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Heart Failure Associate Professor Rob Doughty Dept of Medicine, The University of Auckland & Green Lane Cardiovascular Service, Auckland City Hospital • Acute Heart Failure • Chronic heart failure – Pharmacotherapy – “failed” therapies – Device-based therapies – Newer therapeutics The Rotterdam Study Bleumink GS et al. Euro Heart J 2004;25:1614-19 • Population-based cohort of 7,983 people age 55 • 30% of individuals age 55 years will develop HF in their remaining life Hospital Admissions for Heart Failure • Incidence and prevalence data are relatively difficult to obtain • Hospitalisation data are often used as surrogates • Rely on discharge coding • Reasonable reflection of the burden of heart failure • Used for planning healthcare delivery Aging Population 90+ 90+ 85-89 85-89 Male Female 90+ Male Female 85-89 80-84 80-84 80-84 75-79 75-79 75-79 70-74 70-74 70-74 65-69 65-69 65-69 60-64 60-64 60-64 55-59 55-59 55-59 50-54 50-54 50-54 45-49 45-49 45-49 40-44 40-44 40-44 35-39 35-39 35-39 30-34 30-34 30-34 25-29 25-29 25-29 20-24 20-24 20-24 15 - 19 15 - 19 15 - 19 10 - 14 10 - 14 10 - 14 5-9 5-9 5-9 0-4 0-4 0-4 Male Female 7 6 5 4 3 2 1 0 1 2 3 4 5 6 7 7 6 5 4 3 2 1 0 1 2 3 4 5 6 7 7 6 5 4 3 2 1 0 1 2 3 4 5 6 7 Percent Percent Percent 2001 2021 1986 Source: Statistics NZ Mortality from Cardiovascular Disease Source: NZ Heart Foundation Technical Report No 82 Jan 2004 Incidence and Prevalence of HF Levy D et al. NEJM 2002;347:1397 • Incidence & prevalence strongly age related • Incidence – 50’s 2 per 1000, 80’s 40 per 1000 • Prevalence – 2-3%, increasing to 8-10% in elderly populations Trends in Hospitalisations for HF Stewart S et al. EHJ 2001;22:209-217 Acute Heart Failure • • • • Definition Incidence and prevalence Hospitalisations Management – Patient characteristics – Aetiology – Treatment Definition of Heart Failure ESC HF Guidelines EHJ 2005;26:1115-1140 1. Symptoms of heart failure (rest or exercise) 2. Objective evidence of cardiac dysfunction and in cases where diagnosis remains in doubt 3. Response to treatment directed at HF Definition of Heart Failure ESC Acute HF Guidelines EHJ 2005;26:384-416 Acute heart failure defined as rapid onset of symptoms and signs, secondary to abnormal cardiac function • With or without previous cardiac disease • Systolic or diastolic dysfunction, abnormal rhythm, preload and afterload mismatch • Often life-threatening Several Distinct Clinical Conditions ESC Acute HF Guidelines EHJ 2005;26:384-416 1. Acute decompensated HF May be de novo or as decompensated HF Symptoms relatively mild and not 2-4 below 2. Hypertensive AHF 3. Pulmonary oedema and severe respiratory distress 4. Cardiogenic shock 5. High output HF 6. Right-sided acute HF Low output syndrome with increased JVP, hepatomegaly and hypotension Patient Characteristics Cleland JGF et al. EHJ 2003;24:442-463 Survey of 11,327 HF cases in Europe • Mean age 71 yrs, 47% women • 65% prior diagnosis of HF • 44% prior admission for HF Presentation • 40% acute dyspnoea • 35% exertional dyspnoea / oedema • 19% acute coronary syndrome • 9% atrial fibrillation Patient Characteristics Cleland JGF et al. EHJ 2003;24:442-463 Admission • 50% general medical wards • 11 days average length of stay Death rates: • 6.9% during index admission • 13.5% at 3 months Aetiology of