4.3 Article

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

Journal

BMJ OPEN RESPIRATORY RESEARCH
Volume 9, Issue 1, Pages -

Publisher

BMJ PUBLISHING GROUP
DOI: 10.1136/bmjresp-2022-001363

Keywords

rare lung diseases; interstitial fibrosis

Funding

  1. Oulu University Hospital
  2. Research Foundation of Pulmonary Diseases, Helsinki, Finland
  3. Research Foundation of North Finland

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The prevalence of idiopathic pulmonary fibrosis (IPF) in specialised care in Finland was higher than expected and had increased from 2016 to 2021. The number of patients with IPF using antifibrotic drugs, such as pirfenidone and nintedanib, had also increased during the follow-up period. This increase in antifibrotic drug use may have led to a decrease in the number of IPF-related hospitalisations.
Introduction The previous data concerning the prevalence of idiopathic pulmonary fibrosis (IPF) and the frequency of antifibrotic drug use in Finland were based on research registries and medical records whereas nationwide data on the number of patients with IPF in specialised care and those on antifibrotic treatment have not been published. Methods We made an information request to the Finnish National Hospital Discharge Register (Hilmo) covering the whole population of Finland to find out the annual numbers of patients with IPF treated in specialised care in 2016-2021. The numbers of the patients initiating and using pirfenidone and nintedanib were requested from the Social Insurance Institution of Finland (Kela) for the same time period. Results The estimated prevalence of IPF in specialised care was 36.0 per 100 000 in 2021, having increased since 2016. The number of antifibrotic drug users and their proportion of outpatients with IPF had also risen during the follow-up period. In 2021, 35% of the patients with IPF used pirfenidone or nintedanib. The number of inpatients treated in specialised care because of IPF had declined during 2016-2021. Conclusions The prevalence of IPF was higher than expected in Finnish specialised care and had increased during the 6-year follow-up time. The increase in the number of patients with IPF using antifibrotic drugs might have diminished the need for IPF-related hospitalisations.

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