Cargando…

Comorbidity burden and survival in patients with idiopathic pulmonary fibrosis: the EMPIRE registry study

BACKGROUND: Patients with idiopathic pulmonary fibrosis (IPF) frequently have multiple comorbidities, which may influence survival but go under-recognised in clinical practice. We therefore report comorbidity, antifibrotic treatment use and survival of patients with IPF observed in the multi-nationa...

Descripción completa

Detalles Bibliográficos
Autores principales:	Jovanovic, Dragana M., Šterclová, Martina, Mogulkoc, Nesrin, Lewandowska, Katarzyna, Müller, Veronika, Hájková, Marta, Studnicka, Michael, Tekavec-Trkanjec, Jasna, Littnerová, Simona, Vašáková, Martina
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2022
Materias:	Research
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9145164/ https://www.ncbi.nlm.nih.gov/pubmed/35624513 http://dx.doi.org/10.1186/s12931-022-02033-6

Ejemplares similares

Differences in Baseline Characteristics and Access to Treatment of Newly Diagnosed Patients With IPF in the EMPIRE Countries
por: Kolonics-Farkas, Abigél Margit, et al.
Publicado: (2021)

Anticoagulant Use and Bleeding Risk in Central European Patients with Idiopathic Pulmonary Fibrosis (IPF) Treated with Antifibrotic Therapy: Real-World Data from EMPIRE
por: Kolonics-Farkas, Abigél M., et al.
Publicado: (2020)

The European MultiPartner IPF registry (EMPIRE): validating long-term prognostic factors in idiopathic pulmonary fibrosis
por: Tran, Tanja, et al.
Publicado: (2020)

Survival and lung function decline in patients with definite, probable and possible idiopathic pulmonary fibrosis treated with pirfenidone
por: Májek, Ondřej, et al.
Publicado: (2022)

Biomarkers of Fibroproliferative Healing in Fibrosing Idiopathic Interstitial Pneumonias
por: Vasakova, Martina, et al.
Publicado: (2012)

Interstitial Score and Concentrations of IL-4Rα, PAR-2, and MMP-7 in Bronchoalveolar Lavage Fluid Could Be Useful Markers for Distinguishing Idiopathic Interstitial Pneumonias
por: Bruzova, Magdalena, et al.
Publicado: (2021)

Effect of genotype on the disease course in idiopathic pulmonary fibrosis despite antifibrotic treatment
por: Sterclova, Martina, et al.
Publicado: (2021)

The effect of nintedanib on lung functions and survival in idiopathic pulmonary fibrosis: real-life analysis of the Czech EMPIRE registry
por: Štefániková, Marianna, et al.
Publicado: (2023)

A young man with transitory hemiparesis and lung infiltrates
por: Ljilja, Anja, et al.
Publicado: (2021)

Role of interleukin 4 and its receptor in clinical presentation of chronic extrinsic allergic alveolitis: a pilot study
por: Sterclova, Martina, et al.
Publicado: (2013)

Bronchoalveolar lavage cell profiles and proteins concentrations can be used to phenotype extrinsic allergic alveolitis patients
por: Sterclova, Martina, et al.
Publicado: (2019)

PAR-2, IL-4R, TGF-β and TNF-α in bronchoalveolar lavage distinguishes extrinsic allergic alveolitis from sarcoidosis
por: MATĚJ, RADOSLAV, et al.
Publicado: (2014)

Effect of pirfenidone on lung function decline and survival: 5-yr experience from a real-life IPF cohort from the Czech EMPIRE registry
por: Zurkova, Monika, et al.
Publicado: (2019)

Comorbidities and survival in patients with chronic hypersensitivity pneumonitis
por: Wälscher, Julia, et al.
Publicado: (2020)

The European IPF registry (eurIPFreg): baseline characteristics and survival of patients with idiopathic pulmonary fibrosis
por: Guenther, Andreas, et al.
Publicado: (2018)

Investigating the role of obstructive pulmonary diseases and eosinophil count at admission on all-cause mortality in SARS-CoV-2 patients: A single center registry-based retrospective cohort study
por: Salai, Grgur, et al.
Publicado: (2023)