Heart Failure • Heart failure clinical syndrome with underlying cause • Underlying cause often not focused on • Hypertension & coronary disease commonest causes Aetiology of Heart Failure Fox KF et al. EHJ 2001;22:228-236 Acute HF: Levosimendan • Levosimendan calcium sensitiser and vasodilator • Previous trials showing efficacy SURVIVE • Levosimendan vs. Dobutamine in patients with acute decompensated HF • 1327 patients • Primary end point: – all cause mortality at 180 days Mebazza A et al. JAMA 2007;297:1883 SURVIVE Trial Mebazza A et al. JAMA 2007;297:1883 Proposed Effects of Nesiritide Hemodynamic Vasodilation: • Veins • Arteries • Coronary arteries BNP Cardiac • Lusitropic • Anti-remodeling • Anti-fibrotic Neurohormonal • Aldosterone • Endothelin-1 • Noradrenaline Renal • Diuresis • Natriuresis Nesiritide • Smaller trials demonstrating short term efficacy • FDA approval in 2001 • Acute decompensated HF • Subsequent meta-analyses suggesting potential adverse effects Nesiritide Hauptman PJ, et al. JAMA 2005;296:1877 Data from 491 US hospitals, 385,627 admissions for HF Any iv Vasodilator Nesiritide GTN FUSION II Trial Out-patient based treatment, nesiritide 1 or 2 weekly LVEF <40%, Class III/IV HF Event Free Survival 1 Week 12 All Nesiritide All Placebo 0.8 0.6 0.4 P=0.791 HR (95% CI) 1.03 (0.82, 1.30) 0.2 0 0 2 4 6 8 10 12 14 Weeks 16 18 20 22 24 Chronic Heart Failure Neurohormonal Status in Heart Failure • SNS • RAAS • Vasopressin • Endothelin-1 • ?Urotensin II CONSTRICTION DILATATION • Natriuretic peptides • Nitric oxide • Vasodilatory PGs • Adrenomedullin • Urocortin Neurohormonal Antagonists Annual Mortality (%) 10 5 0 Diuretics + Digoxin + ACEi + ACEi + b-blocker Cleland meta-analysis; Lechat meta-analysis Secular Trends in Survival For Patients with HF Patients with Reduced LVEF Patients with Preserved LVEF Owan TE, et al. N Engl J Med 2006;355:251-9 C O SE 19 N 86 SU S 19 8 19 8 SO 1 89 LV 99 D 0 R 19 x 92 19 9 19 3 9 19 4 95 19 9 19 6 97 19 R M A 98 ER LE IT S -H 20 F 0 20 1 02 20 0 20 3 04 N % Mortality Mortality After Hospital Admission for HF Wasywich C. CSANZ 2007 45 40 35 30 12-month 25 6-month 20 15 30-day 10 5 0 Year CHARM Trial Programme: Summary CHARM Alternative CHARM Added ACEi intolerant pt Candesartan + ACEi Lancet 2003;362:772 Lancet 2003;362:767 ARB suitable alternative to ACEi Some additive benefit of addition of ARB to ACEi but…..beware adverse effects Long-Term Effects of Treatment CONSENSUS I Trial 10-year FU 1-year FU Recent “Failed” Phase III HF Trials Class Drug Trial TNF blockade Etanercept RENEWAL Packer Circ 2002;106:920 Vasopeptidase Omapatrilat OVERTURE inhibition Mann Circ 2004;1091594 Endothelin blockade Bosentan ENABLE “Failed” Drugs in Heart Failure Increase mortality (sudden death) with: • • • • • Milrinone Flosequinan Ibopamine Moxonidine Class I antiarrhythmics Emerging Drug Therapies in HF • Ranolazine (metabolic agent) • Ivabradine (If channel inhibitor) • Erythropoietin • Eplerenone • HMGcoA reductase inhibitors • Levosimendan • Adenosine agonists • NEP/ECE inhibitors • AGE cross-link breakers • Vasopressin antagonists • Immune modulation therapy • Nesiritide • Rosuvastatin • Copper chelation agents Vasopressin System Arterial underfilling Hyperosmolality Baroreceptors • Left atrium Hypothalamus • Carotid sinus • Supraoptic nucleus • Aortic arch • Paraventricular