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Investigating significant health trends in progressive fibrosing interstitial lung disease (INSIGHTS-ILD): rationale, aims and design of a nationwide prospective registry.
Behr, Juergen; Bonella, Francesco; Günther, Andreas; Koschel, Dirk; Prasse, Antje; Pittrow, David; Klotsche, Jens; Kreuter, Michael.
Afiliação
  • Behr J; Department of Medicine V, Comprehensive Pneumology Center, Member of the German Center for Lung Research (DZL), University Hospital, LMU Munich, Munich, Germany. juergen.behr@med.uni-muenchen.de.
  • Bonella F; Center for Interstitial and Rare Lung Diseases, Pneumology Department, Ruhrlandklinik University Hospital, Duisburg-Essen University, Essen, Germany.
  • Günther A; Universities of Giessen and Marburg Lung Center (UGMLC), Member of the German Center for Lung Research (DZL), Giessen, Germany.
  • Koschel D; Medical Department I, Division of Pneumology, University Hospital Carl Gustav Carus, and Department of Pulmonology, Fachkrankenhaus Coswig GmbH, Lung Center, Coswig, Germany.
  • Prasse A; Department of Respiratory Medicine, Hannover Medical School, Hannover, Germany.
  • Pittrow D; Institute for Clinical Pharmacology, Medical Faculty, Technical University, Dresden, Germany.
  • Klotsche J; German Rheuma Research Center (DRFZ), Epidemiology, Berlin, Germany.
  • Kreuter M; Center for Interstitial and Rare Lung Diseases, and Interdisciplinary Center for Sarcoidosis, Pneumology, Thoraxklinik, University Hospital Heidelberg, German Center for Lung Research, Heidelberg, Germany.
BMC Pulm Med ; 23(1): 64, 2023 Feb 11.
Article em En | MEDLINE | ID: mdl-36774483
BACKGROUND: The progressive course of pulmonary fibrosis (PPF) is observed with variable prevalence in different entities of fibrosing interstitial lung disease (fILD). PPF is characterised by worsening respiratory symptoms, declining lung function and increasing extent of fibrosis on high-resolution computer tomography. In Germany, data are limited on the characteristics and management of such patients. METHODS/DESIGN: INSIGHTS-ILD is a prospective observational longitudinal registry designed to describe characteristics, management and course of newly diagnosed (incident) and prevalent patients with fILD on the long term. The registry uses a non-probability sampling approach to collect data on characteristics, therapeutic interventions, health-related quality of life and health economic parameters. It is planned to include 900 patients in ambulatory care in about 30 expert sites over three years. The study has been initiated in December 2021, and currently (January 2023) follows 360 patients. DISCUSSION: The registry is expected to provide much-needed data on the characteristics, management, and trajectories of patients fILD in Germany. The start of the study comes at a time when new treatment options are available for PPF. We hypothesize that PPF represents a broad clinical phenotype that is differentially influenced by inflammatory and fibrotic pathomechanisms that need to be treated with anti-inflammatory and/or anti-fibrotic treatment strategies. This registry will allow comparisons with other countries. Gap analyses based on current guidelines for management of these patients will be possible. Trial registration DRKS00027389 (registered on 7.12.2021), BfArM NIS 7562.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fibrose Pulmonar / Doenças Pulmonares Intersticiais / Fibrose Pulmonar Idiopática Tipo de estudo: Guideline / Observational_studies / Qualitative_research / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fibrose Pulmonar / Doenças Pulmonares Intersticiais / Fibrose Pulmonar Idiopática Tipo de estudo: Guideline / Observational_studies / Qualitative_research / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article