Survey
* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
SMDC Vitamin K-Warfarin Reversal Guidelines For Overanticoagulation, Bleeding, and Emergent Invasive Procedures I. Caveats (specific recommendations start on page 2) General Remember that patients receive anticoagulation to prevent life-threatening thrombosis. Consider the patient’s future anticoagulation needs when planning the reversal of warfarin anticoagulation. Vitamin K The effect of vitamin K on reversing warfarin anticoagulation is delayed, reaching its full effect at about 24 hours. Excessively large doses of vitamin K do not reverse anticoagulation faster and may cause weeks of warfarin resistance. Any dose of vitamin K greater than 10 mg should be considered excessive. Oral vitamin K is the preferred preparation to be used in most situations. Oral vitamin K is more predictable in its bioavailability and has a quicker onset of action than subcutaneous vitamin K; it also offers additional convenience and safety in comparison to other dosage forms. Intramuscular vitamin K will not be used per SMDC policy to avoid hematoma risk. Intravenous vitamin K has a more predictable response and faster onset of action than other forms of vitamin K. However, IV vitamin K may cause anaphylaxis, and slow infusion rates have never been proven to prevent anaphylaxis. It should be diluted in 50 mL and given via piggyback infusion over at least 30 minutes. It is the preferred route of administration for severe bleeding situations. Subcutaneous vitamin K is not as effective on a mg-to-mg basis as IV vitamin K and does not work as quickly; but it does not carry the anaphylaxis risk of IV vitamin K. It is an alternative when a patient cannot take oral vitamin K and the situation is not emergent. Fresh Frozen Plasma (FFP) FFP is a blood product containing a concentration of clotting factors. All of the risks of blood product transfusions apply to FFP. FFP replaces depleted clotting factors and is therefore the fastest way to reverse warfarin anticoagulation. It begins to work immediately with a full effect in 6 hours. FFP is usually given in doses of 2 to 4 units and is repeated every 6 to 12 hours as needed. 4 units should be used in a severe bleeding situation. Vitkrecs8.doc II. Management of overanticoagulation in patients without bleeding INR above target but less than 5 Lower the dose or omit the dose, monitor more frequently, and resume therapy at a lower dose when the INR is at a therapeutic level. INR 5 to 9 Low Thrombotic Risk2 High Thrombotic Risk3 1 No risk factors for bleeding Omit the next 1 to 2 doses of Omit the next 1 to 2 doses of warfarin. warfarin. Risk factors for bleeding present1 Hold warfarin, give 1 to 2.5 Omit the next 1 to 2 doses of mg oral vitamin K. warfarin and monitor closely for bleeding OR hold warfarin, give 1 to 2.5 mg oral vitamin K. INR greater than 9 Low Thrombotic Risk2 High Thrombotic Risk3 1 No risk factors for bleeding Hold warfarin, give 5 mg oral Hold warfarin, give 5 mg oral vitamin K vitamin K Risk factors for bleeding present1 Hold warfarin, give 10 mg Hold warfarin, give 5 to 10 oral vitamin K mg oral vitamin K In all above cases, monitor more frequently and resume therapy at a lower dose when the INR is at a therapeutic level if a reversible reason for the elevation cannot be identified 1. Risk factors for bleeding: History of GI bleed (not peptic ulcer disease WITHOUT bleeding), hypertension, cerebrovascular disease, ischemic stroke, congestive heart failure, renal insufficiency, concurrent aspirin, age greater than 75 years, and recent major surgery. 