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Risk Factor and Mortality in Patients with Pulmonary Embolism Combined with Infectious Disease

BACKGROUND: Infectious conditions may increase the risk of venous thromboembolism. The purpose of this study was to evaluate the risk factor for combined infectious disease and its influence on mortality in patients with pulmonary embolism (PE). METHODS: Patients with PE diagnosed based on spiral co...

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Autores principales: Lee, Gi Dong, Ju, Sunmi, Kim, Ju-Young, Kim, Tae Hoon, Yoo, Jung-Wan, Lee, Seung Jun, Cho, Yu Ji, Jeong, Yi Yeong, Jeon, Kyung Nyeo, Lee, Jong Deog, Kim, Ho Cheol
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Academy of Tuberculosis and Respiratory Diseases 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7105430/
https://www.ncbi.nlm.nih.gov/pubmed/32185917
http://dx.doi.org/10.4046/trd.2019.0037
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author Lee, Gi Dong
Ju, Sunmi
Kim, Ju-Young
Kim, Tae Hoon
Yoo, Jung-Wan
Lee, Seung Jun
Cho, Yu Ji
Jeong, Yi Yeong
Jeon, Kyung Nyeo
Lee, Jong Deog
Kim, Ho Cheol
author_facet Lee, Gi Dong
Ju, Sunmi
Kim, Ju-Young
Kim, Tae Hoon
Yoo, Jung-Wan
Lee, Seung Jun
Cho, Yu Ji
Jeong, Yi Yeong
Jeon, Kyung Nyeo
Lee, Jong Deog
Kim, Ho Cheol
author_sort Lee, Gi Dong
collection PubMed
description BACKGROUND: Infectious conditions may increase the risk of venous thromboembolism. The purpose of this study was to evaluate the risk factor for combined infectious disease and its influence on mortality in patients with pulmonary embolism (PE). METHODS: Patients with PE diagnosed based on spiral computed tomography findings of the chest were retrospectively analyzed. They were classified into two groups: patients who developed PE in the setting of infectious disease or those with PE without infection based on review of their medical charts. RESULTS: Of 258 patients with PE, 67 (25.9%) were considered as having PE combined with infectious disease. The sites of infections were the respiratory tract in 52 patients (77.6%), genitourinary tract in three patients (4.5%), and hepatobiliary tract in three patients (4.5%). Underlying lung disease (odds ratio [OR], 3.69; 95% confidence interval [CI], 1.926–7.081; p<0.001), bed-ridden state (OR, 2.84; 95% CI, 1.390–5.811; p=0.004), and malignant disease (OR, 1.867; 95% CI, 1.017–3.425; p=0.044) were associated with combined infectious disease in patients with PE. In-hospital mortality was higher in patients with PE combined with infectious disease than in those with PE without infection (24.6% vs. 11.0%, p=0.006). In the multivariate analysis, combined infectious disease (OR, 4.189; 95% CI, 1.692–10.372; p=0.002) were associated with non-survivors in patients with PE. CONCLUSION: A substantial portion of patients with PE has concomitant infectious disease and it may contribute a mortality in patients with PE.
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spelling pubmed-71054302020-04-09 Risk Factor and Mortality in Patients with Pulmonary Embolism Combined with Infectious Disease Lee, Gi Dong Ju, Sunmi Kim, Ju-Young Kim, Tae Hoon Yoo, Jung-Wan Lee, Seung Jun Cho, Yu Ji Jeong, Yi Yeong Jeon, Kyung Nyeo Lee, Jong Deog Kim, Ho Cheol Tuberc Respir Dis (Seoul) Original Article BACKGROUND: Infectious conditions may increase the risk of venous thromboembolism. The purpose of this study was to evaluate the risk factor for combined infectious disease and its influence on mortality in patients with pulmonary embolism (PE). METHODS: Patients with PE diagnosed based on spiral computed tomography findings of the chest were retrospectively analyzed. They were classified into two groups: patients who developed PE in the setting of infectious disease or those with PE without infection based on review of their medical charts. RESULTS: Of 258 patients with PE, 67 (25.9%) were considered as having PE combined with infectious disease. The sites of infections were the respiratory tract in 52 patients (77.6%), genitourinary tract in three patients (4.5%), and hepatobiliary tract in three patients (4.5%). Underlying lung disease (odds ratio [OR], 3.69; 95% confidence interval [CI], 1.926–7.081; p<0.001), bed-ridden state (OR, 2.84; 95% CI, 1.390–5.811; p=0.004), and malignant disease (OR, 1.867; 95% CI, 1.017–3.425; p=0.044) were associated with combined infectious disease in patients with PE. In-hospital mortality was higher in patients with PE combined with infectious disease than in those with PE without infection (24.6% vs. 11.0%, p=0.006). In the multivariate analysis, combined infectious disease (OR, 4.189; 95% CI, 1.692–10.372; p=0.002) were associated with non-survivors in patients with PE. CONCLUSION: A substantial portion of patients with PE has concomitant infectious disease and it may contribute a mortality in patients with PE. The Korean Academy of Tuberculosis and Respiratory Diseases 2020-04 2020-03-10 /pmc/articles/PMC7105430/ /pubmed/32185917 http://dx.doi.org/10.4046/trd.2019.0037 Text en Copyright©2020. The Korean Academy of Tuberculosis and Respiratory Diseases http://creativecommons.org/licenses/by-nc/4.0/ It is identical to the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/)
spellingShingle Original Article
Lee, Gi Dong
Ju, Sunmi
Kim, Ju-Young
Kim, Tae Hoon
Yoo, Jung-Wan
Lee, Seung Jun
Cho, Yu Ji
Jeong, Yi Yeong
Jeon, Kyung Nyeo
Lee, Jong Deog
Kim, Ho Cheol
Risk Factor and Mortality in Patients with Pulmonary Embolism Combined with Infectious Disease
title Risk Factor and Mortality in Patients with Pulmonary Embolism Combined with Infectious Disease
title_full Risk Factor and Mortality in Patients with Pulmonary Embolism Combined with Infectious Disease
title_fullStr Risk Factor and Mortality in Patients with Pulmonary Embolism Combined with Infectious Disease
title_full_unstemmed Risk Factor and Mortality in Patients with Pulmonary Embolism Combined with Infectious Disease
title_short Risk Factor and Mortality in Patients with Pulmonary Embolism Combined with Infectious Disease
title_sort risk factor and mortality in patients with pulmonary embolism combined with infectious disease
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7105430/
https://www.ncbi.nlm.nih.gov/pubmed/32185917
http://dx.doi.org/10.4046/trd.2019.0037
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