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Study of IPF relatives as a method of early diagnosis of ILD disease

Olaia Bronte Moreno, Myriam Aburto, Amaia Urrutia, Carmen Jaca, Maria Iciar Arrizubieta, Miren Begoñe Salinas, Laura Tomás, Iñaki Salegui
European Respiratory Journal 2020 56: 447; DOI: 10.1183/13993003.congress-2020.447
Olaia Bronte Moreno
1Basque Public Respiratory Service. Respiratory Department, Galdakao, Spain
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  • For correspondence: olaiabronte@gmail.com
Myriam Aburto
1Basque Public Respiratory Service. Respiratory Department, Galdakao, Spain
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Amaia Urrutia
2Basque Public Respiratory Service. Respiratory Department, Barakaldo, Spain
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Carmen Jaca
2Basque Public Respiratory Service. Respiratory Department, Barakaldo, Spain
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Maria Iciar Arrizubieta
1Basque Public Respiratory Service. Respiratory Department, Galdakao, Spain
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Miren Begoñe Salinas
3Basque Public Respiratory Service. Respiratory Department, Bilbao, Spain
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Laura Tomás
4Basque Public Respiratory Service. Respiratory Department, Vitoria, Spain
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Iñaki Salegui
5Basque Public Respiratory Service. Respiratory Department, Donostia, Spain
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Abstract

Introduction: Early diagnosis of IPF is needed,but except the role of primary care physicians to suspect-detect early signs-symptoms and the radiologists' warning of incidental finding of ILD at HCRT preformed for other reason,there´s no screening program to promote the early detection.

Aims: evaluate cost-effectiveness of implementing an active program to screen new ILD cases in early stages among relatives of IPF patients.

Methods: Jan.2017-Sept.2019,first-degree relatives >40 years,of patients with IPF,assisted in Basque Health Service´s ILD Units,were invited to participate.Demographic and clinical variables were collected.Patients underwent:functional respiratory Test,6-min walking test and HRCT.

Results: 164 relatives of 94 IPF index cases were studied (results are summarized in figure 1).

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Cluster analysis divided sample in 3 groups (fig.2)

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Conclusions:

  1. FPF affects 31.9% families of patients initially diagnosed as sporadic IPF.

  2. 47.8% of siblings has fibrosing disease.

  3. Cluster analysis identified 3 groups:(a)healthy,(b)IPF and(c)fibrotic ILA-Inconsistent with NIU.

  4. Study of relatives of the same generation as IPF patients could be useful as ILD screening.

  • Idiopathic pulmonary fibrosis
  • Diagnosis
  • Orphan diseases

Footnotes

Cite this article as: European Respiratory Journal 2020; 56: Suppl. 64, 447.

This abstract was presented at the 2020 ERS International Congress, in session “Respiratory viruses in the "pre COVID-19" era”.

This is an ERS International Congress abstract. No full-text version is available. Further material to accompany this abstract may be available at www.ers-education.org (ERS member access only).

  • Copyright ©the authors 2020
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Study of IPF relatives as a method of early diagnosis of ILD disease
Olaia Bronte Moreno, Myriam Aburto, Amaia Urrutia, Carmen Jaca, Maria Iciar Arrizubieta, Miren Begoñe Salinas, Laura Tomás, Iñaki Salegui
European Respiratory Journal Sep 2020, 56 (suppl 64) 447; DOI: 10.1183/13993003.congress-2020.447

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Study of IPF relatives as a method of early diagnosis of ILD disease
Olaia Bronte Moreno, Myriam Aburto, Amaia Urrutia, Carmen Jaca, Maria Iciar Arrizubieta, Miren Begoñe Salinas, Laura Tomás, Iñaki Salegui
European Respiratory Journal Sep 2020, 56 (suppl 64) 447; DOI: 10.1183/13993003.congress-2020.447
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