COVID-19-associated Coagulopathy Characterization using Rotational Thromboelastometry in a Prospective, Observational Cohort Study: The HemoCoV Study
Autor(a) principal: | |
---|---|
Data de Publicação: | 2023 |
Outros Autores: | , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/19475 |
Resumo: | Introduction: COVID-19-associated coagulopathy includes systemic and endothelial inflammation with coagulation dysregulation related to immunothrombosis. The aim of this study was to characterize this complication of SARS-CoV-2 infection in patients with moderate to severe COVID-19. Methods: An open-label, prospective observational study conducted in patients with COVID-19 moderate to severe acute respiratory failure admitted to an intensive care unit (ICU). Coagulation testing, including thromboelastometry, biochemical analysis and clinical variables, were collected at prespecified time points during the 30 days of ICU stay.Results: The study included 145 patients, 73.8% male, with a median age of 68 years (interquartile range - IQR 55 - 74). The most prevalent comorbidities were arterial hypertension (63.4%), obesity (44.1%) and diabetes (22.1%). Simplified acute physiology score II (SAPS II) was on average 43.5 (11 - 105) and sequential organ failure assessment (SOFA) at admission was 7.5 (0 - 14). During ICU stay, 66.9% of patients underwent invasive mechanical ventilation and 18.4% extracorporeal membrane oxygenation support; thrombotic and hemorrhagic events occurred in 22.1% and 15.1% of the patients respectively; anticoagulation with heparin was present in 99.2% of patients since early ICU stay. Death occurred in 35% of patients. Longitudinal studies revealed changes in almost all coagulation tests during the ICU stay. SOFA score, lymphocyte counts, some biochemical, inflammatory and coagulation parameters, including hypercoagulability and hypofibrinolysis seen in thromboelastometry, differed significantly (p < 0.05), between ICU admission and discharge. Hypercoagulability and hypofibrinolysis persisted throughout ICU hospitalization, showing higher incidence and severity in non-survivors.Conclusion: COVID-19-associated coagulopathy is characterized by hypercoagulability and hypofibrinolysis from ICU admission, and persisted throughout the clinical course in severe COVID-19. These changes were more pronounced in patients with higher disease burden and in non-survivors. |
id |
RCAP_1b29157e2f2c1bf8e3e845a8cb81303e |
---|---|
oai_identifier_str |
oai:ojs.www.actamedicaportuguesa.com:article/19475 |
network_acronym_str |
RCAP |
network_name_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
repository_id_str |
7160 |
spelling |
COVID-19-associated Coagulopathy Characterization using Rotational Thromboelastometry in a Prospective, Observational Cohort Study: The HemoCoV StudyCaracterização da Coagulopatia Associada ao COVID-19 usando Tromboelastometria Rotacional num Estudo Observacional de Coorte Prospetivo: Estudo HemoCovBlood Coagulation DisordersCOVID-19FibrinolysisThromboelastometryThrombosisCOVID-19FibrinólisePerturbações da Coagulação SanguíneaTromboelastometriaTromboseIntroduction: COVID-19-associated coagulopathy includes systemic and endothelial inflammation with coagulation dysregulation related to immunothrombosis. The aim of this study was to characterize this complication of SARS-CoV-2 infection in patients with moderate to severe COVID-19. Methods: An open-label, prospective observational study conducted in patients with COVID-19 moderate to severe acute respiratory failure admitted to an intensive care unit (ICU). Coagulation testing, including thromboelastometry, biochemical analysis and clinical variables, were collected at prespecified time points during the 30 days of ICU stay.Results: The study included 145 patients, 73.8% male, with a median age of 68 years (interquartile range - IQR 55 - 74). The most prevalent comorbidities were arterial hypertension (63.4%), obesity (44.1%) and diabetes (22.1%). Simplified acute physiology score II (SAPS II) was on average 43.5 (11 - 105) and sequential organ failure assessment (SOFA) at admission was 7.5 (0 - 14). During ICU stay, 66.9% of patients underwent invasive mechanical ventilation and 18.4% extracorporeal membrane oxygenation support; thrombotic and hemorrhagic events occurred in 22.1% and 15.1% of the patients respectively; anticoagulation with heparin was present in 99.2% of patients since early ICU stay. Death occurred in 35% of patients. Longitudinal studies revealed changes in almost all coagulation tests during the ICU stay. SOFA score, lymphocyte counts, some biochemical, inflammatory and coagulation parameters, including hypercoagulability and hypofibrinolysis seen in thromboelastometry, differed significantly (p < 0.05), between ICU admission and discharge. Hypercoagulability and hypofibrinolysis persisted throughout ICU hospitalization, showing higher incidence and severity in non-survivors.Conclusion: COVID-19-associated