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Jan 30, 2014
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About This Presentation
New oral anticoagulants (NOAC) WATAG guidelines
Size: 1.22 MB
Language: en
Added: Jan 30, 2014
Slides: 23 pages
Slide Content
New Oral
Anticoagulants
Guidelines
KAI YAP
What’s wrong with traditional
anticoagulants???
Development
Traditional anticoagulants have 2 major limitations:
-Narrow therapeutic window of adequate anticoagulation without
bleeding
-Highly variable dose-response, requiring monitoring by lab testing
These limitations have provided impetus for development of other
antithrombotic agents.
3 new oral anticoagulants (NOAC) dagibatran, rivaroxaban, apixaban
listed on PBS.
Mechanism
Dagibatran – direct thrombin inhibitor
Rivaroxaban – factor Xa inhibitor
Apixaban – factor Xa inhibitor
Indications
1. Prevention of venous thromboembolism in a patient undergoing
total hip or knee replacement
2. Prevention of stroke or systemic embolism in patients who have
non-valvular atrial fibrillation and has one or more risk factors for
developing stroke or systemic embolism
3. Rivaroxaban for the prevention of recurrent venous
thromboembolism and for the treatment of deep vein thrombosis
and pulmonary embolism.
Contraindications
Known hypersensitivity to ingredients of NOAC
Clinically significant active bleeding
Renal impairment <30ml/min
Hepatic disease (child pugh – C)
Recent high risk bleeding lesion (eg. ICH < 6 months)
Pregnancy or breast feeding
Recent stroke, surgery, GI bleed or ulcer
Recent fibronolytic therapy <10days
Concomitant warfarin therapy
Features of NOAC
Features to consider
-Faster onset
-Shorter ½ life
-Less drug-drug interactions
-No need for monitoring with NOACs
-No antidotes
Dosing – Total hip / knee
replacement (VTE prophylaxis)
Dagibatran Rivaroxaban Apixaban
Crcl > 50ml / min220mg once daily 10mg once daily
Crcl 30–50ml / min150mg once daily 10mg once daily 2.5mg
once daily
Crcl 15-30ml / mincontraindicated contraindicated
Dosing – Non-valvular Atrial
Fibrillation
Dagibatran Rivaroxaban Apixaban
Crcl > 50ml / min150mg twice daily20mg once daily
Crcl 30-50ml / min110mg twice daily15mg once daily 5mg twice daily
Crcl 15-30ml / minContraindicated Contraindicated
Special
populations
Older than 75
years old
110mg twice daily
Not applicable
At least two of
following:
-older than 80 yo
-Weight less than 60kg
-Scr > 133micromol/L
-2.5mg twice daily
Dosing – treatment of DVT / PE
Rivaroxaban
Crcl > 30ml / min
15mg twice daily for three weeks, followed by 20mg daily
Switching anticoagulants
Switching from Switching to Instructions
LMW Heparin NOACs When next dose of LMW
Heparin is due
Heparin NOACs Immediately when heparin
ceased
Warfarin NOACs Start once INR < 2
Dagibatran LMW heparin / UFH No bolus required. Start 12
hrs after last dose
Rivaroxaban / Apixaban LMW heparin / UFH No bolus required. Start 24
hrs after last dose
NOACs Warfarin Continue NOAC and give
warfarin ≤ 5 mg
Stop NOAC once INR ≥ 2 on
2 consecutive days
What do we do when patients
bleed?
Management of bleeding (Initial Ix)
Seek early haematology advice
Dagibatran:
Measure: FBC, U&E, LFT, coagulation profile, Haemoclot and
dabigatran level
normal TT excludes dabigatran activity
normal aPTT suggests bleeding not due to dabigatran
Management of bleeding (Initial Ix)
Rivaroxaban / Apixaban:
Measure: FBC, U&E, LFT, coagulation profile, anti-Xa and
rivaroxaban level
normal PT suggests rivaroxaban level not high
aPTT cannot predict anticoagulant effect
tests are currently inconclusive for apixaban
Management of bleeding (mild)
Mild bleeding -
- local haemostatic measures
- delay or discontinue NOAC as required
Management of bleeding
(clinically significant)
reduction in Hb >20 g/L or requiring RBC transfusion > 2 units
Stop NOAC therapy
Give oral charcoal if NOAC ingested < 2 hours ago
Maintain adequate hydration to aid drug clearance
Local haemostatic measures: mechanical compression
Transfusion support: RBC transfusion as per Hb level
Consider platelet transfusion if on antiplatelet therapy or if platelets
< 50 x 109/L
Consider radiological and surgical interventions to identify and treat
source of bleeding
Management of life threatening
bleeding
bleeding in critical area or organ, loss of Hb > 50 g/L, hypotension not
responding to resuscitation
Get advice of haematologist!!!
T/f to SCGH or RPH
a)FEIBA (factor eight inhibitor bypass activity) 25 -100 International
Units/kg, repeat at 12 hours (probably beneficial)
b)rVIIa 90 microgram/kg every 2-3 hours (possibly beneficial)
c)prothrombinex – VF 25-50 International Units/kg (if not administered
earlier)
d)tranexamic acid 15-30 mg/kg IV for mucosal bleeds
Prescribing a new oral
anticoagulant
1. Lab tests – FBC, EUC, LFTs
Contraindications:
-Poor renal function (CrCl ≤ 30 mL/ min, apixaban: ≤ 15 mL/min)
-Liver disease (e.g. ALT > 3x upper limit of normal)
-Hb ≤ 100 g/L (assess risk vs. benefit)
Prescribing a new oral
anticoagulant
2. Detailed History
EXCLUSION Criteria:
-Known hypersensitivity to NOAC preparation
-Pregnant or breastfeeding
-Stable warfarin therapy
-Prosthetic heart valve
-Recent stroke
Prescribing a new oral
anticoagulant
3. Assess bleeding risk
-Disorder of haemostasis
-Recent surgery (≤ 1 month ago)
-GI bleed ≤ 12 months ago
-Ulcer ≤ 30 days ago
-Fibrinolytic treatment last 10 days
-Dual antiplatelet therapy
Prescribing a new oral
anticoagulant
4. Consider contaminant medications
Rivaroxaban / apixaban
-Systemic azole antifungals (except fluconazole)
-HIV-protease inhibitors
Dabigatran
-Systemic azole antifungals (except fluconazole)
-dronedarone
-Simultaneous initiation with verapamil
-cyclosporin and tacrolimus
Prescribing a new oral
anticoagulant
Is patient on warfarin?
Stop warfarin
Start NOAC once INR < 2
Western Australia Therapeutic
Advisory Group Guidelines
Please visit
http://www.watag.org.au/watag/publications.cfm#guidelines