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Vocal Biomarker Is Associated With Hospitalization and Mortality Among Heart Failure Patients

BACKGROUND: The purpose of this article is to evaluate the association of voice signal analysis with adverse outcome among patients with congestive heart failure (CHF). METHODS AND RESULTS: The study cohort included 10 583 patients who were registered to a call center of patients who had chronic con...

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Autores principales: Maor, Elad, Perry, Daniella, Mevorach, Dana, Taiblum, Nimrod, Luz, Yotam, Mazin, Israel, Lerman, Amir, Koren, Gideon, Shalev, Varda
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/PMC7428646/
https://www.ncbi.nlm.nih.gov/pubmed/32233754
http://dx.doi.org/10.1161/JAHA.119.013359
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author Maor, Elad
Perry, Daniella
Mevorach, Dana
Taiblum, Nimrod
Luz, Yotam
Mazin, Israel
Lerman, Amir
Koren, Gideon
Shalev, Varda
author_facet Maor, Elad
Perry, Daniella
Mevorach, Dana
Taiblum, Nimrod
Luz, Yotam
Mazin, Israel
Lerman, Amir
Koren, Gideon
Shalev, Varda
author_sort Maor, Elad
collection PubMed
description BACKGROUND: The purpose of this article is to evaluate the association of voice signal analysis with adverse outcome among patients with congestive heart failure (CHF). METHODS AND RESULTS: The study cohort included 10 583 patients who were registered to a call center of patients who had chronic conditions including CHF in Israel between 2013 and 2018. A total of 223 acoustic features were extracted from 20 s of speech for each patient. A biomarker was developed based on a training cohort of non‐CHF patients (N=8316). The biomarker was tested on a mutually exclusive CHF study cohort (N=2267) and was evaluated as a continuous and ordinal (4 quartiles) variable. Median age of the CHF study population was 77 (interquartile range 68–83) and 63% were men. During a median follow‐up of 20 months (interquartile range 9–34), 824 (36%) patients died. Kaplan–Meier survival analysis showed higher cumulative probability of death with increasing quartiles (23%, 29%, 38%, and 54%; P<0.001). Survival analysis with adjustment to known predictors of poor survival demonstrated that each SD increase in the biomarker was associated with a significant 32% increased risk of death during follow‐up (95% CI, 1.24–1.41, P<0.001) and that compared with the lowest quartile, patients in the highest quartile were 96% more likely to die (95% CI, 1.59–2.42, P<0.001). The model consistently demonstrated an independent association of the biomarker with hospitalizations during follow‐up (P<0.001). CONCLUSIONS: Noninvasive vocal biomarker is associated with adverse outcome among CHF patients, suggesting a possible role for voice analysis in telemedicine and CHF patient care.
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spelling pubmed-74286462020-08-17 Vocal Biomarker Is Associated With Hospitalization and Mortality Among Heart Failure Patients Maor, Elad Perry, Daniella Mevorach, Dana Taiblum, Nimrod Luz, Yotam Mazin, Israel Lerman, Amir Koren, Gideon Shalev, Varda J Am Heart Assoc Original Research BACKGROUND: The purpose of this article is to evaluate the association of voice signal analysis with adverse outcome among patients with congestive heart failure (CHF). METHODS AND RESULTS: The study cohort included 10 583 patients who were registered to a call center of patients who had chronic conditions including CHF in Israel between 2013 and 2018. A total of 223 acoustic features were extracted from 20 s of speech for each patient. A biomarker was developed based on a training cohort of non‐CHF patients (N=8316). The biomarker was tested on a mutually exclusive CHF study cohort (N=2267) and was evaluated as a continuous and ordinal (4 quartiles) variable. Median age of the CHF study population was 77 (interquartile range 68–83) and 63% were men. During a median follow‐up of 20 months (interquartile range 9–34), 824 (36%) patients died. Kaplan–Meier survival analysis showed higher cumulative probability of death with increasing quartiles (23%, 29%, 38%, and 54%; P<0.001). Survival analysis with adjustment to known predictors of poor survival demonstrated that each SD increase in the biomarker was associated with a significant 32% increased risk of death during follow‐up (95% CI, 1.24–1.41, P<0.001) and that compared with the lowest quartile, patients in the highest quartile were 96% more likely to die (95% CI, 1.59–2.42, P<0.001). The model consistently demonstrated an independent association of the biomarker with hospitalizations during follow‐up (P<0.001). CONCLUSIONS: Noninvasive vocal biomarker is associated with adverse outcome among CHF patients, suggesting a possible role for voice analysis in telemedicine and CHF patient care. John Wiley and Sons Inc. 2020-04-01 /pmc/articles/PMC7428646/ /pubmed/32233754 http://dx.doi.org/10.1161/JAHA.119.013359 Text en © 2020 The Authors and Vocalis Health. Published on behalf of the American Heart Association, Inc., by Wiley. 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
Maor, Elad
Perry, Daniella
Mevorach, Dana
Taiblum, Nimrod
Luz, Yotam
Mazin, Israel
Lerman, Amir
Koren, Gideon
Shalev, Varda
Vocal Biomarker Is Associated With Hospitalization and Mortality Among Heart Failure Patients
title Vocal Biomarker Is Associated With Hospitalization and Mortality Among Heart Failure Patients
title_full Vocal Biomarker Is Associated With Hospitalization and Mortality Among Heart Failure Patients
title_fullStr Vocal Biomarker Is Associated With Hospitalization and Mortality Among Heart Failure Patients
title_full_unstemmed Vocal Biomarker Is Associated With Hospitalization and Mortality Among Heart Failure Patients
title_short Vocal Biomarker Is Associated With Hospitalization and Mortality Among Heart Failure Patients
title_sort vocal biomarker is associated with hospitalization and mortality among heart failure patients
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7428646/
https://www.ncbi.nlm.nih.gov/pubmed/32233754
http://dx.doi.org/10.1161/JAHA.119.013359
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