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AF: Management and Stroke Prevention Disclaimer Bristol-Myers Squibb and Pfizer abide by the Medicines Australia Code of Conduct and our own internal policies, and as such, will not engage in the promotion of unregistered products or unapproved indications. The statements, conclusions and opinions contained in the following presentations are those of the presenter and do not necessarily reflect those of the sponsor Bristol-Myers Squibb or Pfizer. Please refer to the appropriate approved Product Information before prescribing any agents mentioned in this presentation. The Product Information is available through the BMS Australia and Pfizer Australia websites, the trade display or from your BMS or Pfizer representative. Bristol-Myers Squibb Australia Pty Ltd, ABN 33 004 333 322, Level 2, 4 Nexus Court, Mulgrave, VIC, Australia. Pfizer Australia Pty Ltd, ABN 50 008 422 348 38-42 Wharf Road, West Ryde, NSW, AUSTRALIA. 432AU1700005-03. PP-ELI-AUS-0418 AF: Range of Presentations1 • Asymptomatic or minimal symptoms (25–40%) – Symptoms felt do not correlate well with episodes of AF and patients can have symptomatic and silent episodes over time • • • • Severe or disabling symptoms (15–30%)* Chronic, paroxysmal Chronic, persistent Acute, haemodynamically unstable * Maximum symptom score of intermediate or frequent for palpitations, fatigue, dizziness, dyspnea, chest pain, anxiety.2 Reference: 1. Kirchhof P et al. Eur Heart J 2016; 37: 2893-962. 2. Kirchhof P et al. Europace 2014; 16: 6-14. Types and Patterns of Atrial Fibrillation1,2 NonValvular AF AF in the absence of rheumatic mitral stenosis or a mechanical prosthetic heart valve Paroxysmal AF AF that terminates spontaneously usually within 48 hours, may continue for up to 7 days Episodes may recur with variable frequency Persistent AF Continuous AF that is sustained for longer than 7 days Long-standing persistent AF Continuous AF > 12 months in duration AF associated with rheumatic heart disease and mechanical valves require vitamin K antagonists References: 1. Kirchhof P et al. Eur Heart J 2016; 37: 2893-962. 2. January CT et al. Circulation 2014; 130: 2071-104. Mr M Aged 67 years Non-smoker, minimal alcohol intake Taking lisinopril 20 mg/day for hypertension Dyslipidaemia treated with statin BMI 30 kg/m2, waist circumference 91 cm Visits reporting general fatigue and that he has noticed occasional feelings of ‘palpitations’ in his chest and dizziness Risk Factors for Atrial Fibrillation Include: • • • • • • Older age Hypertension Diabetes mellitus Myocardial infarction Heart failure Chronic kidney disease Reference: 1. Kirchhof P et al. Eur Heart J 2016; 37: 2893-962. • • • • • • • Obesity Obstructive sleep apnoea Cardiothoracic surgery Smoking Intense exercise Alcohol use Hyperthyroidism Mr M: Atrial Fibrillation? Further History: • When asked about sleep, he reports that his wife complains about his loud snoring • No chest pain, dyspnoea, peripheral oedema or syncope Examination: • Heart rate 74 BPM and pulse regular • Blood pressure 166/100 mmHg • Respiration rate 16 breaths per minute, lung sounds normal Detecting AF • • • • Irregular pulse felt on manual palpation1,2 Confirmed by ECG: irregular R-R intervals, no P waves1 An episode lasting at least 30 seconds is diagnostic for AF1 Detecting paroxysmal AF usual requires:2 – 24-hour ambulatory ECG monitoring – Event recorder ECG for symptomatic episodes more than 24 hours apart References: 1. Kirchhof P et al. Eur Heart J 2016; 37: 2893-962. 2. NICE Clinical Guideline. 2014. www.nice.org.uk/guidance/cg180. Mr M: Atrial Fibrillation? Test results: • 24 hour ECG shows episodes of AF, no other cardiac abnormalities found • Tests including complete blood count, electrolytes, HbA1c, thyroid and liver function were within normal limits AF Management References: 1. Kirchhof P et al. Eur Heart J 2016; 37: 2893-962. 2. NICE Clinical Guideline. 