Survey
* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
CCS Heart Failure Guidelines: 2014 Update On New Therapies, Biomarkers, Anemia Management, And Complex Cases October 2014 Disclaimer The Canadian Cardiovascular Society (CCS) welcomes reuse of our educational slide deck for medical institution internal education or training (i.e. grand rounds, medical college/classroom education, etc.). However, if the material is being used in an industry sponsored CME program, permission must be sought through our publisher Elsevier (www.onlinecjc.com). If your reuse request qualifies as medical institution internal education, you may reuse the material under the following conditions: • • • • www.ccs.ca You must cite the Canadian Journal of Cardiology and the Canadian Cardiovascular Society as references. You may not use any Canadian Cardiovascular Society logos or trademarks on any slides or anywhere in your presentation or publications. Do not modify the slide content. If repeating recommendations from the published guideline, do not modify the recommendation wording. Heart Failure Guidelines Anemia in HF Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines How prevalent is anemia in heart failure? • Rare? • Occasional? • Frequent? It Depends: -on the patient you are seeing (view next slide for range of anemia in patients) -on oms criteria (hemoglobin levels-note difference between male vs female) -characteristic of population; age, sex, race and degree of renal failure -on NYHA class Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines Anemia in patients with heart failure Hb = hemoglobin Hct = hematocrit HF = heart failure The prevalence of anemia in heart failure patients is approximately: – 30% for Inpatients – 20% for Outpatients Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines The prevalence of anemia and the severity of heart failure 70% 60% 56% 52% 60% Patients 50% 44% 40% 40% 30% 19% 14% 8% 13% 6% 2% 29% 21% 20% 20% 10% 30% 29% 11% 12% 4% 2% 0% I (n=158) II (n=467) III (n=340) IV (n=25) NYHA Class Hb<10g/dL (n=32) Hb<=11g/dL (n=97) Hb<=11.5g/dL (n=165) Hb<=12.0g/dL (n=244) Hb<=12.5g/dL (n=337) Source: STAMINA Registry – 45 General Cardiologist sites, n=673, 12 Academic sites (incl. HF Specialists), n=337 Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines What are the causes of anemia in HF patients? 1. 2. 3. 4. 5. Blood tests (too many) Blood lost (anywhere in GI system) Medications CKD Don’t know Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines Figure 1 - Mechanism of the development of anemia in heart failure ↓ Cardiac output ↓ Renal perfusion Activation RAAS Pro inflammatory Cytokines CKD Volume overload ACEi / ARB ↓ EPO secretion ↓ Bone marrow (response) Hemodilution ↓ Production Anemia Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines How important is anemia in your initial work up of a patient with heart failure? • • • • Limited Moderate Important What? Anemia is important because it has been linked to the prognosis of patients with HF: refer to following slides Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines Anemia is associated with increased risk for hospitalization in heart failure patients Study Design Alexander1 Retrospective cohort study of a population based HF database Polanczyk2 Prospective, single center, observational study N Anemia Risk Assessment Limitations 90,316 Anemia was an independent risk factor of 1-year rehospitalization (RR 1.162; 95% CI: 1.134 to 1.191) no confirmation of the HF diagnosis; undercounts of minorities and biased results. 205 Anemia was an independent predictor of 3-month rehospitalization (p=0.002) Too small of a population to resolve a small difference in readmission rates; role of confounding variables due to lack of control 906 Anemia was an independent predictor of 60-day death or rehospitalization (odds ratio of 0.89 per 1 g/dL increase in hemoglobin; 95% CI: 0.82 to 0.97) Anemia may have been caused by hemodilution in hospitalized patients Lack of data on transfusions or other treatments for anemia; study generalizability to non-study population OPTIME-CHF3 Retrospective chart review Kosiborod4 Retrospective chart review 2,281 Patients had 2% higher risk of 1-year rehospitalization for every 1% lower hematocrit (95% CI: 1.01 to 1.03; p=0.0002) COPERNICUS5 Randomized, double blind, placebo controlled trial 2,286 Anemia was an independent risk factor for 1-year morbidity (HF hospitalization) and mortality outcomes 1Alexander M, et al. Am Heart J. 1999;137:919-927 CA, et al. J Card Failure. 2001;7:289-298 3Felker GM, et al. Am J Cardiol. 2003;92:625-628 4Kosiborod M, et al. Am J Med. 2003;114:112-119 5Anker SD, et al. J Am Coll Cardiol. 