Changes in primary care management of atrial fibrillation patients following the shift from warfarin to non-vitamin K antagonist oral anticoagulants: a Norwegian population based study.


Journal

BMC primary care
ISSN: 2731-4553
Titre abrégé: BMC Prim Care
Pays: England
ID NLM: 9918300889006676

Informations de publication

Date de publication:
25 08 2022
Historique:
received: 22 03 2022
accepted: 12 08 2022
entrez: 25 8 2022
pubmed: 26 8 2022
medline: 30 8 2022
Statut: epublish

Résumé

To assess baseline characteristics, drug utilisation and healthcare use for oral anticoagulants (OACs) following the introduction of non-vitamin K antagonist oral anticoagulants among patients with atrial fibrillation in primary care in Norway. In this retrospective longitudinal cohort study, 92,936 patients with atrial fibrillation were identified from the Norwegian Primary Care Registry between 2010 and 2018. Linking to the Norwegian Prescription Database, we identified 64,112 patients (69.0%) treated with OACs and 28,824 (31%) who were untreated. Participants were followed until 15 May 2019, death, or loss to follow-up, whichever came first. For each OAC, predictors of initiation were assessed by modelling the probability of initiating the OAC using logistic regression, and predictors of the first switch after index date were assessed using multivariable Cox proportional hazards models. The numbers of primary care visits per quarter by index OAC were plotted and analysed with negative binomial regression analyses offset for the log of days at risk. Patients treated with OACs were older, had more comorbidities, and higher CHA In this Norwegian primary care study, we found that the shift from warfarin to non-vitamin K antagonist oral anticoagulants was successful with 95% use in patients initiating OACs in 2018, and associated with fewer general practitioner visits. Persistence with OACs was high, particularly for apixaban. However, many patients eligible for treatment with OACs remained untreated.

Sections du résumé

BACKGROUND
To assess baseline characteristics, drug utilisation and healthcare use for oral anticoagulants (OACs) following the introduction of non-vitamin K antagonist oral anticoagulants among patients with atrial fibrillation in primary care in Norway.
METHODS
In this retrospective longitudinal cohort study, 92,936 patients with atrial fibrillation were identified from the Norwegian Primary Care Registry between 2010 and 2018. Linking to the Norwegian Prescription Database, we identified 64,112 patients (69.0%) treated with OACs and 28,824 (31%) who were untreated. Participants were followed until 15 May 2019, death, or loss to follow-up, whichever came first. For each OAC, predictors of initiation were assessed by modelling the probability of initiating the OAC using logistic regression, and predictors of the first switch after index date were assessed using multivariable Cox proportional hazards models. The numbers of primary care visits per quarter by index OAC were plotted and analysed with negative binomial regression analyses offset for the log of days at risk.
RESULTS
Patients treated with OACs were older, had more comorbidities, and higher CHA
CONCLUSION
In this Norwegian primary care study, we found that the shift from warfarin to non-vitamin K antagonist oral anticoagulants was successful with 95% use in patients initiating OACs in 2018, and associated with fewer general practitioner visits. Persistence with OACs was high, particularly for apixaban. However, many patients eligible for treatment with OACs remained untreated.

Identifiants

pubmed: 36008778
doi: 10.1186/s12875-022-01824-6
pii: 10.1186/s12875-022-01824-6
pmc: PMC9404608
doi:

Substances chimiques

Anticoagulants 0
Warfarin 5Q7ZVV76EI

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

214

Informations de copyright

© 2022. The Author(s).

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Auteurs

Sigrun Halvorsen (S)

Department of Cardiology, Oslo University Hospital Ullevål, Nydalen, Postboks 4956, 0424, Oslo, Norway. sigrun.halvorsen@medisin.uio.no.
University of Oslo, Oslo, Norway. sigrun.halvorsen@medisin.uio.no.

Jørgen Anton Smith (JA)

Rykkinn Legekontor (Rykkinn Medical Office), Rykkinn, Norway.

Fabian Söderdahl (F)

Statisticon AB, Uppsala, Sweden.

Marcus Thuresson (M)

Statisticon AB, Uppsala, Sweden.

Oddvar Solli (O)

Health and Value Lead, Pfizer AS, Oslo, Norway.

Maria Ulvestad (M)

Bristol Myers Squibb, Lysaker, Norway.

Christian Jonasson (C)

K. G. Jebsen Center for Genetic Epidemiology, Faculty of Medicine and Health Sciences, NTNU-Norwegian University of Science and Technology, Trondheim, Norway.

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