This study evaluates the role of AZLI in the treatment of acute pulmonary exacerbations of CF. For consecutive exacerbations patients will receive AZLI + IV Colistin, or two IV anti-pseudomonals.
AZLI, marketed as Cayston, is an inhaled beta-lactam antibiotic. It has a license for the chronic suppression of Pseudomonas aeruginosa (PA). Current standard practice dictates the use of two IV antipseudomonal antibiotics for the treatment of acute pulmonary exacerbations. The increasing survival, and hence population, in CF means that newer antimicrobial strategies are required in order to manage antimicrobial resistance, minimise adverse systemic effects of heavy antimicrobial exposure and also make effective use of resources. Inhaled antibiotics are commonly used in the chronic suppression of PA yet their use has not been thoroughly investigated in acute pulmonary exacerbation. Inhaled antibiotics deliver their drugs directly to the target-site with minimal systemic absorbance, making them an attractive candidate for treatment of acute exacerbations. Recently, it has become apparent that the bacterial community is much more complex than initially thought. The microbiome, a term used to describe the polymicrobial community in the lungs, has become apparent due to the use of modern culture-independent methods to detect bacteria. The microbiome changes in composition and structure around the time of exacerbations and in response to treatment, although these changes have not been prospectively characterised. We have designed an open-label randomised, controlled cross-over trial to investigate the clinical effectiveness of of AZLI in the treatment of acute pulmonary exacerbation, whilst simultaneously comparing the effect inhaled and intravenous antibiotics have on the microbiome.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
16
14 days of AZLI: 75mg TDS PLUS IV Colistin
14 days of IV Colistin plus one of Tazocin/Ceftazidime/Meropenem/Aztreonam/Fosfomycin
Liverpool Heart & Chest Hospital NHS Trust
Liverpool, United Kingdom
Average actual change in percent predicted forced expiratory volume at 1 second (FEV1) from Day 1 to Day 14
The actual change in FEV1 (%predicted) from Day 1 of admission to Day 7 \& Day 14
Time frame: 14 days
Time to first pulmonary exacerbation
Time from discharge to next pulmonary exacerbation
Time frame: 12 months
Average change from baseline in the Cystic Fibrosis Quality of Life Questionnaire (CFQ-R)
Average change from baseline (Day 1) in the CFQ-R Respiratory Symptom Score (RSS) at the end (Day 14) of each arm of the study
Time frame: 14 days
Microbiome changes
Changes in the structure and composition of the microbiome at the beginning and end of each treatment arm
Time frame: 14 days
PA sputum counts
Changes in sputum PA counts from the beginning to end of each treatment arm.
Time frame: 14 days
Antimicrobial resistance
Prevalence of resistance to antibiotics at the beginning and end of each treatment arm.
Time frame: 14 days
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