nucleus Vascular smooth muscle AVP Collecting duct of kidney V1a receptors V2 receptors Vasoconstriction Water re-absorption OPC-31260 SR121463 Tolvaptan Lixivaptan VP-343 FR-161282 OPC-21268 Relcovaptan Conivaptan JTV-605 CL-3 85004 Adapted from Sanghi et al Eur Heart J 2005 EVEREST Outcome Trial Konstam MA, et al. JAMA 2007;297:1319 • Efficacy of Vasopressin Antagonism in Heart failure Outcome Study with Tolvaptan • Tolvaptan (30mg/d) vs. placebo • 4133 patients with LVEF < 40% • Outcomes: – All-cause mortality – CVS death or hospitalisation for worsening HF • Follow up minimum 60 days, median 9 months EVEREST Outcome Trial Konstam MA, et al. JAMA 2007;297:1319 All-Cause Mortality CVS Death or Hospitalisation for HF Anaemia and HF Erythropoietin in HF Mancini DM, et al. Circulation 2003;107:294 • 26 patients, EPO vs. placebo, 6 months • End points: Hb and Peak Vo2 Haemoglobin VO2 Potential Benefits of EPO • Prevention of apoptosis • Endothelial progenitor cell mobilisation • Induction of angiogenesis/ neovascularisation • Limitation of ischaemia/reperfusion injury Biventricular Pacing • LBBB common in HF patients • “Dysynchrony” between ventricles • Biventricular pacing (cardiac resynchronisation therapy, CRT) – Pace right and left ventricle (via lead in coronary sinus) – Improved cardiac output in severe HF – Improved quality of life – Improved survival Implantable Defibrillators • Small implantable devices like pacemakers • Able to deliver small electric shock across the heart to terminate ventricular arrhythmias • Improved survival in patients with chronic heart failure SCD-HeFT: Amiodarone or ICD in CHF G Bardy et al. NEJM 2005;352:225-37 • 2521 patients with HF, NYHA II/III, LVEF <35%, ICD vs. amiodarone vs. placebo • Absolute Risk Reduction at 5yrs = 7.2% Device-Based Therapy in HF Cardiac resynchronisation therapy • Patients with sinus rhythm, wide QRS on ECG (>120msec), LVEF <35%, moderate to severe symptom Implantable defibrillators • Prophylactic ICD for patients with LVEF<30% and mild to moderate symptoms HF with Preserved LVEF Inclusion End-Points Duration Drug CHARM CHF, age>70 EF>40% Mortality Hosp 1 yr Candesartan PEP-CHF CHF, age>70 EF>40% Mortality Hosp 2 yrs Perindopril I-PRESERVE CHF, age>60 Mortality EF>45% CVS Hosp 2 yrs Irbesartan TOP CAT CHF EF>45% 3 yrs Aldo antag Mortality Hosp ACEi in HF with Preserved EF CHARM Preserved PEP-CHF CVS Death or HF Hospitalisation Death or HF Hospitalisation Yusuf S, et al. Lancet 2003;362:777-781 Cleland JGF, et al. EHJ 2006;27:2338 Treatment Heart Failure with Preserved LVEF Disease targeted therapy • Hypertension – BP target levels – Prevent / regress LVH • Atrial fibrillation – Control rate, anticoagulation • Coronary artery disease – Prevention / revascularisation • Diabetes / metabolic syndrome • Other – Anaemia, CRF, arrhythmias (esp. AF) Diabetes and HF Haas SJ et al. Am Heart J 2003;146:848 Diabetes worse Diabetes and HF • Specific therapies for patients with diabetes and heart failure – Metformin and improved outcomes in HF (PHANTOM Study) – AGE cross-link breakers in diastolic HF (Alteon) – Copper chelation Summary • Acute heart failure – Pathophysiology – Aetiology – treament • Chronic heart failure – Established therapies – “Failed” therapies – Device-based therapies • Specific patient subgroups – Disease specific – Patient specific