Zobrazeno 1 - 10
of 48
pro vyhledávání: '"Rachael, Curley"'
Autor:
Nikki Totton, Mike Bradburn, Zhe Hui Hoo, Jen Lewis, Daniel Hind, Carla Girling, Elizabeth Shepherd, Julia Nightingale, Thomas Daniels, Jane Dewar, Sophie Dawson, Mary Carroll, Mark Allenby, Frank Edenborough, Rachael Curley, Charlotte Carolan, Martin Wildman
Publikováno v:
Health Science Reports, Vol 4, Iss 4, Pp n/a-n/a (2021)
Abstract Rationale and aims Lung health of people with cystic fibrosis (PwCF) can be preserved by daily use of inhaled therapy. Adherence to inhaled therapy, therefore, provides an important process measure to understand the success of care and can b
Externí odkaz:
https://doaj.org/article/9fddfc54b0214cb7b2af0dee64c156bb
Autor:
Amanda Bevan, Zhe Hui Hoo, Nikki Totton, Carla Girling, India R. Davids, Pauline Whelan, Steven Antrobus, John Ainsworth, Iain Buchan, Alan Anderson, Stephen Bourke, Simon Doe, Carlos Echevarria, Jill Taylor, Nicholas J. Bell, Kathryn Bateman, Carys Jones, Peter Moran, Giles Fitch, Michael Martin, Angela McGowan, Stephen Morrow, Heather Seabridge, Nicki Bush, Tracey Daniels, Katy Lee, Nicola Robson, Dejene Shiferaw, Dimah Sweis, Rebecca Thomas, Jayne Faulkner, William G. Flight, Sarah Poole, Louise Warnock, Mark I. Allenby, Mary Carroll, Thomas V. Daniels, Helen Dunn, Julia A. Nightingale, Elizabeth Shepherd, Chandra Ohri, Jessica Gadsby, Simon Range, Darren Tature, Helen L. Barr, Sophie Dawson, Jane Dewar, Bryony Miller, Gauri Saini, Penny Galey, Jack Johnson, Mark C. Pasteur, David Derry, Harriet Gledhill, Angharad Lawson, Michelle Thomas, David Waine, Josie Cunningham, Annant Damani, Alexandra Higton, Christopher Orchard, Charlotte Carolan, Misbah Tahir, Amanda Plummer, Marlene Hutchings, Frank P Edenborough, Rachael Curley, Martin J. Wildman
Publikováno v:
Journal of Cystic Fibrosis. 21:893-897
Autor:
Elizabeth Shepherd, Mike Bradburn, S. Dawson, Charlotte Clarke, Gauri Saini, Pauline Whelan, Michelle Lowther, Kate Barnett, John Ainsworth, C. Carolan, Rachel Szczepanski, Mark I. Allenby, J.A. Nightingale, F P Edenborough, Madelynne A Arden, Jen Lewis, Sarah Millward, C. Girling, Thomas Daniels, Mary P. Carroll, Zhe Hui Hoo, Jane Dewar, Martin J Wildman, Marlene Hutchings, Helen L. Barr, Rachael Curley, Simon Waterhouse, Nikki Totton
Publikováno v:
Chest. 160:2061-2065
Publikováno v:
F1000Research, Vol 7 (2018)
Background: Forced expiratory volume in one second (FEV1) is an important cystic fibrosis (CF) prognostic marker and an established endpoint for CF clinical trials. FEV1 is also used in observation studies, e.g. to compare different centre’s outcom
Externí odkaz:
https://doaj.org/article/a61169e2c52a48ea87f004b03e84cf1c
Publikováno v:
F1000Research, Vol 6 (2018)
Pulmonary exacerbations in adults with cystic fibrosis (CF) and chronic Pseudomonas aeruginosa (Psae) infection are usually treated with dual intravenous antibiotics for 14 days, despite the lack of evidence for best practice. Intravenous antibiotics
Externí odkaz:
https://doaj.org/article/0971f8b6aefd470a8f54ec86dd964abe
Autor:
