Prognostic classification in acute exacerbation of idiopathic pulmonary fibrosis: a multicentre retrospective cohort study

Abstract Acute exacerbation (AE) in idiopathic pulmonary fibrosis (IPF) is a major prognostic determinant. However, evidence for its prognostic strength is mainly based on the results of small cohort studies with statistical limitations. This retrospective study, which included 108 patients with a f...

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Autores principales: Takahito Suzuki, Hironao Hozumi, Koichi Miyashita, Masato Kono, Yuzo Suzuki, Masato Karayama, Kazuki Furuhashi, Hirotsugu Hasegawa, Tomoyuki Fujisawa, Noriyuki Enomoto, Yutaro Nakamura, Naoki Inui, Koshi Yokomura, Hidenori Nakamura, Takafumi Suda
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Publicado: Nature Portfolio 2021
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spelling oai:doaj.org-article:0e0643371bdb413c96c5184a22bb1dc72021-12-02T13:40:50ZPrognostic classification in acute exacerbation of idiopathic pulmonary fibrosis: a multicentre retrospective cohort study10.1038/s41598-021-88718-22045-2322https://doaj.org/article/0e0643371bdb413c96c5184a22bb1dc72021-04-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-88718-2https://doaj.org/toc/2045-2322Abstract Acute exacerbation (AE) in idiopathic pulmonary fibrosis (IPF) is a major prognostic determinant. However, evidence for its prognostic strength is mainly based on the results of small cohort studies with statistical limitations. This retrospective study, which included 108 patients with a first episode of AE-IPF, aimed to identify prognostic factors and to develop prognostic classification models. Multivariate Cox regression analysis revealed that a lower percent-predicted forced vital capacity within 12 months before AE onset (baseline %FVC) and a lower PaO2/FiO2 ratio at AE onset were independent mortality predictors. If the value of each predictor was lower than the cutoff determined by receiver-operating characteristic analysis, 1 point was assigned. Classification of patients into mild, moderate, and severe groups based on total score showed post-AE 90-day cumulative survival rates of 83.3%, 66.2%, and 22.2%, respectively (model 1: C-index 0.702). Moreover, a decision tree-based model was created with the recursive partitioning method using baseline %FVC and PaO2/FiO2 ratio at AE onset from among multivariable; accordingly, patients were classified into 3 groups with post-AE 90-day cumulative survival rates of 84.1%, 64.3%, and 24.0%, respectively (model 2: C-index 0.735). These models can guide clinicians in determining therapeutic strategies and help design future studies on AE-IPF.Takahito SuzukiHironao HozumiKoichi MiyashitaMasato KonoYuzo SuzukiMasato KarayamaKazuki FuruhashiHirotsugu HasegawaTomoyuki FujisawaNoriyuki EnomotoYutaro NakamuraNaoki InuiKoshi YokomuraHidenori NakamuraTakafumi SudaNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-9 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Takahito Suzuki
Hironao Hozumi
Koichi Miyashita
Masato Kono
Yuzo Suzuki
Masato Karayama
Kazuki Furuhashi
Hirotsugu Hasegawa
Tomoyuki Fujisawa
Noriyuki Enomoto
Yutaro Nakamura
Naoki Inui
Koshi Yokomura
Hidenori Nakamura
Takafumi Suda
Prognostic classification in acute exacerbation of idiopathic pulmonary fibrosis: a multicentre retrospective cohort study
description Abstract Acute exacerbation (AE) in idiopathic pulmonary fibrosis (IPF) is a major prognostic determinant. However, evidence for its prognostic strength is mainly based on the results of small cohort studies with statistical limitations. This retrospective study, which included 108 patients with a first episode of AE-IPF, aimed to identify prognostic factors and to develop prognostic classification models. Multivariate Cox regression analysis revealed that a lower percent-predicted forced vital capacity within 12 months before AE onset (baseline %FVC) and a lower PaO2/FiO2 ratio at AE onset were independent mortality predictors. If the value of each predictor was lower than the cutoff determined by receiver-operating characteristic analysis, 1 point was assigned. Classification of patients into mild, moderate, and severe groups based on total score showed post-AE 90-day cumulative survival rates of 83.3%, 66.2%, and 22.2%, respectively (model 1: C-index 0.702). Moreover, a decision tree-based model was created with the recursive partitioning method using baseline %FVC and PaO2/FiO2 ratio at AE onset from among multivariable; accordingly, patients were classified into 3 groups with post-AE 90-day cumulative survival rates of 84.1%, 64.3%, and 24.0%, respectively (model 2: C-index 0.735). These models can guide clinicians in determining therapeutic strategies and help design future studies on AE-IPF.
format article
author Takahito Suzuki
Hironao Hozumi
Koichi Miyashita
Masato Kono
Yuzo Suzuki
Masato Karayama
Kazuki Furuhashi
Hirotsugu Hasegawa
Tomoyuki Fujisawa
Noriyuki Enomoto
Yutaro Nakamura
Naoki Inui
Koshi Yokomura
Hidenori Nakamura
Takafumi Suda
author_facet Takahito Suzuki
Hironao Hozumi
Koichi Miyashita
Masato Kono
Yuzo Suzuki
Masato Karayama
Kazuki Furuhashi
Hirotsugu Hasegawa
Tomoyuki Fujisawa
Noriyuki Enomoto
Yutaro Nakamura
Naoki Inui
Koshi Yokomura
Hidenori Nakamura
Takafumi Suda
author_sort Takahito Suzuki
title Prognostic classification in acute exacerbation of idiopathic pulmonary fibrosis: a multicentre retrospective cohort study
title_short Prognostic classification in acute exacerbation of idiopathic pulmonary fibrosis: a multicentre retrospective cohort study
title_full Prognostic classification in acute exacerbation of idiopathic pulmonary fibrosis: a multicentre retrospective cohort study
title_fullStr Prognostic classification in acute exacerbation of idiopathic pulmonary fibrosis: a multicentre retrospective cohort study
title_full_unstemmed Prognostic classification in acute exacerbation of idiopathic pulmonary fibrosis: a multicentre retrospective cohort study
title_sort prognostic classification in acute exacerbation of idiopathic pulmonary fibrosis: a multicentre retrospective cohort study
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/0e0643371bdb413c96c5184a22bb1dc7
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