Evidence map›Paper›PMID 24032382›Full record

GuidelineAmerican journal of respiratory and critical care medicine2013

An official American Thoracic Society/European Respiratory Society statement: Update of the international multidisciplinary classification of the idiopathic interstitial pneumonias.

William D Travis, Ulrich Costabel, David M Hansell, Talmadge E King, David A Lynch, Andrew G Nicholson, Christopher J Ryerson, Jay H Ryu, Moisés Selman, Athol U Wells and 27 more

4 registry-linked trialsAbstract readPractice Guideline
In one paragraph

Guideline in American journal of respiratory and critical care medicine, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 4 registered trials, which are not on this map. Cited by 1,976 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1,976citing papers in PubMed, 5 pooled it
–field-weighted citation impact
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.

NCT03440489 naunknown statusnot on this mapstarted 2018, after this paper: background citation

Assessment of Skeletal Muscle Dysfunction in Patient With Idiopathic Pulmonary Fibrosis

TypeinterventionalSponsorAssiut UniversityRan2018 to 2020Enrolled1ConditionsInterstitial Lung Disease, Skeletal Muscle DysfunctionArmsSix-minute walking test, 30 seconds chair stand test
NCT04036721 phase4suspendednot on this mapstarted 2019, after this paper: background citation

Randomized Open-label Study of the Impact of Prolonged Systemic Corticosteroid Therapy on the Course and Relapse Risk of Checkpoint Inhibitor Interstitial Lung Disease (Pneumonitis) Related to the Treatment of Solid Tumors With Anti-programmed-death Type 1 Receptor or Ligand Antibodies

TypeinterventionalSponsorNational Institute for Tuberculosis and Lung Diseases, PolandRan2019 to 2026Enrolled85ConditionsLung Neoplasm Malignant, Interstitial Lung DiseaseArmsProlonged glucocorticosteroid (prednisone) regimen, Short glucocorticosteroid (prednisone) regimen
NCT04946708 nacompletednot on this mapstarted 2021, after this paper: background citation

Using Technology to Engage Patients With Interstitial Lung Disease (ILD) in a Home a Home Exercise Program.

TypeinterventionalSponsorUniversity of ManitobaRan2021 to 2022Enrolled14ConditionsInterstitial Lung DiseaseArmsExercise program (virtual/remote)
NCT07315425 naactive not recruitingnot on this mapstarted 2026, after this paper: background citation

Investigation of the Acute Effects of Blood Flow Restriction Aerobic Exercise on Hemodynamic Responses and Muscle Oxygen in Patients With Interstitial Lung Disease

TypeinterventionalSponsorGazi UniversityRan2026 to 2028Enrolled30ConditionsInterstitial Lung Disease (ILD)ArmsBlood flow restriction (BFR) low-intensity aerobic exercise training, Low-intensity aerobic exercise training
3 · Its place in the literature

Who cites it

1,976 citing papers in PubMed, 5 syntheses or guidelines pooled it.

  1. Pooled it
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  5. Clinical care in interstitial lung disease: a critical appraisal of clinical guidance documents.European respiratory review : an official journal of the European Respiratory Society · 2025
    Pooled it
  6. Article
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  9. Acute exacerbation in fibrotic interstitial lung disease: an international working group report.American journal of respiratory and critical care medicine · 2026
    Review
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1,916 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

37 authors.

William D Travis
Ulrich Costabel
David M Hansell
Talmadge E King
David A Lynch
Andrew G Nicholson
Christopher J Ryerson
Jay H Ryu
Moisés Selman
Athol U Wells
Jurgen Behr
Demosthenes Bouros
Kevin K Brown
Thomas V Colby
Harold R Collard
Carlos Robalo Cordeiro
Vincent Cottin
Bruno Crestani
Marjolein Drent
Rosalind F Dudden
Jim Egan
Kevin Flaherty
Cory Hogaboam
Yoshikazu Inoue
Takeshi Johkoh
Dong Soon Kim
Masanori Kitaichi
James Loyd
Fernando J Martinez
Jeffrey Myers
Shandra Protzko
Ganesh Raghu
Luca Richeldi
Nicola Sverzellati
Jeffrey Swigris
Dominique Valeyre
ATS/ERS Committee on Idiopathic Interstitial Pneumonias

Funding

Innate DNA sensing in rapidly progressing IPFR01HL123899 · NHLBI · CEDARS-SINAI MEDICAL CENTER · PI HOGABOAM, CORY M · 2015 to 2018
$2.0M
6 · The paper itself

Abstract

backgroundIn 2002 the American Thoracic Society/European Respiratory Society (ATS/ERS) classification of idiopathic interstitial pneumonias (IIPs) defined seven specific entities, and provided standardized terminology and diagnostic criteria. In addition, the historical "gold standard" of histologic diagnosis was replaced by a multidisciplinary approach. Since 2002 many publications have provided new information about IIPs. PURPOSE: The objective of this statement is to update the 2002 ATS/ERS classification of IIPs.

methodsAn international multidisciplinary panel was formed and developed key questions that were addressed through a review of the literature published between 2000 and 2011.

resultsSubstantial progress has been made in IIPs since the previous classification. Nonspecific interstitial pneumonia is now better defined. Respiratory bronchiolitis-interstitial lung disease is now commonly diagnosed without surgical biopsy. The clinical course of idiopathic pulmonary fibrosis and nonspecific interstitial pneumonia is recognized to be heterogeneous. Acute exacerbation of IIPs is now well defined. A substantial percentage of patients with IIP are difficult to classify, often due to mixed patterns of lung injury. A classification based on observed disease behavior is proposed for patients who are difficult to classify or for entities with heterogeneity in clinical course. A group of rare entities, including pleuroparenchymal fibroelastosis and rare histologic patterns, is introduced. The rapidly evolving field of molecular markers is reviewed with the intent of promoting additional investigations that may help in determining diagnosis, and potentially prognosis and treatment.

conclusionsThis update is a supplement to the previous 2002 IIP classification document. It outlines advances in the past decade and potential areas for future investigation.

Indexed as

Diagnosis, DifferentialEuropeHumansIdiopathic Interstitial PneumoniasSocieties, MedicalUnited States

Identifiers

PMID24032382
PMCPMC5803655

What OpenQuestion holds

Textmetadata
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.