About: Acute exacerbation of idiopathic pulmonary fibrosis triggered by Aspergillus empyema

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An Entity of Type : schema:ScholarlyArticle, within Data Space : wasabi.inria.fr associated with source document(s)

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type	Academic Article research paper schema:ScholarlyArticle
isDefinedBy	Covid-on-the-Web dataset
title	Acute exacerbation of idiopathic pulmonary fibrosis triggered by Aspergillus empyema
Creator	Kataoka, Kensuke Kimura, Tomoki Kondoh, Yasuhiro Matsuda, Toshiaki Mori, Yuta Suzuki, Atsushi Yokoyama, Toshiki
source	PMC
abstract	Acute exacerbation (AE) is a severe and life-threatening complication of idiopathic pulmonary fibrosis (IPF). In 2016, the definition and diagnostic criteria for AE-IPF were updated by an international working group. The new definition includes any acute, clinically significant respiratory deterioration (both idiopathic and triggered events) characterized by evidence of new widespread alveolar abnormality in patients with IPF. There are no currently proven beneficial management strategies for idiopathic and triggered AE-IPF. This is the first report describing AE-IPF triggered by Aspergillus empyema, which was improved by a combination of corticosteroid, systemic antifungal therapy, local antifungal therapy, and additional pharmacological therapies. Future research may reveal optimal strategies for both idiopathic and triggered AE-IPF.
has issue date	2018-01-31(xsd:dateTime)
bibo:doi	10.1016/j.rmcr.2018.01.004
bibo:pmid	29719792
has license	cc-by-nc-nd
sha1sum (hex)	ec7eb0e096ddb4117326868b33a872bebb52776b
schema:url	https://doi.org/10.1016/j.rmcr.2018.01.004
resource representing a document's title	Acute exacerbation of idiopathic pulmonary fibrosis triggered by Aspergillus empyema
has PubMed Central identifier	PMC5925856
has PubMed identifier	29719792
schema:publication	Respir Med Case Rep
resource representing a document's body	covid:ec7eb0e096ddb4117326868b33a872bebb52776b#body_text
is schema:about of	named entity 'Acute' named entity 'ASPERGILLUS' named entity 'EMPYEMA' named entity 'TRIGGERED BY' named entity 'Acute exacerbation' named entity 'empyema' named entity 'Aspergillus' named entity 'dyspnea' named entity 'natural history of the disease' named entity 'titration' named entity 'inhalation' named entity 'empyema' named entity 'neutrophils' named entity 'mycotoxins' named entity 'idiopathic' named entity 'dyspnea' named entity 'antifungal' named entity 'thoracic cavity' named entity 'cough' named entity 'lung fields' named entity 'idiopathic' named entity 'IPF' named entity 'left lower lobe' named entity 'idiopathic' named entity 'chemotherapy' named entity 'amphotericin-B' named entity 'infection' named entity 'combination therapy' named entity 'respiratory symptoms' named entity 'histopathological' named entity 'Aspergillus' named entity 'chest CT scan' named entity 'idiopathic' named entity 'intrathoracic' named entity 'IPF' named entity 'corticosteroid therapy' named entity 'diffuse alveolar damage' named entity 'CRP' named entity 'empyema' named entity 'pharmacological' named entity '5 December 2017' named entity 'corticosteroid therapy' named entity 'Serum' named entity 'empyema' named entity 'interstitial lung disease' named entity 'pirfenidone' named entity 'bioactive' named entity 'pred' named entity 'serum brain natriuretic peptide' named entity 'infection' named entity 'IPF' named entity 'C-reactive protein' named entity 'computed tomographic' named entity 'vital signs' named entity 'mg/dl' named entity 'corticosteroid' named entity 'IPF' named entity 'pulmonary function' named entity 'Aspergillus' named entity 'IPF' named entity 'infection' named entity 'bacterial pneumonia' named entity 'methylprednisolone' named entity 'combination therapy' named entity 'procalcitonin' named entity 'intravenous' named entity 'white blood cell (WBC) count' named entity 'corticosteroid' named entity 'steroids' named entity 'July 2008' named entity 'IPF' named entity 'IPF' named entity 'IPF' named entity 'sputum smear' named entity 'thrombomodulin'

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