Cystic Fibrosis and Bronchiectasis Research
Cystic Fibrosis is a genetic disorder resulting in damage to the lungs and elsewhere. The resulting changes associated with this disease increase the risk of chronic bacterial infection, lung function decline and overall ill health, both physical and mental.
The Cystic Fibrosis and Bronchiectasis Research Group is investigating how patients may benefit from novel drug therapies, diagnostic imaging techniques, molecular epidemiology of infection and psychosocial interventions.
The group has an excellent track record in attracting competitive research grants, both from Australian and international sources. They are recognised as world leaders and have an extensive collaborative network with the leading researchers in cystic fibrosis throughout Australia and internationally.
The Cystic Fibrosis and Bronchiectasis Research Group are made up of a multi-disciplinary team of doctors, nurses, physiotherapists and allied health staff. The team is committed to assisting in the search for new and improved treatments and providing high-quality care for patients with cystic fibrosis and bronchiectasis.
Current research projects
- Airway Clearance
- High Intensity Interval Training
- Infection with Clostridium difficile
- The Gut Microbiome
- Pseudomonas aeruginosa
The CF Research Unit has several highlights for 2017/18. These include:
- Dr Anna Tai was awarded the Thoracic Society Australia and New Zealand Vertex Adult Cystic Fibrosis Fellowship for 2017/18.
- Wood J, Jenkins S, Putrino D, Mulrennan S, Morey S, Cecins N, Hill K. A smartphone application for reporting symptoms in adults with cystic fibrosis: protocol of a randomised controlled trial. BMJ Open. 2018 Apr 21;8(4):e021136.
- Wood J, Sawyer A, Mulrennan S, Bullock A. Respiratory exacerbation in a young adult with cystic fibrosis and tricuspid atresia. Respirol Case Rep. 2018 Apr 1;6(5):e00318.
- Mulrennan S, Knuiman M, Walsh JP, Hui J, Hunter M, Divitini M, Zhu K, Cooke BR, Musk AWB, James A. Vitamin D and respiratory health in the Busselton Healthy Ageing Study. 2018 Jun;23(6):576-582.
- Wood J, Jenkins S, Putrino D, Mulrennan S, Morey S, Cecins N, Hill K. High usability of a smartphone application for reporting symptoms in adults with cystic fibrosis. J Telemed Telecare. 2018 Sep;24(8):547-552.
Tai AS, Morey S. The open door policy – An important and under-recognised activity of the adult CF centre. J Cyst Fibros. 2018 Sep;17(5):558-559. doi: 10.1016/j.jcf.2018.07.004. Epub 2018 Aug 9. No abstract available.
- Wee BA, Tai AS, Sherrard LJ, Ben Zakour NL, Hanks KR, Kidd TJ, Ramsay KA, Lamont I, Whiley DM, Bell SC, Beatson SA. Whole-genome sequencing reveals the emergence of a Pseudomonas aeruginosa shared strain sub-lineage among patients treated within a single cystic fibrosis centre. BMC Genomics. 2018 Aug 30;19(1):644. doi: 10.1186/s12864-018-5018-x.
- Vale Dr Jenni Ibrahim OAM
- Research could help cystic fibrosis patients breathe easier
- Calorie intake research could improve quality of life for people with cystic fibrosis
- Fundraiser success for research
- L I F E Activities
- World Lung Day 2020: Lung Health Advocacy and Action
- Free Will Service
- Free screening for benchtop workers
- David’s story of living with alpha 1-antitrypsin deficiency
- To wear or not to wear the mask: That is the question
Help us continue our vital research by making a donation today.