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2017 /H/HFS Focused Update of the 2013 F/H 6.3.1 Biomarkers for Prevention: Recommendation OR LOE Recommendation a For patients at risk of developing HF, natriuretic peptide biomarker-based screening followed by team-based care, including a cardiovascular specialist optimizing GDMT, can be useful to prevent the development of left ventricular dysfunction (systolic or diastolic) or new onset HF. NEW: New data suggest that natriuretic peptide biomarker screening and early intervention may prevent HF. 6.3.2 Biomarkers for Diagnosis: Recommendation OR LOE Recommendation n patients presenting with dyspnea, measurement of natriuretic peptide biomarkers is useful to support a diagnosis or exclusion of HF, especially in the setting of clinical uncertainty. MODFED: 2013 acute and chronic recommendations combined into diagnosis section. 6.3.3 Biomarkers for Prognosis or dded Risk Stratification: Recommendations Measurement of BNP or NT-proBNP is useful for establishing prognosis or disease severity in chronic HF. a b Measurement of baseline natriuretic peptide biomarkers and/or cardiac troponin on admission to the hospital is useful to establish a prognosis in acutely decompensated HF. MODFED: Emphasizes that it is admission natriuretic peptide biomarkers levels that are useful. During a HF hospitalization, a pre-discharge natriuretic peptide level can be useful to establish a post-discharge prognosis. NEW: New observational studies. n patients with chronic HF, measurement of other clinically available tests, such as biomarkers of myocardial injury or fibrosis, may be considered for additive risk stratification. MODFED: 2013 recommendations combined into prognosis section resulting in LOE change from to B-NR

2017 /H/HFS Focused Update of the 2013 F/H 7.3.2 Pharmacoloigical Treatment for Stage HF With Reduced Ejection Fraction: Recommendations : : E-: RB: RN: E-: RB: RN: -EO The clinical strategy of inhibition of the renin-angiotensin system with E inhibitors (Level of Evidence: ), OR RBs (Level of Evidence: ), OR RN (Level of Evidence: ) in conjunction with evidence-based beta blockers, and aldosterone antagonists in selected patient, is recommended for patients with chronic HFrEF to reduce morbidity and mortality. NEW: New clinical trial data prompted clarification and important updates The use of E inhibitors is beneficial for patients with prior or current symptoms of chronic HFrEF to reduce morbidity and mortality. NOTE: 2013 recommendation repeated for clarity in this section. The use of RBs to reduce morbidity and mortality is recommended in patients with prior or current symptoms of chronic HFrEF who are intolerant to E inhibitors because of cough or angioedema. NOTE: 2013 recommendation repeated for clarity in this section. n patients with chronic symptomatic HFrEF NYH class or who tolerate an E inhibitor or RB, replacement by an RN is recommended to further reduce morbidity and mortality. NEW: New clinical trial data necessitated this recommendation RN should not be administered concomitantly with E inhibitors or within 36 hours of the last dose of an E inhibitor. NEW: vailable evidence demonstrates a potential signal of harm for a concomitant use of E and RN. RN should not be administered to patients with a history of angioedema. NEW: New clinical trial data. 7.3.2.11 vabradine: Recommendation a vabradine can be beneficial to reduce HF hospitalization for patients with symptomatic (NYH class -) 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. NEW: New clinical trial data.

