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Managing anticoagulation in atrial fibrillation

Managing anticoagulation in atrial fibrillation . Dr Katy Rice June 2011. Atrial fibrillation. Commonest chronic arrhythmia Increasing prevalence - ageing population -improved survival from CHD Morbidity/mortality from stroke, heart failure

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Managing anticoagulation in atrial fibrillation

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  1. Managing anticoagulation in atrial fibrillation Dr Katy Rice June 2011

  2. Atrial fibrillation • Commonest chronic arrhythmia • Increasing prevalence - ageing population -improved survival from CHD • Morbidity/mortality from stroke, heart failure • Stroke risk reduced by warfarin

  3. Themes of talk • AF - the burden of disease • Recognition of those at risk of stroke • Warfarin - current standard of care • Anticoagulant service provision • New oral anticoagulants

  4. Themes of talk • AF - the burden of disease • Recognition of those at risk of stroke • Warfarin - current standard of care • Anticoagulant service provision • New oral anticoagulants

  5. Burden of disease

  6. Prevalence of AF in the Renfrew-Paisley study Cohort of men and women aged 45–64 years (n = 15,406) Reproduced with permission of the BMJ Publishing Group from Stewart S et al, Heart 2001: 86:516-21

  7. Extrapolating to Sutton and Merton population

  8. Themes of talk • AF - the burden of disease • Recognition of those at risk of stroke • Warfarin - current standard of care • Anticoagulant service provision • New oral anticoagulants

  9. Recognition of those at risk of stroke • Patients with AF have x 5 risk of stroke • AF and no risk factors 1% per year • AF and previous stroke/TIA 12% per year • Stroke in AF has poorer outcome

  10. Annual stroke rates in AF according to CHADS2 score

  11. Patients with AF Determine stroke/thromboembolic risk • High risk: • Previous ischaemic stroke/TIA or thromboembolic event • Age >75 with hypertension, diabetes or vascular disease • Clinical evidence of valve disease, heart failure, or impaired left ventricular function on echocardiography • Moderate risk: • Age >65 with no high risk factors • Age <75 with hypertension, diabetes or vascular disease • Low risk: • Age <65 with no moderate or high risk factors

  12. Patients with AF Determine stroke/thromboembolic risk Low risk High risk Moderate risk Consider anticoagulation Consider anticoagulation or aspirin Aspirin 75 to 300 mg/day if no contraindications Contraindications to warfarin? YES NO Reassess risk stratification whenever individual risk factors are reviewed Warfarin, target INR = 2.5 (range 2.0 to 3.0)

  13. New risk scoring systems • CHA(2)DS(2)-Vasc (Cong heart failure, Hypertension, Age≥75,Diabetes, Stroke, Vascular disease, Age 65-74, Sex category) • HAS-BLED - (Hypertension, Abnormal renal/liver function, Stroke, Bleeding history or predisposition, Labile INR, Elderly, Drugs/alcohol concomitantly)

  14. Themes of talk • AF - the burden of disease • Recognition of those at risk of stroke • Warfarin - current standard of care • Anticoagulant service provision • New oral anticoagulants

  15. Warfarin and AF • Oral anticoagulation reduces stroke risk in AF by 2/3………..but only if time in therapeutic range (INR 2-3) is greater than 65% • Oral anticoagulation leads to 2 extra intracranial bleeds per annum per 1000 patients

  16. Stroke risk Valvular AF CHADS2 Bleeding risk >75 years Uncontrolled hypertension History of bleeding or intracranial haemorrhage Anaemia Polypharmacy History of poor anticoagulation control Anti-platelet drugs Benefits versus risks

  17. Advanced age Multiple comorbidities Cognitive impairment Visual impairment History of falls Alcohol Previous bleed on warfarin Recent history of GI bleeding Uncontrolled hypertension Recent major surgery Pregnancy Inherited coagulation defect Thrombocytopenia Warfarin (relative) contraindications

  18. Warfarin preassessment • FBC - anaemia (?bleeding) - platelets <100 x 109/l • INR or APTT ratio >1.4 needs investigation (liver disease, lupus inhibitor, factor deficiency) • Liver function tests

  19. Warfarin determinants of dose • Genetic e.g. VKORC1, CYP2C9 genes • Age • Comorbidities (heart, liver disease, poor nutrition) • Medication

  20. Slow AF No heparin needed Less likely to ‘overshoot’ Less frequent monitoring Fast Acute DVT or PE Need heparin until INR therapeutic Often results in high INRs Frequent tests Warfarin induction protocols

  21. AF Induction Protocol • Start 3mg daily and check INR after one week • If INR <1.4 increase to 5 mg daily and repeat INR in 3 days • If INR 1.4-1.8 increase to 4mg daily and repeat in one week • If INR 1.9-2.5 continue 3mg daily and repeat INR in one week • If INR >2.5 consider dose reduction or omitting dose

