Integration and application of clinical ...
Type de document :
Article dans une revue scientifique: Article de synthèse/Review paper
PMID :
URL permanente :
Titre :
Integration and application of clinical practice guidelines for the diagnosis of idiopathic pulmonary fibrosis and fibrotic hypersensitivity pneumonitis.
Auteur(s) :
Marinescu, D. C. [Auteur]
Raghu, G. [Auteur]
Remy, Martine [Auteur]
METRICS : Evaluation des technologies de santé et des pratiques médicales - ULR 2694
Travis, W. D. [Auteur]
Adegunsoye, A. [Auteur]
Beasley, M. B. [Auteur]
Chung, J. H. [Auteur]
Churg, A. [Auteur]
Cottin, Vincent [Auteur]
Centre de Référence des Maladies Pulmonaires Rares [Hôpital Louis Pradel - HCL]
Egashira, R. [Auteur]
Fernández Pérez, E. R. [Auteur]
Inoue, Y. [Auteur]
Johannson, K. A. [Auteur]
Kazerooni, E. A. [Auteur]
Khor, Y. H. [Auteur]
Lynch, D. A. [Auteur]
Müller, N. L. [Auteur]
Myers, J. L. [Auteur]
Nicholson, A. G. [Auteur]
Rajan, S. [Auteur]
Saito-Koyama, R. [Auteur]
Troy, L. [Auteur]
Walsh, S. L. F. [Auteur]
Wells, A. U. [Auteur]
Wijsenbeek, M. S. [Auteur]
Wright, J. L. [Auteur]
Ryerson, C. J. [Auteur]
Raghu, G. [Auteur]
Remy, Martine [Auteur]
METRICS : Evaluation des technologies de santé et des pratiques médicales - ULR 2694
Travis, W. D. [Auteur]
Adegunsoye, A. [Auteur]
Beasley, M. B. [Auteur]
Chung, J. H. [Auteur]
Churg, A. [Auteur]
Cottin, Vincent [Auteur]
Centre de Référence des Maladies Pulmonaires Rares [Hôpital Louis Pradel - HCL]
Egashira, R. [Auteur]
Fernández Pérez, E. R. [Auteur]
Inoue, Y. [Auteur]
Johannson, K. A. [Auteur]
Kazerooni, E. A. [Auteur]
Khor, Y. H. [Auteur]
Lynch, D. A. [Auteur]
Müller, N. L. [Auteur]
Myers, J. L. [Auteur]
Nicholson, A. G. [Auteur]
Rajan, S. [Auteur]
Saito-Koyama, R. [Auteur]
Troy, L. [Auteur]
Walsh, S. L. F. [Auteur]
Wells, A. U. [Auteur]
Wijsenbeek, M. S. [Auteur]
Wright, J. L. [Auteur]
Ryerson, C. J. [Auteur]
Titre de la revue :
Chest
Nom court de la revue :
Chest
Numéro :
162
Pagination :
P614-629
Date de publication :
2022-06-24
ISSN :
1931-3543
Mot(s)-clé(s) en anglais :
clinical practice guidelines
hypersensitivity pneumonitis
idiopathic pulmonary fibrosis
multidisciplinary discussion
usual interstitial pneumonia
hypersensitivity pneumonitis
idiopathic pulmonary fibrosis
multidisciplinary discussion
usual interstitial pneumonia
Discipline(s) HAL :
Sciences du Vivant [q-bio]
Résumé en anglais : [en]
Recent clinical practice guidelines have addressed the diagnosis of idiopathic pulmonary fibrosis (IPF) and fibrotic hypersensitivity pneumonitis (fHP). These disease-specific guidelines were developed independently, without ...
Lire la suite >Recent clinical practice guidelines have addressed the diagnosis of idiopathic pulmonary fibrosis (IPF) and fibrotic hypersensitivity pneumonitis (fHP). These disease-specific guidelines were developed independently, without clear direction on how to apply their respective recommendations concurrently within a single patient, where discrimination between these two fibrotic interstitial lung diseases represents a frequent diagnostic challenge. The objective of this review, created by an international group of experts, was to suggest a pragmatic approach on how to apply existing guidelines to distinguish IPF and fHP. Key clinical, radiologic, and pathologic features described in previous guidelines are integrated in a set of diagnostic algorithms, which then are placed in the broader context of multidisciplinary discussion to guide the generation of a consensus diagnosis. Although these algorithms necessarily reflect some uncertainty wherever strong evidence is lacking, they provide insight into the current approach favored by experts in the field based on currently available knowledge. The authors further identify priorities for future research to clarify ongoing uncertainties in the diagnosis of fibrotic interstitial lung diseases.Lire moins >
Lire la suite >Recent clinical practice guidelines have addressed the diagnosis of idiopathic pulmonary fibrosis (IPF) and fibrotic hypersensitivity pneumonitis (fHP). These disease-specific guidelines were developed independently, without clear direction on how to apply their respective recommendations concurrently within a single patient, where discrimination between these two fibrotic interstitial lung diseases represents a frequent diagnostic challenge. The objective of this review, created by an international group of experts, was to suggest a pragmatic approach on how to apply existing guidelines to distinguish IPF and fHP. Key clinical, radiologic, and pathologic features described in previous guidelines are integrated in a set of diagnostic algorithms, which then are placed in the broader context of multidisciplinary discussion to guide the generation of a consensus diagnosis. Although these algorithms necessarily reflect some uncertainty wherever strong evidence is lacking, they provide insight into the current approach favored by experts in the field based on currently available knowledge. The authors further identify priorities for future research to clarify ongoing uncertainties in the diagnosis of fibrotic interstitial lung diseases.Lire moins >
Langue :
Anglais
Audience :
Internationale
Vulgarisation :
Non
Établissement(s) :
Université de Lille
CHU Lille
CHU Lille
Date de dépôt :
2023-11-15T03:49:27Z
2024-04-08T12:33:38Z
2024-04-08T12:33:38Z