Cargando…

Development of a Decision Support Tool for Anticoagulation in Critically Ill Patients Admitted for SARS-CoV-2 Infection: The CALT Protocol

Severe COVID-19 infections are at high risk of causing thromboembolic events (TEEs). However, the usual exams may be unavailable or unreliable in predicting the risk of TEEs at admission or during hospitalization. We performed a retrospective analysis of two centers (n = 124 patients) including seve...

Descripción completa

Detalles Bibliográficos
Autores principales: Dubar, Victoria, Pascreau, Tiffany, Dupont, Annabelle, Dubucquoi, Sylvain, Dautigny, Anne-Laure, Ghozlan, Benoit, Zuber, Benjamin, Mellot, François, Vasse, Marc, Susen, Sophie, Poissy, Julien, Gaudet, Alexandre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10295063/
https://www.ncbi.nlm.nih.gov/pubmed/37371599
http://dx.doi.org/10.3390/biomedicines11061504
_version_ 1785063331261841408
author Dubar, Victoria
Pascreau, Tiffany
Dupont, Annabelle
Dubucquoi, Sylvain
Dautigny, Anne-Laure
Ghozlan, Benoit
Zuber, Benjamin
Mellot, François
Vasse, Marc
Susen, Sophie
Poissy, Julien
Gaudet, Alexandre
author_facet Dubar, Victoria
Pascreau, Tiffany
Dupont, Annabelle
Dubucquoi, Sylvain
Dautigny, Anne-Laure
Ghozlan, Benoit
Zuber, Benjamin
Mellot, François
Vasse, Marc
Susen, Sophie
Poissy, Julien
Gaudet, Alexandre
author_sort Dubar, Victoria
collection PubMed
description Severe COVID-19 infections are at high risk of causing thromboembolic events (TEEs). However, the usual exams may be unavailable or unreliable in predicting the risk of TEEs at admission or during hospitalization. We performed a retrospective analysis of two centers (n = 124 patients) including severe COVID-19 patients to determine the specific risk factors of TEEs in SARS-CoV-2 infection at admission and during stays at the intensive care unit (ICU). We used stepwise regression to create two composite scores in order to predict TEEs in the first 48 h (H0–H48) and during the first 15 days (D1–D15) in ICU. We then evaluated the performance of our scores in our cohort. During the period H0–H48, patients with a TEE diagnosis had higher D-Dimers and ferritin values at day 1 (D1) and day 3 (D3) and a greater drop in fibrinogen between D1 and D3 compared with patients without TEEs. Over the period D1-D15, patients with a diagnosis of a TEE showed a more marked drop in fibrinogen and had higher D-Dimers and lactate dehydrogenase (LDH) values at D1 and D3. Based on ROC analysis, the COVID-related acute lung and deep vein thrombosis (CALT) 1 score, calculated at D1, had a diagnostic performance for TEEs at H0–H48, estimated using an area under the curve (AUC) of 0.85 (CI95%: 0.76–0.93, p < 10(−3)). The CALT 2 score, calculated at D3, predicted the occurrence of TEEs over the period D1-D15 with an estimated AUC of 0.85 (CI95%: 0.77–0.93, p < 10(−3)). These two scores were used as the basis for the development of the CALT protocol, a tool to assist in the decision to use anticoagulation during severe SARS-CoV-2 infections. The CALT scores showed good performances in predicting the risk of TEEs in severe COVID-19 patients at admission and during ICU stays. They could, therefore, be used as a decision support protocol on whether or not to initiate therapeutic anticoagulation.
format Online
Article
Text
id pubmed-10295063
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-102950632023-06-28 Development of a Decision Support Tool for Anticoagulation in Critically Ill Patients Admitted for SARS-CoV-2 Infection: The CALT Protocol Dubar, Victoria Pascreau, Tiffany Dupont, Annabelle Dubucquoi, Sylvain Dautigny, Anne-Laure Ghozlan, Benoit Zuber, Benjamin Mellot, François Vasse, Marc Susen, Sophie Poissy, Julien Gaudet, Alexandre Biomedicines Article Severe COVID-19 infections are at high risk of causing thromboembolic events (TEEs). However, the usual exams may be unavailable or unreliable in predicting the risk of TEEs at admission or during hospitalization. We performed a retrospective analysis of two centers (n = 124 patients) including severe COVID-19 patients to determine the specific risk factors of TEEs in SARS-CoV-2 infection at admission and during stays at the intensive care unit (ICU). We used stepwise regression to create two composite scores in order to predict TEEs in the first 48 h (H0–H48) and during the first 15 days (D1–D15) in ICU. We then evaluated the performance of our scores in