Zobrazeno 1 - 10
of 73
pro vyhledávání: '"Gemma Stanford"'
Autor:
Gemma Stanford, Diana Bilton, Winston Banya, Jane C Davies, Omar Usmani, Susan Charman, Mandy Jones, Nicholas J Simmonds
Publikováno v:
BMJ Open Respiratory Research, Vol 7, Iss 1 (2020)
Introduction Airway clearance techniques (ACTs) are a gold standard of cystic fibrosis management; however, the majority of research evidence for their efficacy is of low standard; often attributed to the lack of sensitivity from outcome measures (OM
Externí odkaz:
https://doaj.org/article/1f94608e33704f8f9d5f4f12b0357765
Publikováno v:
BMJ Open Respiratory Research, Vol 6, Iss 1 (2019)
Introduction Non-invasive ventilation (NIV) is used in cystic fibrosis (CF) to support airway clearance techniques (ACTs) by augmenting tidal volumes and reducing patient effort. However, the evidence base for this is limited. We hypothesised that NI
Externí odkaz:
https://doaj.org/article/481a424ddb994cc3acc28a4075fdd9e0
Autor:
Gemma Stanford, Tracey Daniels, Catherine Brown, Katie Ferguson, Ammani Prasad, Penny Agent, Alison Gates, Lisa Morrison
Publikováno v:
Physical Therapy. 103
In looking back on 2020 and 2021, this Perspective reflects on the monumental impacts of the rollout of cystic fibrosis (CF) transmembrane conductance regulator highly effective modulator therapies and the COVID-19 pandemic on the management of CF. A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::716c8feb6c017c29c93fba81335f0490
https://doi.org/10.1093/ptj/pzac136
https://doi.org/10.1093/ptj/pzac136
Publikováno v:
Chest. 159:93-102
Pulmonary exacerbations (PExs) are significant life events in people with cystic fibrosis (CF), associated with declining lung function, reduced quality of life, hospitalizations, and decreased survival. The adult CF population is increasing worldwid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8b7712aa7663982537cdb05751f11fbe
https://doi.org/10.1016/j.chest.2020.09.084
https://doi.org/10.1016/j.chest.2020.09.084
Autor:
Omar S. Usmani, Mandy Jones, Jane C. Davies, Susan C. Charman, Gemma Stanford, Nicholas J. Simmonds, Diana Bilton
Background Airway clearance techniques (ACTs) are integral to cystic fibrosis (CF) management. However, there is no consensus as to which outcome measures (OMs) are best for assessing ACT efficacy. Objectives: To summarise OMs that have been assessed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::49a145ef1acf055a8296c8afd6dcbc79
https://doi.org/10.21203/rs.3.rs-585783/v1
https://doi.org/10.21203/rs.3.rs-585783/v1
Autor:
Mandy Jones, Gemma Stanford, Omar S. Usmani, Nicholas J. Simmonds, Diana Bilton, Winston Banya, Jane C. Davies, Susan C. Charman
Publikováno v:
BMJ Open Respiratory Research
BMJ Open Respiratory Research, Vol 7, Iss 1 (2020)
BMJ Open Respiratory Research, Vol 7, Iss 1 (2020)
IntroductionAirway clearance techniques (ACTs) are a gold standard of cystic fibrosis management; however, the majority of research evidence for their efficacy is of low standard; often attributed to the lack of sensitivity from outcome measures (OMs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b16db6ddbb091d1f7911fc8d0de7266
http://bura.brunel.ac.uk/handle/2438/21874
http://bura.brunel.ac.uk/handle/2438/21874
Autor:
Gemma Stanford, Mandy Jones, Diana Bilton, Jane C. Davies, Z. Beverley, C. Short, F. Cathcart, Nicholas J. Simmonds
Publikováno v:
Cystic fibrosis and bronchiectasis: updates and controversies.
Introduction The best outcome measure (OM) for airway clearance (AC) in CF is unknown. Our National Institute for Health Research funded RCT compares standard OMs (sputum weight, FEV1) to new OMs (electronic impedance tomography (EIT), lung clearance
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4a010546b99850a6623bd3db7bbf1ce1
https://doi.org/10.1136/thorax-2019-btsabstracts2019.386
https://doi.org/10.1136/thorax-2019-btsabstracts2019.386
Publikováno v:
Cochrane Database Syst Rev
BACKGROUND: Cystic fibrosis is the most common autosomal recessive disease in white populations, and causes respiratory dysfunction in the majority of individuals. Numerous types of respiratory muscle training to improve respiratory function and heal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54abed0ce73c377b400f21b9611a7742
https://pubmed.ncbi.nlm.nih.gov/33331663
https://pubmed.ncbi.nlm.nih.gov/33331663
Autor:
Diana Bilton, F. Cathcart, Mandy Jones, Z. Beverley, N.J. Simmonds, Jane C. Davies, C. Short, Gemma Stanford
Publikováno v:
Journal of Cystic Fibrosis. 18:S3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::707b2f89d01e93e037bce8dd850a6108
https://doi.org/10.1016/s1569-1993(19)30123-7
https://doi.org/10.1016/s1569-1993(19)30123-7
Autor:
Nicholas J. Simmonds, Gemma Stanford, Diana Bilton, Penny Agent, Winston Banya, Helen Parrott
Publikováno v:
BMJ Open Respiratory Research
IntroductionNon-invasive ventilation (NIV) is used in cystic fibrosis (CF) to support airway clearance techniques (ACTs) by augmenting tidal volumes and reducing patient effort. However, the evidence base for this is limited. We hypothesised that NIV
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f11d26948e884b2289b37b4307c0cf57
https://doi.org/10.1136/bmjresp-2018-000399
https://doi.org/10.1136/bmjresp-2018-000399