Publications
318 results found
Bilton, 2011, Bronchiectasis, Bronchiectasis, Editors: Floto, Haworth, Publisher: EuropeanRespiratorySociety, ISBN: 9781849840125
This book provides a definitive guide to the management of patients with bronchiectasis.
Bilton D, Jones AL, 2011, Bronchiectasis: epidemiology and causes, BRONCHIECTASIS, Editors: Floto, Haworth, Publisher: EUROPEAN RESPIRATORY SOCIETY, Pages: 1-10
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- Citations: 24
Morgan GE, Parrott H, Bilton D, et al., 2011, POSITIVE PRESSURE - A POSITIVE IMPACT ON AIRWAY CLEARANCE AT HOME, Publisher: WILEY-BLACKWELL, Pages: 351-352, ISSN: 8755-6863
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- Citations: 1
Kernan NG, Cullinan P, Alton EWFW, et al., 2010, ORAL CONTRACEPTIVE USE DOES NOT AFFECT CF DISEASE SEVERITY, Publisher: B M J PUBLISHING GROUP, Pages: A121-A121, ISSN: 0040-6376
Salako M, MacNeill SJ, Gunn E, et al., 2010, DISPARITIES IN CARE OF ADULT CF PATIENTS IN THE UK, Publisher: B M J PUBLISHING GROUP, Pages: A172-A173, ISSN: 0040-6376
Pasteur MC, Bilton D, Hill AT, 2010, British Thoracic Society guideline for non-CF bronchiectasis, THORAX, Vol: 65, Pages: 577-577, ISSN: 0040-6376
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- Citations: 75
Pasteur MC, Bilton D, Hill AT, 2010, British Thoracic Society guideline for non-CF bronchiectasis, THORAX, Vol: 65, Pages: I1-I58, ISSN: 0040-6376
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- Citations: 718
McKeon DJ, Cadwallader KA, Idris S, et al., 2010, Cystic fibrosis neutrophils have normal intrinsic reactive oxygen species generation, EUROPEAN RESPIRATORY JOURNAL, Vol: 35, Pages: 1264-1272, ISSN: 0903-1936
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- Citations: 33
Adler AI, Bilton D, Haworth C, et al., 2010, Hyperglycemia and Death in Cystic Fibrosis Related Diabetes, 70th Annual Meeting of the American-Diabetes-Association, Publisher: AMER DIABETES ASSOC, Pages: A505-A505, ISSN: 0012-1797
Shead EF, Haworth CS, Barker H, et al., 2010, Osteoclast function, bone turnover and inflammatory cytokines during infective exacerbations of cystic fibrosis, JOURNAL OF CYSTIC FIBROSIS, Vol: 9, Pages: 93-98, ISSN: 1569-1993
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- Citations: 66
Chamnan P, Shine BSF, Haworth CS, et al., 2010, Diabetes as a Determinant of Mortality in Cystic Fibrosis, DIABETES CARE, Vol: 33, Pages: 311-316, ISSN: 0149-5992
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- Citations: 99
Srivastava SA, Nguyen TTB, Burgess JC, et al., 2010, Breath glucose as a marker of pulmonary inflammation in adult patients with cystic fibrosis, North American Cystic Fibrosis Conference, Pages: 375-375
Srivastava SA, Burgess JC, Bilton D, et al., 2010, Is HbA1C a useful marker for pulmonary exacerbations in patients with CF but no known diabetes?, North American Cystic Fibrosis Conference, Pages: 375-375
Kernan NG, Cullinan P, Alton EW, et al., 2010, ORAL CONTRACEPTIVE USE DOES NOT AFFECT CF DISEASE SEVERITY, PEDIATRIC PULMONOLOGY, Pages: 250-250, ISSN: 8755-6863
Bilton D, Robinson P, Cooper P, et al., 2010, LONG TERM ADMINISTRATION OF INHALED DRY POWDER MANNITOL IN CF: RESULTS FROM THE OPEN LABEL PHASE III DPM-CF-301 STUDY, Publisher: WILEY, Pages: 321-321, ISSN: 8755-6863
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- Citations: 3
Hurt K, Perrin FM, Gyi K, et al., 2010, RETROSPECTIVE REVIEW AND CASE CONTROL STUDY OF CYSTIC FIBROSIS PATIENTS WITH <i>MYCOBACTERIUM ABSCESSUS</i> INFECTION, PEDIATRIC PULMONOLOGY, Pages: 324-325, ISSN: 8755-6863
Jones A, Bilton D, Evans TW, et al., 2010, PREDICTORS OF OUTCOME IN PATIENTS WITH CYSTIC FIBROSIS REQUIRING ENDOTRACHEAL INTUBATION, Publisher: WILEY, Pages: 364-365, ISSN: 8755-6863
Goldman MD, Nazeran H, Ramos C, et al., 2010, Electrical Circuit Models of the Human Respiratory System Reflect Small Airway Impairment Measured by Impulse Oscillation (IOS), 32nd Annual International Conference of the IEEE Engineering-in-Medicine-and-Biology-Society (EMBC 10), Publisher: IEEE, Pages: 2467-2472, ISSN: 1557-170X
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- Citations: 11
Duff R, Simmonds N, Pantelidis P, et al., 2009, MOLECULAR DETECTION OF COMPLEX MICROBIAL COMMUNITIES IN SPUTA OF PATIENTS WITH CYSTIC FIBROSIS AND NON-CF BRONCHIECTASIS, Winter Meeting of the British-Thoracic-Society, Publisher: B M J PUBLISHING GROUP, Pages: A63-A63, ISSN: 0040-6376
Loebinger MR, Bilton D, Wilson R, 2009, Upper airway . 2: Bronchiectasis, cystic fibrosis and sinusitis, THORAX, Vol: 64, Pages: 1096-1101, ISSN: 0040-6376
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- Citations: 30
Srivastava SA, Burgess JC, Gyi KM, et al., 2009, RELATIONSHIP BETWEEN HBA1C AND LUNG DISEASE IN PATIENTS WITH CYSTIC FIBROSIS NOT KNOWN TO HAVE DIABETES, Winter Meeting of the British-Thoracic-Society, Publisher: B M J PUBLISHING GROUP, Pages: A112-A112, ISSN: 0040-6376
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- Citations: 1
