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Relationship between disease severity and D-dimer levels measured with two different methods in pulmonary embolism patients

Pulmonary embolism (PE) is diagnosed with increasing frequency nowadays due to advances in the diagnostic methods and the increased awareness of the disease. There is a tendency to use non invasive diagnostic methods for all diseases. D-dimer is a fibrin degradation product. We aimed to detect the r...

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Autores principales: Coskun, Funda, Yilmaz, Dilber, Ursavas, Ahmet, Uzaslan, Esra, Ege, Ercument
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3463048/
https://www.ncbi.nlm.nih.gov/pubmed/22958319
http://dx.doi.org/10.1186/2049-6958-5-3-168
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author Coskun, Funda
Yilmaz, Dilber
Ursavas, Ahmet
Uzaslan, Esra
Ege, Ercument
author_facet Coskun, Funda
Yilmaz, Dilber
Ursavas, Ahmet
Uzaslan, Esra
Ege, Ercument
author_sort Coskun, Funda
collection PubMed
description Pulmonary embolism (PE) is diagnosed with increasing frequency nowadays due to advances in the diagnostic methods and the increased awareness of the disease. There is a tendency to use non invasive diagnostic methods for all diseases. D-dimer is a fibrin degradation product. We aimed to detect the relationship between disease severity and the D-dimer levels measured with two different methods. We compared D-dimer levels in cases of massive vs. non-massive PE. A total of 89 patients who were diagnosed between 2006 and 2008 were included in the study. Group 1 included patients whose D-dimer levels were measured with the immunoturbidimetric polyclonal antibody method (D-dimerPLUS(®)), while Group 2 patients made use of the immunoturbidimetric monoclonal antibody method (InnovanceD-DIMER(®)). In each group, the D-dimer levels of those with massive and non-massive PE were compared, using the Mann Whitney U test. The mean age of Group 1 (25 F/26 M) was 56.0 ± 17.9 years, and that of Group 2 (22 F/16 M) was 52.9 ± 17.9 years. There was no statistical difference in gender and mean age between the two groups (p > 0.05). In Group 1, the mean D-dimer level of massive cases (n = 7) was 1444.9 ± 657.9 μg/L and that of nonmassive PE (n = 34) was 1304.7 ± 350.5 μg/L (p > 0.05). In Group 2, the mean D-dimer level of massive cases (n = 6) was 9.7 ± 2.2 mg/L and that of non-massive PE (n = 32) was 5.9 ± 1.3 mg/L (p < 0.05). The mean D-dimer levels of massive cases as measured with the immunoturbidimetric monoclonal antibody method were significantly higher. Pulmonary embolism patients whose D-dimer levels are higher (especially higher than 6.6 mg/L) should be considered as possibly having massive embolism. Diagnostic procedures and management can be planned according to this finding.
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spelling pubmed-34630482012-10-05 Relationship between disease severity and D-dimer levels measured with two different methods in pulmonary embolism patients Coskun, Funda Yilmaz, Dilber Ursavas, Ahmet Uzaslan, Esra Ege, Ercument Multidiscip Respir Med Original Article Pulmonary embolism (PE) is diagnosed with increasing frequency nowadays due to advances in the diagnostic methods and the increased awareness of the disease. There is a tendency to use non invasive diagnostic methods for all diseases. D-dimer is a fibrin degradation product. We aimed to detect the relationship between disease severity and the D-dimer levels measured with two different methods. We compared D-dimer levels in cases of massive vs. non-massive PE. A total of 89 patients who were diagnosed between 2006 and 2008 were included in the study. Group 1 included patients whose D-dimer levels were measured with the immunoturbidimetric polyclonal antibody method (D-dimerPLUS(®)), while Group 2 patients made use of the immunoturbidimetric monoclonal antibody method (InnovanceD-DIMER(®)). In each group, the D-dimer levels of those with massive and non-massive PE were compared, using the Mann Whitney U test. The mean age of Group 1 (25 F/26 M) was 56.0 ± 17.9 years, and that of Group 2 (22 F/16 M) was 52.9 ± 17.9 years. There was no statistical difference in gender and mean age between the two groups (p > 0.05). In Group 1, the mean D-dimer level of massive cases (n = 7) was 1444.9 ± 657.9 μg/L and that of nonmassive PE (n = 34) was 1304.7 ± 350.5 μg/L (p > 0.05). In Group 2, the mean D-dimer level of massive cases (n = 6) was 9.7 ± 2.2 mg/L and that of non-massive PE (n = 32) was 5.9 ± 1.3 mg/L (p < 0.05). The mean D-dimer levels of massive cases as measured with the immunoturbidimetric monoclonal antibody method were significantly higher. Pulmonary embolism patients whose D-dimer levels are higher (especially higher than 6.6 mg/L) should be considered as possibly having massive embolism. Diagnostic procedures and management can be planned according to this finding. BioMed Central 2010-06-30 /pmc/articles/PMC3463048/ /pubmed/22958319 http://dx.doi.org/10.1186/2049-6958-5-3-168 Text en Copyright ©2011 Novamedia srl
spellingShingle Original Article
Coskun, Funda
Yilmaz, Dilber
Ursavas, Ahmet
Uzaslan, Esra
Ege, Ercument
Relationship between disease severity and D-dimer levels measured with two different methods in pulmonary embolism patients
title Relationship between disease severity and D-dimer levels measured with two different methods in pulmonary embolism patients
title_full Relationship between disease severity and D-dimer levels measured with two different methods in pulmonary embolism patients
title_fullStr Relationship between disease severity and D-dimer levels measured with two different methods in pulmonary embolism patients
title_full_unstemmed Relationship between disease severity and D-dimer levels measured with two different methods in pulmonary embolism patients
title_short Relationship between disease severity and D-dimer levels measured with two different methods in pulmonary embolism patients
title_sort relationship between disease severity and d-dimer levels measured with two different methods in pulmonary embolism patients
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3463048/
https://www.ncbi.nlm.nih.gov/pubmed/22958319
http://dx.doi.org/10.1186/2049-6958-5-3-168
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