Evidence map›Paper›PMID 40278040›Full record

ArticleJournal of imaging2025

Evolution of Lung Disease Studied by Computed Tomography in Adults with Cystic Fibrosis Treated with Elexacaftor/Tezacaftor/Ivacaftor.

Susana Hernández-Muñiz, Paloma Caballero, Adrián Peláez, Marta Solís-García, Carmen de Benavides, Javier Collada, Ignacio Díaz-Lorenzo, Cristina Zorzo, Rosa Mar Gómez-Punter, Rosa María Girón

Abstract read
In one paragraph

Article in Journal of imaging, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

10 authors.

Susana Hernández-MuñizRadiology Department, University Hospital La Princesa, Calle Diego de Leon nº 62, 28006 Madrid, Spain.
Paloma CaballeroRadiology Department, University Hospital La Princesa, Calle Diego de Leon nº 62, 28006 Madrid, Spain.ORCID 0000-0002-6352-9994
Adrián PeláezCentro Nacional de Investigaciones Cardiovasculares Carlos III (CNIC), 28029 Madrid, Spain.
Marta Solís-GarcíaPneumonology Department, University Hospital La Princesa, 28006 Madrid, Spain.
Carmen de BenavidesRadiology Department, University Hospital La Princesa, Calle Diego de Leon nº 62, 28006 Madrid, Spain.ORCID 0000-0001-7368-4720
Javier ColladaRadiology Department, University Hospital La Princesa, Calle Diego de Leon nº 62, 28006 Madrid, Spain.
Ignacio Díaz-LorenzoRadiology Department, University Hospital La Princesa, Calle Diego de Leon nº 62, 28006 Madrid, Spain.ORCID 0000-0002-4895-9689
Cristina ZorzoRadiology Department, University Hospital Sanitas La Moraleja, 28050 Madrid, Spain.
Rosa Mar Gómez-PunterPneumonology Department, University Hospital La Princesa, 28006 Madrid, Spain.
Rosa María GirónPneumonology Department, University Hospital La Princesa, 28006 Madrid, Spain.ORCID 0000-0001-7094-0848

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Elexacaftor-tezacaftor-ivacaftor (ETI) has shown clinical and spirometric benefits in cystic fibrosis (CF). CT remains a vital tool for diagnosing and monitoring structural lung disease. This study aimed to assess the evolution of lung disease, as evaluated through CT, in adults with CF after at least one year of ETI treatment. This ambispective observational analysis assessed lung CT scans performed before initiating ETI and after at least one year of treatment, using the modified Bhalla scoring system. For those patients with an earlier CT scan, a pre-treatment phase analysis was performed. Epidemiological, clinical, and functional parameters were evaluated. Results: Sixty-two patients were included (35 males, median age 30.4 ± 7.87 years). After at least one year of ETI, significant improvements were observed in the global CT Bhalla score (12.2 ± 2.8 vs. 14.0 ± 2.8), peribronchial thickening (1.4 ± 0.6 vs. 1.0 ± 0.4), and mucus plugging (1.6 ± 0.7 vs. 0.8 ± 0.6) (

Indexed as

CFTR (cystic fibrosis transmembrane conductance regulator) modulator therapychest imagingcomputed tomographycystic fibrosiselexacaftor/tezacaftor/ivacaftor

Identifiers

PMID40278040
PMCPMC12028220

What Socratic 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 Socratic graph.