Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Ruth, Dentice"'
Autor:
Michael Doumit, Roxanne Strachan, Raynuka Lazarus, Peter Middleton, Ruth Dentice, Jessica Marouvo, Laura Jeffrey, Hiran Selvadurai, Sheila Sivam, Verity Pacey, Adam Jaffe, Kelly Gray
Publikováno v:
Health Services Insights, Vol 16 (2023)
Background: Standard of care recommend that patients with cystic fibrosis (CF) require screening investigations to assess for complications. Changing models of care due to the COVID19 pandemic may have impacted completion of recommended screening. Ob
Externí odkaz:
https://doaj.org/article/6e8d6593b3704b7bb8b0e49f37bd53a9
Autor:
Kathy Stiller, Scott Morrow, Rebecca Chambers, Anne E Holland, Jennifer Bishop, Nathan Ward, Jennifer Corda, Jamie Wood, Margot Green, Amanda Nichols, Jenny Hauser, Andrew Shaw, Kathleen Hall, Ruth Dentice, Brenda M. Button, Jenn Bingham, Hilary Rowe, Rebecca Netluch, Tara Smith, Robyn Cobb, Danielle Shortall
Publikováno v:
Journal of Physiotherapy, Vol 65, Iss 1, Pp 43-50 (2019)
Questions: What airway clearance techniques and exercise regimens are used by adults with cystic fibrosis (CF) in Australia when well or unwell? What proportion of these adults believe that exercise can be used as a substitute for traditional airway
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ebfd92d8e3a3943fa9df9264498cc64f
Autor:
Narelle S Cox, Beverley Eldridge, Sarah Rawlings, Julianna Dreger, Jennifer Corda, Jennifer Hauser, Brenda M Button, Jennifer R Bishop, Amanda Nichols, Anna Middleton, Nathan Ward, Tiffany Dwyer, Ruth Dentice, Raynuka Lazarus, Paul O'Halloran, Joanna Y T Lee, Christie Mellerick, Kelly Mackintosh, Melitta McNarry, Craig Anthony Williams, Anne E Holland
BackgroundPhysical activity levels are known to decline following hospitalisation for people with cystic fibrosis (pwCF). However, optimal physical activity promotion strategies are unclear. This study investigated the effect of a web-based applicati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::888c7e50404eb5abaea118b0f764adda
https://cronfa.swan.ac.uk/Record/cronfa61302/Download/61302__25191__71f2cd1504604e47961df8da2286a0b2.pdf
https://cronfa.swan.ac.uk/Record/cronfa61302/Download/61302__25191__71f2cd1504604e47961df8da2286a0b2.pdf
Autor:
Samantha A Nolan, Edmund M.T. Lau, Keith Kh Wong, Sheila Sivam, Tiffany Dwyer, Jody M Bell, Phillip A. Munoz, Veronica Yozghatlian, Nicole Taylor, Ruth Dentice, Helen E. Jo, Simone K. Visser
Publikováno v:
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society. 21(1)
Spirometry is usually performed under the supervision of a trained respiratory scientist to ensure acceptability and repeatability of results. To evaluate the quality of spirometry performance by adult cystic fibrosis (CF) patients with and without o
Autor:
Mark R. Elkins, Ruth Dentice
Publikováno v:
The Cochrane Library
Cochrane Database Syst Rev
Cochrane Database Syst Rev
BACKGROUND: Inhalation of hypertonic saline improves sputum rheology, accelerates mucociliary clearance and improves clinical outcomes of people with cystic fibrosis. This is an update of a previously published Cochrane Review. OBJECTIVES: To determi
Autor:
Peter T. P. Bye, Veronica Yozghatlian, David Gattas, Paul J. Torzillo, Carmel Moriarty, Sheila Sivam, Nazmeen Reddy, Craig Mellis, Ruth Dentice, Allan R. Glanville
Publikováno v:
Internal Medicine Journal. 48:340-343
Extracorporeal membrane oxygenation (ECMO) support is used in selected patients with cystic fibrosis (CF) as a bridge to transplantation. Our aim was to describe briefly treatment and outcomes of six CF patients who received ECMO. One patient receive
Autor:
Stefan Eberl, Genevieve M Dwyer, Jordan Verschuer, Ruth Dentice, Peter T. P. Bye, Mark R. Elkins
Publikováno v:
BMC Pulmonary Medicine, Vol 19, Iss 1, Pp 1-7 (2019)
BMC Pulmonary Medicine
BMC Pulmonary Medicine
Background In people with and without Cystic Fibrosis (CF), does side lying during nebulisation change: the proportion of the dose loaded in the nebuliser that is deposited in the lungs; the uniformity of deposition throughout the lungs; or the apica
Publikováno v:
Journal of Cystic Fibrosis. 19:S27
Publikováno v:
BMC Pulmonary Medicine
BMC Pulmonary Medicine, Vol 18, Iss 1, Pp 1-6 (2018)
BMC Pulmonary Medicine, Vol 18, Iss 1, Pp 1-6 (2018)
Background Inhalation of nebulised medications is performed in upright sitting to maximise lung volumes. The pattern of deposition is poor for inhaled medications in people with Cystic Fibrosis. The pattern tends to be non-uniform and typically the u
Autor:
Mark R. Elkins, Ruth Dentice
Publikováno v:
Journal of Physiotherapy, Vol 61, Iss 3, Pp 125-134 (2015)
Question: Does inspiratory muscle training improve inspiratory muscle strength in adults receiving mechanical ventilation? Does it improve the duration or success of weaning? Does it affect length of stay, reintubation, tracheostomy, survival, or the