Evidence map›Paper›PMID 38663886›Full record

Observational studyBMJ open respiratory research2024

Antifibrotic treatment adherence, efficacy and outcomes for patients with idiopathic pulmonary fibrosis in Spain: a real-world evidence study.

Ana Dolores Romero Ortiz, Beatriz María Jiménez-Rodríguez, Cecilia López-Ramírez, Ángela López-Bauzá, María Pérez-Morales, José Antonio Delgado-Torralbo, Cristina Villalba Moral, Bernardino Alcazar-Navarrete

Open access · goldAbstract readObservational StudyMulticenter Study
In one paragraph

Observational study in BMJ open respiratory research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 2 pooled it
4.6field-weighted citation impact, top 5% 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

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

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Article
  5. Observational
  6. Article
  7. Article
  8. Survival impact and safety comparison of pirfenidone and nintedanib for idiopathic pulmonary fibrosis: A meta-analysis.Sarcoidosis, vasculitis, and diffuse lung diseases : official journal of WASOG · 2025
    Article
  9. Observational
  10. Article
  11. Article
  12. 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

8 authors at 6 institutions in 1 country.

Ana Dolores Romero OrtizRespiratory Department, Hospital Universitario Virgen de las Nieves, Granada, Spain.
Beatriz María Jiménez-RodríguezRespiratory Department, Hospital Universitario Virgen de las Nieves, Granada, Spain balcazarnavarrete@gmail.com beatriz.jimenez.rodriguez.sspa@juntadeandalucia.es.
Cecilia López-RamírezHospitales Universitarios Virgen del Rocío, Sevilla, Spain.
Ángela López-BauzáHospitales Universitarios Virgen del Rocío, Sevilla, Spain.
María Pérez-MoralesRespiratory Department, Hospital Universitario Costa del Sol, Marbella, Spain.
José Antonio Delgado-TorralboRespiratory Department, Hospital Universitario Virgen Macarena, Sevilla, Spain.
Cristina Villalba MoralRespiratory Department, Complejo Hospitalario de Jaen, Jaen, Andalucía, Spain.
Bernardino Alcazar-NavarreteRespiratory Department, Hospital Universitario Virgen de las Nieves, Granada, Spain balcazarnavarrete@gmail.com beatriz.jimenez.rodriguez.sspa@juntadeandalucia.es.ORCID http://orcid.org/0000-0003-2356-9366
Hospital Universitario Virgen de las Nieves · ESHospital Universitario Virgen del Rocío · ESComplejo Hospitalario de Jaén · ESHospital Costa del Sol · ESHospital Universitario Virgen Macarena · ESUniversidad de Granada · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIdiopathic pulmonary fibrosis (IPF) is a rare disorder associated with increased mortality and morbidity. There are currently two drugs approved for IPF but their safety and efficacy profile in real-world settings in Spain is not well understood.

methodsAn observational, multicentre, prospective study was carried out among patients with IPF who started treatment with pirfenidone or nintedanib from 2015 to 2021. Data regarding clinical characteristics, drug adherence, safety profiles and clinical outcomes between these two drugs were collected.

results232 patients were included in the analysis. There were no meaningful differences between both groups at baseline. Patients who started pirfenidone showed a decreased risk for treatment withdrawal compared with those starting nintedanib (HR 0.65 (95% CI 0.46 to 0.94; p=0.002)). Time to first adverse event and all-cause mortality was similar between study groups. Risk factors for withdrawal were female sex, diarrhoea and photosensitivity.

conclusionsin this real-world study, both pirfenidone and nintedanib showed similar efficacy profiles. Pirfenidone was associated with less treatment discontinuations due to side effects.

Indexed as

Idiopathic Pulmonary FibrosisIndolesPyridonesAgedAged, 80 and overAntifibrotic AgentsDrug MonitoringFemaleHumansMaleMiddle AgedProspective StudiesSpainTreatment OutcomeAntifibrotic AgentsIndolesnintedanibpirfenidonePyridonesinterstitial fibrosis

Identifiers

PMID38663886
PMCPMC11043774
OpenAlexW4395480407

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.