Reversing the New Anticoagulants
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1 Reversing the New Anticoagulants Disclosure Susan C. Lambe, MD Assistant Clinical Professor Department of Emergency Medicine University of California, San Francisco Roadmap for today 1
2 Roadmap for today Characteristics of novel anticoagulants Approach to the bleeding patient Specific reversal agents UCSF guidelines Scope of Problem Prevalence atrial fibrillation 3.03 million in million by 2050 VTE = 900K/yr in US 1-2% of adults take warfarin Warfarin 1920s Outbreak hemorrhagic disease in cattle in northern US and Canada 1933 Isolated by Karl Link 1948 Rodenticde 1954 Approved in humans WARF-arin Wisconsin Alumni Research Foundation Coumarin, plant molecule in sweet clover 2
3 Warfarin Disadvantages Bridging Drug and food interactions Long half-life Close monitoring required Why New Anticoagulants? Rapid onset/shorter half-life Fewer drug and no food interactions No lab monitoring Equivalent to warfarin Prevention of stroke, VTE Bleeding rates New Anticoagulant Disadvantages Limited experience treating bleeding No proven reversal agent No monitoring What s in a name? Direct Thrombin Inhibitors (DTIs) Novel Oral Anticoagulants (NOACS) Target Specific Oral Anticoagulants (TSOACS) 3
4 Roadmap for today Characteristics of novel anticoagulants Approach to the bleeding patient Specific reversal agents UCSF Guidelines New Anticoagulants Dabigatran (Pradaxa ) Rivaroxaban (Xarelto ) Apixaban (Eliquis ) New Anticoagulants Dabigatran (Pradaxa ) Rivaroxaban (Xarelto ) Apixaban (Eliquis ) Dabigatran Indications FDA approved Stroke prevention in non-valvular afib Under FDA review VTE prophylaxis in hip or knee replacement Approved in Europe/Canada 4
5 Dabigatran Dose Stroke prevention 150 mg, po bid Renal insufficiency 75 mg, po bid DVT prophylaxis 220 mg, po qd Dabigatran Mechanism Direct Thrombin (Factor IIa) inhibitor Blocks conversion of fibrinogen to fibrin Dabigatran Pharmacology Dabigatran etexilate = inactive pro-drug Rapidly absorbed Active form binds active site of thrombin Inhibits free and clot-bound thrombin 5
6 Dabigatran Pharmacokinetics Predictable Rapid onset Peak plasma level at 2 hours Half-life hours Dabigatran Pharmacokinetics No food interactions, few drug interactions Fixed dosing can be used No need for routine monitoring or dose adjustment Dabigatran Metabolism Dabigatran Metabolism 85% excreted via the kidneys Use caution with renal dysfunction Low protein binding Eliminated by hemodialysis NOT metabolized by p450 system Substrate of efflux transporter P-glycoprotein Inducers (e.g., rifampin) reduce effect Inhibitors (e.g., verapamil) increase effect 6
7 Dabigatran Metabolism New Anticoagulants Decreased effect with P-gP inducers Rifampin Increased effect with P-gP inhibitors Dronedarone Ketoconazole, Itraconazole Verapamil Amiodarone Quinidine Clarithromycin Dabigatran (Pradaxa ) Rivaroxaban (Xarelto ) Apixaban (Eliquis ) FACTOR Xa INHIBITORS Rivaroxaban (Xarelto )Apixaban (Eliquis ) Indications Rivaroxaban/Apixaban Stroke prevention in non-valvular atrial fib Rivaroxaban only VTE prophylaxis post-joint replacement DVT/PE prophylaxis and treatment 7
8 Rivaroxaban and Apixaban Dose Non-valvular afib Rivaroxaban and Apixaban Mechanism Selective, direct, factor Xa inhibitors Rivaroxaban, 20 mg po qd Apixaban, 5 mg po qd DVT/PE Rivaroxaban, 15 mg po qd DVT prophylaxis Rivaroxaban,10 mg po qd Rivaroxaban and Apixaban Pharmacology Highly protein bound Not easily dialyzed Few drug interactions Rivaroxaban and Apixaban Pharmacokinetics Similar to dabigatran Predictable Not affected by age, sex, body weight Fixed dose Peak at 2 3h Half life 7-14h 8