Jayne Faulkner, Jack Johnson, Carys Jones, Jill Taylor, Simon Range, Pauline Whelan, K. Bateman, Dimah Sweis, Thomas V. Daniels, S. Dawson, Nikki Totton, Helen Dunn, Harriet Gledhill, C. Girling, Elizabeth Shepherd, Darren Tature, Amanda Plummer, Angharad Lawson, Amanda Bevan, Penny Galey, Stephen Bourke, David Waine, Helen L. Barr, Jessica Gadsby, F P Edenborough, Louise Warnock, Michael Martin, Misbah Tahir, John Ainsworth, C. Carolan, Chandra Ohri, Annant Damani, Rebecca Thomas, Stephen Morrow, J.A. Nightingale, Peter Moran, Giles Fitch, Steven Antrobus, David Derry, Christopher Orchard, Jane Dewar, Heather Seabridge, Bryony Miller, William G Flight, Dejene Shiferaw, Sarah Poole, Tracey Daniels, Mark C. Pasteur, Zhe Hui Hoo, Martin J Wildman, Katy Lee, Josie Cunningham, Iain Buchan, Mark I. Allenby, Mary P. Carroll, Alan Anderson, N.J. Bell, Marlene Hutchings, Rachael Curley, Alexandra Higton, Simon Doe, Nicki Bush, India R. Davids, Angela McGowan, Gauri Saini, Michelle Thomas, Carlos Echevarria, Nicola Robson
Background\ud \ud Studies in separate cohorts suggest possible discrepancies between inhaled medicines supplied (median 50-60%) and medicines used (median 30-40%). We performed the first study that directly compares CF medicine supply against use to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eed7e7e1c9fb6c76cd898f54426452a5
Publikováno v:
Journal of Cystic Fibrosis
Background The COVID-19 pandemic has accelerated the transition to telehealth, including the use of home spirometry in cystic fibrosis. Evaluating the accuracy and precision of longitudinal home spirometry is a requisite for telehealth-based research
Autor:
Rachael Curley, Mike Bradburn, Elizabeth Shepherd, Daniel Hind, Jane Dewar, J.A. Nightingale, Zhe Hui Hoo, C. Carolan, Thomas Daniels, Mary P. Carroll, C. Girling, Jen Lewis, Martin J Wildman, Mark I. Allenby, Nikki Totton, S. Dawson, F P Edenborough
Publikováno v:
Health Science Reports, Vol 4, Iss 4, Pp n/a-n/a (2021)
Rationale and aims\ud \ud Lung health of people with cystic fibrosis (PwCF) can be preserved by daily use of inhaled therapy. Adherence to inhaled therapy, therefore, provides an important process measure to understand the success of care and can be
Autor:
Nicole R. Bramley, Stephen J Walters, Rachael Curley, Michael J. Campbell, Zhe Hui Hoo, Martin J Wildman, F P Edenborough
Publikováno v:
Respiratory Medicine. 154:109-115
Introduction In CF, people with higher FEV1 are less aggressively treated with intravenous (IV) antibiotics, with resultant negative impact on their health outcomes. This could be entirely clinician-driven, but patient choice may also influence IV us
Autor:
Nikki, Totton, Mike, Bradburn, Zhe Hui, Hoo, Jen, Lewis, Daniel, Hind, Carla, Girling, Elizabeth, Shepherd, Julia, Nightingale, Thomas, Daniels, Jane, Dewar, Sophie, Dawson, Mary, Carroll, Mark, Allenby, Frank, Edenborough, Rachael, Curley, Charlotte, Carolan, Martin, Wildman
Publikováno v:
Health Science Reports
Rationale and aims Lung health of people with cystic fibrosis (PwCF) can be preserved by daily use of inhaled therapy. Adherence to inhaled therapy, therefore, provides an important process measure to understand the success of care and can be used as