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Prediction of worsening heart failure events and all‐cause mortality using an individualized risk stratification strategy

AIMS: This study aimed to examine the clinical utility of a multisensor, remote, ambulatory diagnostic risk score, TriageHF™, in a real‐world, unselected, large patient sample to predict heart failure events (HFEs) and all‐cause mortality. METHODS AND RESULTS: TriageHF risk score was calculated in p...

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Autores principales: Zile, Michael R., Koehler, Jodi, Sarkar, Shantanu, Butler, Javed
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/PMC7754961/
https://www.ncbi.nlm.nih.gov/pubmed/33118331
http://dx.doi.org/10.1002/ehf2.13077
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author Zile, Michael R.
Koehler, Jodi
Sarkar, Shantanu
Butler, Javed
author_facet Zile, Michael R.
Koehler, Jodi
Sarkar, Shantanu
Butler, Javed
author_sort Zile, Michael R.
collection PubMed
description AIMS: This study aimed to examine the clinical utility of a multisensor, remote, ambulatory diagnostic risk score, TriageHF™, in a real‐world, unselected, large patient sample to predict heart failure events (HFEs) and all‐cause mortality. METHODS AND RESULTS: TriageHF risk score was calculated in patients in the Optum(®) database who had Medtronic implantable cardiac defibrillator device from 2007 to 2016. Patients were categorized into three risk groups based on probability for having an HFE within 6 months (low risk <5.4%, medium risk ≥5.4 < 20%, and high risk ≥20%). Data were analysed using three strategies: (i) scheduled monthly data download; (ii) alert‐triggered data download; and (iii) daily data download. Study population consisted of 22 901 patients followed for 1.8 ± 1.3 years. Using monthly downloads, HFE risk over 30 days incrementally increased across risk categories (odds ratio: 2.8, 95% confidence interval: 2.5–3.2 for HFE, P < 0.001, low vs. medium risk, and odds ratio: 9.2, 95% confidence interval: 8.1–10.3, P < 0.001, medium vs. high risk). Findings were similar using the other two analytic strategies. Using a receiver operating characteristic curve analysis, sensitivity for predicting HFE over 30 days using high‐risk score was 47% (alert triggered) and 51% (daily download) vs. 0.5 per patient year unexplained detection rate. TriageHF risk score also predicted all‐cause mortality risk over 4 years. All‐cause mortality risk was 14% in low risk, 20% in medium risk, and 38% in high risk. CONCLUSIONS: TriageHF risk score provides a multisensor remote, ambulatory diagnostic method that predicts both HFEs and all‐cause mortality.
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spelling pubmed-77549612020-12-23 Prediction of worsening heart failure events and all‐cause mortality using an individualized risk stratification strategy Zile, Michael R. Koehler, Jodi Sarkar, Shantanu Butler, Javed ESC Heart Fail Original Research Articles AIMS: This study aimed to examine the clinical utility of a multisensor, remote, ambulatory diagnostic risk score, TriageHF™, in a real‐world, unselected, large patient sample to predict heart failure events (HFEs) and all‐cause mortality. METHODS AND RESULTS: TriageHF risk score was calculated in patients in the Optum(®) database who had Medtronic implantable cardiac defibrillator device from 2007 to 2016. Patients were categorized into three risk groups based on probability for having an HFE within 6 months (low risk <5.4%, medium risk ≥5.4 < 20%, and high risk ≥20%). Data were analysed using three strategies: (i) scheduled monthly data download; (ii) alert‐triggered data download; and (iii) daily data download. Study population consisted of 22 901 patients followed for 1.8 ± 1.3 years. Using monthly downloads, HFE risk over 30 days incrementally increased across risk categories (odds ratio: 2.8, 95% confidence interval: 2.5–3.2 for HFE, P < 0.001, low vs. medium risk, and odds ratio: 9.2, 95% confidence interval: 8.1–10.3, P < 0.001, medium vs. high risk). Findings were similar using the other two analytic strategies. Using a receiver operating characteristic curve analysis, sensitivity for predicting HFE over 30 days using high‐risk score was 47% (alert triggered) and 51% (daily download) vs. 0.5 per patient year unexplained detection rate. TriageHF risk score also predicted all‐cause mortality risk over 4 years. All‐cause mortality risk was 14% in low risk, 20% in medium risk, and 38% in high risk. CONCLUSIONS: TriageHF risk score provides a multisensor remote, ambulatory diagnostic method that predicts both HFEs and all‐cause mortality. John Wiley and Sons Inc. 2020-10-28 /pmc/articles/PMC7754961/ /pubmed/33118331 http://dx.doi.org/10.1002/ehf2.13077 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
Zile, Michael R.
Koehler, Jodi
Sarkar, Shantanu
Butler, Javed
Prediction of worsening heart failure events and all‐cause mortality using an individualized risk stratification strategy
title Prediction of worsening heart failure events and all‐cause mortality using an individualized risk stratification strategy
title_full Prediction of worsening heart failure events and all‐cause mortality using an individualized risk stratification strategy
title_fullStr Prediction of worsening heart failure events and all‐cause mortality using an individualized risk stratification strategy
title_full_unstemmed Prediction of worsening heart failure events and all‐cause mortality using an individualized risk stratification strategy
title_short Prediction of worsening heart failure events and all‐cause mortality using an individualized risk stratification strategy
title_sort prediction of worsening heart failure events and all‐cause mortality using an individualized risk stratification strategy
topic Original Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7754961/
https://www.ncbi.nlm.nih.gov/pubmed/33118331
http://dx.doi.org/10.1002/ehf2.13077
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