Risk of mortality between warfarin and direct oral anticoagulants: population-based cohort studies.

Risk of mortality between warfarin and direct oral anticoagulants: population-based cohort studies.

Publication date: Dec 23, 2024

Direct oral anticoagulants (DOACs) have been reported to be associated with a higher risk of mortality compared with an older alternative, warfarin using primary care data in the United Kingdom (UK). However, other studies observed contradictory findings. We therefore aimed to investigate the association between mortality and warfarin, compared with DOACs. We conducted cohort studies using UK Clinical Practice Research Datalink (CPRD) Aurum and Hong Kong Clinical Data Analysis and Reporting System (CDARS) to identify the association between warfarin and hazard of mortality, compared to DOACs. Individuals with non-valvular atrial fibrillation aged ≥ 18 years who had first anticoagulant therapy (warfarin or DOAC) during 1/1/2011-31/12/2019 were included. Compared with DOAC use, a lower hazard of all-cause mortality was found in warfarin users (hazard ratio (HR) = 0. 81, 95% confidence interval (CI) = 0. 77-0. 86) in CPRD; while a higher hazard was observed in warfarin users (HR = 1. 31, 95% CI = 1. 24-1. 39) in CDARS, versus DOAC users. In our exploratory analysis, consistent results were seen in both databases when stratified warfarin users by time in therapeutic range (TTR) using post-baseline measurements: a lower hazard of all-cause mortality in warfarin users with TTR ≥ 65% (CPRD: HR = 0. 68, 95% CI = 0. 65-0. 72; CDARS: HR = 0. 86, 95% CI = 0. 77-0. 96) and increased hazard in warfarin users with TTR 

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Concepts Keywords
Aged18years Administration, Oral
Databases Aged
Drugs Aged, 80 and over
Kong Anticoagulants
Therapy Anticoagulants
Atrial Fibrillation
Cohort Studies
Direct anticoagulant
Female
Hong Kong
Humans
Male
Middle Aged
Mortality
United Kingdom
Warfarin
Warfarin
Warfarin

Semantics

Type Source Name
drug DRUGBANK Warfarin
disease MESH atrial fibrillation
pathway REACTOME Reproduction
disease MESH thrombosis
disease MESH ischaemic stroke
drug DRUGBANK Trestolone
disease IDO blood
disease MESH venous thromboembolism
disease MESH myocardial infarction
disease MESH bleeding
drug DRUGBANK Coenzyme M
disease MESH death
disease MESH parasitic diseases
disease MESH neoplasms
disease MESH respiratory diseases
drug DRUGBANK Hydroxyethyl Starch
drug DRUGBANK Imidacloprid
disease IDO quality
disease MESH cardiovascular diseases
drug DRUGBANK Aspartame
disease MESH mitral stenosis
disease MESH antiphospholipid antibody syndrome
drug DRUGBANK Dabigatran
drug DRUGBANK Rivaroxaban
drug DRUGBANK Apixaban
drug DRUGBANK Edoxaban
disease MESH lifestyle
disease MESH high blood pressure
drug DRUGBANK Ethanol
drug DRUGBANK Isoxaflutole
drug DRUGBANK Ilex paraguariensis leaf
disease MESH polyp
disease MESH pulmonary fibrosis
disease MESH chronic kidney disease
disease MESH Underweight
disease MESH Overweight
disease MESH obesity
disease MESH lipid metabolism disorders
disease MESH Alcohol related disorders
disease MESH COPD
disease MESH Chronic renal failure
disease MESH Diabetes mellitus
disease MESH Heart failure
drug DRUGBANK Acetylsalicylic acid
disease IDO algorithm
drug DRUGBANK Medical air
disease MESH COVID 19
disease MESH deep vein thrombosis
disease MESH pulmonary embolism
disease MESH stroke
disease MESH treatment resistant depression
disease MESH Osteoporotic Fractures
disease MESH dementia
disease MESH Atopic eczema
disease MESH Allergy
disease MESH complications
drug DRUGBANK Pentaerythritol tetranitrate
disease MESH Interstitial Lung Disease

Original Article

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