9 Rivaroxaban Excretion 2/3 rd renal 1/3 rd liver Dose adjusted for reduced CrCl Metabolism Apixaban Excretion 2/3 rd liver, biliary 1/3 rd renal Coagulation Assays Not routinely necessary Indications Major bleeding Overdose Emergent surgery Coagulation Assays Coagulation Assays Dabigatran Peak/trough ng/ml aptt Prolonged at >50 ng/ml Normal at 25 ng/ml Dabigatran aptt not useful Thrombin time If normal, dabigatran not present Thrombin time Prolonged at 3 ng/ml Normal at 1 ng/ml 9
10 Coagulation Assays Coagulation Assays Rivaroxaban/Apixaban Peak/trough ng/ml aptt Prolonged at 120 ng/ml Normal at 60 ng/ml Rivaroxaban/Apixaban Anti-factor Xa assay No assay for rivaroxaban available Ask for assay calibrated for enoxaparin Estimate of rivaroxaban/apixaban activity Roadmap for today Characteristics of novel anticoagulants Approach to the bleeding patient Specific reversal agents UCSF guidelines Approach to Bleeding Discontinue anticoagulant Compress Fluid replacement, transfusion 10
11 Approach to Bleeding Consider emergent reversal Intracranial Pericardial Intraspinal Hemorrhagic shock Drug overdose Emergency surgery Roadmap for today Characteristics of novel anticoagulants Approach to the bleeding patient Specific reversal agents UCSF guidelines Reversal Agents NO ROLE FOR VITAMIN K IN REVERSAL OF NEW ORAL ANTICOAGULANTS Reversal: Options Hemodialysis (dabigatran only) Prothombin complex concentrate (PCC) Recombinant Factor VIIa (rfviia) apcc (FEIBA ) 11
12 Reversal: Hemodialysis For reversing dabigatran Evidence 6 healthy volunteers w ESRD 62% removed after 2 hours 68% removed after 4 hours Two preparations Reversal: PCC Kcentra 4-factor PCC (II, VII, IX, X) Bebulin 3-factor PCC (II, IX, X) Rivaroxaban/apixaban too highly proteinbound for HD Stangier, 2010 Reversal: Specific Agents Reversal: Specific Agents Human studies Animal studies Specific Antidotes Human studies Animal studies Specific Antidotes 12
13 Reversal: Specific Agents Reversal: Human Studies Human studies 5 studies, Healthy volunteers Anticoagulants: dabigatran, rivaroxaban, apixaban Reversal agents PCC apcc rfviia Erenberg, 2011 Study design N=12 subjects Dabigatran or rivaroxaban po x 2.5 d Treated with PCC bolus iv Measured PT and ETP over 24 hours Outcome: clotting assays Reversal: Human Studies Erenberg, 2011 Findings PCC reversed PT, ETP in rivaroxaban treated patients PCC did not reverse dabigatran Reversal: Human Studies Marlu, 2012 Study design N=10 men Dabigatran or rivaroxaban po x 1 Collected blood samples Treated blood (PCC, rfviia, apcc) 13
14 Reversal: Human Studies Reversal: Human Studies Marlu, 2012 Findings Dabigatran rfviia most effective Rivaroxaban PCC most effective Khoo, 2013 Dabigatran+aPCC Study design N=8 subjects on dabigatran Blood treated with apcc Reversal: Human Studies Reversal: Human Studies Khoo, 2013 Findings apcc reversed dabigatran Dinklaar, 2013 Rivaroxaban+PCC Study Design N=9 subjects PCC added to rivaroxaban-treated samples Coagulation assays performed 14
15 Reversal: Human Studies Reversal: Human Studies Dinklaar, 2013 Rivaroxaban + PCC Findings mixed results PCC Normalized thrombin generation Did not normalize PT Dose of PCC required depended on type of assay Korber, 2013 Rivaroxaban + PCC/rFVIIa Study design N=10 subjects Blood samples treated with rivaroxaban Added PCC and rviia Performed clotting assays Reversal: Human Studies Human Studies: Summary Korber, 2013 Rivaroxaban + PCC/rVIIa Findings PCC had no effect on clotting tests rviia reversed PT and clotting factor time prolongation Dabigatran Reversed with apcc in 2/2 studies Rivaroxaban Reversed with PCC in 3/4 studies 15
16 Human studies: Limitations Reversal: Specific Agents Variable designs Healthy volunteers Reversal agents added to blood samples Clotting tests proxy for bleeding Human studies Animal studies Specific antidotes Reversal: Animal studies 6 studies, Anticoagulants: Dabigatran Rivaroxaban Apixaban Reversal agents PCC rfviia apcc (FEIBA ) Fibrinogen FFP Outcomes Clotting assays Bleeding Van Ryn, 2008 Study Design Rats infused w high dose dabigatran x 20 min Reversed with rfviia and apcc (FEIBA ) given iv Bleeding measured 5 min after tail incision 16
