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Pilot clinical study of quantitative ultrasound spectroscopy measurements of erythrocyte aggregation within superficial veins

BACKGROUND: An enhanced inflammatory response is a trigger to the production of blood macromolecules involved in abnormally high levels of erythrocyte aggregation. OBJECTIVE: This study aimed at demonstrating for the first time the clinical feasibility of a non-invasive ultrasound-based erythrocyte...

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Autores principales: Chayer, Boris, Allard, Louise, Qin, Zhao, Garcia-Duitama, Julian, Roger, Laurence, Destrempes, François, Cailhier, Jean-François, Denault, André, Cloutier, Guy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7242846/
https://www.ncbi.nlm.nih.gov/pubmed/31476146
http://dx.doi.org/10.3233/CH-180541
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author Chayer, Boris
Allard, Louise
Qin, Zhao
Garcia-Duitama, Julian
Roger, Laurence
Destrempes, François
Cailhier, Jean-François
Denault, André
Cloutier, Guy
author_facet Chayer, Boris
Allard, Louise
Qin, Zhao
Garcia-Duitama, Julian
Roger, Laurence
Destrempes, François
Cailhier, Jean-François
Denault, André
Cloutier, Guy
author_sort Chayer, Boris
collection PubMed
description BACKGROUND: An enhanced inflammatory response is a trigger to the production of blood macromolecules involved in abnormally high levels of erythrocyte aggregation. OBJECTIVE: This study aimed at demonstrating for the first time the clinical feasibility of a non-invasive ultrasound-based erythrocyte aggregation quantitative measurement method for potential application in critical care medicine. METHODS: Erythrocyte aggregation was evaluated using modeling of the backscatter coefficient with the Structure Factor Size and Attenuation Estimator (SFSAE). SFSAE spectral parameters W (packing factor) and D (mean aggregate diameter) were measured within the antebrachial vein of the forearm and tibial vein of the leg in 50 healthy participants at natural flow and reduced flow controlled by a pressurized bracelet. Blood samples were also collected to measure erythrocyte aggregation ex vivo with an erythroaggregometer (parameter S(10)). RESULTS: W and D in vivo measurements were positively correlated with the ex vivo S(10) index for both measurement sites and shear rates (correlations between 0.35–0.81, p < 0.05). Measurement at low shear rate was found to increase the sensitivity and reliability of this non-invasive measurement method. CONCLUSIONS: We behold that the SFSAE method presents systemic measures of the erythrocyte aggregation level, since results on upper and lower limbs were highly correlated.
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spelling pubmed-72428462020-05-27 Pilot clinical study of quantitative ultrasound spectroscopy measurements of erythrocyte aggregation within superficial veins Chayer, Boris Allard, Louise Qin, Zhao Garcia-Duitama, Julian Roger, Laurence Destrempes, François Cailhier, Jean-François Denault, André Cloutier, Guy Clin Hemorheol Microcirc Research Article BACKGROUND: An enhanced inflammatory response is a trigger to the production of blood macromolecules involved in abnormally high levels of erythrocyte aggregation. OBJECTIVE: This study aimed at demonstrating for the first time the clinical feasibility of a non-invasive ultrasound-based erythrocyte aggregation quantitative measurement method for potential application in critical care medicine. METHODS: Erythrocyte aggregation was evaluated using modeling of the backscatter coefficient with the Structure Factor Size and Attenuation Estimator (SFSAE). SFSAE spectral parameters W (packing factor) and D (mean aggregate diameter) were measured within the antebrachial vein of the forearm and tibial vein of the leg in 50 healthy participants at natural flow and reduced flow controlled by a pressurized bracelet. Blood samples were also collected to measure erythrocyte aggregation ex vivo with an erythroaggregometer (parameter S(10)). RESULTS: W and D in vivo measurements were positively correlated with the ex vivo S(10) index for both measurement sites and shear rates (correlations between 0.35–0.81, p < 0.05). Measurement at low shear rate was found to increase the sensitivity and reliability of this non-invasive measurement method. CONCLUSIONS: We behold that the SFSAE method presents systemic measures of the erythrocyte aggregation level, since results on upper and lower limbs were highly correlated. IOS Press 2020-04-01 /pmc/articles/PMC7242846/ /pubmed/31476146 http://dx.doi.org/10.3233/CH-180541 Text en © 2020 – IOS Press and the authors. All rights reserved https://creativecommons.org/licenses/by-nc/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial (CC BY-NC 4.0) License (https://creativecommons.org/licenses/by-nc/4.0/) , which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Chayer, Boris
Allard, Louise
Qin, Zhao
Garcia-Duitama, Julian
Roger, Laurence
Destrempes, François
Cailhier, Jean-François
Denault, André
Cloutier, Guy
Pilot clinical study of quantitative ultrasound spectroscopy measurements of erythrocyte aggregation within superficial veins
title Pilot clinical study of quantitative ultrasound spectroscopy measurements of erythrocyte aggregation within superficial veins
title_full Pilot clinical study of quantitative ultrasound spectroscopy measurements of erythrocyte aggregation within superficial veins
title_fullStr Pilot clinical study of quantitative ultrasound spectroscopy measurements of erythrocyte aggregation within superficial veins
title_full_unstemmed Pilot clinical study of quantitative ultrasound spectroscopy measurements of erythrocyte aggregation within superficial veins
title_short Pilot clinical study of quantitative ultrasound spectroscopy measurements of erythrocyte aggregation within superficial veins
title_sort pilot clinical study of quantitative ultrasound spectroscopy measurements of erythrocyte aggregation within superficial veins
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7242846/
https://www.ncbi.nlm.nih.gov/pubmed/31476146
http://dx.doi.org/10.3233/CH-180541
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