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Effect of Airflow Limitation on Acute Exacerbations in Patients with Destroyed Lungs by Tuberculosis

History of treatment for tuberculosis (TB) is a risk factor for obstructive lung disease. However, it has been unclear whether the clinical characteristics of patients with destroyed lung by TB differ according to the presence or absence of airflow limitation. The objective of the study was to evalu...

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Autores principales: Kim, Soo Jung, Lee, Jinwoo, Park, Young Sik, Lee, Chang-Hoon, Lee, Sang-Min, Yim, Jae-Joon, Kim, Young Whan, Han, Sung Koo, Yoo, Chul-Gyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Academy of Medical Sciences 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4444474/
https://www.ncbi.nlm.nih.gov/pubmed/26028926
http://dx.doi.org/10.3346/jkms.2015.30.6.737
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author Kim, Soo Jung
Lee, Jinwoo
Park, Young Sik
Lee, Chang-Hoon
Lee, Sang-Min
Yim, Jae-Joon
Kim, Young Whan
Han, Sung Koo
Yoo, Chul-Gyu
author_facet Kim, Soo Jung
Lee, Jinwoo
Park, Young Sik
Lee, Chang-Hoon
Lee, Sang-Min
Yim, Jae-Joon
Kim, Young Whan
Han, Sung Koo
Yoo, Chul-Gyu
author_sort Kim, Soo Jung
collection PubMed
description History of treatment for tuberculosis (TB) is a risk factor for obstructive lung disease. However, it has been unclear whether the clinical characteristics of patients with destroyed lung by TB differ according to the presence or absence of airflow limitation. The objective of the study was to evaluate differences in acute exacerbations and forced expiratory volume in 1 second (FEV(1)) decline in patients with destroyed lung by TB according to the presence or absence of airflow limitation. We performed a retrospective cohort study and enrolled patients with destroyed lung by TB. The presence of airflow limitation was defined as FEV(1)/forced vital capacity (FVC) < 0.7. One hundred and fifty-nine patients were enrolled, and 128 (80.5%) had airflow limitation. The proportion of patients who experienced acute exacerbation was higher in patients with airflow limitation compared to those without (89.1 vs. 67.7%, respectively; P = 0.009). The rate of acute exacerbation was higher in patients with airflow limitation (IRR, 1.19; 95% CI, 1.11-1.27). Low body mass index (X vs. X + 1; HR, 0.944; 95% CI, 0.895-0.996) in addition to airflow limitation (HR, 1.634; 95% CI, 1.012-2.638), was an independent risk factor for acute exacerbation. The annual decline of FEV(1) was 2 mL in patients with airflow limitation and 36 mL in those without (P < 0.001). In conclusion, the presence of airflow limitation is an independent risk factor for acute exacerbation in patients with the destroyed lung by TB.
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spelling pubmed-44444742015-06-01 Effect of Airflow Limitation on Acute Exacerbations in Patients with Destroyed Lungs by Tuberculosis Kim, Soo Jung Lee, Jinwoo Park, Young Sik Lee, Chang-Hoon Lee, Sang-Min Yim, Jae-Joon Kim, Young Whan Han, Sung Koo Yoo, Chul-Gyu J Korean Med Sci Original Article History of treatment for tuberculosis (TB) is a risk factor for obstructive lung disease. However, it has been unclear whether the clinical characteristics of patients with destroyed lung by TB differ according to the presence or absence of airflow limitation. The objective of the study was to evaluate differences in acute exacerbations and forced expiratory volume in 1 second (FEV(1)) decline in patients with destroyed lung by TB according to the presence or absence of airflow limitation. We performed a retrospective cohort study and enrolled patients with destroyed lung by TB. The presence of airflow limitation was defined as FEV(1)/forced vital capacity (FVC) < 0.7. One hundred and fifty-nine patients were enrolled, and 128 (80.5%) had airflow limitation. The proportion of patients who experienced acute exacerbation was higher in patients with airflow limitation compared to those without (89.1 vs. 67.7%, respectively; P = 0.009). The rate of acute exacerbation was higher in patients with airflow limitation (IRR, 1.19; 95% CI, 1.11-1.27). Low body mass index (X vs. X + 1; HR, 0.944; 95% CI, 0.895-0.996) in addition to airflow limitation (HR, 1.634; 95% CI, 1.012-2.638), was an independent risk factor for acute exacerbation. The annual decline of FEV(1) was 2 mL in patients with airflow limitation and 36 mL in those without (P < 0.001). In conclusion, the presence of airflow limitation is an independent risk factor for acute exacerbation in patients with the destroyed lung by TB. The Korean Academy of Medical Sciences 2015-06 2015-05-13 /pmc/articles/PMC4444474/ /pubmed/26028926 http://dx.doi.org/10.3346/jkms.2015.30.6.737 Text en © 2015 The Korean Academy of Medical Sciences. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Kim, Soo Jung
Lee, Jinwoo
Park, Young Sik
Lee, Chang-Hoon
Lee, Sang-Min
Yim, Jae-Joon
Kim, Young Whan
Han, Sung Koo
Yoo, Chul-Gyu
Effect of Airflow Limitation on Acute Exacerbations in Patients with Destroyed Lungs by Tuberculosis
title Effect of Airflow Limitation on Acute Exacerbations in Patients with Destroyed Lungs by Tuberculosis
title_full Effect of Airflow Limitation on Acute Exacerbations in Patients with Destroyed Lungs by Tuberculosis
title_fullStr Effect of Airflow Limitation on Acute Exacerbations in Patients with Destroyed Lungs by Tuberculosis
title_full_unstemmed Effect of Airflow Limitation on Acute Exacerbations in Patients with Destroyed Lungs by Tuberculosis
title_short Effect of Airflow Limitation on Acute Exacerbations in Patients with Destroyed Lungs by Tuberculosis
title_sort effect of airflow limitation on acute exacerbations in patients with destroyed lungs by tuberculosis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4444474/
https://www.ncbi.nlm.nih.gov/pubmed/26028926
http://dx.doi.org/10.3346/jkms.2015.30.6.737
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