08025 Barcelona, Spain

5. Cardiovascular Research Chair, Universidad Autónoma Barcelona (UAB), Sant Antoni M. Claret 167, 08025 Barcelona, Spain

6. University of Hertfordshire, College Lane Campus Hatfield, Hertfordshire AL10 9AB, UK

7. National Heart and Lung Institute, Guy Scadding Building, Dovehouse St, London SW3 6LY, UK

8. Division of Cardiology, University of Florida College of Medicine – Jacksonville, 655 West, 8th Street, Jacksonville, FL 32209, USA

9. Leeds Vascular Institute, Leeds General Infirmary, Great George Street, Leeds LS1 3EX, UK

10. Institute of Pharmacology, Catholic University School of Medicine, Rome, Italy

11. Department of Infection, Immunity and Cardiovascular Disease, University of Sheffield, Beech Hill Road, Sheffield S10 2RX, UK

Abstract

Abstract Cardiovascular disease remains the main cause of mortality in individuals with diabetes mellitus (DM) and also results in significant morbidity. Premature and more aggressive atherosclerotic disease, coupled with an enhanced thrombotic environment, contributes to the high vascular risk in individuals with DM. This prothrombotic milieu is due to increased platelet activity together with impaired fibrinolysis secondary to quantitative and qualitative changes in coagulation factors. However, management strategies to reduce thrombosis risk remain largely similar in individuals with and without DM. The current review covers the latest in the field of antithrombotic management in DM. The role of primary vascular prevention is discussed together with options for secondary prevention following an ischaemic event in different clinical scenarios including coronary, cerebrovascular, and peripheral artery diseases. Antiplatelet therapy combinations as well as combination of antiplatelet and anticoagulant agents are examined in both the acute phase and long term, including management of individuals with sinus rhythm and those with atrial fibrillation. The difficulties in tailoring therapy according to the variable atherothrombotic risk in different individuals are emphasized, in addition to the varying risk within an individual secondary to DM duration, presence of complications and predisposition to bleeding events. This review provides the reader with an up-to-date guide for antithrombotic management of individuals with DM and highlights gaps in knowledge that represent areas for future research, aiming to improve clinical outcome in this high-risk population.

Funder

National Institute for Health Research, Diabetes UK

British Heart Foundation

Biotechnology and Biological Sciences Research Council

Abbott Diabetes Care

Avacta Life Sciences

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine

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