Zobrazeno 1 - 10
of 1 037
pro vyhledávání: '"pulmonary exacerbation"'
Autor:
R. Benson Weyant, Barbara J. Waddell, Nicole Acosta, Conrad Izydorczyk, John M. Conly, Deirdre L. Church, Michael G. Surette, Harvey R. Rabin, Christina S. Thornton, Michael D. Parkins
Publikováno v:
BMC Infectious Diseases, Vol 24, Iss 1, Pp 1-9 (2024)
Abstract Background Haemophilus influenzae is prevalent within the airways of persons with cystic fibrosis (pwCF). H. influenzae is often associated with pulmonary exacerbations (PEx) in pediatric cohorts, but in adults, studies have yielded conflict
Externí odkaz:
https://doaj.org/article/9fe01188bd904eb3b73333105c4b3ca1
Autor:
V. V. Shmarin, D. A. Pukhalskaya, S. A. Krasovsky, Yu. M. Chudakova, A. V. Martynov, G. V. Shmarina
Publikováno v:
Медицинская иммунология, Vol 26, Iss 5, Pp 1045-1052 (2024)
Cystic fibrosis (CF) is one of the most common autosomal-recessive inherited diseases. The primary genetic defect in CF is aligned CFTR gene mutation which encodes a membrane protein functioning as cAMP-depended chloride channel. Classic phenotypical
Externí odkaz:
https://doaj.org/article/d2bd8462184245d5921303507e9f8409
Autor:
Matteo De Marchis, Enza Montemitro, Alessandra Boni, Alessandra Federici, Daniele Di Giovanni, Luca Cristiani, Renato Cutrera, Alessandro G. Fiocchi
Publikováno v:
Italian Journal of Pediatrics, Vol 50, Iss 1, Pp 1-7 (2024)
Abstract Background Multiple Breath washout (MBW) represents an important tool to detect early a possible pulmonary exacerbation especially in Cystic Fibrosis (CF) disease. Lung clearance index (LCI) is the most commonly reported multiple breath wash
Externí odkaz:
https://doaj.org/article/ba8900d6dd9940c198ad1eb0d89d6a8e
Autor:
Brandie D. Wagner, Edith T. Zemanick, Scott D. Sagel, Charles E. Robertson, Mark J. Stevens, Nicole Mayer-Hamblett, George Retsch-Bogart, Bonnie W. Ramsey, J. Kirk Harris
Publikováno v:
BMC Microbiology, Vol 23, Iss 1, Pp 1-11 (2023)
Abstract Background Tobramycin inhalation solution (TIS) and chronic azithromycin (AZ) have known clinical benefits for children with CF, likely due to antimicrobial and anti-inflammatory activity. The effects of chronic AZ in combination with TIS on
Externí odkaz:
https://doaj.org/article/d5da65057c594b7ab884fe12599e5df7
Akademický článek
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Publikováno v:
Microbiology Spectrum, Vol 11, Iss 6 (2023)
ABSTRACT Primary ciliary dyskinesia (PCD) is characterized by symptoms such as productive cough, rhinitis, and recurrent infections in both the upper and lower airways, which can lead to chronic infection, bronchiectasis, and decreased pulmonary func
Externí odkaz:
https://doaj.org/article/2c5e9f158f53458aae1bdd6e80f07f77
Autor:
Dana Albon, Lijia Zhang, James Patrie, Marieke Jones, Z. Galvin Li, Emily Noonan, Larry Borish
Publikováno v:
Allergy, Asthma & Clinical Immunology, Vol 19, Iss 1, Pp 1-10 (2023)
Abstract Background The Cystic Fibrosis Foundation Patient Registry (CFFPR) reports a high prevalence of asthma (34.6%) in people with Cystic Fibrosis (PwCF). While our current understanding of this relationship is limited, a type 2 inflammatory (T2)
