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Microcirculation alterations in severe COVID-19 pneumonia

PURPOSE: To assess the presence of sublingual microcirculatory and skin perfusion alterations in COVID-19 pneumonia. MATERIALS AND METHODS: This is a preliminary report of a prospective observational study performed in four teaching intensive care units. We studied 27 mechanically ventilated patient...

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Autores principales: Kanoore Edul, Vanina Siham, Caminos Eguillor, Juan Francisco, Ferrara, Gonzalo, Estenssoro, Elisa, Siles, Daniel Shiovan Páez, Cesio, Cristián Emanuel, Dubin, Arnaldo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7568145/
https://www.ncbi.nlm.nih.gov/pubmed/33096349
http://dx.doi.org/10.1016/j.jcrc.2020.10.002
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author Kanoore Edul, Vanina Siham
Caminos Eguillor, Juan Francisco
Ferrara, Gonzalo
Estenssoro, Elisa
Siles, Daniel Shiovan Páez
Cesio, Cristián Emanuel
Dubin, Arnaldo
author_facet Kanoore Edul, Vanina Siham
Caminos Eguillor, Juan Francisco
Ferrara, Gonzalo
Estenssoro, Elisa
Siles, Daniel Shiovan Páez
Cesio, Cristián Emanuel
Dubin, Arnaldo
author_sort Kanoore Edul, Vanina Siham
collection PubMed
description PURPOSE: To assess the presence of sublingual microcirculatory and skin perfusion alterations in COVID-19 pneumonia. MATERIALS AND METHODS: This is a preliminary report of a prospective observational study performed in four teaching intensive care units. We studied 27 mechanically ventilated patients with acute respiratory distress syndrome secondary to COVID-19. Sublingual microcirculation was assessed by hand-held videomicroscopy. A software-assisted analysis of videos was performed. We also measured capillary refill time. RESULTS: Patients were hemodynamically stable with normal lactate (1.8 [1.6–2.5] mmol/L) and high D-dimer (1.30 [0.58–2.93] μg/mL). Capillary refill time was prolonged (3.5 [3.0–5.0] s). Compared to previously reported normal values, total and perfused vascular density (21.9 ± 3.9 and 21.0 ± 3.5 mm/mm(2)) and heterogeneity flow index (0.91 ± 0.24) were high; and the proportion of perfused vessels (0.96 ± 0.03), microvascular flow index (2.79 ± 0.10), and red blood cell velocity (1124 ± 161 μm/s) were reduced. The proportion of perfused vessels was inversely correlated with total vascular density (Pearson r = −0.41, P = 0.03). CONCLUSIONS: COVID-19 patients showed an altered tissue perfusion. Sublingual microcirculation was characterized by decreases in the proportion of perfused vessel and flow velocity along with high vascular densities. This last finding might be related to enhanced angiogenesis or hypoxia-induced capillary recruitment.
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spelling pubmed-75681452020-10-19 Microcirculation alterations in severe COVID-19 pneumonia Kanoore Edul, Vanina Siham Caminos Eguillor, Juan Francisco Ferrara, Gonzalo Estenssoro, Elisa Siles, Daniel Shiovan Páez Cesio, Cristián Emanuel Dubin, Arnaldo J Crit Care Article PURPOSE: To assess the presence of sublingual microcirculatory and skin perfusion alterations in COVID-19 pneumonia. MATERIALS AND METHODS: This is a preliminary report of a prospective observational study performed in four teaching intensive care units. We studied 27 mechanically ventilated patients with acute respiratory distress syndrome secondary to COVID-19. Sublingual microcirculation was assessed by hand-held videomicroscopy. A software-assisted analysis of videos was performed. We also measured capillary refill time. RESULTS: Patients were hemodynamically stable with normal lactate (1.8 [1.6–2.5] mmol/L) and high D-dimer (1.30 [0.58–2.93] μg/mL). Capillary refill time was prolonged (3.5 [3.0–5.0] s). Compared to previously reported normal values, total and perfused vascular density (21.9 ± 3.9 and 21.0 ± 3.5 mm/mm(2)) and heterogeneity flow index (0.91 ± 0.24) were high; and the proportion of perfused vessels (0.96 ± 0.03), microvascular flow index (2.79 ± 0.10), and red blood cell velocity (1124 ± 161 μm/s) were reduced. The proportion of perfused vessels was inversely correlated with total vascular density (Pearson r = −0.41, P = 0.03). CONCLUSIONS: COVID-19 patients showed an altered tissue perfusion. Sublingual microcirculation was characterized by decreases in the proportion of perfused vessel and flow velocity along with high vascular densities. This last finding might be related to enhanced angiogenesis or hypoxia-induced capillary recruitment. Elsevier Inc. 2021-02 2020-10-17 /pmc/articles/PMC7568145/ /pubmed/33096349 http://dx.doi.org/10.1016/j.jcrc.2020.10.002 Text en © 2020 Elsevier Inc. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Kanoore Edul, Vanina Siham
Caminos Eguillor, Juan Francisco
Ferrara, Gonzalo
Estenssoro, Elisa
Siles, Daniel Shiovan Páez
Cesio, Cristián Emanuel
Dubin, Arnaldo
Microcirculation alterations in severe COVID-19 pneumonia
title Microcirculation alterations in severe COVID-19 pneumonia
title_full Microcirculation alterations in severe COVID-19 pneumonia
title_fullStr Microcirculation alterations in severe COVID-19 pneumonia
title_full_unstemmed Microcirculation alterations in severe COVID-19 pneumonia
title_short Microcirculation alterations in severe COVID-19 pneumonia
title_sort microcirculation alterations in severe covid-19 pneumonia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7568145/
https://www.ncbi.nlm.nih.gov/pubmed/33096349
http://dx.doi.org/10.1016/j.jcrc.2020.10.002
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