Clinimetric analysis of outcome measures for airway clearance in people with cystic fibrosis: a systematic review

Authors: Gemma E. Stanford, Mandy Jones, Susan C. Charman, Diana Bilton, Omar S. Usmani, Jane C. Davies, Nicholas J. Simmonds

Source: Therapeutic Advances in Respiratory Disease, Vol 16 (2022)

Subject Terms: Diseases of the respiratory system, RC705-779

File Description: electronic resource

Relation: https://doaj.org/toc/1753-4666

Access URL: https://doaj.org/article/1935b98869e14fbfa892edc1a5075e54

Real-World Outcomes Among Patients with Cystic Fibrosis Treated with Ivacaftor: 2012–2016 Experience

Authors: Mark Higgins, Nataliya Volkova, Kristin Moy, Bruce C. Marshall, Diana Bilton

Source: Pulmonary Therapy, Vol 6, Iss 1, Pp 141-149 (2020)

Subject Terms: Cystic fibrosis, Ivacaftor, Real-world data, Registry, Long-term safety, Diseases of the respiratory system, RC705-779

File Description: electronic resource

Relation: https://doaj.org/toc/2364-1754; https://doaj.org/toc/2364-1746

Access URL: https://doaj.org/article/4ae508c16f82478fa03fcd3afddc6596

Investigating outcome measures for assessing airway clearance techniques in adults with cystic fibrosis: protocol of a single-centre randomised controlled crossover trial

Authors: Gemma Stanford, Diana Bilton, Winston Banya, Jane C Davies, Omar Usmani, Susan Charman, Mandy Jones, Nicholas J Simmonds

Source: BMJ Open Respiratory Research, Vol 7, Iss 1 (2020)

Subject Terms: Medicine, Diseases of the respiratory system, RC705-779

File Description: electronic resource

Relation: https://bmjopenrespres.bmj.com/content/7/1/e000694.full; https://doaj.org/toc/2052-4439

Access URL: https://doaj.org/article/1f94608e33704f8f9d5f4f12b0357765

Randomised cross-over trial evaluating the short-term effects of non-invasive ventilation as an adjunct to airway clearance techniques in adults with cystic fibrosis

Authors: Gemma Stanford, Helen Parrott, Diana Bilton, Penny Agent, Winston Banya, Nicholas Simmonds

Source: BMJ Open Respiratory Research, Vol 6, Iss 1 (2019)

Subject Terms: Medicine, Diseases of the respiratory system, RC705-779

File Description: electronic resource

Relation: https://bmjopenrespres.bmj.com/content/6/1/e000399.full; https://doaj.org/toc/2052-4439

Access URL: https://doaj.org/article/481a424ddb994cc3acc28a4075fdd9e0

Identifying exceptional cystic fibrosis care services: combining statistical process control with focus groups

Authors: Stephanie J MacNeill, Livia Pierotti, Mohammed A Mohammed, Martin Wildman, Jonathan Boote, Steve Harrison, Siobhán B Carr, Paul Cullinan, Caroline Elston, Diana Bilton

Source: Health Services and Delivery Research, Vol 7, Iss 6 (2019)

Subject Terms: CYSTIC FIBROSIS, QUALITY IMPROVEMENT, CF REGISTRY, FUNNEL PLOTS, Public aspects of medicine, RA1-1270, Medicine (General), R5-920

File Description: electronic resource

Relation: https://doaj.org/toc/2050-4349; https://doaj.org/toc/2050-4357

Access URL: https://doaj.org/article/799df63a29e14e3d95a1237599ef4d35

Results from an online survey of adults with cystic fibrosis: Accessing and using life expectancy information.

Authors: Ruth H Keogh, Diana Bilton, Rebecca Cosgriff, Dominic Kavanagh, Oliver Rayner, Philip M Sedgwick

Source: PLoS ONE, Vol 14, Iss 4, p e0213639 (2019)

Subject Terms: Medicine, Science

File Description: electronic resource

Relation: https://doaj.org/toc/1932-6203

Access URL: https://doaj.org/article/48ec2595905849dd961cb55510b3086d

Longitudinal assessment of sputum microbiome by sequencing of the 16S rRNA gene in non-cystic fibrosis bronchiectasis patients.

