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Diffuse alveolar damage associated mortality in selected acute respiratory distress syndrome patients with open lung biopsy

INTRODUCTION: Diffuse alveolar damage (DAD) is the pathological hallmark of acute respiratory distress syndrome (ARDS), however, the presence of DAD in the clinical criteria of ARDS patients by Berlin definition is little known. This study is designed to investigate the role of DAD in ARDS patients...

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Autores principales: Kao, Kuo-Chin, Hu, Han-Chung, Chang, Chih-Hao, Hung, Chen-Yiu, Chiu, Li-Chung, Li, Shih-Hong, Lin, Shih-Wei, Chuang, Li-Pang, Wang, Chih-Wei, Li, Li-Fu, Chen, Ning-Hung, Yang, Cheng-Ta, Huang, Chung-Chi, Tsai, Ying-Huang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4449559/
https://www.ncbi.nlm.nih.gov/pubmed/25981598
http://dx.doi.org/10.1186/s13054-015-0949-y
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author Kao, Kuo-Chin
Hu, Han-Chung
Chang, Chih-Hao
Hung, Chen-Yiu
Chiu, Li-Chung
Li, Shih-Hong
Lin, Shih-Wei
Chuang, Li-Pang
Wang, Chih-Wei
Li, Li-Fu
Chen, Ning-Hung
Yang, Cheng-Ta
Huang, Chung-Chi
Tsai, Ying-Huang
author_facet Kao, Kuo-Chin
Hu, Han-Chung
Chang, Chih-Hao
Hung, Chen-Yiu
Chiu, Li-Chung
Li, Shih-Hong
Lin, Shih-Wei
Chuang, Li-Pang
Wang, Chih-Wei
Li, Li-Fu
Chen, Ning-Hung
Yang, Cheng-Ta
Huang, Chung-Chi
Tsai, Ying-Huang
author_sort Kao, Kuo-Chin
collection PubMed
description INTRODUCTION: Diffuse alveolar damage (DAD) is the pathological hallmark of acute respiratory distress syndrome (ARDS), however, the presence of DAD in the clinical criteria of ARDS patients by Berlin definition is little known. This study is designed to investigate the role of DAD in ARDS patients who underwent open lung biopsy. METHODS: We retrospectively reviewed all ARDS patients who met the Berlin definition and underwent open lung biopsy from January 1999 to January 2014 in a referred medical center. DAD is characterized by hyaline membrane formation, lung edema, inflammation, hemorrhage and alveolar epithelial cell injury. Clinical data including baseline characteristics, severity of ARDS, clinical and pathological diagnoses, and survival outcomes were analyzed. RESULTS: A total of 1838 patients with ARDS were identified and open lung biopsies were performed on 101 patients (5.5 %) during the study period. Of these 101 patients, the severity of ARDS on diagnosis was mild of 16.8 %, moderate of 56.5 % and severe of 26.7 %. The hospital mortality rate was not significant difference between the three groups (64.7 % vs 61.4 % vs 55.6 %, p = 0.81). Of the 101 clinical ARDS patients with open lung biopsies, 56.4 % (57/101) patients had DAD according to biopsy results. The proportion of DAD were 76.5 % (13/17) in mild, 56.1 % (32/57) in moderate and 44.4 % (12/27) in severe ARDS and there is no significant difference between the three groups (p = 0.113). Pathological findings of DAD patients had a higher hospital mortality rate than non-DAD patients (71.9 % vs 45.5 %, p = 0.007). Pathological findings of DAD (odds ratio: 3.554, 95 % CI, 1.385–9.12; p = 0.008) and Sequential Organ Failure Assessment score on the biopsy day (odds ratio: 1.424, 95 % CI, 1.187–1.707; p<0.001) were significantly and independently associated with hospital mortality. The baseline demographics and clinical characteristics were not significantly different between DAD and non-DAD patients. CONCLUSIONS: The correlation of pathological findings of DAD and ARDS diagnosed by Berlin definition is modest. A pathological finding of DAD in ARDS patients is associated with hospital mortality and there are no clinical characteristics that could identify DAD patients before open lung biopsy.
