Disclosures. Advances in Chronic Heart Failure Management 6/12/2017. Van N Selby, MD UCSF Advanced Heart Failure Program June 19, 2017

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Advances in Chronic Heart Failure Management Van N Selby, MD UCSF Advanced Heart Failure Program June 19, 2017 I have nothing to disclose Disclosures 1

Goal statement To review recently-approved therapies and updates to practice guidelines for chronic heart failure Overview New pharmacologic therapies for heart failure with reduced ejection fraction (HFrEF) New pharmacologic options for heart failure with preserved ejection fraction (HFpEF) Remote hemodynamic monitoring for heart failure Anemia and iron deficiency as a therapeutic target in chronic heart failure 2

Medical Therapy for HFrEF: 2013 Guidelines ACE Inhibitors (Class Ia) o ARB as an alternative (Class Ia) Beta-blockers (Class Ia) Mineralocorticoid receptor antagonists (Class Ia) Hydralazine/Isosorbide for African-Americans (Class Ia) Other: Diuretics, digoxin, etc Yancy CW et al, Circulation 2013 Angiotensin-Neprilysin Inhibition Vardeny O et al, JACC Heart Failure 2014 3

PARADIGM HF 8442 patients with class II, III, or IV chronic heart failure o EF < 35-40% o SBP 95, GFR 30, K 5.4 o Tolerated enalapril 10 mg daily or equivalent for 4 weeks Randomized to enalapril 20 mg daily vs sacubitril-valsartan 400 mg daily Primary outcome was a composite of cardiovascular death or HF hospitalization McMurray JJV et al, N Engl J Med 2014 McMurray JJV et al, N Engl J Med 2014 4

2016 Guideline Update III: Harm B-R p g ( ) ARNI should not be administered concomitantly with ACE inhibitors or within 36 hours of the last dose of an ACE inhibitor (31, 32). Yancy, CW et al. Circulation 2016 Sacubitril/Valsartan (Entresto TM ) Starting dose is 49/51 mg BID o Start with a reduced dose of 24/26 mg for those not previously taking ACE/ARB, or those on a low dose 36 hour washout period Double the dose after 2-4 weeks to a target dose of 97/103 mg The rate of hypotension was slightly higher than with enalapril, but did not lead to higher rates of study drug discontinuation $4500/year 5

Compared to enalapril, sacubitril/valsartan is: Associated with reduced risk of hyperkalemia when combined with al aldosterone antagonist 1 No more likely to cause severe hypotensive events 2 More cost-effective 3 1 Desai AS et al, JAMA Cardiology 2016 2 Vardeny O et al, HFSA Scientific Sessions 2016 3 Gaziano TA et al, JAMA Cardiology 2016 Ivabradine Heart rate is an independent predictor of mortality in heart failure Ivabradine is an inhibitor of the I f current in the SA node The SHIFT trial randomized 6558 patients: o Symptomatic HF with LVEF 35% o HR 70 in sinus rhythm o HF hospitalization in the past year o On background HF therapy including BB if tolerated Ivabradine (titrated to a max of 7.5 mg BID) vs placebo Swedberg K et al, Lancet 2010 6

Ivabradine: SHIFT Trial Swedberg K et al, Lancet 2010 2016 Guideline Update Recommendation for Ivabradine COR LOE Recommendation IIa B-R Ivabradine can be beneficial to reduce HF hospitalization for patients with symptomatic (NYHA class II-III) stable chronic HFrEF (LVEF 35%) who are receiving GDEM, including a beta blocker at maximum tolerated dose, and who are in sinus rhythm with a heart rate of 70 bpm or greater at rest (37-40). Yancy, CW et al. Circulation 2016 7

SHIFT Trial: Considerations No patients enrolled from the US Only 23% were on target dose beta-blocker o o Average systolic BP was 122 mmhg at enrollment There was no significant improvement in the primary outcome among patients taking at least 50% target dose beta-blocker at randomization Spironolactone for HFpEF Approximately 50% of all patients with heart failure have preserved ejection fraction No medical therapy has been proven to improve outcomes for these patients Mineralocorticoid receptor antagonists (MRA) improve outcomes in HFrEF and post-mi with LV dysfunction Small studies suggested MRAs may improve diastolic function 8

TOPCAT: Spironolactone for HFpEF The TOPCAT trial randomized patients with HFpEF to spironolactone vs placebo No significant difference in the primary composite outcome of cardiovascular death, aborted cardiac arrest, or HF hospitalization BUT, there were significant differences in the patient populations depending on country Pitt B, NEJM 2014 TOPCAT: Americas Sub Analysis Patients enrolled from the Americas more likely to have elevated BNP Patients enrolled on the basis of elevated BNP or NT- ProBNP did show a reduction in the primary outcome HR 0.82 HR 0.74 Pfeffer MA et al, Circulation 2014 9

