Key result
In adults with congenital heart disease, HFrEF had higher risk of HF hospitalization (HR 1.52; P=0.005) and cardiovascular death/heart transplantation (HR 1.74; P=0.002) than HFmrEF and HFpEF.
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Why the study?
Data comparing cardiac remodeling, prognostic markers, and cardiovascular outcomes across heart failure phenotypes in adults with congenital heart disease are limited.
Does LVEF-defined heart failure phenotype (HFrEF vs HFmrEF and HFpEF) predict cardiac remodeling and cardiovascular outcomes (HF hospitalization and cardiovascular death/heart transplantation) in adults with congenital heart disease?
Cohort (n=1,303)
Does LVEF-defined heart failure phenotype (HFrEF vs HFmrEF and HFpEF) predict cardiac remodeling and cardiovascular outcomes (HF hospitalization and cardiovascular death/heart transplantation) in adults with congenital heart disease?
In adults with congenital heart disease and heart failure, LVEF-based phenotyping identifies distinct patterns of remodeling and prognosis, with HFrEF carrying the highest risk of hospitalization and death/transplantation and the strongest benefit from HF therapy.
Supports LVEF-based risk stratification in adults with congenital heart disease and HF; leaves open whether phenotype-guided medical therapy improves outcomes in this population.
BACKGROUND: Data comparing cardiac remodeling, prognostic markers, and cardiovascular outcomes across heart failure (HF) phenotypes in adults with congenital heart disease (CHD) are limited. METHODS: In this study, adults with CHD and HF were classified based on left ventricular ejection fraction (LVEF): HF with reduced EF (HFrEF; LVEF < 40%), HF with mildly reduced EF (HFmrEF; LVEF 41%-49%), and HF with preserved EF (HFpEF; LVEF ≥ 50% with pulmonary artery wedge pressure ≥15 mmHg). Cardiac function (strain imaging), prognostic markers (NT-proBNP and peak oxygen consumption), and cardiovascular outcomes (HF hospitalization and cardiovascular death/heart transplantation) were compared across groups. RESULTS: Among 1,303 patients, 304 (23%) had HFrEF, 551 (42%) had HFmrEF, and 448 (34%) had HFpEF. There was a graded worsening of biatrial and right ventricular function from HFpEF to HFmrEF to HFrEF (all P < .001). Despite less severe chamber dysfunction, HFpEF was characterized by higher NT-proBNP levels and lower peak oxygen consumption compared with HFmrEF. HFrEF was associated with the highest adjusted risk of HF hospitalization (hazard ratio, 1.52; P = .005) and cardiovascular death/heart transplantation (hazard ratio, 1.74; P = .002), compared to HFmrEF and HFpEF. HF therapy was associated with lower event rates overall, with the strongest association in HFrEF, a more modest association in HFmrEF, and no significant association in HFpEF. CONCLUSIONS: In adults with CHD and HF, LVEF-defined HF phenotypes identified distinct patterns of cardiac remodeling and prognosis, with worse cardiac remodeling and adverse outcomes observed in the HFrEF phenotype. These findings support use of EF phenotype-based approach to HF management in CHD.
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Moustafa et al. (2026) conducted a cohort in Adults with congenital heart disease (CHD) and heart failure (HF) (n=1,303). HFrEF phenotype (LVEF <40%) vs. HFmrEF (LVEF 41%-49%) and HFpEF (LVEF ≥50%) was evaluated on Cardiovascular death or heart transplantation (HR 1.74, p=0.002). In adults with congenital heart disease, HFrEF had higher risk of HF hospitalization (HR 1.52; P=0.005) and cardiovascular death/heart transplantation (HR 1.74; P=0.002) than HFmrEF and HFpEF.
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