coagulopathy is characterized by hypercoagulability and hypofibrinolysis from ICU admission, and persisted throughout the clinical course in severe COVID-19. These changes were more pronounced in patients with higher disease burden and in non-survivors.Introdução: A coagulopatia associada à COVID-19 inclui inflamação sistémica e endotelial com desregulação da coagulação relacionada com imunotrombose. O objetivo deste estudo foi caracterizar esta complicação da infecção por SARS-CoV-2 em doentes com infeção COVID-19 moderada a grave.Métodos: Estudo prospetivo observacional open-label conduzido em doentes com insuficiência respiratória aguda COVID-19 moderada a grave admitidos numa unidade de cuidados intensivos (UCI). Testes da coagulação, incluindo tromboelastometria, testes de bioquímica e variáveis clínicas foram colhidos em pontos de análise predefinidos durante 30 dias de internamento na UCI.Resultados: Foram incluídos 145 doentes, 73,8% homens, com uma mediana de idade de 68 anos (intervalo interquartílico – IIQ 55 - 74). As comorbilidades mais prevalentes foram hipertensão arterial (63,4%), obesidade (44,1%) e diabetes (22,1%). Na admissão, o simplified acute physiology score II (SAPS II) apresentou uma mediana de 43,5 (11 - 105) e o sequential organ failure assessment (SOFA) de 7,5 (0 - 14). Durante a estadia na UCI, 66,9% dos doentes foram submetidos a ventilação mecânica invasiva e 18,4% a suporte com extracorporeal membrane oxygenation; Eventos trombóticos e hemorrágicos ocorreram em 22,1% e 15,1% dos doentes respetivamente; anticoagulação com heparina esteve presente em 99,2% dos doentes desde precocemente durante a estadia na UCI. A morte ocorreu em 35% dos doentes. Estudos longitudinais revelaram alterações em quase todos os testes da coagulação durante a hospitalização na UCI. O SOFA score, a contagem de linfócitos, alguns parâmetros bioquímicos, inflamatórios e da coagulação, incluindo hipercoagulabilidade e hipofibrinólise observados na tromboelastometria, diferiram significativamente (p < 0,05), entre a admissão e a alta da UCI. A hipercoagulabilidade e a hipofibrinólise persistiram ao longo da hospitalização na ICU, mostrando maior incidência e gravidade nos doentes não sobreviventes.Conclusão: A coagulopatia associada à COVID-19 é caracterizada por hipercoagulabilidade e hipofibrinólise desde a admissão na UCI, as quais persistiram durante o curso clínico na infeção COVID-19 grave. Estas alterações foram mais pronunciadas nos doentes com maior gravidade e nos não sobreviventes.Ordem dos Médicos2023-07-03info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfapplication/pdfapplication/pdfhttps://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/19475Acta Médica Portuguesa; Vol. 36 No. 7-8 (2023): July-August; 496-505Acta Médica Portuguesa; Vol. 36 N.º 7-8 (2023): Julho-Agosto; 496-5051646-07580870-399Xreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAPenghttps://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/19475https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/19475/15174https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/19475/15148https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/19475/15151Direitos de Autor (c) 2023 Acta Médica Portuguesainfo:eu-repo/semantics/openAccessRodrigues, AnabelaDias Domingues, TiagoNobre Jesus, GustavoGarção, AnaRodrigues, Ana RitaJacinto Correia, CatarinaLeal Pereira, CarlaCorreia, DulceBeleza, ÁlvaroRibeiro, João Miguel2023-07-09T03:00:27Zoai:ojs.www.actamedicaportuguesa.com:article/19475Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T18:02:52.592623Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
COVID-19-associated Coagulopathy Characterization using Rotational Thromboelastometry in a Prospective, Observational Cohort Study: The HemoCoV Study Caracterização da Coagulopatia Associada ao COVID-19 usando Tromboelastometria Rotacional num Estudo Observacional de Coorte Prospetivo: Estudo HemoCov |
title |
COVID-19-associated Coagulopathy Characterization using Rotational Thromboelastometry in a Prospective, Observational Cohort Study: The HemoCoV Study |
spellingShingle |
COVID-19-associated Coagulopathy Characterization using Rotational Thromboelastometry in a Prospective, Observational Cohort Study: The HemoCoV Study Rodrigues, Anabela Blood Coagulation Disorders COVID-19 Fibrinolysis Thromboelastometry Thrombosis COVID-19 Fibrinólise Perturbações da Coagulação Sanguínea Tromboelastometria Trombose |
title_short |
COVID-19-associated Coagulopathy Characterization using Rotational Thromboelastometry in a Prospective, Observational Cohort Study: The HemoCoV Study |
title_full |
COVID-19-associated Coagulopathy Characterization using Rotational Thromboelastometry in a Prospective, Observational Cohort Study: The HemoCoV Study |
title_fullStr |
COVID-19-associated Coagulopathy Characterization using Rotational Thromboelastometry in a Prospective, Observational Cohort Study: The HemoCoV Study |