2004;43(suppl A):Abstract 842-2 2Polanczyk Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines - Hemoglobin and mortality in heart failure patients Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines Hemoglobin and mortality % 35 Hgb 11.3 30 All cause mortality Hgb 12.8 25 Hgb 13.6 Hgb 15.7 20 Hgb 14.4 15 10 5 0 I II III IV V Haemoglobin quintiles Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines O’Meara et al. CHARM Investigators. Circulation 2006 What is the rationale for anemia correction? Potential benefits and risks of treating anemia in HF: Potential Benefits • Improved oxygen delivery • Improved exercise tolerance • Attenuate adverse remodeling • Improved Quality of Life • Antiapoptotic? • Decrease in hosp./death? Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines Potential Risks • Increased thrombosis • Platelet activation • Hypertension • Endothelial activation Adapted from Felker and O’Connor J Am Coll Cardiol. 2004;44:959-966. Randomized controlled trials play a critical role in advancing patient care through guidelines Clinical Trials Drug Discovery Guidelines Patient Outcomes Quality Indicators Caregiver Performance Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines Califf, R et al JACC 2002;40(11):1895-1901 Should I treat anemia in a patient with heart failure? 1. Yes 2. No 3. Refer to a) b) c) d) GP GI IM Next cardiologist Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines The decision to treat, not to treat, or to refer the patient is discussed in the 2014 Heart Failure Guidelines. Evidence to support treatment of anemia Table 1 Randomized, controlled studies with intravenous iron in patients with heart failure Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines van Veldhuisen, D. J. et al. (2011) Anemia and iron deficiency in heart failure: mechanisms and therapeutic approaches Nat. Rev. Cardiol. doi:10.1038/nrcardio.2011.77 The FAIR-HF trial Method Study design: The FAIR-HF trial was a randomized, double-blind, multicenter study. Study population: A total of 495 patients were enrolled in this study. Ambulatory patients who had chronic heart failure of NYHA class II or III, a LVEF of 40–45% or less, a hemoglobin level between 95 and 135 g/L and iron deficiency. Uncontrolled hypertension, other significant heart diseases and inflammation were some of the excluding factors. Treatment regimen: Ferric carboxymaltose or saline was administered to the patients randomly as an intravenous bolus injection of 4 ml. Dosing was done every week till repletion of iron was achieved and after that every 4 weeks as maintenance therapy after 8th or 12th week of initiation of therapy. End point: The primary end point was a self-reported Patient Global Assessment (PGA) form and NYHA functional class in the 24th week. Safety end points were serious and non-serious adverse effects, hospitalization and death up to the 26th week of study. Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines Noticed an improvement in intravenous iron, compared to placebo (note: scale is between 30-35 metres). The 6-minute-walk test aims to improve exercise tolerance and perception of symptomology. Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines The administration of ferric carboxymaltose in patients with chronic heart failure and iron deficiency with or without anemia was beneficial (seeing an improvement in symptomology). Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines The effect of intravenous iron Figure 4 Effect of intravenous iron (ferric carboxymaltose) in patients with heart failure and iron deficiency in various subgroups (including those with and without anemia). Seem to be responding to improvement in iron storage. Permission obtained from Massachusetts Medical Society © Anker, S. D. et al. Ferric carboxymaltose in patients with heart failure and iron deficiency. N. Engl. J. Med. 361, 2436–2448 (2009) van Veldhuisen, D. J. et al. (2011) Anemia and iron deficiency in heart failure: mechanisms and therapeutic approaches Nat. Rev. Cardiol. doi:10.1038/nrcardio.2011.77 Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines Anemia recommendations Recommendation We suggest that for patients with documented iron deficiency, oral or intravenous iron supplement be initiated to improve functional capacity (Weak Recommendation, Low-Quality Evidence). Values and Preferences: The iron supplement recommendation was derived mostly from the experience of clinicians, small clinical trials, and 2 large randomized controlled trials (RCTs). Practical Tip: Symptomatic patients with low transferrin and/or ferritin levels should be considered for supplementary iron therapy principally with a goal of improving