Evidence map›Paper›PMID 36052286›Full record

ArticleTherapeutic advances in chronic disease2022

Therapeutic decisions in a cohort of patients with idiopathic pulmonary fibrosis: a multicenter, prospective survey from Poland.

Katarzyna Górska, Marta Maskey-Warzęchowska, Małgorzata Barnaś, Adam Białas, Adam Barczyk, Hanna Jagielska-Len, Ewa Jassem, Aleksander Kania, Katarzyna Lewandowska, Sebastian Majewski and 9 more

Abstract read
In one paragraph

Article in Therapeutic advances in chronic disease, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Review
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

19 authors.

Katarzyna GórskaDepartment of Internal Medicine, Pulmonary Diseases and Allergy, Medical University of Warsaw, Warsaw, Poland.ORCID https://orcid.org/0000-0003-4686-910X
Marta Maskey-WarzęchowskaDepartment of Internal Medicine, Pulmonary Diseases and Allergy, Medical University of Warsaw, Warsaw, Poland.
Małgorzata BarnaśDepartment of Internal Medicine, Pulmonary Diseases and Allergy, Medical University of Warsaw, 02-091 Warsaw, Poland.ORCID https://orcid.org/0000-0003-3545-8401
Adam BiałasDepartment of Pathobiology of Respiratory Diseases, Medical University of Lodz, Lodz, Poland.
Adam BarczykDepartment of Pneumonology, Medical University of Silesia, Katowice, Poland.
Hanna Jagielska-LenClinical Department of Lung Diseases, K. Marcinkowski University Hospital, Zielona Gora, Poland.
Ewa JassemDepartment of Pneumonology, Medical University of Gdańsk, Gdańsk, Poland.
Aleksander KaniaDepartment of Pulmonology, Jagiellonian University Medical College, Kraków, Poland.
Katarzyna Lewandowska1st Lung Diseases Department, National Tuberculosis and Lung Diseases Research Institute, Warsaw, Poland.
Sebastian MajewskiDepartment of Pneumology, Medical University of Lodz, Lodz, Poland.
Magdalena M Martusewicz-Boros3rd Lung Diseases and Oncology Department, National Tuberculosis and Lung Diseases Research Institute, Warsaw, Poland.
Wojciech J PiotrowskiDepartment of Pneumology, Medical University of Lodz, Lodz, Poland.
Alicja SiemińskaDepartment of Allergology, Medical University of Gdańsk, Gdańsk, Poland.
Krzysztof SładekDepartment of Pulmonology, Jagiellonian University Medical College, Kraków, Poland.
Małgorzata Sobiecka1st Lung Diseases Department, National Tuberculosis and Lung Diseases Research Institute, Warsaw, Poland.
Marzena Trzaska-SobczakDepartment of Pneumonology, Medical University of Silesia, Katowice, Poland.
Witold Tomkowski1st Lung Diseases Department, National Tuberculosis and Lung Diseases Research Institute, Warsaw, Poland.
Beata Żołnowska1st Lung Diseases Department, National Tuberculosis and Lung Diseases Research Institute, Warsaw, Poland.
Rafał KrenkeDepartment of Internal Medicine, Pulmonary Diseases and Allergy, Medical University of Warsaw, Warsaw, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Pirfenidone and nintedanib are considered as the standard of care in idiopathic pulmonary fibrosis (IPF), but there is no consensus as to which of these two agents should be regarded as first-line treatment. Objective: To provide real-world data on therapeutic decisions of pulmonary specialists, particularly the choice of the antifibrotic drug in patients with IPF. Methods: This was a multicenter, prospective survey collecting clinical data of patients with IPF considered as candidates for antifibrotic treatment between September 2019 and December 2020. Clinical characteristics and information on the therapeutic approach were retrieved. Statistical evaluation included multiple logistic regression analysis with stepwise model selection. Results: Data on 188 patients [74.5% male, median age 73 (interquartile range, 68-78) years] considered for antifibrotic therapy were collected. Treatment was initiated in 138 patients, while 50 patients did not receive an antifibrotic, mainly due to the lack of consent for treatment and IPF severity. Seventy-two patients received pirfenidone and 66 received nintedanib. Dosing protocol ( Conclusion: This real-world prospective study showed that dose protocol and patient preference were more frequently associated with the choice of nintedanib, while the comorbidity profile and concomitant medication use were more frequently associated with the choice of pirfenidone. Age, TL

Indexed as

antifibrotic treatmentcomorbiditiesdosing protocolnintedanibpirfenidone

Identifiers

PMID36052286
PMCPMC9425901

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