4.3 Article

National data on prevalence of idiopathic pulmonary fibrosis and antifibrotic drug use in Finnish specialised care

Related references

Note: Only part of the references are listed.
Article Critical Care Medicine

Idiopathic Pulmonary Fibrosis (an Update) and Progressive Pulmonary Fibrosis in Adults An Official ATS/ERS/JRS/ALAT Clinical Practice Guideline

Ganesh Raghu et al.

Summary: This article provides updates on the guidelines for idiopathic pulmonary fibrosis (IPF) and addresses the progression of pulmonary fibrosis in patients with interstitial lung diseases (ILDs) other than IPF. The recommendations are based on consensus and systematic reviews, aiming to provide evidence-based guidance for clinicians.

AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE (2022)

Article Respiratory System

Prevalence of idiopathic pulmonary fibrosis in Japan based on a claims database analysis

Yasuhiro Kondoh et al.

Summary: The nationwide prevalence of idiopathic pulmonary fibrosis (IPF) in Japan has been unknown. This study estimated the prevalence of IPF in Japan using a nationwide claims database. The prevalence in Japan was found to be higher than previous reports, and further research is needed to determine the accurate prevalence and compare it with other countries.

RESPIRATORY RESEARCH (2022)

Article Medicine, General & Internal

Differences in Baseline Characteristics and Access to Treatment of Newly Diagnosed Patients With IPF in the EMPIRE Countries

Abigel Margit Kolonics-Farkas et al.

Summary: There are significant differences in IPF patient characteristics and access to antifibrotic therapies among EMPIRE countries, which require further investigation and strategies to improve and harmonize patient care and therapy availability in this region.

FRONTIERS IN MEDICINE (2021)

Article Respiratory System

Global incidence and prevalence of idiopathic pulmonary fibrosis

Toby M. Maher et al.

Summary: IPF is a progressive lung disease with varying reported incidence and prevalence globally. Based on analyzed countries, estimated adjusted incidence and prevalence of IPF range from 0.09-1.30 and 0.33-4.51 per 10,000 persons, respectively. Future epidemiologic studies of IPF should account for age, sex, smoking status, and case definition specificity for consistency.

RESPIRATORY RESEARCH (2021)

Article Respiratory System

Baseline characteristics and survival of patients of idiopathic pulmonary fibrosis: a longitudinal analysis of the Swedish IPF Registry

Jing Gao et al.

Summary: Observational data from the Swedish IPF Registry showed that anti-fibrotic treatment, disease severity, and phenotypes are closely associated with outcomes of patients with idiopathic pulmonary fibrosis (IPF). Treated patients had better survival rates, with specific physiological factors and phenotypes playing a role in predicting outcomes.

RESPIRATORY RESEARCH (2021)

Article Biochemistry & Molecular Biology

Long-Term Follow-Up of Patients With Idiopathic Pulmonary Fibrosis Treated With Pirfenidone or Nintedanib: A Real-Life Comparison Study

Paolo Cameli et al.

FRONTIERS IN MOLECULAR BIOSCIENCES (2020)

Article Respiratory System

Prognosis and causes of death of patients with acute exacerbation of fibrosing interstitial lung diseases

Johanna Salonen et al.

BMJ OPEN RESPIRATORY RESEARCH (2020)

Article Respiratory System

Time to diagnosis of idiopathic pulmonary fibrosis in the IPF-PRO Registry

Laurie D. Snyder et al.

BMJ OPEN RESPIRATORY RESEARCH (2020)

Article Cardiac & Cardiovascular Systems

y Patient journey and treatment patterns in adults with IPF based on health care data in Sweden from 2001 to 2015

C. Magnus Skold et al.

RESPIRATORY MEDICINE (2019)

Article Cardiac & Cardiovascular Systems

Outcomes with newly proposed classification of acute respiratory deterioration in idiopathic pulmonary fibrosis

Ryo Teramachi et al.

RESPIRATORY MEDICINE (2018)

Article Multidisciplinary Sciences

Burden of Idiopathic Pulmonary Fibrosis Progression: A 5-Year Longitudinal Follow-Up Study

Vincent Cottin et al.

PLOS ONE (2017)

Review Critical Care Medicine

Acute Exacerbation of Idiopathic Pulmonary Fibrosis An International Working Group Report

Harold R. Collard et al.

AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE (2016)

Article Infectious Diseases

Incidence and prevalence of idiopathic interstitial pneumonia and idiopathic pulmonary fibrosis in Korea

H-E. Lee et al.

INTERNATIONAL JOURNAL OF TUBERCULOSIS AND LUNG DISEASE (2016)

Article Cardiac & Cardiovascular Systems

Nintedanib in patients with idiopathic pulmonary fibrosis: Combined evidence from the TOMORROW and INPULSIS® trials

Luca Richeldi et al.

RESPIRATORY MEDICINE (2016)

Article Respiratory System

Management of patients with idiopathic pulmonary fibrosis in clinical practice: the INSIGHTS-IPF registry

Juergen Behr et al.

EUROPEAN RESPIRATORY JOURNAL (2015)

Article Medicine, General & Internal

A Phase 3 Trial of Pirfenidone in Patients with Idiopathic Pulmonary Fibrosis

Talmadge E. King et al.

NEW ENGLAND JOURNAL OF MEDICINE (2014)

Review Public, Environmental & Occupational Health

Quality of the Finnish Hospital Discharge Register: A systematic review

Reijo Sund

SCANDINAVIAN JOURNAL OF PUBLIC HEALTH (2012)

Article Critical Care Medicine

An Official ATS/ERSARS/ALAT Statement: Idiopathic Pulmonary Fibrosis: Evidence-based Guidelines for Diagnosis and Management

Ganesh Raghu et al.

AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE (2011)