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Neutrophil-to-lymphocyte ratio for the assessment of hospital mortality in patients with acute pulmonary embolism
INTRODUCTION: Neutrophil-to-lymphocyte ratio (NLR), which is an essential marker of inflammation, has been shown to be associated with adverse outcomes in various cardiovascular diseases in the literature. In this study we sought to evaluate the association between NLR and prognosis of acute pulmona...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Termedia Publishing House
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4754370/ https://www.ncbi.nlm.nih.gov/pubmed/26925123 http://dx.doi.org/10.5114/aoms.2016.57585 |
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author | Soylu, Korhan Gedikli, Ömer Ekşi, Alay Avcıoğlu, Yonca Soylu, Ayşegül İdil Yüksel, Serkan Aksan, Gökhan Gülel, Okan Yılmaz, Özcan |
author_facet | Soylu, Korhan Gedikli, Ömer Ekşi, Alay Avcıoğlu, Yonca Soylu, Ayşegül İdil Yüksel, Serkan Aksan, Gökhan Gülel, Okan Yılmaz, Özcan |
author_sort | Soylu, Korhan |
collection | PubMed |
description | INTRODUCTION: Neutrophil-to-lymphocyte ratio (NLR), which is an essential marker of inflammation, has been shown to be associated with adverse outcomes in various cardiovascular diseases in the literature. In this study we sought to evaluate the association between NLR and prognosis of acute pulmonary embolism (APE). MATERIAL AND METHODS: We retrospectively evaluated blood counts and clinical data of 142 patients with the diagnosis of pulmonary embolism (PE) from Ondokuz Mayis University Hospital between January 2006 and December 2012. The patients were divided into two groups according to NLR: NLR < 4.4 (low NLR group, n = 71) and NLR ≥ 4.4 (high NLR group, n = 71). RESULTS: Massive embolism (66.2% vs. 36.6%, p < 0.001) and in-hospital mortality (21.1%, 1.4%, p < 0.001) were higher in the high NLR group. In multivariate regression analysis NLR ≥ 5.7, systolic blood pressure (BP) < 90 mm Hg, serum glucose > 126 mg/dl, heart rate > 110 beats/min, and PCO(2) < 35 or > 50 mm Hg were predictors of in-hospital mortality. The optimal NLR cutoff value was 5.7 for mortality in receiver operating characteristic (ROC) analysis. Having an NLR value above 5.7 was found to be associated with a 10.8 times higher mortality rate than an NLR value below 5.7. CONCLUSIONS: In patients presenting with APE, NLR value is an independent predictor of in-hospital mortality and may be used for clinical risk classification. |
format | Online Article Text |
id | pubmed-4754370 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Termedia Publishing House |
record_format | MEDLINE/PubMed |
spelling | pubmed-47543702016-02-26 Neutrophil-to-lymphocyte ratio for the assessment of hospital mortality in patients with acute pulmonary embolism Soylu, Korhan Gedikli, Ömer Ekşi, Alay Avcıoğlu, Yonca Soylu, Ayşegül İdil Yüksel, Serkan Aksan, Gökhan Gülel, Okan Yılmaz, Özcan Arch Med Sci Clinical Research INTRODUCTION: Neutrophil-to-lymphocyte ratio (NLR), which is an essential marker of inflammation, has been shown to be associated with adverse outcomes in various cardiovascular diseases in the literature. In this study we sought to evaluate the association between NLR and prognosis of acute pulmonary embolism (APE). MATERIAL AND METHODS: We retrospectively evaluated blood counts and clinical data of 142 patients with the diagnosis of pulmonary embolism (PE) from Ondokuz Mayis University Hospital between January 2006 and December 2012. The patients were divided into two groups according to NLR: NLR < 4.4 (low NLR group, n = 71) and NLR ≥ 4.4 (high NLR group, n = 71). RESULTS: Massive embolism (66.2% vs. 36.6%, p < 0.001) and in-hospital mortality (21.1%, 1.4%, p < 0.001) were higher in the high NLR group. In multivariate regression analysis NLR ≥ 5.7, systolic blood pressure (BP) < 90 mm Hg, serum glucose > 126 mg/dl, heart rate > 110 beats/min, and PCO(2) < 35 or > 50 mm Hg were predictors of in-hospital mortality. The optimal NLR cutoff value was 5.7 for mortality in receiver operating characteristic (ROC) analysis. Having an NLR value above 5.7 was found to be associated with a 10.8 times higher mortality rate than an NLR value below 5.7. CONCLUSIONS: In patients presenting with APE, NLR value is an independent predictor of in-hospital mortality and may be used for clinical risk classification. Termedia Publishing House 2016-02-02 2016-02-01 /pmc/articles/PMC4754370/ /pubmed/26925123 http://dx.doi.org/10.5114/aoms.2016.57585 Text en Copyright © 2016 Termedia & Banach http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license. |
spellingShingle | Clinical Research Soylu, Korhan Gedikli, Ömer Ekşi, Alay Avcıoğlu, Yonca Soylu, Ayşegül İdil Yüksel, Serkan Aksan, Gökhan Gülel, Okan Yılmaz, Özcan Neutrophil-to-lymphocyte ratio for the assessment of hospital mortality in patients with acute pulmonary embolism |
title | Neutrophil-to-lymphocyte ratio for the assessment of hospital mortality in patients with acute pulmonary embolism |
title_full | Neutrophil-to-lymphocyte ratio for the assessment of hospital mortality in patients with acute pulmonary embolism |
title_fullStr | Neutrophil-to-lymphocyte ratio for the assessment of hospital mortality in patients with acute pulmonary embolism |
title_full_unstemmed | Neutrophil-to-lymphocyte ratio for the assessment of hospital mortality in patients with acute pulmonary embolism |
title_short | Neutrophil-to-lymphocyte ratio for the assessment of hospital mortality in patients with acute pulmonary embolism |
title_sort | neutrophil-to-lymphocyte ratio for the assessment of hospital mortality in patients with acute pulmonary embolism |
topic | Clinical Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4754370/ https://www.ncbi.nlm.nih.gov/pubmed/26925123 http://dx.doi.org/10.5114/aoms.2016.57585 |
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