http://circ.ahajournals.org/content/132/Suppl_3/A11919.short
- Victoria Jacobs1;
- Heidi T May1;
- Tami L Bair1;
- Jeffrey L Anderson2;
- Brian G Crandall1;
- Michael Cutler1;
- John D Day1;
- Charles D Mallender1;
- Jeffrey S Osborn1;
- Scott M Stevens1;
- J P Weiss1;
- Scott C Woller1;
- T J Bunch1
+ Author Affiliations
Abstract
Introduction: Patients
with atrial fibrillation (AF) are at an increased risk of developing
dementia, and this risk appears sensitive to
quality of warfarin control. Longstanding
warfarin use predisposes AF patients to the development of microbleeds
if they are
over-anticoagulated and microemboli if they are
under-anticoagulated. The novel oral anticoagulants (NOACs) offer an
alternative
to warfarin with a predictable anticoagulant
effect, and comparatively favorable intracranial bleeding and thrombosis
rates
which may lower the risk of dementia.
Hypothesis: The use of NOACs will be associated with a lower risk of stroke, TIA, and dementia compared to warfarin.
Methods: Patients
receiving long-term anticoagulation therapy with either warfarin or a
single NOAC for thromboembolism prevention
were studied (June 2010-December 2014). NOAC and
warfarin patients were matched 1:1 by index date (± 6 months) and
propensity
score (±0.01). Multivariable Cox hazard
regression was performed to evaluate the association of NOAC compared to
warfarin
use for the composite outcome of dementia,
stroke, and TIA.
Results: A total of
5,254 (2,627 per group) patients were studied, and those receiving NOACs
included: apixaban= 590 (22.5%), dabigatran=583
(22.2%), and rivaroxaban=1,454 (55.3%). Average
age was 72.4±10.9 and 59.0% were male. The majority of patients were
receiving
long-term anticoagulation for AF (warfarin:
96.5% vs. NOAC: 92.7%, p<0.0001). History of a prior stroke/TIA were
similar between
the groups (warfarin: 10.7% vs. NOAC: 10.8%,
p=0.89). Dementia incidence alone was lower in the NOAC group compared
to the
warfarin group (0.3% vs. 1.6%, p<0.0001). The
composite outcome of dementia, stroke, and TIA occurred in 4.7% of
warfarin
patients and 1.8% of NOAC patients
(p<0.0001). After adjustment, patients taking NOACs had a 51%
decreased risk of dementia
incidence or subsequent stroke or TIA compared
to patients taking warfarin (HR=0.49 (0.35, 0.69), p<0.0001).
Conclusions: This study shows the use of NOACs in a community setting to be superior to that of warfarin for the composite outcome of
dementia, stroke, and TIA among patients receiving long-term oral anticoagulation.
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