Externí odkaz:
https://doaj.org/article/2b71294f4f5549d3a5f01c13709ca3b2
Autor:
Muhammad Saleem Khan, Philippa Douglas, Anna L. Hansell, Nicholas J. Simmonds, Frédéric B. Piel
Publikováno v:
Environmental Health, Vol 21, Iss 1, Pp 1-13 (2022)
Abstract Aim To explore the health risk of living near permitted composting sites (PCSs) on disease severity in children and adults with cystic fibrosis (CF) across the UK. Methods A semi-individual cross-sectional study was used to examine the risk
Externí odkaz:
https://doaj.org/article/fd1b62adf5a5479bbf8598e584e52e10
Autor:
Sivagurunathan Sutharsan, Stefanie Dillenhoefer, Matthias Welsner, Florian Stehling, Folke Brinkmann, Manuel Burkhart, Helmut Ellemunter, Anna-Maria Dittrich, Christina Smaczny, Olaf Eickmeier, Matthias Kappler, Carsten Schwarz, Sarah Sieber, Susanne Naehrig, Lutz Naehrlich, Klaus Tenbrock, Claus Pfannenstiel, Dirk Steffen, Jochen Meister, Britta Welzenbach, Anette Scharschinger, Markus Kratz, Maike Pincus, Tobias Tenenbaum, Mirjam Stahl, Kerstin Landwehr, Stefanie Dillenhöfer, Hans Kössel, Petra Kaiser, Manfred Käding, Simone Stolz, Stefan Blaas, Jutta Hammermann, Monika Gappa, Antje Schuster, Dana Spittel, Sabine Zirlik, Sabina Schmitt, Joachim Bargon, Malte Cremer, Sebastian Fähndrich, Andrea Heinzmann, Lutz Nährlich, Stefan Kuhnert, Sebastian Schmidt, Bettina Wollschläger, Anna Nolde, Inka Held, Wolfgang Kamin, Felix C. Ringshausen, Sabine Wege, Olaf Sommerburg, Norbert Geier, Sara Lisa Fleser, Heinrike Wilkens, Michael Lorenz, Paul Vöhringer, Martin Schebek, Christian Timke, Ingrid Bobis, Thomas Nüßlein, Doris Dieninghoff, Ernst Rietschel, Bastian Klinkhammer, Freerk Prenzel, Alexandra Wald, Axel Kempa, Eva Lücke, Ines Adams, Krystyna Poplawska, Simone Lehmkühler, Monika Bauck, Anne Pfülb, Rainald Fischer, Gudrun Schopper, Susanne Nährig, Matthias Griese, Jörg Grosse, Peter Küster, Birte KinderHolger Köster, Susanne Büsing, Margarethe Pohl, Andreas Artlich, Alexander Kiefer, Manfred Ballmann, Nikola Gjorgjevski, Markus A. Rose, Friederike Ruf, Rolf Mahlberg, Wolfgang Thomas, Ute Graepler, Sebastian Bode, hilipp Meyn, Josef Rosenecker, Cordula Koerner, Klaus-Michael Keller, Tina Teßmer, Helge Hebestreit, Gerhild Lohse
Publikováno v:
The Lancet Regional Health. Europe, Vol 32, Iss , Pp 100690- (2023)
Summary: Background: Treatment with elexacaftor/tezacaftor/ivacaftor (ETI) improves multiple clinical outcomes in people with cystic fibrosis (pwCF) with at least one F508del allele. This study evaluated the real-world impact of ETI on lung function,
Externí odkaz:
https://doaj.org/article/cb7f1132ad9145b4909f1a838def4b95
Publikováno v:
Brazilian Journal of Medical and Biological Research, Vol 56 (2023)
There is little information on pulmonary rehabilitation in patients with cystic fibrosis (CF) with pulmonary exacerbation. This study aimed to evaluate the effects of an early rehabilitation program on lung function, muscle strength, inflammatory mar
Externí odkaz:
https://doaj.org/article/3cd20bdf56b74dfd949722df66509e03