Quality of Anticoagulation With Warfarin in Patient With Atrial Fibrillation for Secondary Stroke Prevention in Korea

Inje University

Status: Completed

Conditions: Atrial Fibrillation; Stroke

Study type: Observational

Funder types: Other

Identifiers

NCT02810509

Warfarin TTR-01

Details and patient eligibility

About

The current study aims to assess the quality of anticoagulation with warfarin in real world practice of secondary stroke prevention in Korean patients with Atrial fibrillation (AF) and to explore predictors for poor International Normalized Range (INR) control.

Full description

• To assess the quality of anticoagulation with warfarin in real world practice of Korea for secondary stroke prevention in patients with AF-related Cardioembolic (CE) stroke 1) who initiated warfarin therapy and treatment at least for more than 7 days of warfarin adjustment period (warfarin-initiated cohort), and 2) who initiated and maintained warfarin therapy at least for more than 90 days after the 7 days of warfarin adjustment period (long-term warfarin-treated cohort).
• To explore predictors for poor INR control.

Enrollment: 1,814 patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

Inclusion criteria for the warfarin-initiated cohort

1. Admission due to AF-related ischemic stroke
2. Initiation of warfarin therapy and treatment at least for more than 7 days of warfarin adjustment period
3. For TTR calculation, available consecutive INR values ≥3 after the 7 days of warfarin adjustment

Inclusion criteria for the long-term warfarin-treated cohort

1. Admission due to AF-related ischemic stroke
2. Long-term warfarin therapy at least for more than 90 days after the 7 days of warfarin adjustment period
3. For TTR calculation, available consecutive INR values ≥3 after the 7 days of warfarin adjustment
4. TTR evaluable days ≥ 90 days

Exclusion criteria

1. AF with mechanical valve
2. Enrollment in anticoagulation randomized clinical trial
3. Enrollment in studies affecting the target INR range.

Trial design

1,814 participants in 2 patient groups

Short-term Warfarin-treated cohort

Description:

1. admission due to AF-related ischemic stroke (known AF or newly detected AF) 2. for TTR calculation, the number of consecutive INR measurements ≥3 after the 7 days of warfarin adjustment 3. TTR evaluable days \< 90 days

Long-term Warfarin-treated cohort

Description:

1. admission due to AF-related ischemic stroke (known AF or newly detected AF) 2. long-term warfarin therapy at least for more than 90 days after the 7 days of warfarin adjustment period 3. for TTR calculation, the number of consecutive INR measurements ≥3 after the 7 days of warfarin adjustment 4. TTR evaluable days ≥ 90 days