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Estimation of time to target INR based on initial Warfarin dose in mechanical mitral valve replacement

Estimation of time to target INR based on initial Warfarin dose in mechanical mitral valve replacement

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
TCTR
Registry ID
TCTR20251130003
Enrollment
212
Registered
2025-11-30
Start date
2025-11-14
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients who undergo mechanical mitral valve replacement require lifelong anticoagulation to prevent prosthetic valve thrombosis and systemic thromboembolism. Achieving a therapeutic INR early in the postoperative period is clinically crucial, yet inappropriate initiation doses of warfarin often lead to delayed target INR, bleeding complications, or subtherapeutic anticoagulation. This study focuses on anticoagulation management in postoperative mechanical mitral valve patients and the clinical

Interventions

Patients aged 20 years or older who underwent mechanical mitral valve replacement (MVR) at Lampang Hospital between 2018 and 2023. Patients in this group received an initial Warfarin dose of 1.5, 2.0,
Health Services Research
Mechanical MVR patients receiving initial Warfarin 1.5, 2.0, 2.5 mg/day

Sponsors

Lampang Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 100 Years

Inclusion criteria

Inclusion criteria: Patients aged 20 years or older who underwent mechanical mitral valve replacement surgery at Lampang Hospital between 2018 and 2023. Patients who received an initial warfarin dose of 1.5 mg, 2.0 mg, or 2.5 mg per day.

Exclusion criteria

Exclusion criteria: Patients who received an initial warfarin dose other than 1.5 mg, 2.0 mg, or 2.5 mg per day following mechanical mitral valve replacement surgery. Patients who died during hospitalization or those for whom INR follow-up data were unavailable.

Design outcomes

Primary

MeasureTime frame
Time to target INR Up to 120 days post-surgery (measured at days 3, 14, 30, 90, and 120) The number of days from the initial Warfarin dose until the first INR level falls within the therapeutic range of 2.5 to 3.5

Secondary

MeasureTime frame
INR Control Status Days 3, 14, 30, 90, and 120 post-surgery. Classification of patients into 3 groups based on INR levels: Subtherapeutic, In-target, and Supratherapeutic.

Countries

Thailand

Contacts

Public ContactChanin Prakongyot

Lampang Hospital

chaninp67@nu.ac.th054 237 400

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026