our cohort. During the period H0–H48, patients with a TEE diagnosis had higher D-Dimers and ferritin values at day 1 (D1) and day 3 (D3) and a greater drop in fibrinogen between D1 and D3 compared with patients without TEEs. Over the period D1-D15, patients with a diagnosis of a TEE showed a more marked drop in fibrinogen and had higher D-Dimers and lactate dehydrogenase (LDH) values at D1 and D3. Based on ROC analysis, the COVID-related acute lung and deep vein thrombosis (CALT) 1 score, calculated at D1, had a diagnostic performance for TEEs at H0–H48, estimated using an area under the curve (AUC) of 0.85 (CI95%: 0.76–0.93, p < 10(−3)). The CALT 2 score, calculated at D3, predicted the occurrence of TEEs over the period D1-D15 with an estimated AUC of 0.85 (CI95%: 0.77–0.93, p < 10(−3)). These two scores were used as the basis for the development of the CALT protocol, a tool to assist in the decision to use anticoagulation during severe SARS-CoV-2 infections. The CALT scores showed good performances in predicting the risk of TEEs in severe COVID-19 patients at admission and during ICU stays. They could, therefore, be used as a decision support protocol on whether or not to initiate therapeutic anticoagulation. MDPI 2023-05-23 /pmc/articles/PMC10295063/ /pubmed/37371599 http://dx.doi.org/10.3390/biomedicines11061504 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
Dubar, Victoria
Pascreau, Tiffany
Dupont, Annabelle
Dubucquoi, Sylvain
Dautigny, Anne-Laure
Ghozlan, Benoit
Zuber, Benjamin
Mellot, François
Vasse, Marc
Susen, Sophie
Poissy, Julien
Gaudet, Alexandre
Development of a Decision Support Tool for Anticoagulation in Critically Ill Patients Admitted for SARS-CoV-2 Infection: The CALT Protocol
title Development of a Decision Support Tool for Anticoagulation in Critically Ill Patients Admitted for SARS-CoV-2 Infection: The CALT Protocol
title_full Development of a Decision Support Tool for Anticoagulation in Critically Ill Patients Admitted for SARS-CoV-2 Infection: The CALT Protocol
title_fullStr Development of a Decision Support Tool for Anticoagulation in Critically Ill Patients Admitted for SARS-CoV-2 Infection: The CALT Protocol
title_full_unstemmed Development of a Decision Support Tool for Anticoagulation in Critically Ill Patients Admitted for SARS-CoV-2 Infection: The CALT Protocol
title_short Development of a Decision Support Tool for Anticoagulation in Critically Ill Patients Admitted for SARS-CoV-2 Infection: The CALT Protocol
title_sort development of a decision support tool for anticoagulation in critically ill patients admitted for sars-cov-2 infection: the calt protocol
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10295063/
https://www.ncbi.nlm.nih.gov/pubmed/37371599
http://dx.doi.org/10.3390/biomedicines11061504
work_keys_str_mv AT dubarvictoria developmentofadecisionsupporttoolforanticoagulationincriticallyillpatientsadmittedforsarscov2infectionthecaltprotocol
AT pascreautiffany developmentofadecisionsupporttoolforanticoagulationincriticallyillpatientsadmittedforsarscov2infectionthecaltprotocol
AT dupontannabelle developmentofadecisionsupporttoolforanticoagulationincriticallyillpatientsadmittedforsarscov2infectionthecaltprotocol
AT dubucquoisylvain developmentofadecisionsupporttoolforanticoagulationincriticallyillpatientsadmittedforsarscov2infectionthecaltprotocol
AT dautignyannelaure developmentofadecisionsupporttoolforanticoagulationincriticallyillpatientsadmittedforsarscov2infectionthecaltprotocol
AT ghozlanbenoit developmentofadecisionsupporttoolforanticoagulationincriticallyillpatientsadmittedforsarscov2infectionthecaltprotocol
AT zuberbenjamin developmentofadecisionsupporttoolforanticoagulationincriticallyillpatientsadmittedforsarscov2infectionthecaltprotocol
AT mellotfrancois developmentofadecisionsupporttoolforanticoagulationincriticallyillpatientsadmittedforsarscov2infectionthecaltprotocol
AT vassemarc developmentofadecisionsupporttoolforanticoagulationincriticallyillpatientsadmittedforsarscov2infectionthecaltprotocol
AT susensophie developmentofadecisionsupporttoolforanticoagulationincriticallyillpatientsadmittedforsarscov2infectionthecaltprotocol
AT poissyjulien developmentofadecisionsupporttoolforanticoagulationincriticallyillpatientsadmittedforsarscov2infectionthecaltprotocol
AT gaudetalexandre developmentofadecisionsupporttoolforanticoagulationincriticallyillpatientsadmittedforsarscov2infectionthecaltprotocol