Non-vitamin K antagonist oral anticoagulants
Non-vitamin K antagonist oral anticoagulants has been studied in 13 papers since 2017: 10 observational studies in people, 3 reviews; 1 in the past year. It has not reached trials in people. The newest paper, Oct 13, 2026: “Factors associated with mortality in patients with atrial fibrillation: an umbrella review of systematic reviews and meta-analyses”.
InterventionPreclinical
13 papers study it20 findingsUpdated
1 new paper in 30 daysSee all 13 papers on non-vitamin K antagonist oral anticoagulants
At a glance
Independent labs found the same change in people. 4 independent labs in 7 countries.
“Compared to no OAC, participants receiving a NOAC had a lower risk of incident dementia (hazHR 0.68, 95% CI 0.65-0.71), all-cause mortality (HR 0.49, 95% CI 0.48-0.50)”
2 of its findings point the other way.
- 4 independent labs in 7 countries
- 2 findings against
- Funders: Belgian Health Care Knowledge Centre and 4 more
- 5 of 19 findings with company ties
- Humans10
What did studies of non-vitamin K antagonist oral anticoagulants find?
2Studies of non-vitamin K antagonist oral anticoagulants measured 2 outcomes; the most studied are mortality (1 study) and net clinical benefit (1).
Mortality
downin humans1OR 0.42
1 study
Mortality
downin humans1OR 0.42
Non-vitamin K antagonist oral anticoagulants are linked with lower mortality in humans (compared with non-anticoagulated patients) (5.3% vs. 9.7%; OR 0.42; 95% CI: 0.26-0.70).
“all-cause death (5.3% vs. 9.7%; p = 0.007) were seen in the low-dose group (ORs 0.50; 95% CI: 0.32-0.78, and 0.42; 95% CI: 0.26-0.70, respectively).”
Humanscompared with non-anticoagulated patientsone-year follow-up
International journal of stroke : official journal of the International Stroke Society
Net clinical benefit
upin humans1
1 study
Net clinical benefit
upin humans1
Non-vitamin K antagonist oral anticoagulants improve net clinical benefit in humans (compared with VKAs in high-risk patients with non-valvular AF).
“NOACs may offer a greater net clinical benefit compared with VKAs, particularly in these high-risk patients.”
Reviewcompared with VKAs in high-risk patients with non-valvular AF
Advances in therapy
What is non-vitamin K antagonist oral anticoagulants linked with?
14Studies link non-vitamin K antagonist oral anticoagulants with 14 measures, most often mortality (3 studies), major bleeding (1) and composite outcome (1).
Mortality
downin humans3HR 0.49–0.79
3 studies
Mortality
downin humans3HR 0.49–0.79
Non-vitamin K antagonist oral anticoagulants are linked with a lower risk of mortality in humans (atrial fibrillation) (HR: 0.79, 95% CI: 0.65-0.97).
“Compared with VKA, NOAC use in patients ≥80 years was associated with lower risks of all-cause death”
Humansatrial fibrillation3 years
Age and ageing
Non-vitamin K antagonist oral anticoagulants are linked with a lower risk of mortality in patients with AF and frailty compared with VKAs (aHR 0.88, 95% CI (0.84-0.92)).
“all-cause mortality [aHR 0.88, 95%CI (0.84-0.92)]”
Humansin patients with AF and frailty compared with VKAsn = 71,638
European heart journal. Quality of care & clinical outcomes
Non-vitamin K antagonist oral anticoagulants are linked with a lower risk of mortality in humans (compared to no OAC) (HR 0.49, 95% CI 0.48-0.50).
“Compared to no OAC, participants receiving a NOAC had a lower risk of incident dementia (hazHR 0.68, 95% CI 0.65-0.71), all-cause mortality (HR 0.49, 95% CI 0.48-0.50)”
Humanscompared to no OAC
Journal of the American Geriatrics Society
Major bleeding
downin humans1upin humans1HR 0.88–1.08
1 study
Major bleeding
downin humans1upin humans1HR 0.88–1.08
Non-vitamin K antagonist oral anticoagulants are linked with a lower risk of major bleeding in humans (compared to warfarin) (HR 0.88, 95% CI 0.85-0.90).
“ischaemic stroke (HR 0.86, 95% CI: 0.82-0.90) and major bleeding (HR 0.88, 95% CI: 0.85-0.90).”
Humanscompared to warfarin
Journal of the American Geriatrics Society
Non-vitamin K antagonist oral anticoagulants are linked with a higher risk of major bleeding in humans (compared to no OAC) (HR 1.08, 95% CI 1.05-1.11).
“and a higher risk of major bleeding (HR 1.08, 95% CI 1.05-1.11).”
Humanscompared to no OAC
Journal of the American Geriatrics Society
Composite outcome
downin humans1upin humans1OR 0.5–2.51
1 study
Composite outcome
downin humans1upin humans1OR 0.5–2.51
Non-vitamin K antagonist oral anticoagulants are linked with a lower risk of composite outcome in humans (compared with non-anticoagulated patients) (7.3% vs. 11.3%; OR 0.50; 95% CI: 0.32-0.78).
