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AHA/ACC

2022 AHA/ACC/HFSA heart failure guideline: key recommendations

This guideline updates the classification, prevention, diagnosis, and management of heart failure across the spectrum of ejection fraction, including new stages of heart failure risk and updated pharmacologic and device therapy recommendations. Its central message is that four key drug classes now form the foundation of guideline-directed medical therapy for HFrEF, and that natriuretic peptide-based screening and staging can help prevent progression to symptomatic heart failure.

AHA/ACC2022 editionSummary
Official guideline2022 AHA/ACC/HFSA Guideline for the Management of Heart Failure: A Report of the American College of Cardiology/American Heart Association Joint Committee on Clinical Practice Guidelines. AHA/ACC, 2022.
Read the official guideline · Checked for a newer edition on 2026-10-20
We do not reproduce the guideline text — this page is an independent summary.

Who it applies to

Adults at risk of or diagnosed with heart failure across all ejection fraction categories, in outpatient and inpatient settings.

Key recommendations

  • Heart failure is reclassified into four stages: at risk (A), pre-heart failure (B), symptomatic heart failure (C), and advanced heart failure (D), replacing older terminology.
  • For HFrEF, four pillars of therapy are recommended: an ACE inhibitor, ARB, or ARNI, a beta-blocker, a mineralocorticoid receptor antagonist, and an SGLT2 inhibitor, ideally initiated and titrated promptly rather than sequentially.
    Class 1
  • ARNI (sacubitril-valsartan) is preferred over ACE inhibitors or ARBs for patients with chronic symptomatic HFrEF where appropriate.
    Class 1
  • SGLT2 inhibitors are recommended for HFrEF regardless of diabetes status, reducing heart failure hospitalization and cardiovascular death.
    Class 1
  • In heart failure with mildly reduced or preserved ejection fraction, SGLT2 inhibitors are recommended to reduce hospitalization and cardiovascular mortality.
    Class 2a
  • Mineralocorticoid receptor antagonists and ARNI may be considered in HFmrEF and HFpEF, particularly in patients with lower ejection fractions within these ranges.
    Class 2b
  • Natriuretic peptide biomarker screening followed by multidisciplinary intervention can be useful in patients at risk of heart failure to prevent progression to left ventricular dysfunction or symptomatic disease.
    Class 2a
  • Routine use of vasodilators or inotropes is not recommended outside of specific advanced heart failure or cardiogenic shock scenarios.
  • Hydralazine-isosorbide dinitrate is recommended as an option for self-identified Black patients with NYHA class III-IV HFrEF already on optimal therapy.
    Class 1
  • Patients with advanced heart failure should be referred for specialty evaluation, including consideration of mechanical circulatory support or transplantation, when appropriate.

What is new in this edition

  • Introduction of revised terminology for the existing four-stage classification system (A-D)
  • Simultaneous or rapid sequence initiation of all four GDMT drug classes rather than stepwise titration
  • SGLT2 inhibitors added as a core therapy for HFrEF and extended to HFmrEF/HFpEF
  • Expanded role of ARNI across the ejection fraction spectrum
  • Greater emphasis on natriuretic peptide-based screening for primary prevention

Practice points for students

  • Think of the four pillars of HFrEF therapy as something to start together and titrate quickly, not necessarily one after another.
  • SGLT2 inhibitors now apply across nearly the entire heart failure spectrum, not just in diabetic patients.
  • The A-D staging system emphasizes prevention, so patients with risk factors or asymptomatic structural disease are captured earlier than before.
  • Remember hydralazine-nitrate combination therapy has a specific, guideline-supported role in Black patients with persistent NYHA III-IV symptoms.

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Other guidelines on this topic

Independent educational summary written by the WhiteCoat Pro editorial team with AI assistance and checked by a second AI model. It does not reproduce the guideline text, tables or figures, and it is not affiliated with or endorsed by AHA/ACC. It is not medical advice: always read the original guideline before applying it to patients.