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Trajectories of Vital Signs and Risk of In-Hospital Cardiac Arrest
Background: Little is known about the trajectories of vital signs prior to in-hospital cardiac arrest (IHCA), which could explain the heterogeneous processes preceding this event. We aimed to identify clinically relevant subphenotypes at high risk of IHCA in the emergency department (ED). Methods: T...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8761796/ https://www.ncbi.nlm.nih.gov/pubmed/35047534 http://dx.doi.org/10.3389/fmed.2021.800943 |
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author | Tsai, Chu-Lin Lu, Tsung-Chien Wang, Chih-Hung Fang, Cheng-Chung Chen, Wen-Jone Huang, Chien-Hua |
author_facet | Tsai, Chu-Lin Lu, Tsung-Chien Wang, Chih-Hung Fang, Cheng-Chung Chen, Wen-Jone Huang, Chien-Hua |
author_sort | Tsai, Chu-Lin |
collection | PubMed |
description | Background: Little is known about the trajectories of vital signs prior to in-hospital cardiac arrest (IHCA), which could explain the heterogeneous processes preceding this event. We aimed to identify clinically relevant subphenotypes at high risk of IHCA in the emergency department (ED). Methods: This retrospective cohort study used electronic clinical warehouse data from a tertiary medical center. We retrieved data from 733,398 ED visits over a 7-year period. We selected one ED visit per person and retrieved patient demographics, triage data, vital signs (systolic blood pressure [SBP], heart rate [HR], body temperature, respiratory rate, oxygen saturation), selected laboratory markers, and IHCA status. Group-based trajectory modeling was performed. Results: There were 37,697 adult ED patients with a total of 1,507,121 data points across all vital-sign categories. Three to four trajectory groups per vital-sign category were identified, and the following five trajectory groups were associated with a higher rate of IHCA: low and fluctuating SBP, high and fluctuating HR, persistent hypothermia, recurring tachypnea, and low and fluctuating oxygen saturation. The IHCA-prone trajectory group was associated with a higher triage level and a higher mortality rate, compared to other trajectory groups. Except for the persistent hypothermia group, the other four trajectory groups were more likely to have higher levels of C-reactive protein, lactic acid, cardiac troponin I, and D-dimer. Multivariable analysis revealed that hypothermia (adjusted odds ratio [aOR], 2.20; 95% confidence interval [95%CI], 1.35–3.57) and recurring tachypnea (aOR 2.44; 95%CI, 1.24–4.79) were independently associated with IHCA. Conclusions: We identified five novel vital-sign sub-phenotypes associated with a higher likelihood of IHCA, with distinct patterns in clinical course and laboratory markers. A better understanding of the pre-IHCA vital-sign trajectories may help with the early identification of deteriorating patients. |
format | Online Article Text |
id | pubmed-8761796 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-87617962022-01-18 Trajectories of Vital Signs and Risk of In-Hospital Cardiac Arrest Tsai, Chu-Lin Lu, Tsung-Chien Wang, Chih-Hung Fang, Cheng-Chung Chen, Wen-Jone Huang, Chien-Hua Front Med (Lausanne) Medicine Background: Little is known about the trajectories of vital signs prior to in-hospital cardiac arrest (IHCA), which could explain the heterogeneous processes preceding this event. We aimed to identify clinically relevant subphenotypes at high risk of IHCA in the emergency department (ED). Methods: This retrospective cohort study used electronic clinical warehouse data from a tertiary medical center. We retrieved data from 733,398 ED visits over a 7-year period. We selected one ED visit per person and retrieved patient demographics, triage data, vital signs (systolic blood pressure [SBP], heart rate [HR], body temperature, respiratory rate, oxygen saturation), selected laboratory markers, and IHCA status. Group-based trajectory modeling was performed. Results: There were 37,697 adult ED patients with a total of 1,507,121 data points across all vital-sign categories. Three to four trajectory groups per vital-sign category were identified, and the following five trajectory groups were associated with a higher rate of IHCA: low and fluctuating SBP, high and fluctuating HR, persistent hypothermia, recurring tachypnea, and low and fluctuating oxygen saturation. The IHCA-prone trajectory group was associated with a higher triage level and a higher mortality rate, compared to other trajectory groups. Except for the persistent hypothermia group, the other four trajectory groups were more likely to have higher levels of C-reactive protein, lactic acid, cardiac troponin I, and D-dimer. Multivariable analysis revealed that hypothermia (adjusted odds ratio [aOR], 2.20; 95% confidence interval [95%CI], 1.35–3.57) and recurring tachypnea (aOR 2.44; 95%CI, 1.24–4.79) were independently associated with IHCA. Conclusions: We identified five novel vital-sign sub-phenotypes associated with a higher likelihood of IHCA, with distinct patterns in clinical course and laboratory markers. A better understanding of the pre-IHCA vital-sign trajectories may help with the early identification of deteriorating patients. Frontiers Media S.A. 2022-01-03 /pmc/articles/PMC8761796/ /pubmed/35047534 http://dx.doi.org/10.3389/fmed.2021.800943 Text en Copyright © 2022 Tsai, Lu, Wang, Fang, Chen and Huang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Medicine Tsai, Chu-Lin Lu, Tsung-Chien Wang, Chih-Hung Fang, Cheng-Chung Chen, Wen-Jone Huang, Chien-Hua Trajectories of Vital Signs and Risk of In-Hospital Cardiac Arrest |
title | Trajectories of Vital Signs and Risk of In-Hospital Cardiac Arrest |
title_full | Trajectories of Vital Signs and Risk of In-Hospital Cardiac Arrest |
title_fullStr | Trajectories of Vital Signs and Risk of In-Hospital Cardiac Arrest |
title_full_unstemmed | Trajectories of Vital Signs and Risk of In-Hospital Cardiac Arrest |
title_short | Trajectories of Vital Signs and Risk of In-Hospital Cardiac Arrest |
title_sort | trajectories of vital signs and risk of in-hospital cardiac arrest |
topic | Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8761796/ https://www.ncbi.nlm.nih.gov/pubmed/35047534 http://dx.doi.org/10.3389/fmed.2021.800943 |
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