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

Aspiration Pneumonitis and Aspiration Pneumonia

TL;DR: Aspiration pneumonitis (Mendelson's syndrome), whereas aspiration pneumonia is an infectious process caused by the inhalation of oropharyngeal secretions that are colonized by pathogenic bacteria, are distinct clinical entities.
Journal ArticleDOI

Telomerase Mutations in Families with Idiopathic Pulmonary Fibrosis

TL;DR: In this paper, the authors found that mutations in the genes encoding telomerase components can appear as familial idiopathic pulmonary fibrosis, which is a rare hereditary disorder associated with premature death from aplastic anemia and lung fibrosis.
Journal ArticleDOI

Grading Strength of Recommendations and Quality of Evidence in Clinical Guidelines: Report From an American College of Chest Physicians Task Force

TL;DR: An American College of Chest Physicians task force formulated the criteria for a grading system to be utilized in all ACCP guidelines that included simplicity and transparency, explicitness of methodology, and consistency with current methodological approaches to the grading process.
Journal ArticleDOI

Incidence and Prevalence of Idiopathic Pulmonary Fibrosis

TL;DR: The results suggest that idiopathic pulmonary fibrosis is probably more common in the United States than previously reported.
Journal Article

The Six-Minute Walk Test

TL;DR: The American Thoracic Society has issued guidelines for the 6-minute walk test (6MWT), which is safer, easier to administer, better tolerated, and better reflects activities of daily living than other walk tests.
Related Papers (5)

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