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Chronic kidney disease: Prognostic marker of nonfatal pulmonary thromboembolism
OBJECTIVE: Renal dysfunction is associated with increased cardiovascular morbidity and mortality. The alteration in renal function as a marker of mortality in pulmonary thromboembolism (PTE) has not been studied extensively. METHODS: Four hundred four consecutive patients diagnosed with non-high-ris...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Kare Publishing
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5336947/ https://www.ncbi.nlm.nih.gov/pubmed/25868039 http://dx.doi.org/10.5152/akd.2014.5739 |
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author | Ouatu, Anca Tanase, Daniela Maria Floria, Mariana Ionescu, Simona Daniela Ambaruş, Valentin Arsenescu-Georgescu, Catalina |
author_facet | Ouatu, Anca Tanase, Daniela Maria Floria, Mariana Ionescu, Simona Daniela Ambaruş, Valentin Arsenescu-Georgescu, Catalina |
author_sort | Ouatu, Anca |
collection | PubMed |
description | OBJECTIVE: Renal dysfunction is associated with increased cardiovascular morbidity and mortality. The alteration in renal function as a marker of mortality in pulmonary thromboembolism (PTE) has not been studied extensively. METHODS: Four hundred four consecutive patients diagnosed with non-high-risk PTE (without cardiogenic shock or blood pressure <90 mm Hg) were prospectively enrolled in the study between 2005-2010. Kidney function, based on glomerular filtration rate (GFR), calculated by the simplified modification in diet in renal disease (MDRD) equation (sMDRD); troponin I; B-type natriuretic peptide (BNP); and echocardiographic markers of right ventricular (RV) function were determined in survivors versus non-survivors after a 2-year follow-up. RESULTS: GFR was significantly lower in non-survivors than in survivors: 51.85±19.08 mL/min/1.73 m(2) and 71.65±23.21 mL/min/1.73 m(2), respectively (p=0.000). The highest 2-year mortality rate (20%) was recorded in patients with moderate renal dysfunction associated with RV dysfunction. Using multivariate analysis, we found that GFR is an independent predictor of 2-year mortality (OR 0.973, 95% CI: 0.959-0.987, p=0.000), besides troponin I, dyslipidemia, acceleration time of pulmonary ejection, pericardial effusion, and BNP CONCLUSION: The association of renal dysfunction with right ventricular dysfunction in patients with non-fatal pulmonary thromboembolism resulted in high mortality. Renal dysfunction, assessed by glomerular filtration rate, may be used in the risk stratification of patients with non-high-risk pulmonary thromboembolism, besides troponin I, BNP and right ventricle echocardiographic dysfunction markers. |
format | Online Article Text |
id | pubmed-5336947 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Kare Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-53369472017-06-28 Chronic kidney disease: Prognostic marker of nonfatal pulmonary thromboembolism Ouatu, Anca Tanase, Daniela Maria Floria, Mariana Ionescu, Simona Daniela Ambaruş, Valentin Arsenescu-Georgescu, Catalina Anatol J Cardiol Original Investigation OBJECTIVE: Renal dysfunction is associated with increased cardiovascular morbidity and mortality. The alteration in renal function as a marker of mortality in pulmonary thromboembolism (PTE) has not been studied extensively. METHODS: Four hundred four consecutive patients diagnosed with non-high-risk PTE (without cardiogenic shock or blood pressure <90 mm Hg) were prospectively enrolled in the study between 2005-2010. Kidney function, based on glomerular filtration rate (GFR), calculated by the simplified modification in diet in renal disease (MDRD) equation (sMDRD); troponin I; B-type natriuretic peptide (BNP); and echocardiographic markers of right ventricular (RV) function were determined in survivors versus non-survivors after a 2-year follow-up. RESULTS: GFR was significantly lower in non-survivors than in survivors: 51.85±19.08 mL/min/1.73 m(2) and 71.65±23.21 mL/min/1.73 m(2), respectively (p=0.000). The highest 2-year mortality rate (20%) was recorded in patients with moderate renal dysfunction associated with RV dysfunction. Using multivariate analysis, we found that GFR is an independent predictor of 2-year mortality (OR 0.973, 95% CI: 0.959-0.987, p=0.000), besides troponin I, dyslipidemia, acceleration time of pulmonary ejection, pericardial effusion, and BNP CONCLUSION: The association of renal dysfunction with right ventricular dysfunction in patients with non-fatal pulmonary thromboembolism resulted in high mortality. Renal dysfunction, assessed by glomerular filtration rate, may be used in the risk stratification of patients with non-high-risk pulmonary thromboembolism, besides troponin I, BNP and right ventricle echocardiographic dysfunction markers. Kare Publishing 2016-11 2014-12-31 /pmc/articles/PMC5336947/ /pubmed/25868039 http://dx.doi.org/10.5152/akd.2014.5739 Text en Copyright © 2015 Turkish Society of Cardiology http://creativecommons.org/licenses/by-nc-sa/4.0 This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License |
spellingShingle | Original Investigation Ouatu, Anca Tanase, Daniela Maria Floria, Mariana Ionescu, Simona Daniela Ambaruş, Valentin Arsenescu-Georgescu, Catalina Chronic kidney disease: Prognostic marker of nonfatal pulmonary thromboembolism |
title | Chronic kidney disease: Prognostic marker of nonfatal pulmonary thromboembolism |
title_full | Chronic kidney disease: Prognostic marker of nonfatal pulmonary thromboembolism |
title_fullStr | Chronic kidney disease: Prognostic marker of nonfatal pulmonary thromboembolism |
title_full_unstemmed | Chronic kidney disease: Prognostic marker of nonfatal pulmonary thromboembolism |
title_short | Chronic kidney disease: Prognostic marker of nonfatal pulmonary thromboembolism |
title_sort | chronic kidney disease: prognostic marker of nonfatal pulmonary thromboembolism |
topic | Original Investigation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5336947/ https://www.ncbi.nlm.nih.gov/pubmed/25868039 http://dx.doi.org/10.5152/akd.2014.5739 |
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