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Evaluation of the Hematological Patterns from Up to 985 Days of Long COVID: A Cross-Sectional Study
Long COVID affects many individuals following acute coronavirus disease 2019 (COVID-19), and hematological changes can persist after the acute COVID-19 phase. This study aimed to evaluate these hematological laboratory markers, linking them to clinical findings and long-term outcomes in patients wit...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10142608/ https://www.ncbi.nlm.nih.gov/pubmed/37112859 http://dx.doi.org/10.3390/v15040879 |
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author | Galúcio, Vanessa Costa Alves de Menezes, Daniel Carvalho de Lima, Patrícia Danielle Lima Palácios, Vera Regina da Cunha Menezes Vasconcelos, Pedro Fernando da Costa Quaresma, Juarez Antônio Simões Falcão, Luiz Fábio Magno |
author_facet | Galúcio, Vanessa Costa Alves de Menezes, Daniel Carvalho de Lima, Patrícia Danielle Lima Palácios, Vera Regina da Cunha Menezes Vasconcelos, Pedro Fernando da Costa Quaresma, Juarez Antônio Simões Falcão, Luiz Fábio Magno |
author_sort | Galúcio, Vanessa Costa Alves |
collection | PubMed |
description | Long COVID affects many individuals following acute coronavirus disease 2019 (COVID-19), and hematological changes can persist after the acute COVID-19 phase. This study aimed to evaluate these hematological laboratory markers, linking them to clinical findings and long-term outcomes in patients with long COVID. This cross-sectional study selected participants from a ‘long COVID’ clinical care program in the Amazon region. Clinical data and baseline demographics were obtained, and blood samples were collected to quantify erythrogram-, leukogram-, and plateletgram-related markers. Long COVID was reported for up to 985 days. Patients hospitalized in the acute phase had higher mean red/white blood cell, platelet, and plateletcrit levels and red blood cell distribution width. Furthermore, hematimetric parameters were higher in shorter periods of long COVID than in longer periods. Patients with more than six concomitant long COVID symptoms had a higher white blood cell count, a shorter prothrombin time (PT), and increased PT activity. Our results indicate there may be a compensatory mechanism for erythrogram-related markers within 985 days of long COVID. Increased levels of leukogram-related markers and coagulation activity were observed in the worst long COVID groups, indicating an exacerbated response after the acute disturbance, which is uncertain and requires further investigation. |
format | Online Article Text |
id | pubmed-10142608 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-101426082023-04-29 Evaluation of the Hematological Patterns from Up to 985 Days of Long COVID: A Cross-Sectional Study Galúcio, Vanessa Costa Alves de Menezes, Daniel Carvalho de Lima, Patrícia Danielle Lima Palácios, Vera Regina da Cunha Menezes Vasconcelos, Pedro Fernando da Costa Quaresma, Juarez Antônio Simões Falcão, Luiz Fábio Magno Viruses Article Long COVID affects many individuals following acute coronavirus disease 2019 (COVID-19), and hematological changes can persist after the acute COVID-19 phase. This study aimed to evaluate these hematological laboratory markers, linking them to clinical findings and long-term outcomes in patients with long COVID. This cross-sectional study selected participants from a ‘long COVID’ clinical care program in the Amazon region. Clinical data and baseline demographics were obtained, and blood samples were collected to quantify erythrogram-, leukogram-, and plateletgram-related markers. Long COVID was reported for up to 985 days. Patients hospitalized in the acute phase had higher mean red/white blood cell, platelet, and plateletcrit levels and red blood cell distribution width. Furthermore, hematimetric parameters were higher in shorter periods of long COVID than in longer periods. Patients with more than six concomitant long COVID symptoms had a higher white blood cell count, a shorter prothrombin time (PT), and increased PT activity. Our results indicate there may be a compensatory mechanism for erythrogram-related markers within 985 days of long COVID. Increased levels of leukogram-related markers and coagulation activity were observed in the worst long COVID groups, indicating an exacerbated response after the acute disturbance, which is uncertain and requires further investigation. MDPI 2023-03-29 /pmc/articles/PMC10142608/ /pubmed/37112859 http://dx.doi.org/10.3390/v15040879 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Galúcio, Vanessa Costa Alves de Menezes, Daniel Carvalho de Lima, Patrícia Danielle Lima Palácios, Vera Regina da Cunha Menezes Vasconcelos, Pedro Fernando da Costa Quaresma, Juarez Antônio Simões Falcão, Luiz Fábio Magno Evaluation of the Hematological Patterns from Up to 985 Days of Long COVID: A Cross-Sectional Study |
title | Evaluation of the Hematological Patterns from Up to 985 Days of Long COVID: A Cross-Sectional Study |
title_full | Evaluation of the Hematological Patterns from Up to 985 Days of Long COVID: A Cross-Sectional Study |
title_fullStr | Evaluation of the Hematological Patterns from Up to 985 Days of Long COVID: A Cross-Sectional Study |
title_full_unstemmed | Evaluation of the Hematological Patterns from Up to 985 Days of Long COVID: A Cross-Sectional Study |
title_short | Evaluation of the Hematological Patterns from Up to 985 Days of Long COVID: A Cross-Sectional Study |
title_sort | evaluation of the hematological patterns from up to 985 days of long covid: a cross-sectional study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10142608/ https://www.ncbi.nlm.nih.gov/pubmed/37112859 http://dx.doi.org/10.3390/v15040879 |
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