Perrin FMR, Padley S, Gyi KM, et al., 2009, RECURRENT SEVERE HAEMOPTYSIS IN CYSTIC FIBROSIS, Winter Meeting of the British-Thoracic-Society, Publisher: B M J PUBLISHING GROUP, Pages: A112-A112, ISSN: 0040-6376
Dhasmana DJ, Dack K, Gyi K, et al., 2009, DEVELOPMENT OF AN ADULT "CYSTIC FIBROSIS SWINE FLU TRIAGE SERVICE'' IN A LONDON TERTIARY REFERRAL CENTRE, Winter Meeting of the British-Thoracic-Society, Publisher: B M J PUBLISHING GROUP, Pages: A174-A174, ISSN: 0040-6376
Foweraker JE, Laughton CR, Brown DF, et al., 2009, Comparison of Methods To Test Antibiotic Combinations against Heterogeneous Populations of Multiresistant <i>Pseudomonas aeruginosa</i> from Patients with Acute Infective Exacerbations in Cystic Fibrosis, ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, Vol: 53, Pages: 4809-4815, ISSN: 0066-4804
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- Citations: 46
Tsang KW, Bilton D, 2009, Clinical challenges in managing bronchiectasis, RESPIROLOGY, Vol: 14, Pages: 637-650, ISSN: 1323-7799
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- Citations: 39
Davies JC, Bilton D, 2009, Bugs, biofilms, and resistance in cystic fibrosis., Respir Care, Vol: 54, Pages: 628-640, ISSN: 0020-1324
Bacteria infect the respiratory tract early in the course of cystic fibrosis disease, often fail to be eradicated, and together with an aggressive host inflammatory response, are thought to be key players in the irreversible airway damage from which most patients ultimately die. Although incompletely understood, certain aspects of the cystic fibrosis airway itself appear to favor the development of chronic modes of survival, in particular biofilm formation; this and the development of antibiotic resistance following exposure to multiple antibiotic courses lead to chronic, persistent infection. In addition to the common cystic fibrosis pathogens, such as Staphylococcus aureus, Haemophilus influenzae, and Pseudomonas aeruginosa, several newer species are becoming more common. Furthermore, new molecular techniques have led to the identification of multiple different organisms within respiratory secretions, many of which are not cultured with conventional tools. Future work should aim to develop clinically applicable methods to identify these and to determine which have the potential to impact pulmonary health. We outline the basic tenets of infection control and treatment.
Davies JC, Bilton D, 2009, Bugs, Biofilms, and Resistance in Cystic Fibrosis, 43rd Respiratory Care Journal Conference on Respiratory Care and Cystic Fibrosis, Publisher: DAEDALUS ENTERPRISES INC, Pages: 628-638, ISSN: 0020-1324
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- Citations: 88
Gillham MI, Sundaram S, Laughton CR, et al., 2009, Variable antibiotic susceptibility in populations of <i>Pseudomonas aeruginosa</i> infecting patients with bronchiectasis, Winter Meeting of the British-Thoracic-Society, Publisher: OXFORD UNIV PRESS, Pages: 728-732, ISSN: 0305-7453
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- Citations: 24
Gillham MI, Sundaram S, Laughton CR, et al., 2009, Variable antibiotic susceptibility in populations of Pseudomonas aeruginosa infecting patients with bronchiectasis., J Antimicrob Chemother, Vol: 63, Pages: 728-732
OBJECTIVES: To investigate variability in colony morphology and antibiotic susceptibility in populations of Pseudomonas aeruginosa from sputa of patients with bronchiectasis without cystic fibrosis (CF) compared with P. aeruginosa isolated from patients with CF, and from other infections as controls. METHODS: P. aeruginosa was cultured from 31 patients with non-CF bronchiectasis, 24 with CF, 7 ventilated patients and 9 skin swabs. Four colonies of each morphotype of P. aeruginosa were tested for susceptibility to 12 antibiotics by disc diffusion. The variability in susceptibility between the isolates in each patient's population of P. aeruginosa was investigated. RESULTS: The classic morphotype of P. aeruginosa was cultured from control samples with an average variation in zone size of 2 mm (range 0-4 mm) for the four colonies tested. Non-CF bronchiectasis sputa contained 1-3 colonial morphotypes of P. aeruginosa; the average difference between the largest and smallest zone sizes found in all examples of the morphotypes present in each sample varied from 3 mm (1-9 mm) for colistin to 8 mm (0-24 mm) for piperacillin/tazobactam. CF sputa contained 2-6 morphotypes of P. aeruginosa with a wider variation of susceptibility. There was variation between bacteria of the same morphotype from non-CF bronchiectasis and CF sputa. CONCLUSIONS: Phenotypic variation in colonial form and antibiotic susceptibility is not unique to chronic infection in CF but is also found in non-CF bronchiectasis. This questions the use of current susceptibility testing methods for the complex populations of bacteria found in chronic lung infection.
Sundaram S, Herrod T, Oates K, et al., 2009, Exacerbations in Non CF Bronchiectasis - Defining Clinical Endpoints To Measure Treatment Efficacy in Future Trials., Publisher: AMER THORACIC SOC, ISSN: 1073-449X
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