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[French practical guidelines for the diagnosis and management of IPF - 2021 update, full version].

Authors :
Cottin V
Bonniaud P
Cadranel J
Crestani B
Jouneau S
Marchand-Adam S
Nunes H
Wémeau-Stervinou L
Bergot E
Blanchard E
Borie R
Bourdin A
Chenivesse C
Clément A
Gomez E
Gondouin A
Hirschi S
Lebargy F
Marquette CH
Montani D
Prévot G
Quetant S
Reynaud-Gaubert M
Salaun M
Sanchez O
Trumbic B
Berkani K
Brillet PY
Campana M
Chalabreysse L
Chatté G
Debieuvre D
Ferretti G
Fourrier JM
Just N
Kambouchner M
Legrand B
Le Guillou F
Lhuillier JP
Mehdaoui A
Naccache JM
Paganon C
Rémy-Jardin M
Si-Mohamed S
Terrioux P
Source :
Revue des maladies respiratoires [Rev Mal Respir] 2022 Sep; Vol. 39 (7), pp. e35-e106. Date of Electronic Publication: 2022 Jun 22.
Publication Year :
2022

Abstract

Background: Since the previous French guidelines were published in 2017, substantial additional knowledge about idiopathic pulmonary fibrosis has accumulated.<br />Methods: Under the auspices of the French-speaking Learned Society of Pulmonology and at the initiative of the coordinating reference center, practical guidelines for treatment of rare pulmonary diseases have been established. They were elaborated by groups of writers, reviewers and coordinators with the help of the OrphaLung network, as well as pulmonologists with varying practice modalities, radiologists, pathologists, a general practitioner, a head nurse, and a patients' association. The method was developed according to rules entitled "Good clinical practice" in the overall framework of the "Guidelines for clinical practice" of the official French health authority (HAS), taking into account the results of an online vote using a Likert scale.<br />Results: After analysis of the literature, 54 recommendations were formulated, improved, and validated by the working groups. The recommendations covered a wide-ranging aspects of the disease and its treatment: epidemiology, diagnostic modalities, quality criteria and interpretation of chest CT, indication and modalities of lung biopsy, etiologic workup, approach to familial disease entailing indications and modalities of genetic testing, evaluation of possible functional impairments and prognosis, indications for and use of antifibrotic therapy, lung transplantation, symptom management, comorbidities and complications, treatment of chronic respiratory failure, diagnosis and management of acute exacerbations of fibrosis.<br />Conclusion: These evidence-based guidelines are aimed at guiding the diagnosis and the management in clinical practice of idiopathic pulmonary fibrosis.<br /> (Copyright © 2022 SPLF. Published by Elsevier Masson SAS. All rights reserved.)

Details

Language :
French
ISSN :
1776-2588
Volume :
39
Issue :
7
Database :
MEDLINE
Journal :
Revue des maladies respiratoires
Publication Type :
Academic Journal
Accession number :
35752506
Full Text :
https://doi.org/10.1016/j.rmr.2022.01.014