論文

国際誌
2018年10月

Outcomes with newly proposed classification of acute respiratory deterioration in idiopathic pulmonary fibrosis.

Respiratory medicine
  • Ryo Teramachi
  • Yasuhiro Kondoh
  • Kensuke Kataoka
  • Hiroyuki Taniguchi
  • Toshiaki Matsuda
  • Tomoki Kimura
  • Toshiki Yokoyama
  • Yasuhiko Yamano
  • Taiki Furukawa
  • Koji Sakamoto
  • Naozumi Hashimoto
  • Yoshinori Hasegawa
  • 全て表示

143
開始ページ
147
終了ページ
152
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1016/j.rmed.2018.09.011

BACKGROUND: Respiratory-related hospitalization, in particular acute exacerbation of idiopathic pulmonary fibrosis (AE-IPF), is common and associated with increasing mortality in patients with IPF. We aimed to evaluate the implications of a newly proposed framework of acute respiratory deterioration (ARD) and AE-IPF in hospitalized patients. METHODS: Using the data of an IPF cohort consisting of 225 consecutive patients, we retrospectively studied first hospitalizations from January 2008 to December 2017. We analysed the demographics and 90-day mortality of patients with AE-IPF and those with parenchymal cause of ARD other than AE. RESULTS: Among 122 patients with first hospitalization for ARD, 35 patients were diagnosed with AE-IPF, including 11 patients with triggered AE. Parenchymal cause of ARD other than AE was diagnosed in 71 patients, and extra-parenchymal cause in 16 patients. Almost all hospitalized patients (93%) underwent chest CT, and 83% of patients with AE-IPF underwent bronchoalveolar lavage. There was a significant difference in the anti-inflammatory therapy between the AE-IPF group and parenchymal cause of ARD other than AE group (p < 0.001). AE-IPF was independently associated with poor survival in multivariate Cox proportional regression analysis. CONCLUSIONS: AE-IPF accounted for about 30% of first hospitalizations for ARD, and differentiation between AE-IPF and the other categories in ARD is important from a therapeutic and a prognostic point of view.

リンク情報
DOI
https://doi.org/10.1016/j.rmed.2018.09.011
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/30261987
ID情報
  • DOI : 10.1016/j.rmed.2018.09.011
  • PubMed ID : 30261987

エクスポート
BibTeX RIS