EMPIRE Registry, Czech Part: Impact of demographics, pulmonary function and HRCT on survival and clinical course in idiopathic pulmonary fibrosis

  • Martina Doubková
    Department of Phthisiology Pulmonary Diseases and Tuberculosis Masaryk University Faculty of Medicine and University Hospital Brno Czech Republic
  • Jan Švancara
    Institute of Biostatistics and Analyses, Masaryk University Brno Czech Republic
  • Michal Svoboda
    Institute of Biostatistics and Analyses, Masaryk University Brno Czech Republic
  • Martina Šterclová
    Department of Respiratory Medicine, First Faculty of Medicine Charles University, Thomayer Hospital Prague Czech Republic
  • Vladimír Bartoš
    Department of Pneumology Faculty of Medicine and Charles University Hradec Králové Czech Republic
  • Martina Plačková
    Department of Pneumology University Hospital in Ostrava, Faculty of Medicine, Pilsen, Charles University Czech Republic
  • Ladislav Lacina
    Department of Pneumology and Thoracic Surgery Hospital Na Bulovce Prague Czech Republic
  • Monika Žurková
    Department of Respiratory Medicine Faculty of Medicine and Palacky University Hospital Olomouc Czech Republic
  • Ilona Binková
    Department of Phthisiology Pulmonary Diseases and Tuberculosis Masaryk University Faculty of Medicine and University Hospital Brno Czech Republic
  • Radka Bittenglová
    Department of Respiratory Diseases Faculty of Medicine and Charles University Hospital Pilsen Czech Republic
  • Vladimíra Lošťáková
    Department of Respiratory Medicine Faculty of Medicine and Palacky University Hospital Olomouc Czech Republic
  • Zdeněk Merta
    Department of Phthisiology Pulmonary Diseases and Tuberculosis Masaryk University Faculty of Medicine and University Hospital Brno Czech Republic
  • Lenka Šišková
    Department of Respiratory Diseases Tomáš Baťa Regional Hospital Zlín Czech Republic
  • Richard Tyl
    Department of Respiratory Diseases Nový Jičín Hospital Czech Republic
  • Pavlína Lisá
    Department of Pneumology, Second Faculty of Medicine Charles University in Prague and Motol University Hospital Prague Czech Republic
  • Hana Šuldová
    Pulmonary Department České Budějovice Hospital Czech Republic
  • František Petřík
    Department of Pneumology, Second Faculty of Medicine Charles University in Prague and Motol University Hospital Prague Czech Republic
  • Jana Pšikalová
    PneumoAllergolog Department Kromeříž Hospital Czech Republic
  • Vladimír Řihák
    Department of Respiratory Diseases Tomáš Baťa Regional Hospital Zlín Czech Republic
  • Tomáš Snížek
    Department of Respiratory Diseases Jihlava Hospital Czech Republic
  • Pavel Reiterer
    Department of Pulmonary Diseases and Tuberculosis Masaryk Hospital Ústí nad Labem Czech Republic
  • Jiří Homolka
    First Department of Tuberculosis and Respiratory Diseases General Hospital in Prague and The First Medical Faculty of Charles University Czech Republic
  • Pavlína Musilová
    Department of Respiratory Diseases Jihlava Hospital Czech Republic
  • Jaroslav Lněnička
    Department of Pulmonary Diseases and Tuberculosis Masaryk Hospital Ústí nad Labem Czech Republic
  • Peter Palúch
    Department of Respiratory Medicine, First Faculty of Medicine Charles University, Thomayer Hospital Prague Czech Republic
  • Roman Hrdina
    Department of Respiratory Diseases Znojmo Hospital Czech Republic
  • Renata Králová
    Department of Respiratory Diseases Pardubice Hospital Czech Republic
  • Hana Hortvíková
    Department of Pneumology University Hospital in Ostrava, Faculty of Medicine, Pilsen, Charles University Czech Republic
  • Jana Strenková
    Institute of Biostatistics and Analyses, Masaryk University Brno Czech Republic
  • Martina Vašáková
    Department of Respiratory Medicine, First Faculty of Medicine Charles University, Thomayer Hospital Prague Czech Republic

説明

<jats:title>Summary</jats:title><jats:sec><jats:title>Introduction</jats:title><jats:p>Prognostic factors of idiopathic pulmonary fibrosis (IPF) currently recognized include changes in vital capacity and radiologic findings. However, most of the prognostic studies in IPF are based on clinical studies with preselected IPF populations. Therefore, we decided to analyze the factors influencing IPF prognosis based on the real‐practice data from our IPF registry.</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>Data of 514 subjects consecutively entered since 2012 into Czech EMPIRE IPF registry were analyzed.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>Median age of our patient cohort was 67 years (50–82). Median overall survival (OS) of the cohort was 63.1 months. The clinical course of IPF according to FVC (forced vital capacity) changes was stabilized in 32.8% of patients (29.7% according to DL<jats:sub>CO</jats:sub> [diffuse lung capacity] changes), slowly progressive in 39.5% (45%), rapidly progressive in 23.5% (20.7%); and 1.7% patients had at least one acute exacerbation during follow‐up. Deterioration in FVC of ≥10% at month 12 and in DL<jats:sub>CO</jats:sub> of ≥15% at months 12, 18, and 24 influenced the OS significantly. The fast progressors defined by the DL<jats:sub>CO</jats:sub> decline rate had higher risk of death compared to those defined by the FVC change over time. In multivariate analysis, age ≥70 years, interstitial HRCT scores ≥3, and change in DL<jats:sub>CO</jats:sub> of ≥15% at month 12 were confirmed as factors negatively influencing OS.</jats:p></jats:sec><jats:sec><jats:title>Conclusions</jats:title><jats:p>DL<jats:sub>CO</jats:sub> changes over time were shown as a better predictor of mortality compared with FVC changes in our study. In our opinion it is necessary to implement the DL<jats:sub>CO</jats:sub> analysis into clinical trials and routine practice.</jats:p></jats:sec>

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