Real-world on-treatment and initial treatment absolute risk differences for dabigatran vs warfarin in older US adults.


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 2020
Historique:
received: 15 11 2019
revised: 05 05 2020
accepted: 01 06 2020
pubmed: 16 7 2020
medline: 16 6 2021
entrez: 16 7 2020
Statut: ppublish

Résumé

Trials and past observational work compared dabigatran and warfarin in patients with atrial fibrillation, but few reported estimates of absolute harm and benefit under real-world adherence patterns, particularly in older adults that may have differing benefit-harm profiles. We aimed to estimate risk differences for ischemic stroke, death, and gastrointestinal bleeding after initiating dabigatran and warfarin in older adults (a) when patients adhere to treatment and (b) under real-world adherence patterns. In a 20% sample of nationwide Medicare claims from 2010 to 2015, we identified beneficiaries aged 66 years and older initiating warfarin and dabigatran. We followed individuals from initiation until death or October 2015 (initial treatment, IT) and separately censored individuals' follow-up after drug switches and gaps in supply (on-treatment, OT). We applied inverse probability of treatment and standardized morbidity ratio weights, as well as inverse probability of censoring weights, to estimate two-year risk differences (RDs) for dabigatran vs warfarin. We identified 10,717 dabigatran and 74,891 warfarin initiators. Weighted OT RDs suggested decreased ischemic stroke risk for dabigatran vs warfarin; IT RDs indicated increased or no change in ischemic stroke risk. Regardless of follow-up approach and weighting strategy, risk of death appeared lower and risk of gastrointestinal bleeding appeared higher when comparing dabigatran vs warfarin. Dabigatran use was associated with lower risks of mortality and ischemic stroke in routine care when older adults stayed on treatment. IT analyses suggested that these benefits may be diminished under real-world patterns of switching and discontinuation.

Identifiants

pubmed: 32666678
doi: 10.1002/pds.5069
pmc: PMC8356559
mid: NIHMS1727195
doi:

Substances chimiques

Antithrombins 0
Warfarin 5Q7ZVV76EI
Dabigatran I0VM4M70GC

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

832-841

Subventions

Organisme : NIH HHS
ID : UL1TR002489
Pays : United States
Organisme : NIH HHS
ID : K01AI125087
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR002489
Pays : United States
Organisme : NIAID NIH HHS
ID : K01 AI125087
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG056479
Pays : United States

Informations de copyright

© 2020 John Wiley & Sons Ltd.

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Auteurs

Michael Webster-Clark (M)

Department of Epidemiology, University of North Carolina, Chapel Hill, North Carolina, USA.

Til Stürmer (T)

Department of Epidemiology, University of North Carolina, Chapel Hill, North Carolina, USA.

Jessie K Edwards (JK)

Department of Epidemiology, University of North Carolina, Chapel Hill, North Carolina, USA.

Charles Poole (C)

Department of Epidemiology, University of North Carolina, Chapel Hill, North Carolina, USA.

Ross J Simpson (RJ)

Department of Medicine, University of North Carolina, Chapel Hill, North Carolina, USA.

Jennifer L Lund (JL)

Department of Epidemiology, University of North Carolina, Chapel Hill, North Carolina, USA.

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