Investigating significant health trends in progressive fibrosing interstitial lung disease (INSIGHTS-ILD): rationale, aims and design of a nationwide prospective registry

Author:

Behr Juergen,Bonella Francesco,Günther Andreas,Koschel Dirk,Prasse Antje,Pittrow David,Klotsche Jens,Kreuter Michael,Andreica Ioana,Behr Jürgen,Biller Heike,Claussen Martin,Budweiser Stephan,Eisenmann Stephan,Ewert Ralf,Gesierich Wolfgang,Gläser Sven,Grohé Christian,Grund Daniel,Grünewaldt Achim,Hagmeyer Lars,Held Matthias,Kabitz Hans-Joachim,Kirschner Joachim,Markart Philipp,Neff Ulrich,Neurohr Claus,Reichenberger Frank,Schramm Peter,Schwaiblmair Martin,Seese Bernd,Skowasch Dirk,Wälscher Julia,Weber Michael,Westhoff Michael,Wilkens Heinrike,Wirtz Hubert,

Abstract

Abstract 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.

Funder

Boehringer Ingelheim

Universitätsklinik München

Publisher

Springer Science and Business Media LLC

Subject

Pulmonary and Respiratory Medicine

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