Search Results - "Bittenglova, Radka"
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Effect of pirfenidone on lung function decline and survival: 5-yr experience from a real-life IPF cohort from the Czech EMPIRE registry
Published in Respiratory research (21-01-2019)“…Pirfenidone, an antifibrotic drug, slows-down the disease progression in idiopathic pulmonary fibrosis (IPF) over 12 months, however limited data on the…”
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Adherence to the ISHLT Protocol for the Referral of Patients with Idiopathic Pulmonary Fibrosis to the Transplantation Center among of Czech Centers for Interstitial Lung Diseases
Published in Pulmonary medicine (30-06-2024)“…There are limited data on referral rates and the number of patients with idiopathic pulmonary fibrosis (IPF) who are eligible for lung transplantation. The aim…”
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DSP rs2076295 variants influence nintedanib and pirfenidone outcomes in idiopathic pulmonary fibrosis: a pilot study
Published in Therapeutic advances in respiratory disease (2021)“…Background: The antifibrotic drugs nintedanib and pirfenidone are used for the treatment of idiopathic pulmonary fibrosis (IPF). We analysed the association of…”
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EMPIRE Registry, Czech Part: Impact of demographics, pulmonary function and HRCT on survival and clinical course in idiopathic pulmonary fibrosis
Published in The clinical respiratory journal (01-04-2018)“…Prognostic factors of idiopathic pulmonary fibrosis (IPF) currently recognized include changes in vital capacity and radiologic findings. However, most of the…”
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The European MultiPartner IPF registry (EMPIRE): validating long-term prognostic factors in idiopathic pulmonary fibrosis
Published in Respiratory research (08-01-2020)“…Several registries of idiopathic pulmonary fibrosis (IPF) have been established to better understand its natural history, though their size and duration of…”
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The effect of nintedanib on lung functions and survival in idiopathic pulmonary fibrosis: real-life analysis of the Czech EMPIRE registry
Published in BMC pulmonary medicine (03-05-2023)“…The antifibrotic drug nintedanib is used for the treatment of idiopathic pulmonary fibrosis (IPF). We analysed the effect of nintedanib on antifibrotic…”
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Age-Related Progression of Microvascular Dysfunction in Cystic Fibrosis: New Detection Ways and Clinical Outcomes
Published in Physiological research (30-10-2021)“…There are concerns about altered vascular functions that could play an important role in the pathogenesis and influence the severity of chronic disease,…”
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Biomarkers of extracellular matrix turnover in patients with idiopathic pulmonary fibrosis given nintedanib (INMARK study): a randomised, placebo-controlled study
Published in The lancet respiratory medicine (01-09-2019)“…A hallmark of idiopathic pulmonary fibrosis is the excess accumulation of extracellular matrix in the lungs. Degradation of extracellular matrix generates…”
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Use of pepsin detection to identify airways reflux in a range of pulmonary diseases
Published in The clinical respiratory journal (01-09-2017)Get more information
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rs2076295 variants influence nintedanib and pirfenidone outcomes in idiopathic pulmonary fibrosis: a pilot study
Published in Therapeutic advances in respiratory disease (01-09-2021)“…Background: The antifibrotic drugs nintedanib and pirfenidone are used for the treatment of idiopathic pulmonary fibrosis (IPF). We analysed the association of…”
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P38. Extraesophageal reflux disease and lung cancer
Published in Translational lung cancer research (01-10-2014)Get full text
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Comorbidity burden and survival in patients with idiopathic pulmonary fibrosis: the EMPIRE registry study
Published in Respiratory research (27-05-2022)“…Patients with idiopathic pulmonary fibrosis (IPF) frequently have multiple comorbidities, which may influence survival but go under-recognised in clinical…”
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Diagnostics of cystic fibrosis in adults
Published in Vnitřní lékar̆stvĭ (2016)“…There is an increasing number of cystic fibrosis (CF) patients with the diagnosis established in adulthood worldwide. To give an overview of our experience…”
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Idiopathic pulmonary fibrosis prognostic factors - analysis of the Czech registry
Published in Časopis lékařů českých (2016)“…Idiopathic pulmonary fibrosis (IPF) is a rare, progressive and usually fatal form of idiopathic interstitial pneumonia. IPF is characterized by failure of…”
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