2014. www.nice.org.uk/guidance/cg180. Aims of Management • Prevent stroke1 – Up to a third of ischaemic strokes are due to AF2 – Anticoagulants significantly reduce the risk of stroke due to AF1 • Control arrhythmia; rate control, or rhythm control if symptoms remain1 • Improve quality of life1 – Symptomatic patients can experience limiting lethargy, palpitations, dyspnoea, chest tightness, sleeping difficulties, and psychosocial distress References: 1. Kirchhof P et al. Eur Heart J 2016; 37: 2893-962. 2. Friberg L et al. Stroke 2014; 45: 2599-605. Management of AF Should Include:1 • • • • Awareness of symptoms of stroke /TIA Lifestyle changes to reduce stroke risk Psychological support if needed Comprehensive education and information on: – cause, effects and possible complications of atrial fibrillation – anticoagulation and bleeding risks – management of rate and rhythm and what to expect Reference: 1. NICE Clinical Guideline. 2014. www.nice.org.uk/guidance/cg180. Anticoagulants to Prevent Stroke Anticoagulants to Prevent Stroke • Anticoagulation should be initiated early in all suitable patients regardless of AF pattern or symptoms1,2 • Specialist referral not needed for anticoagulation in uncomplicated patients2 • Evidence supporting antiplatelet monotherapy for stroke prevention in AF is limited2 • The prescription of anticoagulation should be based on stroke risk assessed using the CHA2DS2-VASc scoring system1,2 References: 1. Amerena JV et al. Med J Aust 2013; 199: 592-7. 2. Kirchhof P et al. Eur Heart J 2016; 37: 2893-962. . Aim is to Identify Who Does NOT Need Anticoagulation • Stroke risk in AF is a continuum1 • The aim of risk assessment is to identify truly low-risk patients who do not need any antithrombotic therapy1 • Patients with stroke risk factors should be considered for oral anticoagulation therapy1,2 Understanding this paradigm shift in risk assessment is important to reduce the underuse of anticoagulant treatment that occurs despite evidence of efficacy in reducing stroke risk1,2 References: 1. Lane DA et al. Circulation 2012; 126: 860-5. 2. Kirchhof P et al. Eur Heart J 2016; 37: 2893-962. CHA2DS2-VASc to Assess Stroke Risk1 Risk Factor Score C ongestive heart failure/LV dysfunction H ypertension A ge ≥ 75 years D iabetes mellitus S troke/TIA/TE 1 1 2 1 2 V ascular disease (prior myocardial infarction, peripheral artery disease, or aortic plaque) A ge 6574 y S ex category (ie female gender) 1 1 1 Reference: 1. Lip GY et al. Chest 2010; 137: 263-72. Calculate Mr M’s CHA2DS2-VASc Score Mr M Aged 67 years Non-smoker, minimal alcohol intake Taking lisinopril 20 mg/day for hypertension Dyslipidaemia treated with statin BMI 30 kg/m2, waist circumference 91 cm Parameter Score Congestive Heart Failure/LVD? 0 Hypertension? +1 Age 6574 years +1 Age ≥75 years 0 Diabetes? 0 Stroke, TIA or thromboembolism? 0 Vascular disease? 0 Female gender? 0 Acting on CHA2DS2-VASc Score1,2 • CHA2DS2-VASc score of 0: recommendation is no antithrombotic therapy1,2 • Consider anticoagulation in women if CHA2DS2-VASc score = 2. Anticoagulation recommended if CHA2DS2-VASc score ≥ 3 • Consider anticoagulation in men if CHA2DS2-VASc score = 1. Anticoagulation recommended if CHA2DS2-VASc ≥ 21,2 References: 1. Kirchhof P et al. Eur Heart J 2016; 37: 2893-962. 2. Lane DA et al. Circulation 2012; 126: 860-5. Strategies to Minimise Bleeding Risk* • • • • • • Determine bleeding history1,2 Check for anaemia2 † 1,3 Consider use of PPI in patients with history of GI bleeding or ulcers Ensure good blood pressure control1,2 Avoid medications that increase bleeding risk, e.g. NSAIDs1,2 Patient education:2,4 – – – – Adherence to medication Avoid excessive alcohol consumption Awareness of risks for minor bleeds Signs and symptoms of GI bleed * Stroke and bleeding risk factors overlap, however a high bleeding risk should generally not result in withholding anticoagulation2 † PPIs may accelerate the absorption of warfarin and may reduce dabigatran exposure. PPIs are unlikely to influence the pharmacokinetics of factor Xa inhibitors.3 References: 1. Heidbuchel H et al. Europace 2015; 17: 1467-507. 