Diastolic Dysfunction in Acute and Critical Illness

Heart failure with preserved ejection fraction (HFpEF) is a heterogeneous, multi-organ syndrome driven by comorbidity-induced systemic inflammation. In acute and critical illness, such as sepsis, acute diastolic dysfunction is common. Its prognostic significance is debated and is complicated by hemodynamic instability and diagnostic challenges. Survivors of acute illness face a long-term risk of major adverse cardiovascular events, yet the transition from critical illness to acquired diastolic dysfunction to chronic HFpEF remains an underexplored area requiring further research. Recent landmark trials have established new therapeutic options for chronic HFpEF, including sodium glucose co-transporter 2 inhibitors, mineralocorticoid receptor antagonists, and glucagon-like peptide-1 receptor agonists. Here, we review the pathophysiology of HFpEF across the continuum from chronic stable HFpEF to acute decompensation, identify long-term sequelae, and highlight future advancements.

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Journal
JACC Advances
Published
2026-01-13
DOI
https://doi.org/10.1016/j.jacadv.2025.102532
Primary Topic
Cardiovascular Function and Risk Factors
Type
article
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article

Diastolic Dysfunction in Acute and Critical Illness

Sandeep S Hothi, Thomas E. Ingram, Suneesh Thilak, Cyril Chacko et al.
JACC Advances
Cardiovascular Function and Risk Factors
article

Diastolic Dysfunction in Acute and Critical Illness

Sandeep S Hothi, Thomas E. Ingram, Suneesh Thilak, Cyril Chacko, Marcus Abbawy, Finlay Holden, Kesaven Dhamodaran, James Cotton, Tonny Veenith, Fang Gao-Smith, Tom Fisher
article en

Abstract

Heart failure with preserved ejection fraction (HFpEF) is a heterogeneous, multi-organ syndrome driven by comorbidity-induced systemic inflammation. In acute and critical illness, such as sepsis, acute diastolic dysfunction is common. Its prognostic significance is debated and is complicated by hemodynamic instability and diagnostic challenges. Survivors of acute illness face a long-term risk of major adverse cardiovascular events, yet the transition from critical illness to acquired diastolic dysfunction to chronic HFpEF remains an underexplored area requiring further research. Recent landmark trials have established new therapeutic options for chronic HFpEF, including sodium glucose co-transporter 2 inhibitors, mineralocorticoid receptor antagonists, and glucagon-like peptide-1 receptor agonists. Here, we review the pathophysiology of HFpEF across the continuum from chronic stable HFpEF to acute decompensation, identify long-term sequelae, and highlight future advancements.

JACC AdvancesVol. 5(2)
University College London Hospitals NHS Foundation Trust (GB), New Cross Hospital (GB), Dudley Group NHS Foundation Trust (GB), The Edgbaston Hospital (GB), The Royal Wolverhampton NHS Trust (GB), Wolverhampton Hospital (GB), University College London (GB)
Good health and well-being
Openalex Percentile: Top 89%
Cardiovascular Function and Risk Factors
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Diastolic Dysfunction in Acute and Critical Illness — Sandeep S Hothi, Thomas E. Ingram, et al. · JACC Advances (2026) | TGRS Research Map | TGRS