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)”
Oral anticoagulants and outcomes in adults ≥80 years with atrial fibrillation: A global federated health network analysisJournal of the American Geriatrics Society2022doi:10.1111/jgs.17884

2 of its findings point the other way.

Humans: replicated by independent labs. Cells, worms or flies and mice: nothing yet.
  • 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?

2

Studies 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
  1. 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

    Are low doses of non-vitamin K antagonists effective in Chinese patients with atrial fibrillation? A report from the Optimal Thromboprophylaxis in Elderly Chinese Patients with Atrial Fibrillation (ChiOTEAF) registry

    International journal of stroke : official journal of the International Stroke Society

Net clinical benefit

upin humans1

1 study
  1. 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

    Non-Vitamin K Oral Anticoagulants for Stroke Prevention in Special Populations with Atrial Fibrillation

    Advances in therapy

What is non-vitamin K antagonist oral anticoagulants linked with?

14

Studies 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
  1. 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

    Long-term clinical outcomes of oral anticoagulation in the older patients with atrial fibrillation aged ≥80 years: a report from the GLORIA-AF registry phase III

    Age and ageing

  2. 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

    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

    European heart journal. Quality of care & clinical outcomes

  3. 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

    Oral anticoagulants and outcomes in adults ≥80 years with atrial fibrillation: A global federated health network analysis

    Journal of the American Geriatrics Society

Major bleeding

downin humans1upin humans1HR 0.88–1.08

1 study
  1. 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

    Oral anticoagulants and outcomes in adults ≥80 years with atrial fibrillation: A global federated health network analysis

    Journal of the American Geriatrics Society

  2. 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

    Oral anticoagulants and outcomes in adults ≥80 years with atrial fibrillation: A global federated health network analysis

    Journal of the American Geriatrics Society

More on Major bleeding

Composite outcome

downin humans1upin humans1OR 0.5–2.51

1 study
  1. 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

    Are low doses of non-vitamin K antagonists effective in Chinese patients with atrial fibrillation? A report from the Optimal Thromboprophylaxis in Elderly Chinese Patients with Atrial Fibrillation (ChiOTEAF) registry

    International journal of stroke : official journal of the International Stroke Society

  2. 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

    Are low doses of non-vitamin K antagonists effective in Chinese patients with atrial fibrillation? A report from the Optimal Thromboprophylaxis in Elderly Chinese Patients with Atrial Fibrillation (ChiOTEAF) registry

    International journal of stroke : official journal of the International Stroke Society

Cognitive decline

downin humans1OR 0.322

1 study
  1. 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

    The Impact of NOACS versus VKAS on Absolute and Relative Cognitive Function Decline Over Time: A Machine Learning Approach

    Thrombosis and haemostasis

Major bleeding

downin humans1HR 0.66

1 study
  1. 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

    Long-term clinical outcomes of oral anticoagulation in the older patients with atrial fibrillation aged ≥80 years: a report from the GLORIA-AF registry phase III

    Age and ageing

Major adverse cardiovascular events

downin humans1HR 0.72

1 study
  1. 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

    Long-term clinical outcomes of oral anticoagulation in the older patients with atrial fibrillation aged ≥80 years: a report from the GLORIA-AF registry phase III

    Age and ageing

Cardiovascular death

downin humans1HR 0.7

1 study
  1. 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

    Long-term clinical outcomes of oral anticoagulation in the older patients with atrial fibrillation aged ≥80 years: a report from the GLORIA-AF registry phase III

    Age and ageing

Gastrointestinal bleeding

upin humans1

1 study
  1. 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

    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

    European heart journal. Quality of care & clinical outcomes

More on Gastrointestinal bleeding

Intracranial bleeding

downin humans1

1 study
  1. 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

    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

    European heart journal. Quality of care & clinical outcomes

More on Intracranial bleeding

Stroke or systemic embolism

downin humans1

1 study
  1. 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

    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

    European heart journal. Quality of care & clinical outcomes

More on Stroke or systemic embolism

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See all 13 papers on non-vitamin K antagonist oral anticoagulants