EMPIRE Registry, Czech Part: Impact of demographics, pulmonary function and HRCT on survival and clinical course in idiopathic pulmonary fibrosis
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- Martina Doubková
- Department of Phthisiology Pulmonary Diseases and Tuberculosis Masaryk University Faculty of Medicine and University Hospital Brno Czech Republic
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- Jan Švancara
- Institute of Biostatistics and Analyses, Masaryk University Brno Czech Republic
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- Michal Svoboda
- Institute of Biostatistics and Analyses, Masaryk University Brno Czech Republic
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- Martina Šterclová
- Department of Respiratory Medicine, First Faculty of Medicine Charles University, Thomayer Hospital Prague Czech Republic
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- Vladimír Bartoš
- Department of Pneumology Faculty of Medicine and Charles University Hradec Králové Czech Republic
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- Martina Plačková
- Department of Pneumology University Hospital in Ostrava, Faculty of Medicine, Pilsen, Charles University Czech Republic
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- Ladislav Lacina
- Department of Pneumology and Thoracic Surgery Hospital Na Bulovce Prague Czech Republic
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- Monika Žurková
- Department of Respiratory Medicine Faculty of Medicine and Palacky University Hospital Olomouc Czech Republic
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- Ilona Binková
- Department of Phthisiology Pulmonary Diseases and Tuberculosis Masaryk University Faculty of Medicine and University Hospital Brno Czech Republic
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- Radka Bittenglová
- Department of Respiratory Diseases Faculty of Medicine and Charles University Hospital Pilsen Czech Republic
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- Vladimíra Lošťáková
- Department of Respiratory Medicine Faculty of Medicine and Palacky University Hospital Olomouc Czech Republic
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- Zdeněk Merta
- Department of Phthisiology Pulmonary Diseases and Tuberculosis Masaryk University Faculty of Medicine and University Hospital Brno Czech Republic
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- Lenka Šišková
- Department of Respiratory Diseases Tomáš Baťa Regional Hospital Zlín Czech Republic
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- Richard Tyl
- Department of Respiratory Diseases Nový Jičín Hospital Czech Republic
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- Pavlína Lisá
- Department of Pneumology, Second Faculty of Medicine Charles University in Prague and Motol University Hospital Prague Czech Republic
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- Hana Šuldová
- Pulmonary Department České Budějovice Hospital Czech Republic
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- František Petřík
- Department of Pneumology, Second Faculty of Medicine Charles University in Prague and Motol University Hospital Prague Czech Republic
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- Jana Pšikalová
- PneumoAllergolog Department Kromeříž Hospital Czech Republic
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- Vladimír Řihák
- Department of Respiratory Diseases Tomáš Baťa Regional Hospital Zlín Czech Republic
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- Tomáš Snížek
- Department of Respiratory Diseases Jihlava Hospital Czech Republic
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- Pavel Reiterer
- Department of Pulmonary Diseases and Tuberculosis Masaryk Hospital Ústí nad Labem Czech Republic
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- Jiří Homolka
- First Department of Tuberculosis and Respiratory Diseases General Hospital in Prague and The First Medical Faculty of Charles University Czech Republic
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- Pavlína Musilová
- Department of Respiratory Diseases Jihlava Hospital Czech Republic
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- Jaroslav Lněnička
- Department of Pulmonary Diseases and Tuberculosis Masaryk Hospital Ústí nad Labem Czech Republic
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- Peter Palúch
- Department of Respiratory Medicine, First Faculty of Medicine Charles University, Thomayer Hospital Prague Czech Republic
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- Roman Hrdina
- Department of Respiratory Diseases Znojmo Hospital Czech Republic
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- Renata Králová
- Department of Respiratory Diseases Pardubice Hospital Czech Republic
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- Hana Hortvíková
- Department of Pneumology University Hospital in Ostrava, Faculty of Medicine, Pilsen, Charles University Czech Republic
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- Jana Strenková
- Institute of Biostatistics and Analyses, Masaryk University Brno Czech Republic
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- 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>
収録刊行物
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- The Clinical Respiratory Journal
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The Clinical Respiratory Journal 12 (4), 1526-1535, 2017-09-26
Wiley