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spelling pubmed-44495592015-05-31 Diffuse alveolar damage associated mortality in selected acute respiratory distress syndrome patients with open lung biopsy Kao, Kuo-Chin Hu, Han-Chung Chang, Chih-Hao Hung, Chen-Yiu Chiu, Li-Chung Li, Shih-Hong Lin, Shih-Wei Chuang, Li-Pang Wang, Chih-Wei Li, Li-Fu Chen, Ning-Hung Yang, Cheng-Ta Huang, Chung-Chi Tsai, Ying-Huang Crit Care Research INTRODUCTION: Diffuse alveolar damage (DAD) is the pathological hallmark of acute respiratory distress syndrome (ARDS), however, the presence of DAD in the clinical criteria of ARDS patients by Berlin definition is little known. This study is designed to investigate the role of DAD in ARDS patients who underwent open lung biopsy. METHODS: We retrospectively reviewed all ARDS patients who met the Berlin definition and underwent open lung biopsy from January 1999 to January 2014 in a referred medical center. DAD is characterized by hyaline membrane formation, lung edema, inflammation, hemorrhage and alveolar epithelial cell injury. Clinical data including baseline characteristics, severity of ARDS, clinical and pathological diagnoses, and survival outcomes were analyzed. RESULTS: A total of 1838 patients with ARDS were identified and open lung biopsies were performed on 101 patients (5.5 %) during the study period. Of these 101 patients, the severity of ARDS on diagnosis was mild of 16.8 %, moderate of 56.5 % and severe of 26.7 %. The hospital mortality rate was not significant difference between the three groups (64.7 % vs 61.4 % vs 55.6 %, p = 0.81). Of the 101 clinical ARDS patients with open lung biopsies, 56.4 % (57/101) patients had DAD according to biopsy results. The proportion of DAD were 76.5 % (13/17) in mild, 56.1 % (32/57) in moderate and 44.4 % (12/27) in severe ARDS and there is no significant difference between the three groups (p = 0.113). Pathological findings of DAD patients had a higher hospital mortality rate than non-DAD patients (71.9 % vs 45.5 %, p = 0.007). Pathological findings of DAD (odds ratio: 3.554, 95 % CI, 1.385–9.12; p = 0.008) and Sequential Organ Failure Assessment score on the biopsy day (odds ratio: 1.424, 95 % CI, 1.187–1.707; p<0.001) were significantly and independently associated with hospital mortality. The baseline demographics and clinical characteristics were not significantly different between DAD and non-DAD patients. CONCLUSIONS: The correlation of pathological findings of DAD and ARDS diagnosed by Berlin definition is modest. A pathological finding of DAD in ARDS patients is associated with hospital mortality and there are no clinical characteristics that could identify DAD patients before open lung biopsy. BioMed Central 2015-05-15 2015 /pmc/articles/PMC4449559/ /pubmed/25981598 http://dx.doi.org/10.1186/s13054-015-0949-y Text en © Kao et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Kao, Kuo-Chin
Hu, Han-Chung
Chang, Chih-Hao
Hung, Chen-Yiu
Chiu, Li-Chung
Li, Shih-Hong
Lin, Shih-Wei
Chuang, Li-Pang
Wang, Chih-Wei
Li, Li-Fu
Chen, Ning-Hung
Yang, Cheng-Ta
Huang, Chung-Chi
Tsai, Ying-Huang
Diffuse alveolar damage associated mortality in selected acute respiratory distress syndrome patients with open lung biopsy
title Diffuse alveolar damage associated mortality in selected acute respiratory distress syndrome patients with open lung biopsy
title_full Diffuse alveolar damage associated mortality in selected acute respiratory distress syndrome patients with open lung biopsy
title_fullStr Diffuse alveolar damage associated mortality in selected acute respiratory distress syndrome patients with open lung biopsy
title_full_unstemmed Diffuse alveolar damage associated mortality in selected acute respiratory distress syndrome patients with open lung biopsy
title_short Diffuse alveolar damage associated mortality in selected acute respiratory distress syndrome patients with open lung biopsy
title_sort diffuse alveolar damage associated mortality in selected acute respiratory distress syndrome patients with open lung biopsy
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4449559/
https://www.ncbi.nlm.nih.gov/pubmed/25981598
http://dx.doi.org/10.1186/s13054-015-0949-y
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