Aims: Patients with subclinical hypotension are common but underrepresented in acute decompensated heart failure (ADHF) clinical studies. Whether low baseline systolic blood pressure (SBP) impacts long-term prognosis or limits guideline-directed medical therapy (GDMT) remains uncertain. Methods and results: We analyzed 2105 ADHF admissions from the TRI-AHF registry; after excluding patients on inotropes/vasopressors or mechanical support, 1590 were included (96 hypotensive, SBP ≤100 mmHg; 1494 normotensive). Propensity score-matching yielded 92 hypotensive and 216 normotensive patients (effective ratio ≈1:2.35). The primary endpoint was 1-year all-cause mortality or first HF hospitalization; secondary analyses were at 5 years. GDMT prescription and uptitration (RAASi/ARNI, beta-blockers, MRAs) were assessed, in the HFrEF population, at discharge and 1 year. In the matched cohort, admission hypotension was associated with higher 1-year risk (HR 2.16, 95% CI 1.47-3.17) and persisted at 5 years (HR 1.80, 95% CI 1.32-2.46); the association was stronger in women (p-interaction=0.032). Spline analysis showed a non-linear risk increase below ∼100 mmHg. In HFrEF, admission hypotension was not independently associated with reduced GDMT prescription or uptitration at discharge or 1 year; optimization was more strongly influenced by renal dysfunction, absence of prior therapy, and older age, with secular increases in MRA use/composite optimization and a modest decline in RAASi/ARNI ≥50% at discharge. Conclusion: Subclinical hypotension at ADHF admission identifies a fragile, high-risk phenotype with adverse outcomes, without clear evidence of independently impaired GDMT implementation. Recognition of this profile should prompt individualized, physiology-guided strategies to safely optimize therapy.

Subclinical hypotension in acute decompensated heart failure: prognosis and treatment implementation / Savonitto, G., Stolfo, D., Biber, M.E., Cocianni, D., Contessi, S., Perotto, M., Rizzi, J.G., Soranzo, E., Masè, M., Merlo, M., Sinagra, G.. - In: EUROPEAN JOURNAL OF INTERNAL MEDICINE. - ISSN 0953-6205. - (2026), pp. "-"-"-". [Epub ahead of print] [10.1016/j.ejim.2026.107080]

Subclinical hypotension in acute decompensated heart failure: prognosis and treatment implementation

Savonitto, Giulio;Stolfo, Davide;Biber, Mattia Emanuele;Cocianni, Daniele;Contessi, Stefano;Perotto, Maria;Rizzi, Jacopo Giulio;Soranzo, Elisa;Masè, Marco;Merlo, Marco;Sinagra, Gianfranco
2026-01-01

Abstract

Aims: Patients with subclinical hypotension are common but underrepresented in acute decompensated heart failure (ADHF) clinical studies. Whether low baseline systolic blood pressure (SBP) impacts long-term prognosis or limits guideline-directed medical therapy (GDMT) remains uncertain. Methods and results: We analyzed 2105 ADHF admissions from the TRI-AHF registry; after excluding patients on inotropes/vasopressors or mechanical support, 1590 were included (96 hypotensive, SBP ≤100 mmHg; 1494 normotensive). Propensity score-matching yielded 92 hypotensive and 216 normotensive patients (effective ratio ≈1:2.35). The primary endpoint was 1-year all-cause mortality or first HF hospitalization; secondary analyses were at 5 years. GDMT prescription and uptitration (RAASi/ARNI, beta-blockers, MRAs) were assessed, in the HFrEF population, at discharge and 1 year. In the matched cohort, admission hypotension was associated with higher 1-year risk (HR 2.16, 95% CI 1.47-3.17) and persisted at 5 years (HR 1.80, 95% CI 1.32-2.46); the association was stronger in women (p-interaction=0.032). Spline analysis showed a non-linear risk increase below ∼100 mmHg. In HFrEF, admission hypotension was not independently associated with reduced GDMT prescription or uptitration at discharge or 1 year; optimization was more strongly influenced by renal dysfunction, absence of prior therapy, and older age, with secular increases in MRA use/composite optimization and a modest decline in RAASi/ARNI ≥50% at discharge. Conclusion: Subclinical hypotension at ADHF admission identifies a fragile, high-risk phenotype with adverse outcomes, without clear evidence of independently impaired GDMT implementation. Recognition of this profile should prompt individualized, physiology-guided strategies to safely optimize therapy.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11368/3141981
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