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Published in 2020 at "Pediatric Pulmonology"
DOI: 10.1002/ppul.24917
Abstract: Individuals with cystic fibrosis (CF) require higher dosages of aminoglycosides due to an increased volume of distribution (Vd) and clearance. Optimal dosing of aminoglycosides in the CF population is essential as repeated exposure to aminoglycosides… read more here.
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Published in 2021 at "Pediatric Pulmonology"
DOI: 10.1002/ppul.25353
Abstract: Acute pulmonary exacerbations are complications of cystic fibrosis (CF) and are associated with increased morbidity and mortality. Methicillin‐resistant Staphylococcus aureus (MRSA) and Aspergillus fumigatus are organisms that have been detected in the lungs of CF… read more here.
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Published in 2021 at "Pediatric pulmonology"
DOI: 10.1002/ppul.25441
Abstract: Aminoglycosides are commonly used for the treatment of Pseudomonas aeruginosa (PsA) in the setting of acute pulmonary exacerbations (PEx) in pediatric patients with cystic fibrosis (CF). There are controversies and practice differences between institutions related… read more here.
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Published in 2021 at "Pediatric Pulmonology"
DOI: 10.1002/ppul.25552
Abstract: We are writing this letter to provide an update of published information on antibiotics for cystic fibrosis (CF) pulmonary exacerbations to the State of the Art articles by Zobell et al. Information on meropenem‐vaborbactam and… read more here.
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Published in 2022 at "Pediatric Pulmonology"
DOI: 10.1002/ppul.26136
Abstract: Pulmonary exacerbations (PEx), pathogens colonizing the respiratory tract, and patients' age are associated with progressive worsening of lung function among patients with cystic fibrosis (CF). However, the effect of these factors on longitudinal changes of… read more here.
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Published in 2022 at "Pediatric Pulmonology"
DOI: 10.1002/ppul.26267
Abstract: Viral respiratory infections trigger pulmonary exacerbations (PEs) in children with cystic fibrosis (CF), but their clinical impact is not well understood. read more here.
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Published in 2019 at "Journal of proteome research"
DOI: 10.1021/acs.jproteome.9b00443
Abstract: The most common cause of death in cystic fibrosis (CF) patients is progressive lung function decline, which is punctuated by acute pulmonary exacerbations (APEs). A major challenge is to discover biomarkers for detecting an oncoming… read more here.
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Published in 2017 at "Scientific Reports"
DOI: 10.1038/s41598-017-10945-3
Abstract: Pulmonary exacerbations (PEx) in Cystic Fibrosis (CF) are associated with an increased morbidity and even mortality. We investigated whether early detection of PEx in children with CF is possible by electronic home monitoring of symptoms… read more here.
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Published in 2019 at "Scientific Reports"
DOI: 10.1038/s41598-019-53759-1
Abstract: Pulmonary exacerbations (PEx) are clinically impactful events for individuals with CF. Unfortunately, many CF individuals with PEx fail to regain their baseline lung function despite treatment. The objective of this study was to use unbiased… read more here.
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Published in 2023 at "Expert Review of Respiratory Medicine"
DOI: 10.1080/17476348.2023.2202852
Abstract: ABSTRACT Introduction Pulmonary exacerbations are common events in children with cystic fibrosis (CF) and are usually treated with oral antibiotics on an outpatient basis. Even these mild clinical events are clinically meaningful and contribute to… read more here.
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Published in 2018 at "Current Opinion in Pulmonary Medicine"
DOI: 10.1097/mcp.0000000000000519
Abstract: Purpose of review Pulmonary exacerbations are described as worsening of the daily symptoms of cystic fibrosis airways disease, typically with increased cough and sputum production. There are often associated signs such as weight loss and… read more here.