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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 Dr Katy Rice June 2011
Atrial fibrillation • Commonest chronic arrhythmia • Increasing prevalence - ageing population -improved survival from CHD • Morbidity/mortality from stroke, heart failure • Stroke risk reduced by warfarin
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
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
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
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
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
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
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)
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)
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
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
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
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
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
Warfarin determinants of dose • Genetic e.g. VKORC1, CYP2C9 genes • Age • Comorbidities (heart, liver disease, poor nutrition) • Medication
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
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
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
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%)
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
Anticoagulant service provision • General practice • Secondary care • Self monitoring -and various combinations of the above!
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
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
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
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
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
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
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)
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
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
MI, Death and Net clinical Benefit Net Clinical Benefit includes vascular events, death and major bleed
Dabigatran 150 mg vs. 110 mg *Net Clinical Benefit includes vascular events, death and major bleed
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
Common Adverse Events *Occurred more commonly on dabigatran p<0.001
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
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
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
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?
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