Scope of this summary
Adults at risk for heart failure or with chronic symptomatic heart failure, classified by ACC/AHA stage and left-ventricular ejection-fraction phenotype. Acute pulmonary edema, cardiogenic shock and other decompensated presentations require the acute-heart-failure pathway; pregnancy, congenital disease and pediatric heart failure require specialist guidance.
sources for this section:AHA/ACC/HFSA 2022
The Bottom Line
- Classify ACC/AHA stage and ejection-fraction phenotype; when ejection fraction is above 40%, objective evidence of increased filling pressures is important to confirm heart failure.
- For HFrEF, guideline-directed medical therapy includes four foundational medication classes, one of which is an SGLT2 inhibitor; initiate and titrate as tolerated rather than waiting for sequential failure.
- The guideline also recommends SGLT2 inhibitors for selected patients across mildly reduced and preserved ejection-fraction phenotypes, with other therapies individualized by phenotype and comorbidity.
- Address hypertension, coronary disease, atrial fibrillation, diabetes, kidney disease, iron deficiency, sleep disorders, vaccination, exercise and self-care as part of the heart-failure plan.
- Refer patients with advanced heart failure who wish to prolong survival to a specialist team for advanced-therapy assessment and goal-concordant palliative care.
sources for this section:AHA/ACC/HFSA 2022
Practical clinical workflow
1
Confirm the syndrome with history, examination, natriuretic peptide testing and cardiac imaging as appropriate; identify ischemic, valvular, rhythm, toxic and systemic contributors.
2
Record stage, ejection-fraction phenotype, congestion, functional limitation, kidney function, electrolytes, blood pressure and comorbidity burden.
3
Start and titrate phenotype-appropriate guideline-directed therapy, providing practical education about adherence, daily symptoms, weight, sodium, activity and when to seek help.
4
Recheck blood pressure, kidney function, potassium, volume status, symptoms and adverse effects after initiation or dose change; repeat imaging when the result will change management.
5
Assess device eligibility, cardiac rehabilitation, multidisciplinary support and timely advanced-heart-failure referral when symptoms progress despite treatment.
sources for this section:AHA/ACC/HFSA 2022
Safety boundaries and escalation
- New rest dyspnea, hypoxemia, hypotension, confusion, chest pain, syncope, rapidly worsening edema or oliguria may signal acute decompensation and needs urgent assessment.
- Check renal function, potassium, blood pressure, volume status and interactions when adding or titrating renin-angiotensin-system, mineralocorticoid, diuretic or SGLT2 therapies.
- Verify pregnancy potential and current FDA labeling; several foundational HFrEF medicines can cause fetal harm.
- Do not abruptly withdraw effective heart-failure therapy solely because ejection fraction improves; reassess the complete guideline and patient context.
sources for this section:AHA/ACC/HFSA 2022
Localization
The 2022 AHA/ACC/HFSA guideline supplies the US clinical framework. US FDA indications, insurer authorization, device coverage and local specialty access determine implementation.
sources for this section:AHA/ACC/HFSA 2022
Source documents
Use the linked source documents for complete recommendations, evidence grading, exclusions and implementation detail.
- American Heart Association, American College of Cardiology, and Heart Failure Society of America2022 AHA/ACC/HFSA Guideline for the Management of Heart FailureDOI 10.1161/CIR.0000000000001063 路 published 2022-04-01 路 accessed 2026-08-20view source
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