The purpose of the study is to estimate the impact of bleeding events in patients in the UK with non-valvular atrial fibrillation (NVAF) treated with vitamin K antagonists (VKA).
Study Type
OBSERVATIONAL
Enrollment
16,513
Impact of bleeding events on the risk of subsequent clinical events including subsequent bleeds assessed based on hazard ratios
Time frame: Up to 24 months after initial treatment with VKA
Impact of bleeding events on the rate of health-care resource utilization (HCRU) assessed based on incidence rate ratios
Time frame: Up to 24 months after initial treatment with VKA
Impact of bleeding events on the health-care costs in NVAF patients treated by VKAs assessed based on ratios of costs associated with number of bleeding events
Time frame: Up to 24 months after initial treatment with VKA
Variation of impact of bleeding events on clinical events, the rate of HCRU, and health-care costs over time following each bleeding event in NVAF patients treated by VKA
Time frame: Upto 24 months after initial treatment with VKA
Characteristics of NVAF patients newly treated with VKA who experience bleeding events
Time frame: Up to 24 months after initial treatment with VKA
Characteristics of NVAF patients newly treated with VKA who do not experience bleeding events
Time frame: Up to 24 months after initial treatment with VKA
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