Cargando…
Clinical phenotypes from fatal cases of acute respiratory distress syndrome caused by pneumonia
There have been no report of objective clinical characteristics or prognostic factors that predict fatal outcome of acute respiratory distress syndrome (ARDS) since the Berlin definition was published. The aim of this study is to identify clinically available predictors that distinguish between two...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8501115/ https://www.ncbi.nlm.nih.gov/pubmed/34625618 http://dx.doi.org/10.1038/s41598-021-99540-1 |
_version_ | 1784580585933504512 |
---|---|
author | Ichikado, Kazuya Kawamura, Kodai Johkoh, Takeshi Fujimoto, Kiminori Shintani, Ayumi Hashimoto, Satoru Eguchi, Yoshitomo Yasuda, Yuko Anan, Keisuke Shingu, Naoki Sakata, Yoshihiko Hisanaga, Junpei Nitawaki, Tatsuya Iio, Miwa Sekido, Yuko Nishiyama, Kenta Nakamura, Kazunori Suga, Moritaka Ichiyasu, Hidenori Sakagami, Takuro |
author_facet | Ichikado, Kazuya Kawamura, Kodai Johkoh, Takeshi Fujimoto, Kiminori Shintani, Ayumi Hashimoto, Satoru Eguchi, Yoshitomo Yasuda, Yuko Anan, Keisuke Shingu, Naoki Sakata, Yoshihiko Hisanaga, Junpei Nitawaki, Tatsuya Iio, Miwa Sekido, Yuko Nishiyama, Kenta Nakamura, Kazunori Suga, Moritaka Ichiyasu, Hidenori Sakagami, Takuro |
author_sort | Ichikado, Kazuya |
collection | PubMed |
description | There have been no report of objective clinical characteristics or prognostic factors that predict fatal outcome of acute respiratory distress syndrome (ARDS) since the Berlin definition was published. The aim of this study is to identify clinically available predictors that distinguish between two phenotypes of fatal ARDS due to pneumonia. In total, 104 cases of Japanese patients with pneumonia-induced ARDS were extracted from our prospectively collected database. Fatal cases were divided into early (< 7 days after diagnosis) and late (≥ 7 days) death groups, and clinical variables and prognostic factors were statistically evaluated. Of the 50 patients who died within 180 days, 18 (36%) and 32 (64%) were in the early (median 2 days, IQR [1, 5]) and late (median 16 days, IQR [13, 29]) death groups, respectively. According to multivariate regression analyses, the APACHE II score (HR 1.25, 95%CI 1.12–1.39, p < 0.001) and the disseminated intravascular coagulation score (HR 1.54, 95%CI 1.15–2.04, p = 0.003) were independent prognostic factors for early death. In contrast, late death was associated with high-resolution computed tomography (HRCT) score indicating early fibroproliferation (HR 1.28, 95%CI 1.13–1.42, p < 0.001) as well as the disseminated intravascular coagulation score (HR 1.24, 95%CI 1.01–1.52, p = 0.039). The extent of fibroproliferation on HRCT, and the APACHE II scores along with coagulation abnormalities, should be considered for use in predictive enrichment and personalized medicine for patients with ARDS due to pneumonia. |
format | Online Article Text |
id | pubmed-8501115 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-85011152021-10-12 Clinical phenotypes from fatal cases of acute respiratory distress syndrome caused by pneumonia Ichikado, Kazuya Kawamura, Kodai Johkoh, Takeshi Fujimoto, Kiminori Shintani, Ayumi Hashimoto, Satoru Eguchi, Yoshitomo Yasuda, Yuko Anan, Keisuke Shingu, Naoki Sakata, Yoshihiko Hisanaga, Junpei Nitawaki, Tatsuya Iio, Miwa Sekido, Yuko Nishiyama, Kenta Nakamura, Kazunori Suga, Moritaka Ichiyasu, Hidenori Sakagami, Takuro Sci Rep Article There have been no report of objective clinical characteristics or prognostic factors that predict fatal outcome of acute respiratory distress syndrome (ARDS) since the Berlin definition was published. The aim of this study is to identify clinically available predictors that distinguish between two phenotypes of fatal ARDS due to pneumonia. In total, 104 cases of Japanese patients with pneumonia-induced ARDS were extracted from our prospectively collected database. Fatal cases were divided into early (< 7 days after diagnosis) and late (≥ 7 days) death groups, and clinical variables and prognostic factors were statistically evaluated. Of the 50 patients who died within 180 days, 18 (36%) and 32 (64%) were in the early (median 2 days, IQR [1, 5]) and late (median 16 