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D-Dimer as a potential biomarker for disease severity in COVID-19

INTRODUCTION: This study seeks to determine the utility of D-dimer levels as a biomarker in determining disease severity and prognosis in COVID-19. METHODS: Clinical, imaging and laboratory data of 120 patients whose COVID-19 diagnosis based on RT-PCR were evaluated retrospectively. Clinically, the...

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Autores principales: Ozen, Mert, Yilmaz, Atakan, Cakmak, Vefa, Beyoglu, Resad, Oskay, Alten, Seyit, Murat, Senol, Hande
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7837156/
https://www.ncbi.nlm.nih.gov/pubmed/33348224
http://dx.doi.org/10.1016/j.ajem.2020.12.023
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author Ozen, Mert
Yilmaz, Atakan
Cakmak, Vefa
Beyoglu, Resad
Oskay, Alten
Seyit, Murat
Senol, Hande
author_facet Ozen, Mert
Yilmaz, Atakan
Cakmak, Vefa
Beyoglu, Resad
Oskay, Alten
Seyit, Murat
Senol, Hande
author_sort Ozen, Mert
collection PubMed
description INTRODUCTION: This study seeks to determine the utility of D-dimer levels as a biomarker in determining disease severity and prognosis in COVID-19. METHODS: Clinical, imaging and laboratory data of 120 patients whose COVID-19 diagnosis based on RT-PCR were evaluated retrospectively. Clinically, the severity of COVID-19 was classified as noncomplicated or mild or severe pneumonia. Radiologically, the area of affected lungs compatible with viral pneumonia in each patient's computed tomography was classified as either 0–30% or ≥ 31% of the total lung area. The D-dimer values and laboratory data of patients with COVID-19 were compared with inpatient status, duration of hospitalization, and lung involvement during treatment and follow-up. To assess the predictive value of D-dimer, receiver operating characteristic (ROC) analysis was conducted. RESULTS: D-dimer elevation (> 243 ng/ml) was detected in 63.3% (76/120) of the patients. The mean D-dimer value was calculated as 3144.50 ± 1709.4 ng/ml (1643–8548) for inpatients with severe pneumonia in the intensive care unit. D-Dimer values showed positive correlations with age, duration of stay, lung involvement, fibrinogen, neutrophil count, neutrophil lymphocyte ratio (NLR) and platelet lymphocyte ratio (PLR). When the threshold D-dimer value was 370 ng/ml in the ROC analysis, this value was calculated to have 77% specificity and 74% sensitivity for lung involvement in patients with COVID-19. CONCLUSION: D-Dimer levels in patients with COVID-19 correlate with outcome, but further studies are needed to see how useful they are in determining prognosis.
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spelling pubmed-78371562021-01-26 D-Dimer as a potential biomarker for disease severity in COVID-19 Ozen, Mert Yilmaz, Atakan Cakmak, Vefa Beyoglu, Resad Oskay, Alten Seyit, Murat Senol, Hande Am J Emerg Med Article INTRODUCTION: This study seeks to determine the utility of D-dimer levels as a biomarker in determining disease severity and prognosis in COVID-19. METHODS: Clinical, imaging and laboratory data of 120 patients whose COVID-19 diagnosis based on RT-PCR were evaluated retrospectively. Clinically, the severity of COVID-19 was classified as noncomplicated or mild or severe pneumonia. Radiologically, the area of affected lungs compatible with viral pneumonia in each patient's computed tomography was classified as either 0–30% or ≥ 31% of the total lung area. The D-dimer values and laboratory data of patients with COVID-19 were compared with inpatient status, duration of hospitalization, and lung involvement during treatment and follow-up. To assess the predictive value of D-dimer, receiver operating characteristic (ROC) analysis was conducted. RESULTS: D-dimer elevation (> 243 ng/ml) was detected in 63.3% (76/120) of the patients. The mean D-dimer value was calculated as 3144.50 ± 1709.4 ng/ml (1643–8548) for inpatients with severe pneumonia in the intensive care unit. D-Dimer values showed positive correlations with age, duration of stay, lung involvement, fibrinogen, neutrophil count, neutrophil lymphocyte ratio (NLR) and platelet lymphocyte ratio (PLR). When the threshold D-dimer value was 370 ng/ml in the ROC analysis, this value was calculated to have 77% specificity and 74% sensitivity for lung involvement in patients with COVID-19. CONCLUSION: D-Dimer levels in patients with COVID-19 correlate with outcome, but further studies are needed to see how useful they are in determining prognosis. Elsevier Inc. 2021-02 2020-12-14 /pmc/articles/PMC7837156/ /pubmed/33348224 http://dx.doi.org/10.1016/j.ajem.2020.12.023 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
Ozen, Mert
Yilmaz, Atakan
Cakmak, Vefa
Beyoglu, Resad
Oskay, Alten
Seyit, Murat
Senol, Hande
D-Dimer as a potential biomarker for disease severity in COVID-19
title D-Dimer as a potential biomarker for disease severity in COVID-19
title_full D-Dimer as a potential biomarker for disease severity in COVID-19
title_fullStr D-Dimer as a potential biomarker for disease severity in COVID-19
title_full_unstemmed D-Dimer as a potential biomarker for disease severity in COVID-19
title_short D-Dimer as a potential biomarker for disease severity in COVID-19
title_sort d-dimer as a potential biomarker for disease severity in covid-19
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7837156/
https://www.ncbi.nlm.nih.gov/pubmed/33348224
http://dx.doi.org/10.1016/j.ajem.2020.12.023
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