Online home spirometry in national pulmonary fibrosis care: insights from daily practice

Online home spirometry is feasible on a large scale in daily clinical practice to monitor disease trajectories in patients with IPF and PF. Online home spirometry could guide management decisions and improve care access for a majority of patients with pulmonary fibrosis.

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Publication Details

Journal
ERJ Open Research
Published
2025-02-27
DOI
https://doi.org/10.1183/23120541.01234-2024
Citations
3
Primary Topic
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
Type
article
Field-Weighted Citation Impact
4.56
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article

Online home spirometry in national pulmonary fibrosis care: insights from daily practice

Suzan F. M. Nijman, Gizal Nakshbandi, Tonia Magrì, Rémy L.M. Mostard et al.
3 citations
ERJ Open Research
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
4.56
article

Online home spirometry in national pulmonary fibrosis care: insights from daily practice

Suzan F. M. Nijman, Gizal Nakshbandi, Tonia Magrì, Rémy L.M. Mostard, Luca Richeldi, Marcel Veltkamp, Marlies Wijsenbeek, J.J. Miranda Geelhoed, Paul Bresser, Sara J. Baart, Catharina C. Moor, Adriane D.M. Vorselaars, René E. Jonkers, Lian Trapman, Maria J. Overbeek
article en
3 citations

Abstract

Online home spirometry is feasible on a large scale in daily clinical practice to monitor disease trajectories in patients with IPF and PF. Online home spirometry could guide management decisions and improve care access for a majority of patients with pulmonary fibrosis.

ERJ Open ResearchVol. 11(5)
Università Cattolica del Sacro Cuore (IT), Leiden University (NL), University Medical Center Utrecht (NL), Maastricht University (NL), Medisch Centrum Haaglanden (NL), St. Antonius Ziekenhuis (NL), OLVG (NL), Zuyderland Medisch Centrum (NL), GGD Amsterdam (NL), Amsterdam University Medical Centers (NL), Istituti di Ricovero e Cura a Carattere Scientifico (IT), Amsterdam UMC Location Vrije Universiteit Amsterdam (NL), Erasmus University Rotterdam (NL)
Openalex Percentile: Top 6%
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
4.56
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