To determine if there is any difference in the effectiveness and safety outcomes of patients with NVAF newly treated with apixaban, dabigatran, rivaroxaban and vitamin K antagonists
Study Type
OBSERVATIONAL
Adults receiving apixaban
Adults receiving dabigatran
Adults receiving rivaroxaban
stroke/systemic embolism event
To compare the risk of stroke (either ischemic or hemorrhagic) or SE among patients newly treated with each NOAC separately (apixaban, dabigatran, rivaroxaban) versus VKAs.
Time frame: between 2014 and 2018
major bleeding event
To compare the risk of major bleeding (gastrointestinal \[GI\], intracranial \[IC\] and other) among patients newly treated with each NOAC separately (apixaban, dabigatran, rivaroxaban) versusVKAs.
Time frame: between 2014 and 2018
ischemic stroke event
To compare the risk of ischemic stroke among patients newly treated with each NOAC separately (apixaban, dabigatran, rivaroxaban) versus VKAs.
Time frame: between 2014 and 2018
hemorrhagic stroke event
To compare the risk of hemorrhagic stroke among patients newly treated with each NOAC separately (apixaban, dabigatran, rivaroxaban) versus VKAs.
Time frame: between 2014 and 2018
systemic embolism event
To compare the risk of systemic embolism among patients newly treated with each NOAC separately (apixaban, dabigatran, rivaroxaban) versus VKAs.
Time frame: 2014-2018
major GI bleeding event
To compare the risk of major GI bleeding among patients newly treated with each NOAC separately (apixaban, dabigatran, rivaroxaban) versus VKAs.
Time frame: 2014-2018
major IC bleeding event
To compare the risk of major IC bleeding among patients newly treated with each NOAC separately (apixaban, dabigatran, rivaroxaban) versus VKAs.
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Adults receiving VKA
Time frame: 2014-2018
other major bleeding event
To compare the risk of other major bleeding among patients newly treated with each NOAC separately (apixaban, dabigatran, rivaroxaban) versus VKAs.
Time frame: 2014-2018