“lower rates of the composite outcome (7.3% vs. 11.3%; p = 0.025) and all-cause death (5.3% vs. 9.7%; p = 0.007) were seen in the low-dose group (ORs 0.50; 95% CI: 0.32-0.78,”
Humanscompared with non-anticoagulated patientsone-year follow-up
International journal of stroke : official journal of the International Stroke Society
Non-vitamin K antagonist oral anticoagulants are linked with a higher risk of composite outcome in humans (compared with standard dose NOACs) (OR: 2.51; 95% CI: 1.11-5.71).
“The use of low-dose NOACs was independently associated with higher odds of the composite outcome (OR: 2.51; 95% CI: 1.11-5.71)”
Humanscompared with standard dose NOACsone-year follow-up38.9% femalesn = 1,310
International journal of stroke : official journal of the International Stroke Society
Cognitive decline
downin humans1OR 0.322
1 study
Cognitive decline
downin humans1OR 0.322
Non-vitamin K antagonist oral anticoagulants are linked with a lower risk of cognitive decline in humans (elderly patients with atrial fibrillation) (OR 0.322, 95% CI 0.221-0.469).
“In logistic regression, NOAC use was independently associated with a lower risk of cognitive decline (odds ratio: 0.322; 95% confidence interval: 0.221-0.469; p < 0.0001).”
Humanselderly patients with atrial fibrillationmean follow-up of 7.2 ± 3.4 yearsn = 983
Thrombosis and haemostasis
Major bleeding
downin humans1HR 0.66
1 study
Major bleeding
downin humans1HR 0.66
Non-vitamin K antagonist oral anticoagulants are linked with a lower risk of major bleeding in humans (atrial fibrillation) (HR: 0.66, 95% CI: 0.48-0.92).
“and major bleeding (HR: 0.66, 95% CI: 0.48-0.92)”
Humansatrial fibrillation3 years
Age and ageing
Major adverse cardiovascular events
downin humans1HR 0.72
1 study
Major adverse cardiovascular events
downin humans1HR 0.72
Non-vitamin K antagonist oral anticoagulants are linked with a lower risk of major adverse cardiovascular events in humans (atrial fibrillation) (HR: 0.72, 95% CI: 0.56-0.92).
“MACE (HR: 0.72, 95% CI: 0.56-0.92)”
Humansatrial fibrillation3 years
Age and ageing
Cardiovascular death
downin humans1HR 0.7
1 study
Cardiovascular death
downin humans1HR 0.7
Non-vitamin K antagonist oral anticoagulants are linked with a lower risk of cardiovascular death in humans (atrial fibrillation) (HR: 0.70, 95% CI: 0.51-0.96).
“cardiovascular death (HR: 0.70, 95% CI: 0.51-0.96)”
Humansatrial fibrillation3 years
Age and ageing
Gastrointestinal bleeding
upin humans1
1 study
Gastrointestinal bleeding
upin humans1
Non-vitamin K antagonist oral anticoagulants are linked with a higher risk of gastrointestinal bleeding in patients with AF and frailty compared with VKAs (aHR 1.19, 95% CI (1.06-1.33)).
“higher gastrointestinal bleeding risk [aHR 1.19, 95%CI (1.06-1.33)] compared with VKAs”
Humansin patients with AF and frailty compared with VKAsn = 71,638
European heart journal. Quality of care & clinical outcomes
Intracranial bleeding
downin humans1
1 study
Intracranial bleeding
downin humans1
Non-vitamin K antagonist oral anticoagulants are linked with a lower risk of intracranial bleeding in patients with AF and frailty compared with VKAs (aHR 0.78, 95% CI (0.66-0.91)).
“and intracranial bleeding [aHR 0.78, 95%CI (0.66-0.91)]”
Humansin patients with AF and frailty compared with VKAsn = 71,638
European heart journal. Quality of care & clinical outcomes
Stroke or systemic embolism
downin humans1
1 study
Stroke or systemic embolism
downin humans1
Non-vitamin K antagonist oral anticoagulants are linked with a lower risk of stroke or systemic embolism in patients with AF and frailty compared with VKAs (aHR 0.77, 95% CI (0.70-0.86)).
“NOACs were associated with lower risks of stroke or systemic embolism (stroke/SE) [aHR 0.77, 95%CI (0.70-0.86)]”
Humansin patients with AF and frailty compared with VKAsn = 71,638
European heart journal. Quality of care & clinical outcomes
All 14Fewer
Latest
1 paper in 12 monthsFactors associated with mortality in patients with atrial fibrillation: an umbrella review of systematic reviews and meta-analyses
The Impact of NOACS versus VKAS on Absolute and Relative Cognitive Function Decline Over Time: A Machine Learning Approach
Impact of frailty on the effectiveness and safety of non-vitamin K antagonist oral anticoagulants (NOACs) in patients with atrial fibrillation: a nationwide cohort study
Epidemiology and impact of frailty in patients with atrial fibrillation in Europe
Oral anticoagulants and outcomes in adults ≥80 years with atrial fibrillation: A global federated health network analysis
2021 Focused Update Consensus Guidelines of the Asia Pacific Heart Rhythm Society on Stroke Prevention in Atrial Fibrillation: Executive Summary
One-year Follow-up Results of the Optimal Thromboprophylaxis in Elderly Chinese Patients with Atrial Fibrillation (ChiOTEAF) registry
See all 13 papers on non-vitamin K antagonist oral anticoagulants