Antifibrotic therapy combined with pulmonary vasodilator therapy may improve survival in patients with pulmonary fibrosis and pulmonary hypertension: a retrospective cohort study

We found a potential survival benefit when pulmonary vasodilator therapy was given in combination with antifibrotic therapy in patients with pulmonary fibrosis and pulmonary hypertension. This may be reflective of a pulmonary vascular phenotype among those with pulmonary fibrosis and pulmonary hypertension. Further trials are needed to better elucidate which patients benefit from combination therapy.

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Publication Details

Journal
Therapeutic Advances in Respiratory Disease
Published
2025-01-01
DOI
https://doi.org/10.1177/17534666251326743
Citations
1
Primary Topic
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
Type
article
Field-Weighted Citation Impact
1.52
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article

Antifibrotic therapy combined with pulmonary vasodilator therapy may improve survival in patients with pulmonary fibrosis and pulmonary hypertension: a retrospective cohort study

Gerard J. Criner, S. Gayen, Christian Cardillo
1 citations
Therapeutic Advances in Respiratory Disease
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
1.52
article

Antifibrotic therapy combined with pulmonary vasodilator therapy may improve survival in patients with pulmonary fibrosis and pulmonary hypertension: a retrospective cohort study

Gerard J. Criner, S. Gayen, Christian Cardillo
article en
1 citations

Abstract

We found a potential survival benefit when pulmonary vasodilator therapy was given in combination with antifibrotic therapy in patients with pulmonary fibrosis and pulmonary hypertension. This may be reflective of a pulmonary vascular phenotype among those with pulmonary fibrosis and pulmonary hypertension. Further trials are needed to better elucidate which patients benefit from combination therapy.

Therapeutic Advances in Respiratory DiseaseVol. 19
Temple University Hospital (US)
Good health and well-being
Openalex Percentile: Top 21%
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
1.52
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