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Phenogrouping heart failure with preserved or mildly reduced ejection fraction using electronic health record data

Phenogrouping heart failure with preserved or mildly reduced ejection fraction using electronic health record data
Phenogrouping heart failure with preserved or mildly reduced ejection fraction using electronic health record data
Background: heart failure (HF) with preserved or mildly reduced ejection fraction includes a heterogenous group of patients. Reclassification into distinct phenogroups to enable targeted interventions is a priority. This study aimed to identify distinct phenogroups, and compare phenogroup characteristics and outcomes, from electronic health record data.

Methods: 2,187 patients admitted to five UK hospitals with a diagnosis of HF and a left ventricular ejection fraction ≥ 40% were identified from the NIHR Health Informatics Collaborative database. Partition-based, model-based, and density-based machine learning clustering techniques were applied. Cox Proportional Hazards and Fine-Gray competing risks models were used to compare outcomes (all-cause mortality and hospitalisation for HF) across phenogroups.

Results: three phenogroups were identified: (1) Younger, predominantly female patients with high prevalence of cardiometabolic and coronary disease; (2) More frail patients, with higher rates of lung disease and atrial fibrillation; (3) Patients characterised by systemic inflammation and high rates of diabetes and renal dysfunction. Survival profiles were distinct, with an increasing risk of all-cause mortality from phenogroups 1 to 3 (p < 0.001). Phenogroup membership significantly improved survival prediction compared to conventional factors. Phenogroups were not predictive of hospitalisation for HF.

Conclusions: applying unsupervised machine learning to routinely collected electronic health record data identified phenogroups with distinct clinical characteristics and unique survival profiles.

1471-2261
Soltani, Fardad
b9ccc750-c325-4d3a-a693-e6f45adc2ebb
Jenkins, David A.
e71717f2-82a1-46ca-aac8-cd89d0c3bd00
Kaura, Amit
a9878db1-caed-486b-b5cc-0ad07c503eb5
Curzen, Nick
70f3ea49-51b1-418f-8e56-8210aef1abf4
et al.
Soltani, Fardad
b9ccc750-c325-4d3a-a693-e6f45adc2ebb
Jenkins, David A.
e71717f2-82a1-46ca-aac8-cd89d0c3bd00
Kaura, Amit
a9878db1-caed-486b-b5cc-0ad07c503eb5
Curzen, Nick
70f3ea49-51b1-418f-8e56-8210aef1abf4

et al. (2024) Phenogrouping heart failure with preserved or mildly reduced ejection fraction using electronic health record data. BMC Cardiovascular Disorders, 24 (1), [343]. (doi:10.1186/s12872-024-03987-9).

Record type: Article

Abstract

Background: heart failure (HF) with preserved or mildly reduced ejection fraction includes a heterogenous group of patients. Reclassification into distinct phenogroups to enable targeted interventions is a priority. This study aimed to identify distinct phenogroups, and compare phenogroup characteristics and outcomes, from electronic health record data.

Methods: 2,187 patients admitted to five UK hospitals with a diagnosis of HF and a left ventricular ejection fraction ≥ 40% were identified from the NIHR Health Informatics Collaborative database. Partition-based, model-based, and density-based machine learning clustering techniques were applied. Cox Proportional Hazards and Fine-Gray competing risks models were used to compare outcomes (all-cause mortality and hospitalisation for HF) across phenogroups.

Results: three phenogroups were identified: (1) Younger, predominantly female patients with high prevalence of cardiometabolic and coronary disease; (2) More frail patients, with higher rates of lung disease and atrial fibrillation; (3) Patients characterised by systemic inflammation and high rates of diabetes and renal dysfunction. Survival profiles were distinct, with an increasing risk of all-cause mortality from phenogroups 1 to 3 (p < 0.001). Phenogroup membership significantly improved survival prediction compared to conventional factors. Phenogroups were not predictive of hospitalisation for HF.

Conclusions: applying unsupervised machine learning to routinely collected electronic health record data identified phenogroups with distinct clinical characteristics and unique survival profiles.

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More information

Accepted/In Press date: 19 June 2024
Published date: 5 July 2024

Identifiers

Local EPrints ID: 492656
URI: http://eprints.soton.ac.uk/id/eprint/492656
ISSN: 1471-2261
PURE UUID: 3dc23b30-722b-40ea-ae3f-4e459c7c9f6b
ORCID for Nick Curzen: ORCID iD orcid.org/0000-0001-9651-7829

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Date deposited: 09 Aug 2024 16:45
Last modified: 10 Aug 2024 01:40

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Contributors

Author: Fardad Soltani
Author: David A. Jenkins
Author: Amit Kaura
Author: Nick Curzen ORCID iD
Corporate Author: et al.

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