Evidence map›Paper›PMID 30578335›Full record

ReviewEuropean respiratory review : an official journal of the European Respiratory Society2018

Presentation, diagnosis and clinical course of the spectrum of progressive-fibrosing interstitial lung diseases.

Vincent Cottin, Nikhil A Hirani, David L Hotchkin, Anoop M Nambiar, Takashi Ogura, María Otaola, Dirk Skowasch, Jong Sun Park, Hataya K Poonyagariyagorn, Wim Wuyts and 1 more

3 registry-linked trialsOpen access · diamondAbstract readReview
In one paragraph

Review in European respiratory review : an official journal of the European Respiratory Society, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 317 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
317citing papers in PubMed, 6 pooled it
38.3field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT04675619 phase2completednot on this mapstarted 2019, after this paper: background citation

Evaluation of the Efficacy of Pirfenidone in Progressive Chronic Hypersensitivity Pneumonitis

TypeinterventionalSponsorZagazig UniversityRan2019 to 2020Enrolled40ConditionsHypersensitivity PneumonitisArmsOral pirfenidone, Standard care
NCT06844331 enrolling by invitationnot on this mapstarted 2024, after this paper: background citation

ULtrasOund Applicability in the Assessment of Patients With fibRosing Interstitial Lung Disease (LORD): A Research Protocol of a Single Center, Real-life, Prospective Observational Study

TypeobservationalSponsorOdense University HospitalRan2024 to 2026Enrolled117ConditionsFibrosing Interstitial Lung Diseases, Thoracic UltrasoundArmsThoracic ultrasound
NCT07577115 active not recruitingnot on this mapstarted 2026, after this paper: background citation

Occupational and Environmental Exposures Analysis in Interstitial Lung Diseases: a Prospective Observational Study.

Typeobservational_patient_registrySponsorIstituto Clinico HumanitasRan2026 to 2034Enrolled1,000ConditionsInterstitial Lung Disease Due to Systemic Disease (Disorder), Interstitial Lung Disease Due to Systemic Disease (Telomere Biology Disorder), Exposure Occupational, Occupational ExposureArmsstandard interview
3 · Its place in the literature

Who cites it

317 citing papers in PubMed, 6 syntheses or guidelines pooled it, 640 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. A systematic review of procedural and sampling techniques for cryobiopsy in interstitial lung disease.European respiratory review : an official journal of the European Respiratory Society · 2024
    Pooled it
  5. Pooled it
  6. Guideline
  7. Trial
  8. Trial
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Dual pathology, dual burden: Functional impact of emphysema and fibrosis in Hypersensitivity Pneumonitis.Sarcoidosis, vasculitis, and diffuse lung diseases : official journal of WASOG · 2026
    Article
  15. Observational
  16. Article
  17. Article
  18. Review
  19. Article
  20. Review

257 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 9 institutions in 7 countries.

Vincent CottinLouis Pradel Hospital, Reference Center for Rare Pulmonary Diseases, Hospices Civils de Lyon, UMR 754, Université Claude Bernard Lyon 1, Lyon, France.ORCID https://orcid.org/0000-0002-5591-0955
Nikhil A HiraniEdinburgh Lung Fibrosis Clinic and MRC Centre for Inflammation Research, The Queen's Medical Research Centre, The University of Edinburgh, Edinburgh, UK.
David L HotchkinDivision of Pulmonary and Critical Care Medicine, Oregon Clinic, Portland, OR, USA.
Anoop M NambiarDivision of Pulmonary and Critical Care Medicine, Dept of Medicine, University of Texas Health Science Center San Antonio and the South Texas Veterans Health Care System, San Antonio, TX, USA.ORCID http://orcid.org/0000-0003-2778-0433
Takashi OguraKanagawa Cardiovascular and Respiratory Center, Kanagawa, Japan.
María OtaolaFundación FUNEF, Instituto de Rehabilitacion Psicofísica (IREP Hospital), Buenos Aires, Argentina.
Dirk SkowaschDept of Internal Medicine II, Cardiology, Pneumology and Angiology, University Hospital Bonn, Bonn, Germany.
Jong Sun ParkDivision of Pulmonary and Critical Care Medicine, Dept of Internal Medicine and Lung Institute of Medical Research Center, Seoul National University College of Medicine, Seoul National University Bundang Hospital, Seongnam, Republic of Korea.
Hataya K PoonyagariyagornDivision of Pulmonary and Critical Care Medicine, Oregon Clinic, Portland, OR, USA.
Wim WuytsUnit for Interstitial Lung Diseases, University Hospitals Leuven, Leuven, Belgium.
Athol U WellsInterstitial Lung Disease Unit, Royal Brompton Hospital, London, UK.
Oregon Clinic · USKanagawa Cardiovascular and Respiratory Center · JPKU Leuven · BEQueen's Medical Centre · GBRoyal Brompton Hospital · GBSeoul National University Bundang Hospital · KRThe University of Texas Health Science Center at San Antonio · USUniversité Claude Bernard Lyon 1 · FRUniversity Hospital Bonn · DE

Funding

San Antonio OAIC - Research Education Component (REC)P30AG044271 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Adam Salmon, Elena Volpi · 2015 to 2026
$14.1M
NIA NIH HHS P30 AG044271
6 · The paper itself

Abstract

Although these conditions are rare, a proportion of patients with interstitial lung diseases (ILDs) may develop a progressive-fibrosing phenotype. Progressive fibrosis is associated with worsening respiratory symptoms, lung function decline, limited response to immunomodulatory therapies, decreased quality of life and, potentially, early death. Idiopathic pulmonary fibrosis may be regarded as a model for other progressive-fibrosing ILDs. Here we focus on other ILDs that may present a progressive-fibrosing phenotype, namely idiopathic nonspecific interstitial pneumonia, unclassifiable idiopathic interstitial pneumonia, connective tissue disease-associated ILDs (

Indexed as

AdultAgedDiagnosis, DifferentialDisease ProgressionFemaleHumansLungLung Diseases, InterstitialMaleMiddle AgedPhenotypePredictive Value of TestsPulmonary FibrosisQuality of LifeRisk FactorsSeverity of Illness Index

Identifiers

PMID30578335
PMCPMC9489068
OpenAlexW2906077632

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.