Synopsis
Start and monitor warfarin safely, interpret INR in clinical context, manage interruptions and reverse excessive anticoagulation according to bleeding severity and urgency.
- Warfarin inhibits vitamin-K recycling and lowers functional factors II, VII, IX and X; the delayed fall and recovery mean INR changes lag behind dose changes.
- Use an indication-specific target, commonly target INR 2.5 with range 2.0–3.0 for VTE and AF; mechanical valve targets depend on valve type, position and additional embolic risks.
- Monitor INR more frequently during initiation and after illness, interacting medicine, diet or alcohol change, missed doses or unstable control; stable patients can move to longer locally defined intervals.
- Major bleeding: stop warfarin and give four-factor PCC plus 5–10 mg slow IV phytomenadione; vitamin K alone is too slow and plasma is not routine first-line replacement when PCC is available.
- No bleeding with INR above 8: omit warfarin and give 1–5 mg oral phytomenadione, then recheck promptly and repeat if necessary according to the UK protocol and patient risk.
- No bleeding with INR 5–8: omit one or two doses and investigate the cause; vitamin K is not routinely required unless individual bleeding risk is high.
- PCC dosing is product and INR based: for Beriplex, 25, 35 or 50 IU factor IX/kg for INR 2–3.9, 4–6 or above 6 respectively, with stated maximum doses.
- Bridge acute VTE with therapeutic heparin for at least 5 days and until the INR has been therapeutic for the protocol-defined period because early protein C depletion is not immediate protection.
- Provide an anticoagulant record and consistent advice on missed doses, vitamin-K-containing food, alcohol, interacting medicines, pregnancy and when to seek urgent help.
Key red flags
New neurological deficit, severe headache, collapse or head injury while taking warfarin requires emergency intracranial imaging and reversal assessment irrespective of an apparently modest INR.
Haemodynamic instability, ongoing gastrointestinal bleeding, haemoptysis, haematuria with obstruction or a rapid haemoglobin fall requires major-haemorrhage escalation and source control.
An INR above 8, interacting antibiotic, acute liver or renal failure, inability to take nutrition or repeated dosing error predicts further INR rise even when bleeding is not yet visible.
Investigation priorities
Quantify anticoagulant intensity and detect haemoglobin or platelet consequences.
Management branches
Bleeding is life-threatening, at a critical site, haemodynamically significant or uncontrolled.
- Stop warfarin, use ABCDE resuscitation, activate major-haemorrhage and obtain urgent INR, FBC, fibrinogen, renal, liver and group samples.
- Give four-factor PCC using the stocked product's INR and weight schedule plus 5–10 mg slow IV phytomenadione.
- Control the anatomical source, repeat INR and clinical assessment, then create a multidisciplinary anticoagulation restart plan.
An invasive procedure is planned in a patient taking stable warfarin.
- Obtain procedure bleeding risk, indication, target INR, recent thrombosis and exact mechanical-valve details.
- Continue for supported low-risk procedures or stop at the locally specified interval and confirm pre-procedure INR; use bridging only when thrombotic risk justifies it.
- Restart when haemostasis permits, with a written timing and any bridging plan communicated across teams.