Educational draft · awaiting clinical reviewUse Rapid for revision, not patient-care decisions. Check current national and local guidance and the BNF or BNFC before acting.
2 min synopsisUK scopeSources checked 27 Aug 2026Clinical review pending
!
Escalate
Acute dyspnoea, shock, embolism or a new/muffled prosthetic click suggests obstructive thrombosis; major bleeding on warfarin requires immediate reversal and specialist input. Neither should wait for routine clinic review.
Synopsis
Select and monitor antithrombotic therapy, recognise prosthetic dysfunction and act safely on thrombosis or bleeding.
Every mechanical valve requires lifelong vitamin K antagonist therapy; a DOAC is not an acceptable substitute.
The INR target is valve- and patient-specific: a modern bileaflet mechanical aortic valve commonly targets 2.5, while a mechanical mitral valve or added thromboembolic risk commonly targets 3.0; older high-thrombogenicity valves need higher targets.
A low INR risks valve thrombosis and embolism; a high INR risks bleeding. Use the implant record, valve position/type and risk factors to document one target explicitly.
Key red flags
Obstructive valve thrombosis
Acute dyspnoea, pulmonary oedema, shock, embolus, new murmur or a softer/absent mechanical click is an emergency.
Investigation priorities
01
INR with anticoagulation recordFirst step
Measure current VKA effect and time in therapeutic range.
Management branches
RoutineSelect antithrombotic therapy
After valve replacement or when reviewing an established prosthesis.
Identify valve type, manufacturer, position, implant date and separate indications for anticoagulation.
For any mechanical valve, use lifelong warfarin with a written target INR; do not use a DOAC.
Key medicines
WarfarinSmPC typical induction 10 mg once daily for 2 days and usual maintenance 3-9 mg once daily, but prosthetic-valve dosing must be individualised to INR; common targets are 2.5 for a modern bileaflet aortic valve and 3.0 for a mechanical mitral valve or added risk.
National guidance is shown before implementation-dependent detail. Typical adult dose examples remain subject to patient factors, contraindications and the live BNF or specialist protocol. Source check completed 27 Aug 2026; clinical approval remains outstanding.