2017 /H/HFS Focused Update of the 2013 F/H 7.3.3 Pharmacological Treatment for Stage HFpEF: Recommendations a a a a B Systolic and diastolic blood pressure should be controlled in patients with HFpEF in accordance with published clinical practice guidelines to prevent morbidity. Diuretics should be used for relief of symptoms due to volume overload in patients with HFpEF. oronary revascularization is reasonable in patients with D in whom symptoms (angina) or demonstrable myocardial ischemia is judged to be having an adverse effect on symptomatic HFpEF despite GDMT. Management of F according to published clinical practice guidelines in patients with HFpEF is reasonable to improve symptomatic HF (Section 9.1 in the 2013 HF guideline). NOTE: 2013 Recommendation remain current. The use of beta-blocking agents, E inhibitors, and RBs in patients with hypertension is reasonable to control blood pressure in patients with HFpEF. n appropriately selected patients with HFpEF (with EF >45%, elevated BNP or HF admission within 1 year, estimated glomerular filtration rate >30 and creatinine <2.5 mg/dl, potassium <5.0 meq /L), aldosterone receptor antagonists might be considered to decrease hospitalizations. NEW: New RT data. a : No : No B The use of RBs might be considered to decrease hospitalizations for patients with HFpEF. Routine use of nitrates or phosphodiesterase-5 inhibitors to increase activity or QoL in patients with HFpEF is not effective. NEW: New data from RTs. NET-HFpEF based on the results of this trial, the routine use of nitrates in patients with HF[EF is not recommended. This recommendation does not apply to people with HFpEF and symptomatic D for whol nitrates may provide symptomatic relief. The RELX (phosphodiesterase-5 inhibition) This study failed to show an improvement in oxygen consumption or exercise tolerance. Routine use of nutritional supplements is not recommended for patients with HFpEF. NOTE: 2013 recommendation remains current

2017 /H/HFS Focused Update of the 2013 F/H 9. mportant omorbidities in HF 9.2 nemia: Recommendations a : No n patients with NYH class and HF and iron deficiency (ferritin <100 ng/ml or 100 to 300 ng/ml if transferrin saturation <20%), intravenous iron replacement might be reasonable to improve functional status and QoL. NEW: New evidence consistent with therapeutic benefit. n patients with HF and anemia, erythropoietin stimulating agents should not be used. NEW: New evidence demonstrating absence of therapeutic benefit. 9.5 Hypertension (New Section) 9.5.1 Treating Hypertension to Reduce the ncidence of HF: Recommendation n patients at increased risk, Stage HF, the optimal blood pressure in those with hypertension should be less than 130/80 mm Hg. NEW: New RT data. 9.5.2 Treating Hypertension in Stage HFrEF: Recommendation -LD Patients with HFrEF and hypertension should be prescribed GDMT titrated to attain systolic blood pressure less than 130 mm Hg. NEW: dapted from recent clinical trial data but not specifically tested per se in a randomized trial of patients with HF. 9.5.3 Treating Hypertension in Stage HFpEF: Recommendation -LD Patients with HFpEF and persistent hypertension after management of volume overload should be prescribed GDMT titrated to attain systolic blood pressure less than 130 mm Hg. NEW: New target goal blood pressure based on updated interpretation of recent clinical trial data.

2017 /H/HFS Focused Update of the 2013 F/H 9.6 Sleep Disordered Breathing: Recommendation a b : -LD n patients with NYH class V HF and suspicion of sleep disordered breathing or excessive daytime sleepiness, a formal sleep assessment is reasonable. NEW: linical necessity to distinguish obstructive versus central sleep apnea. n patients with cardiovascular disease and obstructive sleep apnea, PP may be reasonable to improve sleep quality and daytime sleepiness. NEW: New data demonstrate the limited scope of benefit expected from PP for obstructive sleep apnea. n patients with NYH class V HFrEF and central sleep apnea, adaptive servo-ventilation causes harm. NEW: New data demonstrate a signal of harm when adaptive servo-ventilation (SV) is used for central sleep apnea. Sleep apnea occurs more often in people with heart failure than in the general population. Sleep disordered breathing is common in people who have HF with reduced EF (prevalence rates of 50%-75%). This recommendation is based off of the SERVE-HF study. This study showed that while SV effectively treated central sleep apnea, it did not have a significant effect on the composite end point of death from any cause. owie MR, Woehrle H, Wegscheider K, et al. daptive Servo-Ventilation for entral Sleep pnea in Systolic Heart Failure. N Engl J Med. 2015;373:1095-105.