symptoms Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines EPO therapy Advantages of EPO Therapy Disadvantages of EPO Therapy 1. Increase hemoglobin level 2. Increases peak O2 consumption 3. Improve functional class 4. Decreases ventricular remodeling 5. Improve cardiac and renal functions 6. Reduce diuretic dose 7. Reduce hospitalizations 8. Reduce mortality rate (small study) 1. Increase hypertension 2. Increase thrombosis 3. Increase endothelin activation 4. Expensive Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines RED-HF trial (Reduction of Events by Darbepoetin Alfa in Heart Failure) Available online at NEJM.org Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines I was hoping I’d be in the active therapy group. Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines Well, I was hoping I’d be in the placebo group. RED-HF trial Study Population •Hemoglobin 9 to 12 g/dL •LVEF ≤ 35% •NYHA Class II to IV Timelines Darbepoetin alfa group (target hemoglobin 13.0 to 14.5 g/dL) N = 1200 1:1 randomization Placebo group N = 1200 Follow-up Site Evaluation & Selection Approximately 620 global sites Began enrolling June 2006 Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines Event driven: ~1150 events Study End September 1 2012 KCCQ primary analysis: Change from baseline to month 6 KCCQ Overall Summary Score Mean Change From Baseline to Month 6 KCCQ Symptom Frequency Score Mean Change From Baseline to Month 6 10 P = 0.005 9 8 6.68 7 6 5 4.48 4 3 2 1 0 Placebo (n = 929) Darbepoetin alfa (n = 928) 2.46 95% CI: (0.90, 4.02) Change from Baseline in KCCQ Symptom Frequency Score Change from Baseline in KCCQ Overall Summary Score 2.20 95% CI: (0.65, 3.75) 10 P = 0.011 9 8 7 6.20 6 5 3.91 4 3 2 1 0 Placebo (n = 927) Darbepoetin alfa (n = 925) Mixed effects model estimating treatment effect adjusted for region, type of device, and baseline KCCQ score; scale scores range from 0 to 100, with higher scores indicating better functioning. Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines Data on file, Amgen. Prop. of Subject With Event (%) Primary outcome: All cause death or first hospitalization for worsening heart failure 100 Placebo Darbepoetin alfa Stratified Log-rank, p = 0.87 80 60 40 20 0 0 1 Subjects at risk: 1142 956 1136 975 2 4 5 Years of Randomization 818 855 695 712 591 581 Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca 3 Heart Failure Guidelines 497 473 395 385 290 281 211 212 154 161 92 101 Selected adverse events of interest Darbepoetin alfa (N = 1133) n (%) Ischaemic cerebrovascular conditions Embolic and thrombotic events Placebo Risk difference (N = 1140) (95% CI) p-value 51 (4.5) 32 (2.8) 1.7 (0.2, 3.2) 0.031 153 (13.5) 114 (10.0) 3.5 (0.9, 6.1) 0.009 Hypertension 81 (7.1) 69 (6.1) 1.1 (-0.9, 3.1) 0.292 Malignancies 69 (6.1) 68 (6.0) 0.1 (-1.8, 2.1) 0.900 Hypersensitivity reactions 99 (8.7) 96 (8.4) 0.3 (-2.0, 2.6) 0.787 Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines EPO recommendation Recommendation We recommend erythropoiesis stimulating agents not be routinely used to treat anemia in HF (Strong Recommendation, High-Quality Evidence). Values and Preferences: The recommendations against the use of erythropoiesis-stimulating agents (ESAs) were derived from robust data from RCTs. Practical Tip: Patients with severe chronic kidney disease and anemia should be referred to a nephrologist to seek the optimal therapy for anemia. Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines Conclusion 1. Identify anemia and potential causes; anemia is a marker of the severity of the disease (HF) 2. Evaluate 3. Consider treatment options Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines Biomarkers Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines Optimal use of biomarkers • Establishing diagnosis and selecting optimal therapy for any given patient are current challenges, as costs associated with HF diagnostic and therapeutic strategies continue to rise • Biomarkers may help stratify risk and individualize therapy • This update will review the role of circulating biomarkers for the management of patients with HF with a focus on its role in the monitoring for disease progression Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines B-type natriuretic peptides Increased myocardial wall stress due to volume or pressure overload activates the B-type natriuretic peptide (BNP) gene in cardiac myocytes, producing the intracellular precursor propeptide (proBNP). Cleavage releases the biologically active BNP and biologically inert amino-terminal fragment (NT-proBNP). BNP stimulates natriuresis and vasodilation with consequent afterload reduction, inhibits renin-angiotensin-aldosterone release and sympathetic nervous activity, and reduces fibrosis. Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines Diagnosis of heart failure • A 74 y.o. lady presents to ER with increased shortness of breath on exertion for 2 months, no chest pain • Known for hypertension and diabetes but has never had angina or a notion of coronary artery disease. No family history of CAD and stopped smoking 15 years ago but smoked 30 cigarettes a day for 40 years • Medications: Perindopril 4mg qd, Metformin 500mg bid, Calcium and Vitamin D • P/E: Pulse 82 bpm, BP 150/85mmHg, T 37.1, RR 16, JVP and carotids normal, S4 but otherwise cardiac auscultation is normal, mild bibasal crackles, unremarkable abdominal exam and no peripheral oedema Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines Optimal use of biomarkers • • • • Chest X-Ray: COPD, no clear signs of HF CBC normal E+, BUN, creatinine: normal High sensitivity troponin T: 21 µg/L (gives normal in your lab) Do you believe BNP or NT-proBNP could help you make the proper diagnosis? A) I really do not see how B) I know for sure what her diagnosis is C) I would rather check procalcitonin, as this must be infectious D) Yes, they could help me clarify whether or not this is HF E) It’s really too expensive and does not really help Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines Optimal use of biomarkers • Her NT-proBNP levels: 1600 pg/mL Recommendation We recommend that B-type NP (BNP)/amino-terminal fragment of propeptide BNP (NT-proBNP) levels be measured to help confirm or rule out a diagnosis of HF in the acute or ambulatory care setting in patients in whom the clinical diagnosis is in doubt (Strong Recommendation, High-Quality Evidence). Values and Preferences: These recommendations remain unchanged from previous CCS HF guidelines. Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines Natriuretic peptides for HF diagnosis Table 2. Natriuretic peptides cut points for the diagnosis of heart failure Age (years) HF is unlikely HF is very likely < 100 pg/ml HF is possible but other diagnoses need to be considered 100-500 pg/ml BNP All NT-proBNP < 50 < 300 pg/ml 300-450 pg/ml > 450 pg/ml 50 - 75 < 300 pg/ml 450-900 pg/ml > 900 pg/ml > 75 < 300 pg/ml 900 - 1800 pg/ml > 1800 pg/ml HF, heart failure Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines > 500 pg/ml The troubling case of Mr. B • Mr. B. is 70 y.o. and comes in your office in May 2012 for his follow-up (q 4 months). He lives 7 hours from your hospital and is followed by his GP and you, his cardiologist, for HF due to ischemic cardiomyopathy. The last echo (4 months) showed and EF of 25%, severe functional MR, Mild RV dysfunction, moderate to severe TR, PAPs 55mmHg • He still smokes 10 cigarettes/day, has COPD, respects his water and salt intake limits and takes his medications • He has had prior myocardial infarctions and coronary bypasses in 2001, has no ischemia but a large scar on his nuclear scan done 4 months ago. His ICD was implanted in primary prevention in 2005, he had a narrow QRS. He never had ICD therapies. Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines The troubling case of Mr. B • Current medications: ASA 80mg qd, Bisoprolol 10mg qd, Candesartan 16mg bid, Spironolactone 25mg qd, Furosemide 80mg bid • Mr. B’s NYHA class often varies between 2 and 3. Today he reports being more short of breath (definitely NYHA 3) for about 6 weeks but he is stressed with financial and family issues. He seems depressed and worried • He did not cough more than usual and did not have fever • On physical examination: well perfused, very thin, pulse 60 (NSR), BP 95/55mmHg (usual), JVP 12 (V wave nadir), S3+, holosystolic apical murmur 3/6, clear lungs, mild peripheral oedema. ECG: SR, right ventricular pacing • His last labs were done with his GP 3 weeks ago and showed stable Hb 125g/L and creatinine 120umol/L, K 4.0 Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines What would you do? A) Increase furosemide to 120mg bid and send him back to his GP until next time (4 months) B) Ask for NP levels today at your hospital and then decide what to do C) Add digitalis to his therapy D) Refer him for Mitra-Clip evaluation E) All of the above Note: There is no HF clinic closer to where he lives and his GP seems him every 3-4 weeks Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines What we did: His NT-proBNP level was 7500 (prior was 3700) and his creatinine up to 142umoL/L. We did increase his diuretics but also reevaluated all potential means of improving his outcome (was referred for Mitra-Clip evaluation). Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines Recommendations Recommendation We recommend measurement of BNP/NT-proBNP levels be considered in patients with an established diagnosis of HF for prognostic stratification (Strong Recommendation, High-Quality Evidence). We suggest, in ambulatory patients with HF due to systolic dysfunction, measurement of BNP or NT-proBNP to guide management should be considered to decrease HF-related hospitalizations and potentially reduce mortality. The benefit is uncertain in individuals older than 75 years of age (Weak Recommendation, Moderate-Quality Evidence). Values and Preferences: These recommendations are based on multiple small RCTs, most of which demonstrated benefit, and 3 meta-analyses, which universally demonstrated benefit. It is realized that there is still a large RCT ongoing that might modify the conclusions. Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines Evidence for NP-guided therapy • In the available trials, 3 systematic reviews and meta-analyses (Figures) synthesizing the RCT results, NP-guided therapy has been shown to improve survival and reduce hospitalizations • In these studies, NP-guided therapy had no benefits in 2 subgroups: age >75 years and those with HFpEF • Consequently, a larger multicenter trial of a single-target NP level (NTproBNP 1000 pg/ml) and the use of guideline-approved therapies in both treatment arms is now underway, the Guiding Evidence Based Therapy Using Biomarker Intensified Treatment (GUIDE-IT, NCT01685840) • The ongoing single-centre EX-IMPROVE-CHF, NCT00601679) will also help clarify the role of NP-guided therapy in HF management Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines Effect of NP-guided management on mortality: hazard ratios from meta-analysis Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines Effect of NP-guided management on HF hospitalizations: HRs from meta-analysis Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines What’s a significant change in NP level? • A change of 30% in NP level likely exceeds the day to day variation and is in general considered relevant. • For ambulatory patients with HF evaluated in the clinic, a NP level that increases more than 30% should therefore call for more intensive follow up and/or intensified medical treatments, even if they are not congested clinically. • The latter can include diuretic therapy or intensification of ACE inhibitors, β-blockers and mineralocorticoid receptor antagonists if their doses are not yet at the targets defined by clinical trials. Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines Pre-discharge NP levels • Besides predicting prognosis of patients in general, BNP level obtained pre-discharge has been associated with mortality and rehospitalization. • Indeed, predischarge NP in conjunction with change in NP has now been incorporated into a risk score for death and readmission of HF in patients admitted with HF. Salah K, Kok WE, Eurlings LW et al. ELAN-HF Score. Heart 2014;100(2):115-125. Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines Pre-discharge NP levels Recommendation We suggest that measurement of BNP or NT-proBNP in patients hospitalized for HF should be considered before discharge, because of the prognostic value of these biomarkers in predicting rehospitalization and mortality (Strong Recommendation, Moderate-Quality Evidence). Values and Preferences: This recommendation is based on multiple small RCTs, all of which demonstrated an association with clinical outcomes. Although the risk of readmission is decreased with lower NP levels, clinicians should also consider the limitations of delaying discharge from the hospital for this purpose. Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines Preventing heart failure • The preliminary results of STOP-HF and PONTIAC trials suggest that a NP guided strategy for at-risk individuals may provide benefit in both preventing and treating HF, leading to reductions in cardiac mortality and hospitalizations. • Asymptomatic individuals at high risk for the development of HF but without established heart disease: Subjects with hypertension, hypercholesterolemia, obesity, known vascular disease, diabetes, arrhythmia requiring treatment, valvular abnormalities. Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines Preventing heart failure Practical Tip: We suggest that individuals with risk factors for the development of HF, NP levels be used to implement strategies to prevent HF. An increased level of NP of BNP > 100 pg/mL and NT-proBNP > 300 pg/mL, higher values than those used in the 2 trials discussed below to avoid over screening, along with the presence of risk factors for HF, should at least trigger more intensive follow up (See Prevention of HF in CJC Published Article). Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines Algorithm of the use of natriuretic peptides Patient Population Risk factors for HF Natriuretic Peptide Level Actions NT-proBNP > 300 g/mL More frequent follow up, consideration of intensification of existing therapy BNP > 100 g/mL Stable ambulatory HF > 30% from clinic baseline value More frequent follow up ± intensification of HF therapy Hospitalized for HF and before discharge > 30% from admission value Discharge if relatively free from congestion Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines Other biomarkers ready for clinic? Biomarkers Pathophysiological HF populations Advantages targeted pathways / comorbid conditions with prognostic implications Potential benefits Challenges before implementation NGAL Renal Function Acute HF Early detection of renal function deterioration Adjusting therapy to improve prognosis by avoiding acute renal failure progression Unclear if using NGAL in acute HF to modify therapies improves clinical outcomes Cystatin C Renal Function Acute and chronic HF More sensitive detection of changes in renal function Same as above Unclear if using Cystatin C, over using eGFR, to modify clinical management provides further clinical benefit Cardiac hstroponins Myocyte death Acute and Chronic HF Very sensitive marker predicting higher risk of CV events regardless of etiology Optimization of therapy in patients with elevated hs-cTn should be more aggressive Prognostication improves only for mortality and use to modify therapy has not been tested ST2 Fibrosis / inflammation / immunity Acute and chronic HFrEF, HFpEF and previously low EF recovered Additional prognostic value beyond NPs suspected Low week-to-week variations Could provide additional value for short and long term prognostication, regardless of LVEF Unclear if using ST2 in acute HF to modify therapies improves clinical outcomes; Galectin-3 Cardiac and vascular fibrosis Incident HF, HFrEEF and HFpEF Early detection of risk and long term prognostication in HF Preventive measures and therapy optimization based on levels could improve outcomes Recent study showed ST2 superior to Galectin-3 in a multivariable prediction model Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines Clinical trials that might influence practice Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines HF – Preserved ejection fraction • No therapy specifically recommended for HF-PEF with “strong” • Complicated phenotype(s) and trial design(s) • Different patient demographics • Many pharmacologic and non-pharmacologic interventions have been tried: • ACE, ARB, BB, exercise, etc • Recently: mineralocorticoid antagonists (TOPCAT) Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines TOPCAT • International, multi-center, double-blind, placebo-controlled RCT • NIH Sponsored • Significant CAN involvement: Sites, Exec, Country Leaders • Randomization, 1:1 – Spironolactone, 15, 30, 45 mg daily – matching placebo • Primary outcome: CV death, HF hosp, or aborted cardiac arrest • Assumed: 3-year placebo rate of 17.4% Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines Desai, Rationale and design, Am Heart J 2011 Pfeffer, TOPCAT NEJM 2013 TOPCAT: Eligibility criteria • Inclusion: – – – – Symptomatic Heart Failure Age ≥ 50 LVEF ≥ 45% stratified according to: • HF Hospitalization within the past year, or • Elevated natriuretic peptides • Major Exclusion: – eGFR<30 mL/min/1.7m2 – potassium ≥5 mmol/L – uncontrolled hypertension, AF with rate > 90/min, recent ACS, restrictive, infiltrative, or hypertrophic cardiomyopathy – BNP ≥100 pg/mL – NT-proBNP ≥360 pg/mL Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines Desai, Rationale and design, Am Heart J 2011 Pfeffer, TOPCAT NEJM 2013 TOPCAT: Baseline characteristics N=3445 pts Age, median (IQR), years 67 (61-76) Female, % 52 Ejection Fraction, median, % 56 Diabetes, % 33 Atrial Fibrillation, % 35 eGFR, median, IQR 65 (54, 79) < 60 (ml/min/1.73m2) 39% Eligibility Stratum, % Hosp. for HF Natriuretic Peptide 72 29 ACE-I or ARB Beta-blocker Diuretic 84 78 81 Medications, % Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines S. Shah Circ HF 2012 TOPCAT: Primary outcome (CV Death, HF Hosp, or Resuscitated Cardiac Arrest) 351/1723 (20.4%) Placebo 320/1722 (18.6%) Placebo Spironolactone HR = 0.89 (0.77 – 1.04) p=0.138 Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines Pfeffer, TOPCAT NEJM 2013 TOPCAT: Enrollment strata • BNP/NT-proBNP: • Prior HF hosp: 28.5% 71.5% Spiro event rate Placebo event rate Hazard Ratio (95% CI) P-value Natriuretic peptide 15.9% 23.6% 0.65 (0.49-0.87) 0.003 Heart Failure Hosp 19.6% 19.1% 1.01 (0.84-1.21) 0.923 Enrolled by: *P=0.013 for