EMPIRE Registry, Czech Part: Impact of Demographics, Pulmonary Function and HRCT on Survival and Clinical Course in Idiopathic Pulmonary Fibrosis

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Authors	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
Year of publication	2018
Type	Article in Periodical
Magazine / Source	CLINICAL RESPIRATORY JOURNAL
MU Faculty or unit	Faculty of Medicine
Citation
Doi	http://dx.doi.org/10.1111/crj.12700
Field	Pneumology
Keywords	idiopathic pulmonary fibrosis; prognosis; pulmonary funcions; registry; survival
Description	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. Data of 514 subjects consecutively entered since 2012 into Czech EMPIRE IPF registry were analyzed.