Why the study?
Patients with HFpEF are not a homogenous population, and different phenotypes can differ in prognosis and optimal management strategies.
Does machine learning-based clustering of clinical electronic health record and echocardiographic variables identify distinct phenotypes associated with death and cardiovascular hospitalization in patients with HFpEF?
Cohort (n=2,500)
No
Does machine learning-based clustering of clinical electronic health record and echocardiographic variables identify distinct phenotypes associated with death and cardiovascular hospitalization in patients with HFpEF?
Answers are grounded in this paper and cite their sources.
Machine learning applied to routine electronic health record and echocardiographic data can classify HFpEF patients into four distinct phenotypic clusters with differing prognoses, potentially enabling more personalized follow-up and targeted therapy.
Aims: Patients presenting symptoms of heart failure with preserved ejection fraction (HFpEF) are not a homogenous population. Different phenotypes can differ in prognosis and optimal management strategies. We sought to identify phenotypes of HFpEF by using the medical information database from a large university hospital centre using machine learning. Methods and results: We explored the use of clinical variables from electronic health records in addition to echocardiography to identify different phenotypes of patients with HFpEF. The proposed methodology identifies four phenotypic clusters based on both clinical and echocardiographic characteristics, which have differing prognoses (death and cardiovascular hospitalization). Conclusion: This work demonstrated that artificial intelligence-derived phenotypes could be used as a tool for physicians to assess risk and to target therapies that may improve outcomes.
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Pierre‐Jean et al. (2023) conducted a cohort in Heart failure with preserved ejection fraction (HFpEF) (n=2,500). Machine learning-derived clinical and echocardiographic phenotyping (4 clusters) vs. Comparison across four distinct phenogroups (Clusters 1, 2, 3, and 4) was evaluated on Combined endpoint of death and/or cardiovascular hospitalization.
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