Evidence map›Paper›PMID 42477604›Full record

ArticleBMC pulmonary medicine2026

Development and internal validation of a nomogram to predict pulmonary hypertension in fibrosing interstitial lung diseases.

David Rodríguez-Plaza, Jesús Ribas, Isabel Alfaya, Sonia López-Monzoni, Guadalupe Bermudo, Vanesa Vicens-Zygmunt, Yolanda Ruiz, Marta Hernández-Argudo, Judith Peñafiel, Belén Del Río and 4 more

Abstract readValidation Study
In one paragraph

Article in BMC pulmonary medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

14 authors.

David Rodríguez-Plaza *Respiratory Department, Bellvitge University Hospital, Barcelona, Spain. drodriguezp@bellvitgehospital.cat.
Jesús Ribas *Respiratory Department, Bellvitge University Hospital, Barcelona, Spain.
Isabel AlfayaRespiratory Department, Bellvitge University Hospital, Barcelona, Spain.
Sonia López-MonzoniInstitute of Biomedical Research of Bellvitge (IDIBELL), Barcelona, Spain.
Guadalupe BermudoRespiratory Department, Bellvitge University Hospital, Barcelona, Spain.
Vanesa Vicens-ZygmuntRespiratory Department, Bellvitge University Hospital, Barcelona, Spain.
Yolanda RuizRespiratory Department, Bellvitge University Hospital, Barcelona, Spain.
Marta Hernández-ArgudoRespiratory Department, Bellvitge University Hospital, Barcelona, Spain.
Judith PeñafielBarcelona University (UB), Barcelona, Spain.
Belén Del RíoRadiology Department, Bellvitge University Hospital, Barcelona, Spain.
Ángela DíazRadiology Department, Bellvitge University Hospital, Barcelona, Spain.
Lara FuentesCardiology Department, Bellvitge University Hospital, Barcelona, Spain.
Salud SantosRespiratory Department, Bellvitge University Hospital, Barcelona, Spain.
María Molina-MolinaRespiratory Department, Bellvitge University Hospital, Barcelona, Spain.

Funding

Sociedad Española de Neumología y Cirugía Torácica 1551-2024
6 · The paper itself

Abstract

backgroundPulmonary hypertension (PH) is a common comorbidity in patients with interstitial lung disease (ILD), with a negative prognostic impact. The main objective of this study was to develop and internally validate a nomogram to predict PH using real-life data from patients with fibrosing ILD.

methodsRetrospective, cross-sectional, single-centre study including adult patients with a diagnosis of fibrosing ILD undergoing right heart catheterization (RHC). Bootstrap was used to select clinical, radiological, and functional predictors of precapillary PH. LASSO, Elastic Net, and CART were also performed to enhance robustness. The final model was presented using a nomogram and PH risk was stratified into three categories according to CART.

resultsNinety patients were included. The most frequent ILD diagnoses were idiopathic pulmonary fibrosis (20%), connective tissue diseases-ILD (18.9%) and combined pulmonary fibrosis and emphysema (17.8%). Echocardiography identified high PH probability in 54.4% of patients. RHC confirmed PH in 64 (71%) patients and ruled out PH in 26 (29%). Pulmonary artery diameter, transfer coefficient of the lung for carbon monoxide (KCO) and six-minute walking test distance (meters) were retained in the final model, with an AUC [95% CI] of 0.857 [0.779-0.935]. PH predicted risk was classified in low- (< 36%), intermediate- (≥ 36-<73%) or high-risk (≥ 73%) categories.

conclusionA simple model based on three non-invasive objective variables obtained during the routine care of patients with fibrosing ILD showed good internal discrimination in our derivation cohort. Following external validation, the proposed nomogram could support PH-ILD suspicion and optimize echocardiography and RHC referrals.

Indexed as

Hypertension, PulmonaryLung Diseases, InterstitialNomogramsPulmonary FibrosisAgedCardiac CatheterizationCross-Sectional StudiesEchocardiographyFemaleHumansIdiopathic Pulmonary FibrosisMaleMiddle AgedPulmonary ArteryRetrospective StudiesWalk TestInterstitial lung diseasesPredictive modelPulmonary fibrosisPulmonary hypertension

Identifiers

PMID42477604
PMCPMC13663256

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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.