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

Varování

Publikace nespadá pod Filozofickou fakultu, ale pod Lékařskou fakultu. Oficiální stránka publikace je na webu muni.cz.

Autoři	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
Rok publikování	2018
Druh	Článek v odborném periodiku
Časopis / Zdroj	CLINICAL RESPIRATORY JOURNAL
Fakulta / Pracoviště MU	Lékařská fakulta
Citace
Doi	http://dx.doi.org/10.1111/crj.12700
Obor	Pneumologie
Klíčová slova	idiopathic pulmonary fibrosis; prognosis; pulmonary funcions; registry; survival
Popis	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.