Open AccessEMPIRE Registry, Czech Part: Impact of demographics, pulmonary function and HRCT on survival and clinical course in idiopathic pulmonary fibrosis
Author(s) -
Doubková Martina,
Švancara Jan,
Svoboda Michal,
Šterclová Martina,
Bartoš Vladimír,
Plačková Martina,
Lacina Ladislav,
Žurková Monika,
Binková Ilona,
Bittenglová Radka,
Lošťáková Vladimíra,
Merta Zdeněk,
Šišková Lenka,
Tyl Richard,
Lisá Pavlína,
Šuldová Hana,
Petřík František,
Pšikalová Jana,
Řihák Vladimír,
Snížek Tomáš,
Reiterer Pavel,
Homolka Jiří,
Musilová Pavlína,
Lněnička Jaroslav,
Palúch Peter,
Hrdina Roman,
Králová Renata,
Hortvíková Hana,
Strenková Jana,
Vašáková Martina
Publication year - 2018
Publication title -
the clinical respiratory journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.789
H-Index - 33
eISSN - 1752-699X
pISSN - 1752-6981
DOI - 10.1111/crj.12700
Subject(s) - dlco , medicine , idiopathic pulmonary fibrosis , exacerbation , pulmonary function testing , vital capacity , cohort , pirfenidone , interstitial lung disease , diffusing capacity , lung , lung function
Summary Introduction 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. Methods Data of 514 subjects consecutively entered since 2012 into Czech EMPIRE IPF registry were analyzed. Results 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 CO [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 CO of ≥15% at months 12, 18, and 24 influenced the OS significantly. The fast progressors defined by the DL CO 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 CO of ≥15% at month 12 were confirmed as factors negatively influencing OS. Conclusions DL CO 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 CO analysis into clinical trials and routine practice.