Evidence map›Paper›PMID 39065780›Full record

ArticlePharmaceuticals (Basel, Switzerland)2024

Pirfenidone in Idiopathic Pulmonary Fibrosis: Real-World Observation on Efficacy and Safety, Focus on Patients Undergoing Antithrombotic and Anticoagulant.

Nicolò Reccardini, Maria Chernovsky, Francesco Salton, Paola Confalonieri, Lucrezia Mondini, Mariangela Barbieri, Antonio Romallo, Marta Maggisano, Chiara Torregiani, Pietro Geri and 6 more

Abstract read
In one paragraph

Article in Pharmaceuticals (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 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.

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

8 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. 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

16 authors.

Nicolò ReccardiniDepartment of Pulmonology, University Hospital of Cattinara, 34149 Trieste, Italy.ORCID 0009-0004-5792-3655
Maria ChernovskyDepartment of Pulmonology, University Hospital of Cattinara, 34149 Trieste, Italy.
Francesco SaltonDepartment of Pulmonology, University Hospital of Cattinara, 34149 Trieste, Italy.ORCID 0000-0002-0864-9766
Paola ConfalonieriDepartment of Pulmonology, University Hospital of Cattinara, 34149 Trieste, Italy.ORCID 0000-0002-7284-5016
Lucrezia MondiniDepartment of Pulmonology, University Hospital of Cattinara, 34149 Trieste, Italy.ORCID 0000-0002-7043-9639
Mariangela BarbieriDepartment of Pulmonology, University Hospital of Cattinara, 34149 Trieste, Italy.
Antonio RomalloDepartment of Pulmonology, University Hospital of Cattinara, 34149 Trieste, Italy.
Marta MaggisanoDepartment of Pulmonology, University Hospital of Cattinara, 34149 Trieste, Italy.
Chiara TorregianiDepartment of Pulmonology, University Hospital of Cattinara, 34149 Trieste, Italy.ORCID 0000-0001-9110-3029
Pietro GeriDepartment of Pulmonology, University Hospital of Cattinara, 34149 Trieste, Italy.
Michael HughesDivision of Musculoskeletal and Dermatological Sciences, Faculty of Biology, Medicine and Healt, The University of Manchester & Salford Royal NHS Foundation Trust, Manchester M6 8HD, UK.ORCID 0000-0003-3361-4909
Corrado CampochiaroUnit of Immunology, Rheumatology, Allergy and Rare Diseases (UnIRAR), IRCCS San Raffaele Hospital, 20132 Milan, Italy.ORCID 0000-0001-6806-3794
Marco ConfalonieriDepartment of Pulmonology, University Hospital of Cattinara, 34149 Trieste, Italy.ORCID 0000-0002-4791-768X
Angelo ScardaPulmonology Unit, General Hospital "Santa Maria degli Angeli", 33170 Pordenone, Italy.
Umberto ZucconPulmonology Unit, General Hospital "Santa Maria degli Angeli", 33170 Pordenone, Italy.
Barbara RuaroDepartment of Pulmonology, University Hospital of Cattinara, 34149 Trieste, Italy.ORCID 0000-0001-8990-859X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Idiopathic pulmonary fibrosis (IPF) is a rare and progressive interstitial lung disease characterized by irreversible distortion of lung architecture and subsequent loss of pulmonary function. Pirfenidone is an antifibrotic agent associated with increased progression-free survival and overall survival rates, but it carries multiple side effects. The aim of the study was to examine the efficacy and safety profile of pirfenidone in a real-life context, with a focus on the concomitant use of antithrombotic and/or anticoagulant treatments. The clinical and functional data (forced vital capacity [FVC], forced expiratory volume in 1 s [FEV1], diffusing lung capacity for carbon monoxide [DLCO], and 6 min walking test distance [6MWD]) of all IPF patients treated with pirfenidone and referred to our two centers between 2019 and 2022 were retrospectively analyzed at baseline, 6 and 12 months after the start of treatment. A total of 55 IPF subjects undergoing pirfenidone treatment were included in the analysis (45.5% females, median [IQR] age at disease onset 68.0 [10.0] years, median [IQR] age at baseline 69.0 [10.8] years). Compared to baseline, at 12 months, FVC (86.0% vs. 80.0%;

Indexed as

anticoagulantsantithrombotic treatmentidiopathic pulmonary fibrosis (IPF)interstitial lung disease (ILD)pirfenidonepulmonary function test (PFT)

Identifiers

PMID39065780
PMCPMC11280355

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.