Non-vitamin K antagonist oral anticoagulant (NOAC) use and dosing in Canadian practice: Insights from the optimising pharmacotherapy in the management approach to lowering risk in atrial fibrillation (OPTIMAL AF) Programme.


Journal

International journal of clinical practice
ISSN: 1742-1241
Titre abrégé: Int J Clin Pract
Pays: India
ID NLM: 9712381

Informations de publication

Date de publication:
Dec 2020
Historique:
received: 20 04 2020
accepted: 15 07 2020
entrez: 15 1 2021
pubmed: 16 1 2021
medline: 6 3 2021
Statut: ppublish

Résumé

To estimate the rate of non-vitamin K oral anticoagulant (NOAC) dosing that is lower- and higher-than-recommended and to describe the reasons for NOAC dose discordance with Health Canada prescribing information. The OPTIMAL AF Programme was an observational cohort quality assessment initiative in which primary and specialty care physicians in eight provinces provided a snapshot of their anticoagulated non-valvular atrial fibrillation (NVAF) patients through either an electronic medical record (EMR) system or standardised, paper-based data collection methods. Data on 1681 NVAF patients receiving oral anticoagulation (OAC) for stroke prevention was provided by 102 physicians. A NOAC was prescribed in 1379 patients (8%). The standard recommended dose was prescribed in 849 (76%) and reduced dose in 264 (24%). Concordance of the reduced dose with Health Canada prescribing information occurred in 154 patients (58%). The standard dose was concordant in 805 (95%). The main reasons for the use of discordant reduced doses were age of 80 years or more, elevated creatinine, prior bleeding or dose recommended by specialist. The vast majority of Canadian patients meeting the Canadian Cardiovascular Society (CCS) guideline recommendations for OAC to decrease AF-related stroke risk were receiving product monograph-concordant NOAC dosing (85%). Nonetheless, this highlights the fact that an important proportion of patients were prescribed doses that are discordant and opportunities remain to improve NOAC dosing to optimise stroke prevention.

Identifiants

pubmed: 33448547
doi: 10.1111/ijcp.13625
doi:

Substances chimiques

Anticoagulants 0
Vitamin K 12001-79-5

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

e13625

Subventions

Organisme : BMS Pfizer Alliance

Informations de copyright

© 2020 John Wiley & Sons Ltd.

Références

Macle L, Cairns J, Leblanc K, et al. 2016 focused update of the canadian cardiovascular society guidelines for the management of atrial fibrillation. Can J Cardiol. 2016;32:1170‐1185.
Steinberg BA, Shrader P, Thomas L, et al. Off‐label dosing of non‐vitamin K antagonist oral anticoagulants and adverse outcomes. J Am Coll Cardiol. 2016;68:2597‐2604.
Patel AD, Tan MK, Angaran P, et al. Risk stratification and stroke prevention therapy care gaps in canadian atrial fibrillation patients (from the co‐ordinated national network to engage physicians in the care and treatment of patients with atrial fibrillation chart audit). Am J Cardiol. 2015;115:641‐646.
Bell AD, Gross P, Heffernan M, et al. Appropriate use of antithrombotic medication in Canadian patients with nonvalvular atrial fibrillation. Am J Cardiol. 2016;117:1107‐1111.
Labos C, Ha A, Kajil M, et al. Appropriateness of non‐vitamin K oral anticoagulant dosing among Canadian atrial fibrillation patients. Can J Cardiol. 2017;33:S189.
Santos J, Antonio N, Rocha M, Fortuna A. Impact of direct oral anticoagulant off‐label doses on clinical outcomes of atrial fibrillation: a systematic review. Br J Clin Pharmacol. 2019;86:533‐547.
Weitz JI, Eikelboom JW. Appropriate apixaban dosing: prescribers take note. JAMA Cardiology. 2016;1:635‐636.
Steinberg BA, Shrader P, Pieper K, et al. Frequency and outcomes of reduced dose non‐vitamin K antagonist anticoagulants: results From ORBIT‐AF II (the outcomes registry for better informed treatment of atrial fibrillation II). J Am Heart Assoc. 2018;7:e007633.
McAlister FA, Garrison S, Kosowan L, Ezekowitz JA, Singer A. Use of direct oral anticoagulants in canadian primary care practice 2010–2015: a cohort study from the Canadian primary care sentinel surveillance network. J Am Heart Assoc. 2018;7:e007603.
Alexander JH, Andersson U, Lopes RD, et al. Apixaban 5 mg twice daily and clinical outcomes in patients with atrial fibrillation and advanced age, low body weight, or high creatinine: a secondary analysis of a randomized clinical trial. JAMA Cardiology. 2016;1:673‐681.
Granger CB, Alexander JH, McMurray JJV, et al. Apixaban versus warfarin in patients with atrial fibrillation. N Engl J Med. 2011;365:981‐992.

Auteurs

Kori Leblanc (K)

University Health Network, Toronto, ON, Canada.
Leslie Dan Faculty of Pharmacy, University of Toronto, Toronto, ON, Canada.

Alan D Bell (AD)

University of Toronto, Toronto, ON, Canada.

Justin A Ezekowitz (JA)

Canadian VIGOUR Centre, University of Alberta, Edmonton, AB, Canada.

Mary K Tan (MK)

Canadian Heart Research Centre, Toronto, ON, Canada.

David Laflamme (D)

Hôpital Charles-LeMoyne, Greenfield Park, QC, Canada.

Lianne Goldin (L)

Canadian Heart Research Centre, Toronto, ON, Canada.

Jeffrey Habert (J)

University of Toronto, Toronto, ON, Canada.

Peter J Lin (PJ)

Canadian Heart Research Centre, Toronto, ON, Canada.

Kevin Saunders (K)

Seven Oaks General Hospital, Winnipeg, MB, Canada.

Daniel Ngui (D)

University of British Columbia, Vancouver, BC, Canada.

Albert P Ng (AP)

Windsor Regional Hospital, Windsor, ON, Canada.

Jacques Desroches (J)

St Pie, QC, Canada.

Shaun G Goodman (SG)

University of Toronto, Toronto, ON, Canada.
Canadian VIGOUR Centre, University of Alberta, Edmonton, AB, Canada.
Canadian Heart Research Centre, Toronto, ON, Canada.
Terrence Donnelly Heart Centre, St Michael's Hospital, Toronto, ON, Canada.

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