Yancy, CW et al. Circulation 2017 Remote Hemodynamic Monitoring for HF Adapted from Adamson PB, et al. Curr Heart Fail Reports, 2009. 10

CardioMEMS 11

CHAMPION TRIAL NYHA Class III heart failure Previous HF hospitalization No ejection fraction criteria Randomized to a wireless implantable hemodynamic monitoring system vs control At least 6 months follow-up Primary outcome: re-hospitalization Abraham WT et al, Lancet 2011 CHAMPION Risk reduction: 36% Risk reduction: 29% Abraham WT et al, Lancet 2011 12

CardioMEMS Inserted via venous catheter, requires selective pulmonary angiogram (10 cc) No batteries or leads FDA approved May 2014 Indication: o Wirelessly measuring and monitoring PA and HR o In patients with functional class III heart failure with at least one hospitalization in the past year o Hemodynamic data are used by physicians with the goal of better HF management and to reduce hospitalization Abraham WT et al, Lancet 2011 Remote PA Pressure Monitoring: NNT Compared to Other HF Therapies Intervention Trial Mean Duration of Randomized Follow-Up Annualized Reduction in HF Hospitalization Rates NNT per year to Prevent 1 HF Hospitalization Beta-blocker COPERNICUS 10 months 33% 7 Aldosterone antagonist RALES 24 months 36% 7 CRT CARE-HF 29 months 52% 7 Beta-blocker MERIT-HF 12 months 29% 15 ACE inhibitor SOLVD 41 months 30% 15 Aldosterone antagonist EMPHASIS-HF 21 months 38% 16 Digoxin DIG 37 months 24% 17 Angiotensin receptor blocker Val-HeFT 23 months 23% 18 Angiotensin receptor blocker CHARM 40 months 27% 19 PA pressure monitoring CHAMPION 17 months 33% 4 13

CHAMPION According to LVEF Iron Deficiency: A therapeutic Target in HF Anemia is common in HF Treatment of mild to moderate anemia with Epo agents shows no clear benefit and is associated with increased risk of VTE in HF patients Up to 50% of patients with HF have also have iron deficiency o Defective absorption o Reduced availability of iron recycled in the reticuloendothelial system 14

Iron Deficiency in Heart Failure van Veldhuisen, D. J. et al. Nat. Rev. Cardiol 2011 FAIR HF Trial 459 patients with chronic HF and NYHA Class II or III symptoms LVEF 40% if class II or 45% if class III Hgb between 9.5 and 13.5 g/dl Iron deficiency: o Ferritin < 100 μg/l, or: o Ferritin 100-299 μg/l if transferrin % sat < 20% Randomized to ferric carboxymaltose vs placebo o 200 mg weekly until iron stores normal, then q 4 weeks Anker SD et al, NEJM 2009 15

CONFIRM-HF Ponikowski P et al. Eur Heart J 2015 16

Yancy, CW et al. Circulation 2017 Targeting Iron Deficiency in Heart Failure No significant difference in adverse events among those receiving IV iron vs placebo o No allergic reactions with newer formulations The benefits are seen regardless of serum hemoglobin High dose oral iron has not shown the same benefit in clinical trials FAIR-HF 2, a larger trial of IV iron in HF, is underway Lewis GD et al, JAMA 2017 17

Advanced Heart Failure: Know the Signs NYHA Class IIIB/IV symptoms Worsening renal function Systolic BP < 90 mmhg Multiple hospitalizations Inability to tolerate ACE inhibitors or beta-blockers o Need to stop or decrease LV ejection fraction < 25% High diuretic dose (> 100 mg/day of furosemide) Left Ventricular Assist Device Therapy 18

Adult Heart Transplant: Survival by Era All pair-wise comparisons were significant at p < 0.05. Median survival (years): 1982-1991=8.5; 1992-2001=10.4; 2002-2008=11.9; 2009-6/2014=NA J Heart and Lung Trans 2016 Conclusions New therapies continue to improve outcomes for patients with HFrEF o Sacubitril/valsartan improves HFrEF outcomes compared to ACEi o Ivabradine may be useful in selected HFrEF patients Consider aldosterone antagonists for appropriately selected patients with HFpEF Remote hemodynamic monitoring reduces heart failure rehospitalizations in patients at risk Patients with chronic HF should be screened for iron deficiency and those who meet criteria should be treated with IV iron Prompt referral to a HF center for those with signs of advanced disease 19

Thank you van.selby@ucsf.edu 20