Adherence to direct oral anticoagulant treatment for atrial fibrillation in the Netherlands: A surveillance study.


Journal

Pharmacoepidemiology and drug safety
ISSN: 1099-1557
Titre abrégé: Pharmacoepidemiol Drug Saf
Pays: England
ID NLM: 9208369

Informations de publication

Date de publication:
08 2021
Historique:
received: 06 08 2020
accepted: 30 03 2021
pubmed: 7 4 2021
medline: 25 11 2021
entrez: 6 4 2021
Statut: ppublish

Résumé

Adherence to direct oral anticoagulants (DOACs) in patients with atrial fibrillation in every day practice may be less than in clinical trials. To assess adherence to DOACs in atrial fibrillation patients in every day practice and identify predictors for non-adherence. Individual linked dispensing data of atrial fibrillation patients who used DOACs were obtained from the Foundation for Pharmaceutical Statistics covering the Netherlands between 2012 and 2016. One year adherence to DOAC was calculated for initial DOAC as proportion of days covered (PDC) ≥80% and the association between clinical variables and adherence was assessed using logistic regression. In addition, we measured non-persistence, that is, patients who completely stopped their initial DOAC within 1 year follow-up. A total of 4797 apixaban-, 20 454 rivaroxaban- and 18 477 dabigatran users were included. The mean age was 69 years (n = 43 910), which was similar for the DOAC types. The overall proportion of patients with PDC ≥80% was 76%, which was highest for apixaban- (87%), followed by dabigatran- (80%) and rivaroxaban (69%) users. Multivariable analyses revealed that age ≤60 years, no concomitant drug use were predictors for non-adherence. Of atrial fibrillation patients who continued treatment, 97% had a PDC ≥80%, compared with only 56% for those who discontinued their DOAC treatment within 1 year. Non-adherence to DOACs was associated with age ≤60 years and no concomitant drugs use. Non-adherence was higher in patients who later discontinued DOAC treatment. Results of our study support research into interventions to improve adherence.

Sections du résumé

BACKGROUND
Adherence to direct oral anticoagulants (DOACs) in patients with atrial fibrillation in every day practice may be less than in clinical trials.
AIMS
To assess adherence to DOACs in atrial fibrillation patients in every day practice and identify predictors for non-adherence.
METHODS
Individual linked dispensing data of atrial fibrillation patients who used DOACs were obtained from the Foundation for Pharmaceutical Statistics covering the Netherlands between 2012 and 2016. One year adherence to DOAC was calculated for initial DOAC as proportion of days covered (PDC) ≥80% and the association between clinical variables and adherence was assessed using logistic regression. In addition, we measured non-persistence, that is, patients who completely stopped their initial DOAC within 1 year follow-up.
RESULTS
A total of 4797 apixaban-, 20 454 rivaroxaban- and 18 477 dabigatran users were included. The mean age was 69 years (n = 43 910), which was similar for the DOAC types. The overall proportion of patients with PDC ≥80% was 76%, which was highest for apixaban- (87%), followed by dabigatran- (80%) and rivaroxaban (69%) users. Multivariable analyses revealed that age ≤60 years, no concomitant drug use were predictors for non-adherence. Of atrial fibrillation patients who continued treatment, 97% had a PDC ≥80%, compared with only 56% for those who discontinued their DOAC treatment within 1 year.
CONCLUSIONS
Non-adherence to DOACs was associated with age ≤60 years and no concomitant drugs use. Non-adherence was higher in patients who later discontinued DOAC treatment. Results of our study support research into interventions to improve adherence.

Identifiants

pubmed: 33822401
doi: 10.1002/pds.5242
pmc: PMC8360064
doi:

Substances chimiques

Anticoagulants 0
Pyridones 0
Rivaroxaban 9NDF7JZ4M3
Dabigatran I0VM4M70GC

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1027-1036

Informations de copyright

© 2021 The Authors. Pharmacoepidemiology and Drug Safety published by John Wiley & Sons Ltd.

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Auteurs

Gilda D Zielinski (GD)

Department of Clinical Epidemiology, Leiden University Medical Center, Leiden, The Netherlands.

Nienke van Rein (N)

Department of Clinical Epidemiology, Leiden University Medical Center, Leiden, The Netherlands.
Department of Clinical Pharmacy & Toxicology, Leiden University Medical Center, Leiden, The Netherlands.

Martina Teichert (M)

Department of Clinical Pharmacy & Toxicology, Leiden University Medical Center, Leiden, The Netherlands.

Frederikus A Klok (FA)

Department of Thrombosis and Haemostasis, Leiden University Medical Center, Leiden, The Netherlands.

Frits R Rosendaal (FR)

Department of Clinical Epidemiology, Leiden University Medical Center, Leiden, The Netherlands.

Felix J M van der Meer (FJM)

Department of Thrombosis and Haemostasis, Leiden University Medical Center, Leiden, The Netherlands.

Menno V Huisman (MV)

Department of Thrombosis and Haemostasis, Leiden University Medical Center, Leiden, The Netherlands.

Suzanne C Cannegieter (SC)

Department of Clinical Epidemiology, Leiden University Medical Center, Leiden, The Netherlands.
Department of Thrombosis and Haemostasis, Leiden University Medical Center, Leiden, The Netherlands.

Willem M Lijfering (WM)

Department of Clinical Epidemiology, Leiden University Medical Center, Leiden, The Netherlands.

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