Literature DB >> 15741443

Inhaled fluticasone in bronchiectasis: a 12 month study.

K W Tsang1, K C Tan, P L Ho, G C Ooi, J C Ho, J Mak, G L Tipoe, C Ko, C Yan, W K Lam, M Chan-Yeung.   

Abstract

BACKGROUND: The clinical efficacy of inhaled corticosteroid (ICS) treatment has not been evaluated in bronchiectasis, despite the presence of chronic airway inflammation.
METHODS: After three consecutive weekly visits, 86 patients were randomised to receive either fluticasone 500 mug twice daily (n = 43, 23F, mean (SD) age 57.7 (14.4) years) or matched placebo (n = 43, 34F, 59.2 (14.2) years) and reviewed regularly for 52 weeks in a double blind fashion.
RESULTS: 35 and 38 patients in the fluticasone and placebo groups completed the study. Significantly more patients on ICS than on placebo showed improvement in 24 hour sputum volume (OR 2.5, 95% CI 1.1 to 6.0, p = 0.03) but not in exacerbation frequency, forced expiratory volume in 1 second, forced vital capacity, or sputum purulence score. Significantly more patients with Pseudomonas aeruginosa infection receiving fluticasone showed improvement in 24 hour sputum volume (OR 13.5, 95% CI 1.8 to 100.2, p = 0.03) and exacerbation frequency (OR 13.3, 95% CI 1.8 to 100.2, p = 0.01) than those given placebo. Logistic regression models revealed a significantly better response in sputum volume with fluticasone treatment than with placebo among subgroups of patients with 24 hour sputum volume <30 ml (p = 0.04), exacerbation frequency </=2/year (p = 0.04), and sputum purulence score >5 (p = 0.03).
CONCLUSIONS: ICS treatment is beneficial to patients with bronchiectasis, particularly those with P. aerurginosa infection.

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Year:  2005        PMID: 15741443      PMCID: PMC1747352          DOI: 10.1136/thx.2002.003236

Source DB:  PubMed          Journal:  Thorax        ISSN: 0040-6376            Impact factor:   9.139


  27 in total

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Review 2.  Bronchiectasis.

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Review 3.  Glucocorticoid-regulated transcription factors.

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4.  Validation of the Hong Kong Chinese version of the St. George Respiratory Questionnaire in patients with bronchiectasis.

Authors:  Shelley L Chan; Moira M Chan-Yeung; Gaik C Ooi; Cindy L Lam; Tung F Cheung; Wah K Lam; Kenneth W Tsang
Journal:  Chest       Date:  2002-12       Impact factor: 9.410

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6.  Computed tomography of bronchiectasis.

Authors:  D P Naidich; D I McCauley; N F Khouri; F P Stitik; S S Siegelman
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7.  Sputum elastase in steady-state bronchiectasis.

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9.  Alternate-day prednisone reduces morbidity and improves pulmonary function in cystic fibrosis.

Authors:  H S Auerbach; M Williams; J A Kirkpatrick; H R Colten
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10.  Chronic Pseudomonas aeruginosa lung infection in cystic fibrosis. A longitudinal study of immune complex activity and inflammatory response in sputum sol-phase of cystic fibrosis patients with chronic Pseudomonas aeruginosa lung infections: influence of local steroid treatment.

Authors:  P O Schiøtz; M Jørgensen; E W Flensborg; O Faerø; S Husby; N Høiby; S V Jacobsen; H Nielsen; S E Svehag
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  28 in total

Review 1.  [Treatment of not-with cystic fibrosis associated forms bronchiectasis (non-CF bronchiectasis)].

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Review 2.  Treatment of bronchiectasis in adults.

Authors:  Nick H T ten Hacken; Peter J Wijkstra; Huib A M Kerstjens
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Review 3.  A review of non-cystic fibrosis pediatric bronchiectasis.

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Review 5.  Pharmacological treatment options for bronchiectasis: focus on antimicrobial and anti-inflammatory agents.

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6.  Bronchodilator response in adults with bronchiectasis: correlation with clinical parameters and prognostic implications.

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Review 7.  Diagnosis and management of bronchiectasis.

Authors:  Maeve P Smith
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8.  Sputum purulence-associated microbial community compositions in adults with bronchiectasis.

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Review 9.  Bronchiectasis--diagnosis and treatment.

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Review 10.  Is there a role for inhaled corticosteroids and macrolide therapy in bronchiectasis?

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