2. Kirchhof P et al. Eur Heart J 2016; 37: 2893-962. 3. Agewall S et al. Eur Heart J 2013; 34: 1708-13, 13a-13b. 4. Abraham NS. Am J Gastroenterol Suppl 2016; 3: 2-12. Minor Bleeding • Minor bleeding, usually classified as ‘nuisance bleeding’, can occur with anticoagulant use: – Bleeds are usually temporary – Does not usually require anticoagulant discontinuation or dose adjustment – Is not predictive of major bleeding risk • If required can consider preventive interventions, e.g.: – Cauterisation of the intranasal arteries – Haemorrhoidectomy Reference: 1. Heidbuchel H et al. Europace 2015; 17: 1467-507. . Controlling Arrhythmia Address any Reversible Precipitating Causes1 • Weight loss in obese patients reduces AF episodes and symptoms2 – Obesity may also be a risk factor for ischaemic stroke, thrombo-embolism, and death in AF patients2 • AF is associated with obstructive sleep apnoea2 – Treatment of obstructive sleep apnoea reduces the recurrence of AF3 • Lifestyle factors2 – Smoking, alcohol and caffeine intake can precipitate AF4 References: 1. January CT et al. Circulation 2014; 130: 2071-104. 2. Kirchhof P et al. Eur Heart J 2016; 37: 2893-962. 3. Lavergne F et al. J Thorac Dis 2015; 7: E575-84. 4. NICE Clinical Guideline. 2014. www.nice.org.uk/guidance/cg180. Rate or Rhythm Control • Rate control and rhythm control:1 – can both improve AF-related symptoms – may preserve cardiac function, but neither have demonstrated a reduction in long-term morbidity or mortality • Selecting between these approaches depends on patient characteristics and preference e.g.:2 Rate control Rhythm control Advanced age Younger age Longstanding persistent AF More frequent episodes with severe symptoms References: 1. Kirchhof P et al. Eur Heart J 2016; 37: 2893-962. 2. Amerena JV et al. Med J Aust 2013; 199: 592-7. Rate Control • Rate control is an integral part of the management of AF patients, and is often sufficient to improve AF-related symptoms1 • Rate control should be considered as a first-line strategy except:2 – Where there is a reversible cause – In heart failure caused by atrial fibrillation – In new-onset atrial fibrillation – If atrial flutter is present that may require an ablation strategy to restore sinus rhythm References: 1. Kirchhof P et al. Eur Heart J 2016; 37: 2893-962. 2. NICE Clinical Guideline. 2014. www.nice.org.uk/guidance/cg180. Treatment for Rate Control1,2 • Initial monotherapy:1,2 – beta-blocker – nondihydropyridine calcium-channel blocker (e.g. verapamil, diltiazem) • If monotherapy does not control symptoms, combination therapy with any 2 of the following:1,2 – beta-blocker – diltiazem – digoxin • A target resting heart rate <110 bpm is reasonable if patients remain asymptomatic and left ventricular systolic function is preserved2,3 References: 1. January CT et al. Circulation 2014; 130: 2071-104. 2. NICE Clinical Guideline. 2014. www.nice.org.uk/guidance/cg180. 3. Kirchhoff P, Benussi S, Kotecha D et al. Eur Heart J.2016; 37 2893–962. Rhythm Control1,2 • Pharmacological and/or electrical options are available if rhythm control is required to restore sinus rhythm and reduce symptoms • Referral to a cardiologist may be required to determine the optimal approach to rhythm control for the patient References: 1. Kirchhof P et al. Eur Heart J 2016; 37: 2893-962. 2. Amerena JV et al. Med J Aust 2013; 199: 592-7. Summary • The different risk factors, aetiologies and presentations of AF that determine management • Stroke prevention and rate or rhythm control are the main approaches to management in stable patients Discussion among tables What would you now do for Mr M regarding his ongoing management? Summary Integrated Management of Patients with AF Reference: 1. Kirchhof P et al. Eur Heart J 2016; 37: 2893-962. Q&A Presentation end