  22. Cardioversion for persistent AF • NICE guidance : INR 2.5 (range 2-3) for 3 weeks prior and 4 weeks after • At Epsom & St Helier we aim for target 2.5-3.5 to reduce likelihood of cancellation due to low INR • Monitor weekly • Cardiologists insist on venous samples (but probably no need if using Coaguchek) • For urgent cardioversion give therapeutic LMWH before and warfarin for 4 weeks after

  23. Aspirin for AF • Alternative to warfarin if contraindications or intolerance or patient preference • Less effective than warfarin • Reduces stroke risk by 22% compared with placebo (warfarin 68%)

  24. Themes of talk • AF - the burden of disease • Recognition of those at risk of stroke • Warfarin - current standard of care • Anticoagulant service provision • New oral anticoagulants

  25. Anticoagulant service provision • General practice • Secondary care • Self monitoring -and various combinations of the above!

  26. Anticoagulant service provision

  27. Anticoagulation service at St Helier • Estimated AF patients on books • new AF patients per month • Pressure to reduce ‘new:follow-up ratios’ • Need to work with GPs to transfer patients to primary care

  28. Themes of talk • AF - the burden of disease • Recognition of those at risk of stroke • Warfarin - current standard of care • Anticoagulant service provision • New oral anticoagulants

  29. The new anticoagulants • Oral • Wide therapeutic index • Predictable pharmacokinetics and dynamics negating need for monitoring • Rapid onset of action • Antidote • Minimal non-anticoagulant side-effects • Minimal interactions with other drugs and food

  30. The new oral anticoagulant drugs • Dabigatran (Pradaxa - Boehringer-Ingelheim) • Rivaroxaban (Xarelto - Bayer) - both licensed in UK for thromboprophylaxis post knee and hip replacement. Dabigatran licence for AF expected late June 2011. • Apixaban (Pfizer)- awaiting FDA approval

  31. Dabigatran Dabigatran etexilate, a pro-drug, is rapidly converted to dabigatran 80% excreted by kidney Half-life of 12-17 hours Phase 2 data identified 110 mg BID and 150 mg BID as viable doses

  32. RE-LY: A Non-inferiority Trial Atrial fibrillation ≥1 Risk Factor Absence of contra-indications 951 centers in 44 countries R Blinded Event Adjudication. Open Blinded Dabigatran Etexilate 150 mg BID N=6000 Warfarin adjusted (INR 2.0-3.0) N=6000 Dabigatran Etexilate 110 mg BID N=6000

  33. Trial Execution • Performed December 2005-March 2009 • Median Follow up 2.0 years • Follow up 99.9% complete • Mean time in therapeutic range = 64% (patients on warfarin)

  34. Ischaemic/Unspecified Stroke 0.08 0.06 Cumulative Hazard Rates 0.04 Dabigatran110 Warfarin 0.02 Dabigatran150 0.0 0 0.5 1.0 1.5 2.0 2.5 Years of Follow-up

  35. Hemorrhagic Stroke 0.04 0.03 Cumulative Hazard Rates 0.02 Warfarin 0.01 Dabigatran110 Dabigatran150 0.0 0 0.5 1.0 1.5 2.0 2.5 Years of Follow-up

  36. Bleeding

  37. MI, Death and Net clinical Benefit Net Clinical Benefit includes vascular events, death and major bleed

  38. Dabigatran 150 mg vs. 110 mg *Net Clinical Benefit includes vascular events, death and major bleed

  39. Permanent Discontinuation 0.4 0.3 Dabigatran150 Stopping Rates Dabigatran110 0.2 Warfarin 0.1 0.0 0 0.5 1.0 1.5 2.0 2.5 Years of Follow-up

  40. Common Adverse Events *Occurred more commonly on dabigatran p<0.001

  41. RE-LY Study Conclusions • Dabigatran 150 mg significantly reduced stoke compared to warfarin with similar risk of major bleeding • Dabigatran 110 mg had a similar rate of stroke as warfarin with significantly reduced major bleeding • Both doses reduced intra-cerebral, life-threatening and total bleeding • Dabigatran had no major toxicity, but did increase dyspepsia and GI bleeding

  42. Conclusions Both Dabigatran doses offer advantages over warfarin Dabigatran 150 is more effective and dabigatran 110 has a better safety profile Taken twice daily No reversal agent

  43. Dabigatran - financial impact • £2.50/day • £912.50/year • Warfarin cost £383/year(NICE)? • Annual cost pressure for S London £6 - 10.3 million Planned introduction needed

  44. S & M implementation scenarios

  45. Key issues • Can a budget be identified from June 2011? • Can subgroups be specified pending NICE HTA? • How can clinicians be encouraged to comply with guidance? • Can money be released from anticoag services for 2012/13? • How should public pressure be dealt with if no money for widespread use?

  46. Recommendations from S London Cardiac and Stroke Network • Warfarin to remain agent of choice in short term • Dabigatran in patients with contraindications to warfarin • Establish S London working group to ensure consistent approach and develop prescribing guidance • Develop communication plan and patient information strategy

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