2. Low Atrial fibrillation WITHOUT: thrombotic history of severe left ventricular dysfunction (ejection fraction less than risk: 25%) clinically significant rheumatic heart disease previous thromboembolic events within 6 months cardioversion in the last month bioprosthetic heart valve severe left atrial enlargement More than 1 month since arterial thromboembolism Deep vein thrombosis prophylaxis More than 3 months since deep vein thrombosis or pulmonary embolism 3. High Atrial fibrillation WITH: thrombotic history of severe left ventricular dysfunction (ejection fraction less than risk: 25%) clinically significant rheumatic heart disease previous thromboembolic events within 6 months cardioversion in the last month bioprosthetic heart valve severe left atrial enlargement Less than 1 month since arterial thromboembolism Mechanical heart valves Less than 3 months since deep vein thrombosis or pulmonary embolism III. Management of anticoagulated patients with bleeding Minor bleeding: INR is low or in target range: make no changes and observe carefully INR above target but less than 5 (high): adjust warfarin appropriately, no vitamin K INR 5 to 9 (very high): hold warfarin, give 1 to 2.5 mg oral vitamin K INR greater than 9 (critical high): hold warfarin, give 5 to 10 mg oral vitamin K Major bleeding: Any INR: clinical circumstances such as the severity of bleeding, risk of thrombosis, and the INR value will dictate the course of action. Generally in this situation the advice would be to hold warfarin, give 4 units FFP, and supplement FFP with 10 mg vitamin K by slow piggyback IV infusion over at least 30 minutes Vitkrecs8.doc In all above cases, monitor more frequently and resume therapy at a lower dose when the INR is at a therapeutic level if a reversible reason for the elevation cannot be identified. Minor bleeding example: bleeding gums Major bleeding example: major GI bleed, CNS bleed, retroperitoneal bleed, etc. IV. Management of anticoagulated patients for emergent invasive procedures Important facts to remember: 1. The peak effect of vitamin K on reversing warfarin anticoagulation takes 24 hours, although you may start to see effects in 6 to 12 hours. 2. FFP replaces depleted clotting factors and is therefore the fastest way to reverse warfarin anticoagulation. It begins to work immediately, with a full effect in 6 hours. Low surgical risk of bleeding: Goal is low therapeutic INR (INR= 2 to 2.5) INR above target but less than 5: hold warfarin, consider giving 2.5 mg oral vitamin K, consider giving FFP INR 5 to 9 (very high): hold warfarin, give 2.5 mg oral vitamin K, consider giving FFP INR greater than 9 (critical high): hold warfarin, give 5 mg oral vitamin K, consider giving FFP In all cases, recheck INR in 12 hours and re-administer vitamin K and/or FFP if needed. Moderate surgical risk of bleeding: Goal is subtherapeutic INR (INR 1.5) INR above 1.5 but less than upper target range: hold warfarin, give 2.5 mg oral vitamin K, consider giving FFP INR above target but less than 5: hold warfarin, give 2.5 mg oral vitamin K and FFP INR 5 to 9 (very high): hold warfarin, give 5 to 10 mg oral vitamin K and FFP INR greater than 9 (critical high): hold warfarin, give 10 mg oral vitamin K and FFP In all cases, recheck INR in 12 hours and re-administer vitamin K and/or FFP if needed. High surgical risk of bleeding: Goal is complete reversal of anticoagulation (INR=1) Hold warfarin, give FFP and 10 mg oral vitamin K In all cases, recheck INR in 12 hours and re-administer vitamin K and/or FFP if needed. Refer to the SMDC bridging guidelines for appropriate management of emergent invasive procedure patients post-op. Low surgical risk of bleeding example: accessible laceration of the arm. Moderate surgical risk of bleeding example: major abdominal surgery (bowel resection). High surgical risk of bleeding example: brain surgery. References: Ansell J, Hirsh J, Poller L, et al. The pharmacology and management of the vitamin K antagonists. CHEST 2004; 126;204S-233S. Crowther MA, Douketis JD, Schnurr T, et al. Oral vitamin K lowers the international normalized ratio more rapidly than subcutaneous vitamin K in the treatment of warfarin-associated coagulopathy. Ann Intern Med 2002; 137:251-254. Whitling AM, Bussey HI, Lyons RM. Comparing different routes and doses of phytonadione for reversing excessive anticoagulation. Arch Intern Med 1998; 158:2136-2140. Vitkrecs8.doc