Search Results - "Plant, Barry J."
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The effects of freezing on faecal microbiota as determined using MiSeq sequencing and culture-based investigations
Published in PloS one (06-03-2015)“…High-throughput sequencing has enabled detailed insights into complex microbial environments, including the human gut microbiota. The accuracy of the…”
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Individualized approach to elexacaftor/tezacaftor/ivacaftor dosing in cystic fibrosis, in response to self-reported anxiety and neurocognitive adverse events: A case series
Published in Frontiers in pharmacology (27-04-2023)“…The prevalence of mental health disorders is high among people with Cystic Fibrosis. The psychological symptoms in CF are associated with poor adherence, worse…”
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Effects of Ivacaftor in Patients With Cystic Fibrosis Who Carry the G551D Mutation and Have Severe Lung Disease
Published in Chest (01-07-2014)“…BACKGROUND The development of ivacaftor represents a significant advance in therapeutics for patients with cystic fibrosis (CF) who carry the G551D mutation…”
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Microbiota and metabolite profiling reveal specific alterations in bacterial community structure and environment in the cystic fibrosis airway during exacerbation
Published in PloS one (17-12-2013)“…Chronic polymicrobial infections of the lung are the foremost cause of morbidity and mortality in cystic fibrosis (CF) patients. The composition of the…”
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Bacterial cis-2-unsaturated fatty acids found in the cystic fibrosis airway modulate virulence and persistence of Pseudomonas aeruginosa
Published in The ISME Journal (01-05-2012)“…There is an increasing appreciation of the polymicrobial nature of many bacterial infections such as those associated with cystic fibrosis (CF) and of the…”
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Management of comorbidities in older patients with cystic fibrosis
Published in The lancet respiratory medicine (01-04-2013)“…Summary Several key advances have been made in the treatment and management of people with cystic fibrosis in the past two decades. Substantial improvements in…”
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Creatine kinase levels in asthma patients receiving interleukin-5 therapy
Published in Therapeutic advances in respiratory disease (2022)Get full text
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Considerations for the use of inhaled antibiotics for Pseudomonas aeruginosa in people with cystic fibrosis receiving CFTR modulator therapy
Published in BMJ open respiratory research (03-05-2024)“…The major cause of mortality in people with cystic fibrosis (pwCF) is progressive lung disease characterised by acute and chronic infections, the accumulation…”
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Real-World clinical outcomes of asthma patients switched from reslizumab to mepolizumab or benralizumab
Published in Frontiers in allergy (04-01-2023)“…Approximately 3%-10% of asthma patients will remain uncontrolled despite maximum, optimal conventional therapy. Treatment of severe refractory asthma often…”
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Virtual monitoring in CF - the importance of continuous monitoring in a multi-organ chronic condition
Published in Frontiers in digital health (04-05-2023)“…Cystic Fibrosis (CF) is a chronic life-limiting condition that affects multiple organs within the body. Patients must adhere to strict medication regimens,…”
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Biologically Relevant Murine Models of Chronic Pseudomonas aeruginosa Respiratory Infection
Published in Pathogens (Basel) (17-08-2023)“…Pseudomonas aeruginosa (P. aeruginosa) is an opportunistic pathogen and the leading cause of infection in patients with cystic fibrosis (CF). The ability of P…”
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The Role of Ivacaftor in Severe Cystic Fibrosis in a Patient With the R117H Mutation
Published in Chest (01-09-2015)“…Cystic fibrosis (CF) conductance transmembrane regulator functions as a chloride (Cl– ) channel in multiple organs, including the lungs. More than 1,800…”
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Peri-Lung Transplant Renal Issues in Patients With Cystic Fibrosis
Published in Chest (2013)Get full text
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VX-659–Tezacaftor–Ivacaftor in Patients with Cystic Fibrosis and One or Two Phe508del Alleles
Published in The New England journal of medicine (25-10-2018)“…This companion article to the VX-445 report shows that VX-659, a new CFTR potentiator, when administered with tezacaftor and ivacaftor improved lung function,…”
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Telehealth and virtual health monitoring in cystic fibrosis
Published in Current opinion in pulmonary medicine (01-11-2021)“…At many institutions, the Covid-19 pandemic made it necessary to rapidly change the way services are provided to patients, including those with cystic fibrosis…”
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Current and emerging comorbidities in cystic fibrosis
Published in La Presse médicale (1983) (01-06-2017)“…Cystic fibrosis transmembrane conductance regulator (CFTR) is expressed ubiquitously throughout the body. Thus, while respiratory manifestations dominate much…”
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CORK Study in Cystic Fibrosis: Sustained Improvements in Ultra-Low-Dose Chest CT Scores After CFTR Modulation With Ivacaftor
Published in Chest (01-02-2018)“…Ivacaftor produces significant clinical benefit in patients with cystic fibrosis (CF) with the G551D mutation. Prevalence of this mutation at the Cork CF…”
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Editorial: A future focus on cystic fibrosis in an era of uncertainty despite opportunity
Published in Current opinion in pulmonary medicine (01-11-2021)Get full text
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