Anticoagulation Therapeutic Ranges and Clinical Outcomes in Patients with a Mechanical Heart Valve Treated with Vitamin K Antagonists—a Nationwide Linked-data Dutch Study
To examine the impact of different therapeutic international normalized ratio (INR) ranges on anticoagulation control and clinical outcomes in patients with mechanical heart valves (MHVs) treated with vitamin K antagonists (VKAs) in the Netherlands.Data from 17 anticoagulation clinics (2013-2019) were linked to nation-wide data from Statistics Netherlands. Anticoagulation control metrics included significant dose adjustments, INR variance growth rate, and time in therapeutic range. Cause-specific Cox regression models were used to assess associations between therapeutic ranges and clinical outcomes, accounting for death as competing risk. Stratified analyses were performed for significant interactions by type of MHV recipient.Among 3,473 MHV patients (median age: 67.0 [IQR: 58.0-76.0], 61.7% male, 68.2% acenocoumarol, 26.5% phenprocoumon), patients with lower therapeutic ranges (<i>N</i> = 1,866) (2.0-3.0 for isolated aortic valve without risk factors; 2.5-3.5 for all remaining MHV patients) had poorer anticoagulation control compared to those with higher ranges (<i>N</i> = 1,607) (2.5-3.5 and 3.0-4.0, respectively). No association was found between therapeutic ranges and major/clinically relevant bleeding (fully adjusted hazard ratio [aHR]: 0.80 [95%CI: 0.57-1.1]). However, in patients with a non-aortic valve and/or additional risk factors a lower therapeutic range was potentially associated with increased thromboembolic risk (aHR: 1.3 [95%CI: 0.94-1.9]), while no association was observed in patients with an isolated aortic valve (aHR: 0.71 [95%CI: 0.38-1.3]).A lower therapeutic range does not apparently increase thromboembolic risk in most MHV patients but may be associated with a higher thromboembolic risk in higher risk patients. Lower therapeutic ranges were not associated with lower bleeding risk.
Authors
- Martin E W Hemels (ORCID: https://orcid.org/0000-0002-2373-9858)
- Jaap Seelig (ORCID: https://orcid.org/0000-0003-0191-0244)
- Melchior C. Nierman (ORCID: https://orcid.org/0000-0002-8647-7509)
- Nynke M. Wiersma
- Eva K Kempers (ORCID: https://orcid.org/0000-0001-9458-8674)
- Frederikus Albertus Klok (ORCID: https://orcid.org/0000-0001-9961-0754)
- Maryam Kavousi (ORCID: https://orcid.org/0000-0001-5976-6519)
- F. Leebeek
- Maarten Beinema (ORCID: https://orcid.org/0000-0001-6533-5416)
- Chantal A.N. Visser
- Alexander Stork
- Laura M. Faber
- Henk Adriaansen
- Ron Pisters
- Sjef van de Leur
- Raffaele De Caterina
- Qingui Chen
- Hugo ten Cate
- Arina ten Cate
- Roger Schindhelm
- Suzanne C Cannegieter
- Marieke J.H.A. Kruip
Institutions
- University of Pisa (IT)
- Radboud University Nijmegen (NL)
- Leiden University Medical Center (NL)
- Maastricht University Medical Centre (NL)
- Erasmus MC (NL)
- Radboud University Medical Center (NL)
- Maastricht University (NL)
- Stichting Artsenlaboratorium en Trombosedienst (NL)
- Thrombosis Research Institute (GB)
- Isala (NL)
- Tergooi (NL)
- Medicines Evaluation Board (NL)
- Amsterdam University Medical Centers (NL)
- Rijnstate Hospital (NL)
- Deventer Ziekenhuis (NL)
- St. Anna Ziekenhuis (NL)
- Medisch Centrum Alkmaar (NL)
- Erasmus University Rotterdam (NL)
Publication Details
- Journal
- Thrombosis and Haemostasis
- Published
- 2026-01-02
- DOI
- https://doi.org/10.1055/a-2773-5810
- Primary Topic
- Atrial Fibrillation Management and Outcomes
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Bristol-Myers Squibb
- Pfizer
- AstraZeneca
- Sanofi
- CSL Behring
- Amarin Corporation
- Kompetenznetz Vorhofflimmern
- ZonMw
- Daiichi-Sankyo
- Trombosestichting Nederland
- Swedish Orphan Biovitrum
- LEO Pharma
- HORIZON EUROPE Framework Programme
- CARIM School for Cardiovascular Diseases, Universiteit Maastricht