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Time and frequency domain analysis of physiological features during autonomic dysreflexia after spinal cord injury

INTRODUCTION: Autonomic dysreflexia (AD) affects about 70% of individuals with spinal cord injury (SCI) and can have severe consequences, including death if not promptly detected and managed. The current gold standard for AD detection involves continuous blood pressure monitoring, which can be incon...

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Autores principales: Kirby, Ana Karina, Pancholi, Sidharth, Anderson, Zada, Chesler, Caroline, Everett, Thomas H., Duerstock, Bradley S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10493396/
https://www.ncbi.nlm.nih.gov/pubmed/37700754
http://dx.doi.org/10.3389/fnins.2023.1210815
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author Kirby, Ana Karina
Pancholi, Sidharth
Anderson, Zada
Chesler, Caroline
Everett, Thomas H.
Duerstock, Bradley S.
author_facet Kirby, Ana Karina
Pancholi, Sidharth
Anderson, Zada
Chesler, Caroline
Everett, Thomas H.
Duerstock, Bradley S.
author_sort Kirby, Ana Karina
collection PubMed
description INTRODUCTION: Autonomic dysreflexia (AD) affects about 70% of individuals with spinal cord injury (SCI) and can have severe consequences, including death if not promptly detected and managed. The current gold standard for AD detection involves continuous blood pressure monitoring, which can be inconvenient. Therefore, a non-invasive detection device would be valuable for rapid and continuous AD detection. METHODS: Implanted rodent models were used to analyze autonomic dysreflexia after spinal cord injury. Skin nerve activity (SKNA) features were extracted from ECG signals recorded non-invasively, using ECG electrodes. At the same time, blood pressure and ECG data sampled was collected using an implanted telemetry device. Heart rate variability (HRV) features were extracted from these ECG signals. SKNA and HRV parameters were analyzed in both the time and frequency domain. RESULTS: We found that SKNA features showed an increase approximately 18 seconds before the typical rise in systolic blood pressure, indicating the onset of AD in a rat model with upper thoracic SCI. Additionally, low-frequency components of SKNA in the frequency domain were dominant during AD, suggesting their potential inclusion in an AD detection system for improved accuracy. DISCUSSION: Utilizing SKNA measurements could enable early alerts to individuals with SCI, allowing timely intervention and mitigation of the adverse effects of AD, thereby enhancing their overall well-being and safety.
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spelling pubmed-104933962023-09-12 Time and frequency domain analysis of physiological features during autonomic dysreflexia after spinal cord injury Kirby, Ana Karina Pancholi, Sidharth Anderson, Zada Chesler, Caroline Everett, Thomas H. Duerstock, Bradley S. Front Neurosci Neuroscience INTRODUCTION: Autonomic dysreflexia (AD) affects about 70% of individuals with spinal cord injury (SCI) and can have severe consequences, including death if not promptly detected and managed. The current gold standard for AD detection involves continuous blood pressure monitoring, which can be inconvenient. Therefore, a non-invasive detection device would be valuable for rapid and continuous AD detection. METHODS: Implanted rodent models were used to analyze autonomic dysreflexia after spinal cord injury. Skin nerve activity (SKNA) features were extracted from ECG signals recorded non-invasively, using ECG electrodes. At the same time, blood pressure and ECG data sampled was collected using an implanted telemetry device. Heart rate variability (HRV) features were extracted from these ECG signals. SKNA and HRV parameters were analyzed in both the time and frequency domain. RESULTS: We found that SKNA features showed an increase approximately 18 seconds before the typical rise in systolic blood pressure, indicating the onset of AD in a rat model with upper thoracic SCI. Additionally, low-frequency components of SKNA in the frequency domain were dominant during AD, suggesting their potential inclusion in an AD detection system for improved accuracy. DISCUSSION: Utilizing SKNA measurements could enable early alerts to individuals with SCI, allowing timely intervention and mitigation of the adverse effects of AD, thereby enhancing their overall well-being and safety. Frontiers Media S.A. 2023-08-28 /pmc/articles/PMC10493396/ /pubmed/37700754 http://dx.doi.org/10.3389/fnins.2023.1210815 Text en Copyright © 2023 Kirby, Pancholi, Anderson, Chesler, Everett and Duerstock. 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 Neuroscience
Kirby, Ana Karina
Pancholi, Sidharth
Anderson, Zada
Chesler, Caroline
Everett, Thomas H.
Duerstock, Bradley S.
Time and frequency domain analysis of physiological features during autonomic dysreflexia after spinal cord injury
title Time and frequency domain analysis of physiological features during autonomic dysreflexia after spinal cord injury
title_full Time and frequency domain analysis of physiological features during autonomic dysreflexia after spinal cord injury
title_fullStr Time and frequency domain analysis of physiological features during autonomic dysreflexia after spinal cord injury
title_full_unstemmed Time and frequency domain analysis of physiological features during autonomic dysreflexia after spinal cord injury
title_short Time and frequency domain analysis of physiological features during autonomic dysreflexia after spinal cord injury
title_sort time and frequency domain analysis of physiological features during autonomic dysreflexia after spinal cord injury
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10493396/
https://www.ncbi.nlm.nih.gov/pubmed/37700754
http://dx.doi.org/10.3389/fnins.2023.1210815
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