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Predicting tachycardia as a surrogate for instability in the intensive care unit

Tachycardia is a strong though non-specific marker of cardiovascular stress that proceeds hemodynamic instability. We designed a predictive model of tachycardia using multi-granular intensive care unit (ICU) data by creating a risk score and dynamic trajectory. A subset of clinical and numerical sig...

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Autores principales: Yoon, Joo Heung, Mu, Lidan, Chen, Lujie, Dubrawski, Artur, Hravnak, Marilyn, Pinsky, Michael R., Clermont, Gilles
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6823304/
https://www.ncbi.nlm.nih.gov/pubmed/30767136
http://dx.doi.org/10.1007/s10877-019-00277-0
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author Yoon, Joo Heung
Mu, Lidan
Chen, Lujie
Dubrawski, Artur
Hravnak, Marilyn
Pinsky, Michael R.
Clermont, Gilles
author_facet Yoon, Joo Heung
Mu, Lidan
Chen, Lujie
Dubrawski, Artur
Hravnak, Marilyn
Pinsky, Michael R.
Clermont, Gilles
author_sort Yoon, Joo Heung
collection PubMed
description Tachycardia is a strong though non-specific marker of cardiovascular stress that proceeds hemodynamic instability. We designed a predictive model of tachycardia using multi-granular intensive care unit (ICU) data by creating a risk score and dynamic trajectory. A subset of clinical and numerical signals were extracted from the Multiparameter Intelligent Monitoring in Intensive Care II database. A tachycardia episode was defined as heart rate ≥ 130/min lasting for ≥ 5 min, with ≥ 10% density. Regularized logistic regression (LR) and random forest (RF) classifiers were trained to create a risk score for upcoming tachycardia. Three different risk score models were compared for tachycardia and control (non-tachycardia) groups. Risk trajectory was generated from time windows moving away at 1 min increments from the tachycardia episode. Trajectories were computed over 3 hours leading up to the episode for three different models. From 2809 subjects, 787 tachycardia episodes and 707 control periods were identified. Patients with tachycardia had increased vasopressor support, longer ICU stay, and increased ICU mortality than controls. In model evaluation, RF was slightly superior to LR, which accuracy ranged from 0.847 to 0.782, with area under the curve from 0.921 to 0.842. Risk trajectory analysis showed average risks for tachycardia group evolved to 0.78 prior to the tachycardia episodes, while control group risks remained < 0.3. Among the three models, the internal control model demonstrated evolving trajectory approximately 75 min before tachycardia episode. Clinically relevant tachycardia episodes can be predicted from vital sign time series using machine learning algorithms.
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spelling pubmed-68233042019-11-06 Predicting tachycardia as a surrogate for instability in the intensive care unit Yoon, Joo Heung Mu, Lidan Chen, Lujie Dubrawski, Artur Hravnak, Marilyn Pinsky, Michael R. Clermont, Gilles J Clin Monit Comput Original Research Tachycardia is a strong though non-specific marker of cardiovascular stress that proceeds hemodynamic instability. We designed a predictive model of tachycardia using multi-granular intensive care unit (ICU) data by creating a risk score and dynamic trajectory. A subset of clinical and numerical signals were extracted from the Multiparameter Intelligent Monitoring in Intensive Care II database. A tachycardia episode was defined as heart rate ≥ 130/min lasting for ≥ 5 min, with ≥ 10% density. Regularized logistic regression (LR) and random forest (RF) classifiers were trained to create a risk score for upcoming tachycardia. Three different risk score models were compared for tachycardia and control (non-tachycardia) groups. Risk trajectory was generated from time windows moving away at 1 min increments from the tachycardia episode. Trajectories were computed over 3 hours leading up to the episode for three different models. From 2809 subjects, 787 tachycardia episodes and 707 control periods were identified. Patients with tachycardia had increased vasopressor support, longer ICU stay, and increased ICU mortality than controls. In model evaluation, RF was slightly superior to LR, which accuracy ranged from 0.847 to 0.782, with area under the curve from 0.921 to 0.842. Risk trajectory analysis showed average risks for tachycardia group evolved to 0.78 prior to the tachycardia episodes, while control group risks remained < 0.3. Among the three models, the internal control model demonstrated evolving trajectory approximately 75 min before tachycardia episode. Clinically relevant tachycardia episodes can be predicted from vital sign time series using machine learning algorithms. Springer Netherlands 2019-02-14 2019 /pmc/articles/PMC6823304/ /pubmed/30767136 http://dx.doi.org/10.1007/s10877-019-00277-0 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Research
Yoon, Joo Heung
Mu, Lidan
Chen, Lujie
Dubrawski, Artur
Hravnak, Marilyn
Pinsky, Michael R.
Clermont, Gilles
Predicting tachycardia as a surrogate for instability in the intensive care unit
title Predicting tachycardia as a surrogate for instability in the intensive care unit
title_full Predicting tachycardia as a surrogate for instability in the intensive care unit
title_fullStr Predicting tachycardia as a surrogate for instability in the intensive care unit
title_full_unstemmed Predicting tachycardia as a surrogate for instability in the intensive care unit
title_short Predicting tachycardia as a surrogate for instability in the intensive care unit
title_sort predicting tachycardia as a surrogate for instability in the intensive care unit
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6823304/
https://www.ncbi.nlm.nih.gov/pubmed/30767136
http://dx.doi.org/10.1007/s10877-019-00277-0
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