title_full_unstemmed |
COVID-19-associated Coagulopathy Characterization using Rotational Thromboelastometry in a Prospective, Observational Cohort Study: The HemoCoV Study |
title_sort |
COVID-19-associated Coagulopathy Characterization using Rotational Thromboelastometry in a Prospective, Observational Cohort Study: The HemoCoV Study |
author |
Rodrigues, Anabela |
author_facet |
Rodrigues, Anabela Dias Domingues, Tiago Nobre Jesus, Gustavo Garção, Ana Rodrigues, Ana Rita Jacinto Correia, Catarina Leal Pereira, Carla Correia, Dulce Beleza, Álvaro Ribeiro, João Miguel |
author_role |
author |
author2 |
Dias Domingues, Tiago Nobre Jesus, Gustavo Garção, Ana Rodrigues, Ana Rita Jacinto Correia, Catarina Leal Pereira, Carla Correia, Dulce Beleza, Álvaro Ribeiro, João Miguel |
author2_role |
author author author author author author author author author |
dc.contributor.author.fl_str_mv |
Rodrigues, Anabela Dias Domingues, Tiago Nobre Jesus, Gustavo Garção, Ana Rodrigues, Ana Rita Jacinto Correia, Catarina Leal Pereira, Carla Correia, Dulce Beleza, Álvaro Ribeiro, João Miguel |
dc.subject.por.fl_str_mv |
Blood Coagulation Disorders COVID-19 Fibrinolysis Thromboelastometry Thrombosis COVID-19 Fibrinólise Perturbações da Coagulação Sanguínea Tromboelastometria Trombose |
topic |
Blood Coagulation Disorders COVID-19 Fibrinolysis Thromboelastometry Thrombosis COVID-19 Fibrinólise Perturbações da Coagulação Sanguínea Tromboelastometria Trombose |
description |
Introduction: COVID-19-associated coagulopathy includes systemic and endothelial inflammation with coagulation dysregulation related to immunothrombosis. The aim of this study was to characterize this complication of SARS-CoV-2 infection in patients with moderate to severe COVID-19. Methods: An open-label, prospective observational study conducted in patients with COVID-19 moderate to severe acute respiratory failure admitted to an intensive care unit (ICU). Coagulation testing, including thromboelastometry, biochemical analysis and clinical variables, were collected at prespecified time points during the 30 days of ICU stay.Results: The study included 145 patients, 73.8% male, with a median age of 68 years (interquartile range - IQR 55 - 74). The most prevalent comorbidities were arterial hypertension (63.4%), obesity (44.1%) and diabetes (22.1%). Simplified acute physiology score II (SAPS II) was on average 43.5 (11 - 105) and sequential organ failure assessment (SOFA) at admission was 7.5 (0 - 14). During ICU stay, 66.9% of patients underwent invasive mechanical ventilation and 18.4% extracorporeal membrane oxygenation support; thrombotic and hemorrhagic events occurred in 22.1% and 15.1% of the patients respectively; anticoagulation with heparin was present in 99.2% of patients since early ICU stay. Death occurred in 35% of patients. Longitudinal studies revealed changes in almost all coagulation tests during the ICU stay. SOFA score, lymphocyte counts, some biochemical, inflammatory and coagulation parameters, including hypercoagulability and hypofibrinolysis seen in thromboelastometry, differed significantly (p < 0.05), between ICU admission and discharge. Hypercoagulability and hypofibrinolysis persisted throughout ICU hospitalization, showing higher incidence and severity in non-survivors.Conclusion: COVID-19-associated coagulopathy is characterized by hypercoagulability and hypofibrinolysis from ICU admission, and persisted throughout the clinical course in severe COVID-19. These changes were more pronounced in patients with higher disease burden and in non-survivors. |
publishDate |
2023 |
dc.date.none.fl_str_mv |
2023-07-03 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/19475 |
url |
https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/19475 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/19475 https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/19475/15174 https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/19475/15148 https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/19475/15151 |
dc.rights.driver.fl_str_mv |
Direitos de Autor (c) 2023 Acta Médica Portuguesa info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
Direitos de Autor (c) 2023 Acta Médica Portuguesa |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
Ordem dos Médicos |
publisher.none.fl_str_mv |
Ordem dos Médicos |
dc.source.none.fl_str_mv |
Acta Médica Portuguesa; Vol. 36 No. 7-8 (2023): July-August; 496-505 Acta Médica Portuguesa; Vol. 36 N.º 7-8 (2023): Julho-Agosto; 496-505 1646-0758 0870-399X reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
instname_str |
Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
instacron_str |
RCAAP |
institution |
RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
collection |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
repository.name.fl_str_mv |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
repository.mail.fl_str_mv |
|
_version_ |
1799131694187413504 |