Antibiotic Prophylaxis in Patients Undergoing Lung Transplant: Single-Center Cohort Study

Autor: Renato Pascale, Beatrice Tazza, Armando Amicucci, Elena Salvaterra, Giampiero Dolci, Filippo Antonacci, Massimo Baiocchi, Saverio Pastore, Simone Ambretti, Maddalena Peghin, Pierluigi Viale, Maddalena Giannella

Publikováno v: Transplant International, Vol 37 (2024)

Perioperative antibiotic prophylaxis (PAP) in lung transplant recipients (LuTRs) has high heterogeneity between centers. Our aim was to investigate retrospectively the approach to PAP in our center over a 20-year period (2002–2023), and its impact

Externí odkaz: https://doaj.org/article/9cbe34e292a346fa968c80b26d1e73d7

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UIP-net: a decoder-encoder CNN for the detection and quantification of usual interstitial pneumoniae pattern in lung CT scan images

Autor: Annalisa De Liperi, Chiara Romei, Danila Germanese, Rossana Buongiorno, Sara Colantonio, Laura Tavanti

Publikováno v: ICPR 2021: Pattern Recognition. ICPR International Workshops and Challenges, pp. 389–405, Milan, Italy-Virtual event, 10-15/01/2021
info:cnr-pdr/source/autori:Buongiorno R.; Germanese D.; Romei C.; Tavanti L.; De Liperi A.; Colantonio S./congresso_nome:ICPR 2021: Pattern Recognition. ICPR International Workshops and Challenges/congresso_luogo:Milan, Italy-Virtual event/congresso_data:10-15%2F01%2F2021/anno:2021/pagina_da:389/pagina_a:405/intervallo_pagine:389–405
Pattern Recognition. ICPR International Workshops and Challenges ISBN: 9783030687625
ICPR Workshops (1)

A key step of the diagnosis of Idiopathic Pulmonary Fibrosis (IPF) is the examination of high-resolution computed tomography images (HRCT). IPF exhibits a typical radiological pattern, named Usual Interstitial Pneumoniae (UIP) pattern, which can be d

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a499396de8961b15a0378a72db878c90
http://www.cnr.it/prodotto/i/447541

Insights from the German Compassionate Use Program of Nintedanib for the Treatment of Idiopathic Pulmonary Fibrosis

Autor: Bonella, Francesco, Kreuter, Michael, Hagmeyer, Lars, Neurohr, Claus, Keller, Claus, Kohlhaeufl, Martin J., Müller-Quernheim, Joachim, Milger, Katrin, Prasse, Antje, Behr, J., Hetzel, J., Idzko, M., Kardos, P., Koch, A., Markart, P., Reichenberger, F., Schumann, C., Westhoff, M., Windisch, W.

BACKGROUND: Nintedanib is approved for the treatment of idiopathic pulmonary fibrosis (IPF) and has been shown to slow disease progression by reducing annual lung function decline. OBJECTIVE: To evaluate the results of a large cohort of IPF patients

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_______610::e7a17bc81231933ce6be426d08742ac7
https://publica.fraunhofer.de/handle/publica/246390

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