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About:
Survival in Idiopathic pulmonary fibrosis acute exacerbations: the non-steroid approach
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An Entity of Type :
schema:ScholarlyArticle
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covidontheweb.inria.fr
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Academic Article
research paper
schema:ScholarlyArticle
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
has title
Survival in Idiopathic pulmonary fibrosis acute exacerbations: the non-steroid approach
Creator
Kotanidou, Anastasia
Argentos, Stylianos
Baou, Katerina
Karakatsani, Anna
Kagouridis, Konstantinos
Kolilekas, Likurgos
Malagari, Katerina
Manali, Effrosyni
Papaioannou, Andriana
Papiris, Spyros
Roussou, Aneza
Triantafillidou, Christina
Source
PMC
abstract
BACKGROUND: Idiopathic pulmonary fibrosis acute exacerbation (IPF-AE) constitutes IPF’s most devastating event, representing the unexpected superimposition of diffuse alveolar damage of unknown etiology. Guidelines recommend high-dose steroids treatment despite unproven benefit. We hypothesized that previous immunosuppression and the administration of high-dose steroids adversely affect IPF-AE outcome. METHODS: We studied all consecutive patients hospitalized in our department for IPF deterioration from 2007 to June 2013. Our protocol consisted of immediate cessation of immunosuppression (if any), best supportive care, broad-spectrum antimicrobials and thorough evaluation to detect reversible causes of deterioration. Patients were followed-up for survival; post-discharge none received immunosuppression. RESULTS: Twenty-four out of 85 admissions (28 %) fulfilled IPF-AE criteria. IPF-AE were analyzed both as unique events and as unique patients. As unique events 50 % survived; 3 out of 12 (25 %) in the group previously treated with immunosuppression whereas nine out of 12 (75 %) in the group not receiving immunosuppression (p = 0.041). As unique patients 35.3 % survived; 3 out of 6 (50 %) in the never treated group whereas three out of 11 (27.3 %) in the group receiving immunosuppression (p = 0.685). The history of immunosuppression significantly and adversely influenced survival (p = 0.035). Survival was greater in the never treated group compared to the immunosuppressed patients (p = 0.022). Post-discharge, our IPF-AE survivors had an 83 % 1-year survival. CONCLUSIONS: By applying the above mentioned protocol half of our patients survived. The history of immunosuppression before IPF-AE adversely influences survival. Avoiding steroids in IPF patients may favor the natural history of the disease even at the moment of its most devastating event.
has issue date
2015-12-14
(
xsd:dateTime
)
bibo:doi
10.1186/s12890-015-0146-4
bibo:pmid
26666385
has license
cc-by
sha1sum (hex)
a3e7f6f86be44d7e5cad642fc7ac1c22308b44e8
schema:url
https://doi.org/10.1186/s12890-015-0146-4
resource representing a document's title
Survival in Idiopathic pulmonary fibrosis acute exacerbations: the non-steroid approach
has PubMed Central identifier
PMC4678631
has PubMed identifier
26666385
schema:publication
BMC Pulm Med
resource representing a document's body
covid:a3e7f6f86be44d7e5cad642fc7ac1c22308b44e8#body_text
is
schema:about
of
named entity 'survival'
named entity 'protocol'
named entity 'representing'
named entity 'receiving'
named entity 'receiving'
named entity 'Guidelines'
named entity 'hypothesized'
named entity 'events'
named entity 'IPF'
named entity '0.035'
named entity 'SURVIVAL'
named entity 'FOLLOWED'
named entity 'IMMUNOSUPPRESSION'
named entity 'RESULTS'
named entity 'STEROIDS'
named entity 'IMMUNOSUPPRESSED PATIENTS'
named entity '2007'
named entity 'received'
named entity 'Our'
named entity 'etiology'
named entity 'survival'
named entity 'group'
named entity 'compared'
named entity 'immunosuppression'
named entity 'The'
named entity 'immunosuppression'
named entity 'treated'
named entity 'steroids'
named entity 'group'
named entity 'events'
named entity 'history'
named entity 'cessation'
named entity 'steroids'
named entity 'IPF'
named entity 'immunosuppression'
named entity 'adversely affect'
named entity 'IPF'
named entity 'diffuse alveolar damage'
named entity 'immunosuppression'
named entity 'natural history of the disease'
named entity 'patients'
named entity 'lung'
named entity 'IPF'
named entity 'IPF'
named entity 'sputum'
named entity 'IPF'
named entity 'lymphocytes'
named entity 'acute respiratory distress syndrome'
named entity 'acute exacerbation'
named entity 'antimicrobials'
named entity 'Chlamydophila Pneumoniae'
named entity 'methotrexate'
named entity 'TLC'
named entity 'immunosuppressive therapy'
named entity 'Heart failure'
named entity 'diffusing capacity'
named entity 'steroids'
named entity 'IPF'
named entity 'invasive mechanical ventilation'
named entity 'IPF'
named entity 'supportive care'
named entity 'pulmonary embolism'
named entity 'IPF'
named entity 'pulmonary hypertension'
named entity 'pharmacological treatment'
named entity 'pneumonia'
named entity 'IPF'
named entity 'Altrincham'
named entity 'lung injuries'
named entity 'antimicrobials'
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