scispace - formally typeset
Open AccessJournal ArticleDOI

An Official ATS/ERS/JRS/ALAT Statement: Idiopathic Pulmonary Fibrosis: Evidence-Based Guidelines for Diagnosis and Management

TLDR
This document represents the current state of knowledge regarding idiopathic pulmonary fibrosis, and contains sections on definition and epidemiology, risk factors, diagnosis, natural history, staging and prognosis, treatment, and monitoring disease course.
Abstract
This document is an international evidence-based guideline on the diagnosis and management of idiopathic pulmonary fibrosis, and is a collaborative effort of the American Thoracic Society, the European Respiratory Society, the Japanese Respiratory Society, and the Latin American Thoracic Association. It represents the current state of knowledge regarding idiopathic pulmonary fibrosis (IPF), and contains sections on definition and epidemiology, risk factors, diagnosis, natural history, staging and prognosis, treatment, and monitoring disease course. For the diagnosis and treatment sections, pragmatic GRADE evidence-based methodology was applied in a question-based format. For each diagnosis and treatment question, the committee graded the quality of the evidence available (high, moderate, low, or very low), and made a recommendation (yes or no, strong or weak). Recommendations were based on majority vote. It is emphasized that clinicians must spend adequate time with patients to discuss patients' values and preferences and decide on the appropriate course of action.

read more

Citations
More filters
Journal ArticleDOI

An Official American Thoracic Society/European Respiratory Society Statement: Update of the International Multidisciplinary Classification of the Idiopathic Interstitial Pneumonias

TL;DR: This update is a supplement to the previous 2002 IIP classification document and outlines advances in the past decade and potential areas for future investigation.
References
More filters
Journal ArticleDOI

Transbronchial biopsy in usual interstitial pneumonia.

TL;DR: In this article, the authors found that characteristic histologic features of idiopathic interstitial pneumonia can be identified on TBB specimens more often than previously appreciated, and that TBB may be more useful in confirming UIP than previously recognized.
Journal ArticleDOI

Familial Idiopathic Pulmonary Fibrosis: Clinical Features and Outcome

TL;DR: Although uncommon, FIPF represents a distinct syndrome, which has clinical features and patient survival rates that are similar to those of nonfamilial IPF.
Journal ArticleDOI

Analysis of Tumor Necrosis Factor- α , Lymphotoxin- α , Tumor Necrosis Factor Receptor II, and Interleukin-6 Polymorphisms in Patients with Idiopathic Pulmonary Fibrosis

TL;DR: Twelve biallelic polymorphisms in the genes for tumor necrosis factor-receptor 2 (TNF-RII), lymphotoxin (LT)- α, and interleukin- (IL)-6 are examined, finding them candidates for the pathogenesis of IPF.
Journal ArticleDOI

Early Interstitial Lung Disease in Familial Pulmonary Fibrosis

TL;DR: Asymptomatic ILD in individuals at risk of developing familial IPF can be identified using high-resolution computed tomography scan of the chest, especially in those with a history of smoking.
Journal ArticleDOI

Prognostic Determinants among Clinical, Thin-Section CT, and Histopathologic Findings for Fibrotic Idiopathic Interstitial Pneumonias: Tertiary Hospital Study

TL;DR: Patients with UIP or fibrotic NSIP who have a high fib Rotic score determined at thin-section CT and a low Dlco level appear to have ahigh death risk.
Related Papers (5)

American thoracic society/European respiratory society international multidisciplinary consensus classification of the idiopathic interstitial pneumonias