days, IQR [13, 29]) death groups, respectively. According to multivariate regression analyses, the APACHE II score (HR 1.25, 95%CI 1.12–1.39, p < 0.001) and the disseminated intravascular coagulation score (HR 1.54, 95%CI 1.15–2.04, p = 0.003) were independent prognostic factors for early death. In contrast, late death was associated with high-resolution computed tomography (HRCT) score indicating early fibroproliferation (HR 1.28, 95%CI 1.13–1.42, p < 0.001) as well as the disseminated intravascular coagulation score (HR 1.24, 95%CI 1.01–1.52, p = 0.039). The extent of fibroproliferation on HRCT, and the APACHE II scores along with coagulation abnormalities, should be considered for use in predictive enrichment and personalized medicine for patients with ARDS due to pneumonia. Nature Publishing Group UK 2021-10-08 /pmc/articles/PMC8501115/ /pubmed/34625618 http://dx.doi.org/10.1038/s41598-021-99540-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Ichikado, Kazuya Kawamura, Kodai Johkoh, Takeshi Fujimoto, Kiminori Shintani, Ayumi Hashimoto, Satoru Eguchi, Yoshitomo Yasuda, Yuko Anan, Keisuke Shingu, Naoki Sakata, Yoshihiko Hisanaga, Junpei Nitawaki, Tatsuya Iio, Miwa Sekido, Yuko Nishiyama, Kenta Nakamura, Kazunori Suga, Moritaka Ichiyasu, Hidenori Sakagami, Takuro Clinical phenotypes from fatal cases of acute respiratory distress syndrome caused by pneumonia |
title | Clinical phenotypes from fatal cases of acute respiratory distress syndrome caused by pneumonia |
title_full | Clinical phenotypes from fatal cases of acute respiratory distress syndrome caused by pneumonia |
title_fullStr | Clinical phenotypes from fatal cases of acute respiratory distress syndrome caused by pneumonia |
title_full_unstemmed | Clinical phenotypes from fatal cases of acute respiratory distress syndrome caused by pneumonia |
title_short | Clinical phenotypes from fatal cases of acute respiratory distress syndrome caused by pneumonia |
title_sort | clinical phenotypes from fatal cases of acute respiratory distress syndrome caused by pneumonia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8501115/ https://www.ncbi.nlm.nih.gov/pubmed/34625618 http://dx.doi.org/10.1038/s41598-021-99540-1 |
work_keys_str_mv | AT ichikadokazuya clinicalphenotypesfromfatalcasesofacuterespiratorydistresssyndromecausedbypneumonia AT kawamurakodai clinicalphenotypesfromfatalcasesofacuterespiratorydistresssyndromecausedbypneumonia AT johkohtakeshi clinicalphenotypesfromfatalcasesofacuterespiratorydistresssyndromecausedbypneumonia AT fujimotokiminori clinicalphenotypesfromfatalcasesofacuterespiratorydistresssyndromecausedbypneumonia AT shintaniayumi clinicalphenotypesfromfatalcasesofacuterespiratorydistresssyndromecausedbypneumonia AT hashimotosatoru clinicalphenotypesfromfatalcasesofacuterespiratorydistresssyndromecausedbypneumonia AT eguchiyoshitomo clinicalphenotypesfromfatalcasesofacuterespiratorydistresssyndromecausedbypneumonia AT yasudayuko clinicalphenotypesfromfatalcasesofacuterespiratorydistresssyndromecausedbypneumonia AT anankeisuke clinicalphenotypesfromfatalcasesofacuterespiratorydistresssyndromecausedbypneumonia AT shingunaoki clinicalphenotypesfromfatalcasesofacuterespiratorydistresssyndromecausedbypneumonia AT sakatayoshihiko clinicalphenotypesfromfatalcasesofacuterespiratorydistresssyndromecausedbypneumonia AT hisanagajunpei clinicalphenotypesfromfatalcasesofacuterespiratorydistresssyndromecausedbypneumonia AT nitawakitatsuya clinicalphenotypesfromfatalcasesofacuterespiratorydistresssyndromecausedbypneumonia AT iiomiwa clinicalphenotypesfromfatalcasesofacuterespiratorydistresssyndromecausedbypneumonia AT sekidoyuko clinicalphenotypesfromfatalcasesofacuterespiratorydistresssyndromecausedbypneumonia AT nishiyamakenta clinicalphenotypesfromfatalcasesofacuterespiratorydistresssyndromecausedbypneumonia AT nakamurakazunori clinicalphenotypesfromfatalcasesofacuterespiratorydistresssyndromecausedbypneumonia AT sugamoritaka clinicalphenotypesfromfatalcasesofacuterespiratorydistresssyndromecausedbypneumonia AT ichiyasuhidenori clinicalphenotypesfromfatalcasesofacuterespiratorydistresssyndromecausedbypneumonia AT sakagamitakuro clinicalphenotypesfromfatalcasesofacuterespiratorydistresssyndromecausedbypneumonia |