interaction Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines Pfeffer, TOPCAT NEJM 2013 TOPCAT: Placebo event rates Placebo: 280/881 (31.8%) US, Canada, Argentina, Brazil 12.6 per 100 pt-yr Russia, Rep Georgia 2.3 per 100 pt-yr Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines Placebo: 71/842 (8.4%) Pfeffer, TOPCAT NEJM 2013 TOPCAT: Regional strata Placebo: 280/881 (31.8%) US, Canada, Argentina, Brazil HR=0.82 (0.69-0.98) Interaction p=0.122 Placebo: 71/842 (8.4%) Russia, Rep Georgia HR=1.10 (0.79-1.51) Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines Pfeffer, TOPCAT NEJM 2013 TOPCAT: Regional strata • Fully adjusted model for primary endpoint including region and other variables: – HR 0.85, 95%CI 0.73 to 0.99, p=0.043 – “15% relative risk reduction for the primary endpoint in favor of spironolactone” Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines Pfeffer, TOPCAT NEJM 2013 TOPCAT: Safety • Doubling in the rate of hyperkalemia: • 9.1% in the placebo group • 18.7% in the spironolactone group – no deaths due to hyperkalemia • Fewer events of hypokalemia • No renal failure leading to dialysis Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines HF-PEF Recommendation Recommendation We suggest that in individuals with HFpEF, an increased NP level, serum potassium < 5.0 mmol/L, and an estimated glomerular filtration rate (eGFR) ≥ 30 mL/min, a mineralocorticoid receptor antagonist like spironolactone should be considered, with close surveillance of serum potassium and creatinine (Weak Recommendation, Low-Quality Evidence). Values and Preferences: This recommendation is based on a prespecified subgroup analysis of the Treatment of Preserved Cardiac Function Heart Failure with an Aldosterone Antagonist (TOPCAT) trial, which includes analysis of the predefined outcomes according to admission NT-proBNP level, and the corroborating portion of the trial conducted within North and South America. Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines HF – Reduced ejection fraction • Current GDMT (ACE or ARB, BB and MRA) reduces the risk of mortality, hospitalization and improves quality of life • Multiple, adequately powered RCT • Residual risk despite GDMT Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines HF – Reduced ejection fraction • Cumulative reduction in the odds of death over 2 years compared with no treatment Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines Fonarow G C et al. J Am Heart Assoc 2012;1:16-26 PARADIGM-HF • International, multi-center, double-blind, placebo-controlled RCT • Randomization, 1:1 – LCZ696 200 mg BID – Enalapril 10 mg BID • Primary: composite of CV death and/or hospitalization for HF Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines McMurray NEJM 2014 Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines Vardeny CPT 2013 PARADIGM-HF: Eligibility criteria Inclusion: •NYHA II-IV HF •LVEF ≤40 % [≤35% amend] •Elevated NPs – BNP ≥150 pg/mL – NT-proBNP ≥600 pg/mL Inclusion (con’t) Any ACEi or ARB, but able to tolerate stable dose equivalent to at least enalapril 10 mg daily for at least 4 weeks Major Exclusion: •Guideline-recommended use of beta-blockers and mineralocorticoid •SBP < 95 mmHg receptor antagonists •eGFR < 30 ml/min/1.73 m2 •K > 5.4 mEq/L Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines McMurray NEJM 2014 PARADIGM-HF: Design Single-blind run-in period Double-blind period LCZ696 200 mg BID Enalapril LCZ696 Rand’n 10 mg BID 100 mg BID 200 mg BID Enalapril 10 mg BID 2 weeks N=1102 1-2 weeks 2-4 weeks N=977 N=8399 patients Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines McMurray NEJM 2014 PARADIGM-HF: Baseline chars. Age (years) Women (%) Ischemic cardiomyopathy (%) LV ejection fraction (%) NYHA functional class II / III (%) Systolic blood pressure (mm Hg) Heart rate (beats/min) N-terminal pro-BNP (pg/ml) B-type natriuretic peptide (pg/ml) History of diabetes Beta-adrenergic blockers Mineralocorticoid antagonists ICD and/or CRT LCZ696 (n=4187) Enalapril (n=4212) 63.8 ± 11.5 21.0% 59.9% 29.6 ± 6.1 71.6% / 23.1% 122 ± 15 72 ± 12 1631 (885-3154) 255 (155-474) 35% 93.1% 54.2% 16.5% 63.8 ± 11.3 22.6% 60.1% 29.4 ± 6.3 69.4% / 24.9% 121 ± 15 73 ± 12 1594 (886-3305) 251 (153-465) 35% 92.9% 57.0% 16.3% Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines McMurray NEJM 2014 PARADIGM-HF: Primary endpoint Kaplan-Meier Estimate of Cumulative Rates (%) 4 0 3 2 Enalapril 1117 (n=4212) 914 2 4 LCZ696 (n=4187) 1 6 HR = 0.80 (0.73-0.87) P = 0.0000002 Number needed to treat = 21 8 0 0 180 540 4187 4212 3922 3883 3663 3579 3018 2922 Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca 720 900 1080 1260 896 853 249 236 Days After Randomization Patients at Risk LCZ696 Enalapril 