Evidence map›Paper›PMID 26324803›Full record

ReviewEuropean respiratory review : an official journal of the European Respiratory Society2015

Idiopathic pulmonary fibrosis: from clinical trials to real-life experiences.

Sergio Harari, Antonella Caminati

Abstract readReview
In one paragraph

Review in European respiratory review : an official journal of the European Respiratory Society, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
–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.

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

20 citing papers in PubMed.

  1. New analogs of 5-substituted-2(1Acta biochimica Polonica · 2025
    Article
  2. Review
  3. Article
  4. Observational
  5. Article
  6. Observational
  7. Comorbidities in idiopathic pulmonary fibrosis: an underestimated issue.European respiratory review : an official journal of the European Respiratory Society · 2019
    Review
  8. Review
  9. Review
  10. Review
  11. Randomised controlled trials and real-life studies: two answers for one question.European respiratory review : an official journal of the European Respiratory Society · 2018
    Article
  12. Article
  13. Severe idiopathic pulmonary fibrosis: what can be done?European respiratory review : an official journal of the European Respiratory Society · 2017
    Review
  14. Role of pirfenidone in the management of pulmonary fibrosis.Therapeutics and clinical risk management · 2017
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Rare pulmonary diseases and orphan drugs: where do we stand and where are we going to?European respiratory review : an official journal of the European Respiratory Society · 2015
    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

2 authors.

Sergio HarariU.O. di Pneumologia e Terapia Semi-Intensiva Respiratoria, Servizio di Fisiopatologia Respiratoria ed Emodinamica Polmonare, Ospedale San Giuseppe, MultiMedica IRCCS, Milan, Italy sharari@ilpolmone.it.
Antonella CaminatiU.O. di Pneumologia e Terapia Semi-Intensiva Respiratoria, Servizio di Fisiopatologia Respiratoria ed Emodinamica Polmonare, Ospedale San Giuseppe, MultiMedica IRCCS, Milan, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Randomised controlled clinical trials are fundamental in medicine to develop new effective drugs and new therapeutic regimens and are the strength of evidence-based medicine. These studies allow us to avoid the repetition of misleading experiences that have been reported in the past, where drugs or associations were utilised without compelling evidence and ultimately proven to be ineffective. In recent years, randomised clinical trials have been conducted and concluded for many rare diseases, including idiopathic pulmonary fibrosis. However, clinical trials do not always reflect the real-life scenario. Patients selected for clinical trials present fewer comorbidities, they fall between certain age limits, and the severity of their disease is defined; therefore, they do not always reflect the whole of the population affected by a specific disease. These are the reasons why we also need data that mirror real-life experience. The limitations that these kind of studies present are always several and the studies should be interpreted with caution, although they can fill the important gap between efficacy and effectiveness. In this article, we will review the existing clinical data on real-life treatment of idiopathic pulmonary fibrosis.

Indexed as

Research DesignEvidence-Based MedicineHumansIdiopathic Pulmonary FibrosisPyridonesRandomized Controlled Trials as TopicTreatment OutcomepirfenidonePyridones

Identifiers

PMID26324803
PMCPMC9487689

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.