Evidence map›Paper›PMID 30578337›Full record

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

Healthcare utilisation and costs in the diagnosis and treatment of progressive-fibrosing interstitial lung diseases.

Colin Holtze, Kevin Flaherty, Michael Kreuter, Fabrizio Luppi, Teng Moua, Carlo Vancheri, Mary B Scholand

Open 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. Cited by 11 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 2 pooled it
3.7field-weighted citation impact, top 6% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 2 syntheses or guidelines pooled it, 30 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Burden of illness in progressive fibrosing interstitial lung disease.Journal of managed care & specialty pharmacy · 2022
    Article
  6. Article
  7. Article
  8. Article
  9. Observational
  10. Treatment of progressive fibrosing interstitial lung diseases: a milestone in the management of interstitial lung diseases.European respiratory review : an official journal of the European Respiratory Society · 2019
    Article
  11. Beyond idiopathic pulmonary fibrosis: the world of progressive-fibrosing interstitial lung disease.European respiratory review : an official journal of the European Respiratory Society · 2018
    Article
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

7 authors at 5 institutions in 3 countries.

Colin HoltzeDivision of Pulmonary and Critical Care Medicine, University of Michigan, Ann Arbor, MI, USA choltze@med.umich.edu.
Kevin FlahertyDivision of Pulmonary and Critical Care Medicine, University of Michigan, Ann Arbor, MI, USA.
Michael KreuterCenter for Interstitial and Rare Lung Diseases, Pneumology and Respiratory Critical Care Medicine, Thoraxklinik, University of Heidelberg, member of the German Center for Lung Research, Heidelberg, Germany.
Fabrizio LuppiCentre for Rare Lung Disease, University Hospital, Modena, Italy.
Teng MouaDivision of Pulmonary and Critical Care Medicine, Mayo Clinic, Rochester, MN, USA.
Carlo VancheriDept of Clinical and Experimental Medicine, University of Catania, University Hospital "Policlinico - Vitt. Emanuele", Catania, Italy.
Mary B ScholandDept of Internal Medicine, University of Utah School of Medicine, Salt Lake City, UT, USA.
University of Michigan · USGerman Center for Lung Research · DEMayo Clinic · USUniversity of Catania · ITUniversity of Utah · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There are over 200 interstitial lung diseases (ILDs). In addition to patients with idiopathic pulmonary fibrosis (IPF), a percentage of patients with other ILDs also develop progressive fibrosis of the lung during their disease course. Patients with progressive-fibrosing ILDs may show limited response to immunomodulatory therapy, worsening symptoms and lung function and, ultimately, early mortality. There are few data for ILDs that may present a progressive fibrosing phenotype specifically, but we believe the burden and healthcare costs associated with these conditions may be comparable to those reported in IPF. This review discusses the burden of ILDs that may present a progressive fibrosing phenotype and the factors impacting healthcare utilisation.

Indexed as

Health Care CostsComorbidityDisease ProgressionHumansLung Diseases, InterstitialPhenotypePulmonary FibrosisRisk FactorsTreatment Outcome

Identifiers

PMID30578337
PMCPMC9488711
OpenAlexW2905646339

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.