17 Van Ryn, 2008 Findings Both agents reduced bleeding time Neither agent reduced blood loss Zhou, 2011 Study Design Mice were treated with dabigatran po ICH induced Reversed with intravenous PCC Murine FFP rfviia Zhou, 2011 Findings N=96 mice PCC prevented hematoma expansion Murine FFP worked only with high dose dabigatran rfviia did not prevent hematoma expansion Godier, 2012 Study Design (n=83 rabbits) T=0 min, rivaroxaban iv T=1 min, procoagulant iv (PCC, rfviia) Hepatosplenic bleeding induced T=15 min, total blood loss recorded 17
18 Godier, 2012 Findings Neither rfviia nor PCC reduced total blood loss Pragst, 2012 Study Design (n=28 rabbits) T=0 min, dabigatran iv T=5 min, PCC infusion T=10 min, kidney incision Pragst, 2012 Findings PCC reduced blood loss, bleeding time Dose dependent Perzborn, 2013 Study Design rats T=0 min, rivaroxaban iv T=5 min, bleeding induced T=6 min, reversal iv (PCC, apcc, rfviia) 18
19 Perzborn, 2013 Findings rats n=7-12/group All agents reduced bleeding time PCC apcc rfviia Perzborn, 2013 Study Design baboons (n=7) T=0 min, rivaroxaban infusion T=30 min, reversal agent Experimental forearm incision Bleeding time measured Perzborn, 2013 Findings apcc and rviia both reduced bleeding time apcc from twice normal to normal rfviia from 2.5 normal to 1.7 normal Martin, 2013 Study design T=0, simultaneous apixaban bolus and reversal agent bolus T=20 min hepatosplenic section T=30 min, blood loss measured 19
20 Summary of Animal Studies Martin, 2013 Findings rfviia partially corrected bleeding time PCC, rfviia, fibrinogen did NOT reverse blood Dabigatran PCC reversed dabigatran in 3/3 animal studies Rivaroxaban and Apixaban PCC, apcc, rfviia reversed rivaroxaban in 1/3 studies Animal Studies: Limitations Reversal: Specific Agents Wide variability in study design Different doses Different species Different outcomes (coagulation assays, bleeding time, blood loss) Human studies Animal studies Specific antidotes Human clotting factors behave differently in non-humans 20
21 Reversal: Specific Antidotes Reversal: Specific Antidotes r-antidote (PRT064445) adabi-fab PER977 r-antidote (PRT064445) Antidote for rivaroxaban Recombinant protein Binds Xa inhibitor site Reduced blood loss in animal models Not tested in humans Lu, 2013 Reversal: Specific Antidotes Reversal: Specific Antidotes adabi-fab Monoclonal antibody Antidote for dabigatran Reversed anticoagulant assays in rats PER977 Small synthetic molecule Directly binds Xa and IIa Reverses dabigatran, rivaroxaban, apixaban Schiele, 2013 Laulicht,
22 Summary Specific Antidotes Three promising agents None FDA-approved in humans yet Roadmap for today Characteristics of novel anticoagulants Approach to the bleeding patient Specific reversal agents UCSF guidelines UCSF Guidelines UCSF Guidelines Caveat: No proven reversal agents or antidotes 22
23 UCSF Guidelines General Principles Discontinue drug Hemostasis Hemodynamic support Reverse other antithrombotic drugs UCSF Guidelines Consider Hemodialysis (dabigatran only) Activated charcoal UCSF Guidelines If other measures fail Assess thrombotic risk In past 6 wks MI CVA, TIA DVT/PE Severe PVD UCSF Guidelines If all measures fail apcc (FEIBA ) to reverse dabigatran PCC (Kcentra ) to reverse rivaroxaban/apixaban 23
24 FEIBA and Kcentra Cautions Increase risk of thromboembolism Reversal is OFF-LABEL Weigh risk/benefit Blood products Kcentra contains heparin Roadmap for today Characteristics of novel anticoagulants Approach to the bleeding patient Specific reversal agents UCSF guidelines 24
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