The American College of Cardiology (ACC) has published an updated 2026 Expert Consensus Decision Pathway (ECDP) for the management of heart failure with preserved ejection fraction (HFpEF), replacing the 2023 version.1
The document, chaired by Michelle M. Kittleson, MD, PhD, reframes HFpEF as a multisystem syndrome driven by visceral adiposity, inflammatory adipokines, and metabolic dysfunction rather than a single cardiac condition. The update incorporates new trial data on sodium-glucose cotransporter 2 (SGLT2) inhibitors, nonsteroidal mineralocorticoid receptor antagonists (MRAs), and incretin-based therapies.1
Key Facts
What does the 2026 ACC ECDP recommend as foundational pharmacotherapy for HFpEF?
An SGLT2 inhibitor plus a nonsteroidal MRA, with finerenone favored over spironolactone, unless contraindicated.
Which patients with HFpEF should receive incretin-based therapy?
Patients with a body mass index of 30 kg/m² or higher, per STEP-HFpEF and SUMMIT trial data.
How does the updated pathway approach HFpEF diagnosis?
It recommends sequential use of the H2FPEF and HFA-PEFF scoring systems, systematic exclusion of noncardiac and cardiac mimics, and attention to sex-specific presentation differences.
The revision responds to a rapidly evolving therapeutic landscape since 2023, when finerenone, semaglutide, and tirzepatide lacked HFpEF-specific outcomes data. According to the ACC, these agents now offer benefits extending beyond heart failure to broader cardiovascular, kidney, and metabolic health. The writing committee positions accurate diagnosis as a prerequisite for guideline-based therapy, given persistent underrecognition of HFpEF in practice.2
The ECDP outlines three validated scoring systems for establishing diagnostic probability in patients presenting with dyspnea or edema: H2FPEF, HFA-PEFF, and HFpEF-ABA. The writing committee recommends H2FPEF as an initial screening tool followed by HFA-PEFF for confirmation, noting that discordance between the two can prompt further advanced testing. Each carries distinct tradeoffs: H2FPEF offers greater accuracy with fewer input variables and higher sensitivity, while HFA-PEFF is more specific but often requires diastolic stress testing or invasive hemodynamics rarely feasible in routine practice.1
Beyond scoring, the pathway calls for systematic exclusion of noncardiac mimics, including pulmonary disease, kidney disease, high-output states, obesity, and frailty, along with cardiac mimics such as valvular disease, pericardial constriction, infiltrative cardiomyopathies, and ischemic heart disease, before confirming HFpEF as a diagnosis of exclusion. The document also details sex-specific differences in presentation. Women with HFpEF show lower natriuretic peptide levels, greater concentric left ventricular remodeling, and worse symptom burden compared with men.1