360 Heart Failure Guidelines 2257 2123 1544 1488 McMurray NEJM 2014 PARADIGM-HF: CV death Kaplan-Meier Estimate of Cumulative Rates (%) 32 Enalapril HR = 0.80 (0.71-0.89) P = 0.00004 Number need to treat = 32 24 (n=4212) 693 558 16 LCZ696 8 (n=4187) 0 0 180 540 4187 4212 4056 4051 3891 3860 3282 3231 Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca 720 900 1080 1260 1005 994 280 279 Days After Randomization Patients at Risk LCZ696 Enalapril 360 Heart Failure Guidelines 2478 2410 1716 1726 McMurray NEJM 2014 PARADIGM-HF: All cause mortality Kaplan-Meier Estimate of Cumulative Rates (%) 32 Enalapril HR = 0.84 (0.76-0.93) P<0.0001 835 (n=4212) 24 711 16 LCZ696 (n=4187) 8 0 0 180 540 4187 4212 4056 4051 3891 3860 3282 3231 Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca 720 900 1080 1260 1005 994 280 279 Days After Randomization Patients at Risk LCZ696 Enalapril 360 Heart Failure Guidelines 2478 2410 1716 1726 McMurray NEJM 2014 PARADIGM-HF: endpoints LCZ696 (n=4187) Enalapril (n=4212) Hazard Ratio (95% CI) P Value Primary endpoint 914 (21.8%) 1117 (26.5%) 0.80 (0.73-0.87) 0.0000002 Cardiovascular death 558 (13.3%) 693 (16.5%) 0.80 (0.71-0.89) 0.00004 Hospitalization for heart failure 537 (12.8%) 658 (15.6%) 0.79 (0.71- 0.89) 0.00004 Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines McMurray NEJM 2014 PARADIGM-HF: Safety endpoints Prospectively identified adverse events Symptomatic hypotension Serum potassium > 6.0 mmol/l Serum creatinine ≥ 2.5 mg/dl Cough Discontinuation for adverse event Discontinuation for hypotension Discontinuation for hyperkalemia Discontinuation for renal impairment Angioedema (adjudicated) Medications, no hospitalization Hospitalized; no airway compromise Airway compromise Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines LCZ696 (n=4187) Enalapril (n=4212) P Value 588 181 139 474 449 36 11 29 388 236 188 601 516 29 15 59 < 0.001 0.007 0.007 < 0.001 0.02 NS NS 0.001 16 3 0 9 1 0 NS NS ---McMurray NEJM 2014 Is 1 trial enough? Do we need to do another trial to obtain regulatory approval/change clinical practice? Number of trials with P < 0.05 showing efficacy P value required in a single trial to provide same strength of evidence 1 0.05 2 0.00125 3 0.00003125 4 0.00000078 5 0.0000000195 PARADIGM-HF: Effect on primary endpoint PARADIGM-HF: Effect on cardiovascular death 0.00008 0.0000004 Based on formula (0.025)n x2 (personal communication Stuart Pocock) Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines Slide courtesy of J McMurray HF – Reduced ejection fraction Recommendation We recommend that in patients with mild to moderate HF, an EF ≤ 40%, an elevated NP level or hospitalization for HF in the past 12 months, a serum potassium < 5.2 mmol/L and an eGFR ≥ 30 mL/min and treated with appropriate doses of guideline-directed medical therapy should be treated with LCZ696 in place of an ACE inhibitor or an angiotensin receptor blocker, with close surveillance of serum potassium and creatinine (Conditional Recommendation, High-Quality Evidence). Values and Preferences: This recommendation places high value on medications proven in large trials to reduce mortality, HF rehospitalization, and symptoms. It also considers the health economic implications of new medications. The recommendation is conditional because the drug is not yet approved for clinical use in Canada and the price is still not known. Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines Appendix: Useful CCS Heart Failure Guideline Algorithms Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines Algorithm for Prevention and Treatment of Clinically Stable Heart Failure Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines Referral Pathway for Device Therapy in Patients with Chronic Heart Failure Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines Acute Heart Failure – Diagnosis Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines Acute Heart Failure – Acute Management Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines Approach to Assessment for CAD in Patients with HF Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines Decision Regarding Coronary Revascularization in HF Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines Algorithm for Management of Different Stages of HF using Natriuretic Peptides Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines Appendix: CCS Heart Failure Guideline Resources Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines Looking for best practices in heart failure diagnosis and management? To access this tool, and to view all of our guideline resources, please visit www.ccs.ca. Moe GW, Ezekowitz JA et al., Can J Cardiol www.ccs.ca Heart Failure Guidelines