Literature DB >> 32006172

Stratification of long-term outcome in stable idiopathic pulmonary fibrosis by combining longitudinal computed tomography and forced vital capacity.

Nicola Sverzellati1, Mario Silva2, Valeria Seletti2, Carlotta Galeone3, Stefano Palmucci4, Sara Piciucchi5, Carlo Vancheri6, Venerino Poletti7, Sara Tomassetti8, Ronald Karwoski9, Brian J Bartholmai10.   

Abstract

OBJECTIVES: To test HRCT with either visual or quantitative analysis in both short-term and long-term follow-up of stable IPF against long-term (transplant-free) survival, beyond 2 years of disease stability.
METHODS: Fifty-eight IPF patients had FVC measurements and HRCTs at baseline (HRCT0), 10-14 months (HRCT1) and 22-26 months (HRCT2). Visual scoring, CALIPER quantitative analysis of HRCT measures, and their deltas were evaluated against combined all-cause mortality and lung transplantation by adjusted Cox proportional hazard models at each time interval.
RESULTS: At HRCT1, a ≥ 20% relative increase in CALIPER-total lung fibrosis yielded the highest radiological association with outcome (C-statistic 0.62). Moreover, the model combining FVC% drop ≥ 10% and ≥ 20% relative increase of CALIPER-total lung fibrosis improved the stratification of outcome (C-statistic 0.69, high-risk category HR 12.1; landmark analysis at HRCT1 C-statistic 0.66, HR 14.9 and at HRCT2 C-statistic 0.61, HR 21.8). Likewise, at HRCT2, the model combining FVC% decrease trend and ≥ 20% relative increase of CALIPER-pulmonary vessel-related volume (VRS) improved the stratification of outcome (C-statistic 0.65, HR 11.0; landmark analysis at HRCT1 C-statistic 0.62, HR 13.8 and at HRCT2 C-statistic 0.58, HR 12.6). A less robust stratification of outcome distinction was also demonstrated with the categorical visual scoring of disease change.
CONCLUSIONS: Annual combined CALIPER -FVC changes showed the greatest stratification of long-term outcome in stable IPF patients, beyond 2 years. KEY POINTS: • Longitudinal high-resolution computed tomography (HRCT) data is more helpful than baseline HRCT alone for stratification of long-term outcome in IPF. • HRCT changes by visual or quantitative analysis can be added with benefit to the current spirometric reference standard to improve stratification of long-term outcome in IPF. • HRCT follow-up at 12-14 months is more helpful than HRCT follow-up at 23-26 months in clinically stable subjects with IPF.

Entities:  

Keywords:  Idiopathic pulmonary fibrosis; Machine learning; Multidetector computed tomography; Outcome; Usual interstitial pneumonia

Mesh:

Year:  2020        PMID: 32006172     DOI: 10.1007/s00330-019-06619-5

Source DB:  PubMed          Journal:  Eur Radiol        ISSN: 0938-7994            Impact factor:   5.315


  7 in total

1.  Longitudinal change during follow-up of systemic sclerosis: correlation between high-resolution computed tomography and pulmonary function tests.

Authors:  Aldo Carnevale; Mario Silva; Elisa Maietti; Gianluca Milanese; Marta Saracco; Simone Parisi; Elena Bravi; Fabio De Gennaro; Eugenio Arrigoni; Flavio Cesare Bodini; Enrico Fusaro; Carlo Alberto Scirè; Nicola Sverzellati; Alarico Ariani
Journal:  Clin Rheumatol       Date:  2020-09-03       Impact factor: 2.980

2.  Radiographic Progression and Survival of the Different HRCT Patterns of Idiopathic Pulmonary Fibrosis.

Authors:  Marco Mura; Carlotta Rellini; Nada Taha; Francesco Paolo Sbordone; Flavia Rufi; Francesca Montesanto; Roberto Floris; Maurizio Zompatori; Gianluigi Sergiacomi
Journal:  Sarcoidosis Vasc Diffuse Lung Dis       Date:  2022-06-29       Impact factor: 1.803

3.  Several specific high-resolution computed tomography patterns correlate with survival in patients with idiopathic pulmonary fibrosis.

Authors:  Minna E Mononen; Hannu-Pekka Kettunen; Sanna-Katja Suoranta; Miia S Kärkkäinen; Tuomas A Selander; Minna K Purokivi; Riitta L Kaarteenaho
Journal:  J Thorac Dis       Date:  2021-04       Impact factor: 2.895

4.  Longitudinal functional changes with clinically significant radiographic progression in idiopathic pulmonary fibrosis: are we following the right parameters?

Authors:  Nada Taha; Dejanira D'Amato; Karishma Hosein; Tiziana Ranalli; Gianluigi Sergiacomi; Maurizio Zompatori; Marco Mura
Journal:  Respir Res       Date:  2020-05-19

Review 5.  Computer-Aided quantitative analysis in interstitial lung diseases - A pictorial review using CALIPER.

Authors:  Bhavin G Jankharia; Bhoomi A Angirish
Journal:  Lung India       Date:  2021 Mar-Apr

Review 6.  Interstitial lung abnormalities: new insights between theory and clinical practice.

Authors:  Roberta Eufrasia Ledda; Gianluca Milanese; Francesca Milone; Ludovica Leo; Maurizio Balbi; Mario Silva; Nicola Sverzellati
Journal:  Insights Imaging       Date:  2022-01-15

Review 7.  Towards Treatable Traits for Pulmonary Fibrosis.

Authors:  Thijs W Hoffman; Jan C Grutters
Journal:  J Pers Med       Date:  2022-08-03
  7 in total

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