Scoring of the radiological picture of idiopathic interstitial pneumonia: a study to verify the reliability of the method
por: Kocova, Eva, et al.
Publicado: (2015)

Glutathione peroxidase 3 localizes to the epithelial lining fluid and the extracellular matrix in interstitial lung disease
por: Schamberger, Andrea C., et al.
Publicado: (2016)

Burden of comorbid conditions in children and young people with juvenile idiopathic arthritis: a collaborative analysis of 3 JIA registries
por: Kearsley-Fleet, Lianne, et al.
Publicado: (2021)

Effects of Nintedanib on Quantitative Lung Fibrosis Score in Idiopathic Pulmonary Fibrosis
por: Lancaster, Lisa, et al.
Publicado: (2020)

The natural history of progressive fibrosing interstitial lung diseases
por: Kolb, Martin, et al.
Publicado: (2019)

Delphi-Based Consensus on Interstitial Lung Disease Screening in Patients with Connective Tissue Diseases (Croatian National-Based Study)
por: Radić, Mislav, et al.
Publicado: (2022)

Diagnosis, course and management of hypersensitivity pneumonitis
por: Hamblin, Mark, et al.
Publicado: (2022)

Psychometric properties and minimal important differences of SF-36 in Idiopathic Pulmonary Fibrosis
por: Witt, Sabine, et al.
Publicado: (2019)

Long-term effects of complications and vascular comorbidity in idiopathic normal pressure hydrocephalus: a quality registry study
por: Andrén, Kerstin, et al.
Publicado: (2017)

Idiopathic Pulmonary Comorbidities and Mechanisms
por: Pacurari, Maricica, et al.
Publicado: (2021)

Temporal progression of mediastinal lymphadenopathy in idiopathic pulmonary fibrosis
por: Wallis, Tim JM, et al.
Publicado: (2022)

Automated airway quantification associates with mortality in idiopathic pulmonary fibrosis
por: Cheung, Wing Keung, et al.
Publicado: (2023)

An ocular lesion of unknown aetiology
por: Drosslerova, Marie, et al.
Publicado: (2021)

Transition of patients with interstitial lung disease from paediatric to adult care
por: Koucký, Václav, et al.
Publicado: (2021)

Reply to Dutkiewicz and Mackiewicz
por: Raghu, Ganesh, et al.
Publicado: (2023)

Assessment of right ventricular function in patients with pulmonary arterial hypertension-congenital heart disease and repaired and unrepaired defects: Correlation among speckle tracking, conventional echocardiography, and clinical parameters
por: Kemal, Hatice S., et al.
Publicado: (2020)

Managing comorbidities in idiopathic pulmonary fibrosis
por: Fulton, Blair G, et al.
Publicado: (2015)

Comorbidities and Complications in Idiopathic Pulmonary Fibrosis
por: Cano-Jiménez, Esteban, et al.
Publicado: (2018)

Empirical medical therapy for idiopathic male infertility
por: Thaker, Hatim, et al.
Publicado: (2020)

Baseline clinical characteristics, comorbidities and prescribed medication in a real-world population of patients with idiopathic pulmonary fibrosis: the PROOF registry
por: Wuyts, Wim A, et al.
Publicado: (2018)

Comorbidities in the UK Primary Sjögren’s Syndrome Registry
por: Tarn, Jessica, et al.
Publicado: (2022)

Patient Registries in Idiopathic Pulmonary Fibrosis
por: Culver, Daniel A., et al.
Publicado: (2019)

High Comorbidity Burden in Patients with SLE: Data from the Community-Based Lupus Registry of Crete
por: Gergianaki, Irini, et al.
Publicado: (2021)

Biodegradable polydioxanone stents in the treatment of adult patients with tracheal narrowing
por: Stehlik, Ludek, et al.
Publicado: (2015)

Cannot write session to /tmp/vufind_sessions/sess_v1r2g5g750gn4t94moengpq7gs