Authors: Michael J Cox, Elena M Turek, Catherine Hennessy, Ghazala K Mirza, Phillip L James, Meg Coleman, Andrew Jones, Robert Wilson, Diana Bilton, William O C Cookson, Miriam F Moffatt, Michael R Loebinger

Source: PLoS ONE, Vol 12, Iss 2, p e0170622 (2017)

Subject Terms: Medicine, Science

File Description: electronic resource

Relation: https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0170622&type=printable; https://doaj.org/toc/1932-6203

Access URL: https://doaj.org/article/e8c2345d2df24e73b5d786c88430113e

A randomised, double-blind, placebo-controlled trial of repeated nebulisation of non-viral cystic fibrosis transmembrane conductance regulator (CFTR) gene therapy in patients with cystic fibrosis

Authors: Eric WFW Alton, David K Armstrong, Deborah Ashby, Katie J Bayfield, Diana Bilton, Emily V Bloomfield, A Christopher Boyd, June Brand, Ruaridh Buchan, Roberto Calcedo, Paula Carvelli, Mario Chan, Seng H Cheng, David S Collie, Steve Cunningham, Heather E Davidson, Gwyneth Davies, Jane C Davies, Lee A Davies, Maria H Dewar, Ann Doherty, Jackie Donovan, Natalie S Dwyer, Hala I Elgmati, Rosanna F Featherstone, Jemyr Gavino, Sabrina Gea-Sorli, Duncan M Geddes, James SR Gibson, Deborah R Gill, Andrew P Greening, Uta Griesenbach, David M Hansell, Katharine Harman, Tracy E Higgins, Samantha L Hodges, Stephen C Hyde, Laura Hyndman, J Alastair Innes, Joseph Jacob, Nancy Jones, Brian F Keogh, Maria P Limberis, Paul Lloyd-Evans, Alan W Maclean, Michelle C Manvell, Dominique McCormick, Michael McGovern, Gerry McLachlan, Cuixiang Meng, M Angeles Montero, Hazel Milligan, Laura J Moyce, Gordon D Murray, Andrew G Nicholson, Tina Osadolor, Javier Parra-Leiton, David J Porteous, Ian A Pringle, Emma K Punch, Kamila M Pytel, Alexandra L Quittner, Gina Rivellini, Clare J Saunders, Ronald K Scheule, Sarah Sheard, Nicholas J Simmonds, Keith Smith, Stephen N Smith, Najwa Soussi, Samia Soussi, Emma J Spearing, Barbara J Stevenson, Stephanie G Sumner-Jones, Minna Turkkila, Rosa P Ureta, Michael D Waller, Marguerite Y Wasowicz, James M Wilson, Paul Wolstenholme-Hogg, on behalf of the UK Cystic Fibrosis Gene Therapy Consortium

Source: Efficacy and Mechanism Evaluation, Vol 3, Iss 5 (2016)

Subject Terms: cystic fibrosis, gene therapy, liposome, plasmid, clinical trial, randomised controlled trial, cftr, cystic fibrosis transmembrane conductance regulator, Medicine

File Description: electronic resource

Relation: https://doaj.org/toc/2050-4365; https://doaj.org/toc/2050-4373

Access URL: https://doaj.org/article/09b29fe1b155492fba24a177fe4be24c

Prevalence of Nontuberculous Mycobacteria in Cystic Fibrosis Clinics, United Kingdom, 2009

Authors: Paul Seddon, Katy Fidler, Sundhya Raman, Hilary Wyatt, Gary Ruiz, Caroline Elston, Felicity Perrin, Khin Gyi, Diana Bilton, Francis Drobniewski, Melanie Newport

Source: Emerging Infectious Diseases, Vol 19, Iss 7, Pp 1128-1130 (2013)

Subject Terms: nontuberculous mycobacteria, cystic fibrosis, Mycobacterium avium complex, Mycobacterium absessus complex, bacteria, United Kingdom, Medicine, Infectious and parasitic diseases, RC109-216

File Description: electronic resource

Relation: https://wwwnc.cdc.gov/eid/article/19/7/12-0615_article; https://doaj.org/toc/1080-6040; https://doaj.org/toc/1080-6059

Access URL: https://doaj.org/article/d4aa59e697f3474f9d366cb3f9657b10

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Diabetes Mellitus and Impaired Glucose Tolerance Are Associated with Poor Pulmonary Function in Adults with Cystic Fibrosis.

Authors: Adler, Amanda I., Gunn, Elaine, Haworth, Charles S., Shine, Brian S., Diana, Bilton

Source: Diabetes; Jun2007 Supplement 1, Vol. 56, pA267-A267, 1/4p

Subject Terms: DIABETES, BLOOD sugar, LUNG diseases, CYSTIC fibrosis, PEOPLE with diabetes

Geographic Terms: EAST of England

Safety and Efficacy of Recombinant Alpha1‐Antitrypsin Therapy in Cystic FibrosisThere are no known conflicts of interest associated with this manuscript.

Authors: S. Lorraine Martin, Damian Downey, Diana Bilton, Mary T. Keogan, Julia Edgar, J. Stuart Elborn

Source: Pediatric Pulmonology; Feb2006, Vol. 41 Issue 2, p177-183, 0p

Cystic Fibrosis pulmonary disease is not a contra-indication to live-related renal transplantation.

Authors: Damian J. McKeon, Charles Haworth, John R. Bradley, Diana Bilton

Source: Nephrology Dialysis Transplantation; Mar2005, Vol. 20 Issue 3, p664-664, 1p