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1000 Titel
  • Design and baseline characteristics of the ILD-PRO registry in patients with progressive pulmonary fibrosis
1000 Autor/in
  1. Lobo, L Jason |
  2. Liu, Yi |
  3. Li, Peide |
  4. Ramaswamy, Murali |
  5. Swaminathan, Aparna C |
  6. Veeraraghavan, Srihari |
  7. Fan, Yanni |
  8. Neely, Megan L |
  9. Palmer, Scott M |
  10. Olson, Amy L |
  11. on behalf of the ILD-PRO Registry investigators† |
1000 Verlag BioMed Central
1000 Erscheinungsjahr 2024
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2024-09-27
1000 Erschienen in
1000 Quellenangabe
  • 24(1):468
1000 Copyrightjahr
  • 2024
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1186/s12890-024-03247-8 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11438290/ |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • <jats:title>Abstract</jats:title><jats:sec> <jats:title>Background</jats:title> <jats:p>To assess the characteristics of patients enrolled in the ILD-PRO Registry.</jats:p> </jats:sec><jats:sec> <jats:title>Methods</jats:title> <jats:p>The ILD-PRO Registry is a multicentre US registry of patients with progressive pulmonary fibrosis. This registry is enrolling patients with an interstitial lung disease (ILD) other than idiopathic pulmonary fibrosis who have reticular abnormality and traction bronchiectasis on HRCT, and who meet criteria for ILD progression within the prior 24 months. Patient characteristics were analysed based on the number of patients with available data.</jats:p> </jats:sec><jats:sec> <jats:title>Results</jats:title> <jats:p>Of the first 491 patients enrolled, the majority were white (75.4%) and female (60.6%); 47.4% had a history of smoking. Reported ILDs were autoimmune disease-associated ILDs (47.2%), hypersensitivity pneumonitis (17.5%), idiopathic non-specific interstitial pneumonia (9.1%), interstitial pneumonia with autoimmune features (8.9%), unclassifiable ILD (7.6%), other ILDs (9.7%). At enrolment, median (Q1, Q3) FVC % predicted was 62.2 (49.4, 72.4) and DLco % predicted was 39.2 (30.2, 49.2). Median (Q1, Q3) total score on the St. George’s Respiratory Questionnaire was 50.8 (35.9, 64.7). The most common comorbidities were gastroesophageal reflux disease (61.1%) and sleep apnoea (29.6%). Overall, 64.5% of patients were receiving immunosuppressive or cytotoxic therapy, 61.1% proton-pump inhibitors, 53.2% oral steroids, 19.8% nintedanib and 3.6% pirfenidone.</jats:p> </jats:sec><jats:sec> <jats:title>Conclusions</jats:title> <jats:p>Patients enrolled into the ILD-PRO Registry have a variety of ILD diagnoses, marked impairment in lung function and health-related quality of life, and high medication use. Longitudinal data from this registry will further our knowledge of the course of progressive pulmonary fibrosis.</jats:p> </jats:sec><jats:sec> <jats:title>Trial Registration</jats:title> <jats:p>ClinicalTrials.gov, NCT01915511; registered August 5, 2013.</jats:p> </jats:sec>
1000 Sacherschließung
lokal Idiopathic Pulmonary Fibrosis/drug therapy [MeSH]
lokal Disease Progression [MeSH]
lokal Disease progression
lokal Aged [MeSH]
lokal Vital Capacity [MeSH]
lokal Pulmonary Fibrosis/epidemiology [MeSH]
lokal Pyridones/therapeutic use [MeSH]
lokal Tomography, X-Ray Computed [MeSH]
lokal Indoles/therapeutic use [MeSH]
lokal Male [MeSH]
lokal United States/epidemiology [MeSH]
lokal Quality of Life [MeSH]
lokal Idiopathic Pulmonary Fibrosis/epidemiology [MeSH]
lokal Pulmonary fibrosis
lokal Lung Diseases, Interstitial/epidemiology [MeSH]
lokal Female [MeSH]
lokal Pulmonary Fibrosis/complications [MeSH]
lokal Humans [MeSH]
lokal Middle Aged [MeSH]
lokal Multicenter Studies as Topic [MeSH]
lokal Lung Diseases, Interstitial/drug therapy [MeSH]
lokal Idiopathic Pulmonary Fibrosis/physiopathology [MeSH]
lokal Research
lokal Clinical trial
lokal Interstitial lung disease
lokal Registries [MeSH]
1000 Fächerklassifikation (DDC)
1000 Liste der Beteiligten
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  • DeepGreen-ID: 08df39bb2dc244db819a525b8dec2ad9 ; metadata provieded by: DeepGreen (https://www.oa-deepgreen.de/api/v1/), LIVIVO search scope life sciences (http://z3950.zbmed.de:6210/livivo), Crossref Unified Resource API (https://api.crossref.org/swagger-ui/index.html), to.science.api (https://frl.publisso.de/), ZDB JSON-API (beta) (https://zeitschriftendatenbank.de/api/), lobid - Dateninfrastruktur für Bibliotheken (https://lobid.org/resources/search)
1000 Label
1000 Förderer
  1. The IPF-PRO/ILD-PRO Registry is supported by Boehringer Ingelheim Pharmaceuticals, Inc (BIPI) and run in collaboration with the Duke Clinical Research Institute (DCRI) and enrolling centres. |
1000 Fördernummer
  1. -
1000 Förderprogramm
  1. -
1000 Dateien
1000 Förderung
  1. 1000 joinedFunding-child
    1000 Förderer The IPF-PRO/ILD-PRO Registry is supported by Boehringer Ingelheim Pharmaceuticals, Inc (BIPI) and run in collaboration with the Duke Clinical Research Institute (DCRI) and enrolling centres. |
    1000 Förderprogramm -
    1000 Fördernummer -
1000 Objektart article
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1000 Erstellt am 2025-07-05T13:20:51.691+0200
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