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A registry‐based algorithm to predict ejection fraction in patients with heart failure

AIMS: Left ventricular ejection fraction (EF) is required to categorize heart failure (HF) [i.e. HF with preserved (HFpEF), mid‐range (HFmrEF), and reduced (HFrEF) EF] but is often not captured in population‐based cohorts or non‐HF registries. The aim was to create an algorithm that identifies EF su...

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Autores principales: Uijl, Alicia, Lund, Lars H., Vaartjes, Ilonca, Brugts, Jasper J., Linssen, Gerard C., Asselbergs, Folkert W., Hoes, Arno W., Dahlström, Ulf, Koudstaal, Stefan, Savarese, Gianluigi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7524089/
https://www.ncbi.nlm.nih.gov/pubmed/32548911
http://dx.doi.org/10.1002/ehf2.12779
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author Uijl, Alicia
Lund, Lars H.
Vaartjes, Ilonca
Brugts, Jasper J.
Linssen, Gerard C.
Asselbergs, Folkert W.
Hoes, Arno W.
Dahlström, Ulf
Koudstaal, Stefan
Savarese, Gianluigi
author_facet Uijl, Alicia
Lund, Lars H.
Vaartjes, Ilonca
Brugts, Jasper J.
Linssen, Gerard C.
Asselbergs, Folkert W.
Hoes, Arno W.
Dahlström, Ulf
Koudstaal, Stefan
Savarese, Gianluigi
author_sort Uijl, Alicia
collection PubMed
description AIMS: Left ventricular ejection fraction (EF) is required to categorize heart failure (HF) [i.e. HF with preserved (HFpEF), mid‐range (HFmrEF), and reduced (HFrEF) EF] but is often not captured in population‐based cohorts or non‐HF registries. The aim was to create an algorithm that identifies EF subphenotypes for research purposes. METHODS AND RESULTS: We included 42 061 HF patients from the Swedish Heart Failure Registry. As primary analysis, we performed two logistic regression models including 22 variables to predict (i) EF≥ vs. <50% and (ii) EF≥ vs. <40%. In the secondary analysis, we performed a multivariable multinomial analysis with 22 variables to create a model for all three separate EF subphenotypes: HFrEF vs. HFmrEF vs. HFpEF. The models were validated in the database from the CHECK‐HF study, a cross‐sectional survey of 10 627 patients from the Netherlands. The C‐statistic (discrimination) was 0.78 [95% confidence interval (CI) 0.77–0.78] for EF ≥50% and 0.76 (95% CI 0.75–0.76) for EF ≥40%. Similar results were achieved for HFrEF and HFpEF in the multinomial model, but the C‐statistic for HFmrEF was lower: 0.63 (95% CI 0.63–0.64). The external validation showed similar discriminative ability to the development cohort. CONCLUSIONS: Routine clinical characteristics could potentially be used to identify different EF subphenotypes in databases where EF is not readily available. Accuracy was good for the prediction of HFpEF and HFrEF but lower for HFmrEF. The proposed algorithm enables more effective research on HF in the big data setting.
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spelling pubmed-75240892020-10-02 A registry‐based algorithm to predict ejection fraction in patients with heart failure Uijl, Alicia Lund, Lars H. Vaartjes, Ilonca Brugts, Jasper J. Linssen, Gerard C. Asselbergs, Folkert W. Hoes, Arno W. Dahlström, Ulf Koudstaal, Stefan Savarese, Gianluigi ESC Heart Fail Original Research Articles AIMS: Left ventricular ejection fraction (EF) is required to categorize heart failure (HF) [i.e. HF with preserved (HFpEF), mid‐range (HFmrEF), and reduced (HFrEF) EF] but is often not captured in population‐based cohorts or non‐HF registries. The aim was to create an algorithm that identifies EF subphenotypes for research purposes. METHODS AND RESULTS: We included 42 061 HF patients from the Swedish Heart Failure Registry. As primary analysis, we performed two logistic regression models including 22 variables to predict (i) EF≥ vs. <50% and (ii) EF≥ vs. <40%. In the secondary analysis, we performed a multivariable multinomial analysis with 22 variables to create a model for all three separate EF subphenotypes: HFrEF vs. HFmrEF vs. HFpEF. The models were validated in the database from the CHECK‐HF study, a cross‐sectional survey of 10 627 patients from the Netherlands. The C‐statistic (discrimination) was 0.78 [95% confidence interval (CI) 0.77–0.78] for EF ≥50% and 0.76 (95% CI 0.75–0.76) for EF ≥40%. Similar results were achieved for HFrEF and HFpEF in the multinomial model, but the C‐statistic for HFmrEF was lower: 0.63 (95% CI 0.63–0.64). The external validation showed similar discriminative ability to the development cohort. CONCLUSIONS: Routine clinical characteristics could potentially be used to identify different EF subphenotypes in databases where EF is not readily available. Accuracy was good for the prediction of HFpEF and HFrEF but lower for HFmrEF. The proposed algorithm enables more effective research on HF in the big data setting. John Wiley and Sons Inc. 2020-06-17 /pmc/articles/PMC7524089/ /pubmed/32548911 http://dx.doi.org/10.1002/ehf2.12779 Text en © 2020 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of the European Society of Cardiology This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Research Articles
Uijl, Alicia
Lund, Lars H.
Vaartjes, Ilonca
Brugts, Jasper J.
Linssen, Gerard C.
Asselbergs, Folkert W.
Hoes, Arno W.
Dahlström, Ulf
Koudstaal, Stefan
Savarese, Gianluigi
A registry‐based algorithm to predict ejection fraction in patients with heart failure
title A registry‐based algorithm to predict ejection fraction in patients with heart failure
title_full A registry‐based algorithm to predict ejection fraction in patients with heart failure
title_fullStr A registry‐based algorithm to predict ejection fraction in patients with heart failure
title_full_unstemmed A registry‐based algorithm to predict ejection fraction in patients with heart failure
title_short A registry‐based algorithm to predict ejection fraction in patients with heart failure
title_sort registry‐based algorithm to predict ejection fraction in patients with heart failure
topic Original Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7524089/
https://www.ncbi.nlm.nih.gov/pubmed/32548911
http://dx.doi.org/10.1002/ehf2.12779
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