British Thoracic Society guideline for non-CF bronchiectasis

The diagnosis, investigation and particularly management of bronchiectasis has been largely empirical and the subject of relatively few controlled clinical trials. There are no clear guidelines, although an Australian position statement has been published concerning bronchiectasis in children. The p...

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Published in:Thorax Vol. 65 Suppl 1; p. i1
Main Authors: Pasteur, M C, Bilton, D, Hill, A T
Format: Journal Article
Language:English
Published: England 01.07.2010
Subjects:
ISSN:1468-3296, 1468-3296
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Abstract The diagnosis, investigation and particularly management of bronchiectasis has been largely empirical and the subject of relatively few controlled clinical trials. There are no clear guidelines, although an Australian position statement has been published concerning bronchiectasis in children. The purposes of these guidelines were therefore threefold: (1) to identify relevant studies in non-cystic fibrosis (CF) bronchiectasis; (2) to provide guidelines on management based on published studies where possible or a consensus view; and (3) to identify gaps in our knowledge and identify areas for future study.
AbstractList The diagnosis, investigation and particularly management of bronchiectasis has been largely empirical and the subject of relatively few controlled clinical trials. There are no clear guidelines, although an Australian position statement has been published concerning bronchiectasis in children. The purposes of these guidelines were therefore threefold: (1) to identify relevant studies in non-cystic fibrosis (CF) bronchiectasis; (2) to provide guidelines on management based on published studies where possible or a consensus view; and (3) to identify gaps in our knowledge and identify areas for future study.
The diagnosis, investigation and particularly management of bronchiectasis has been largely empirical and the subject of relatively few controlled clinical trials. There are no clear guidelines, although an Australian position statement has been published concerning bronchiectasis in children. The purposes of these guidelines were therefore threefold: (1) to identify relevant studies in non-cystic fibrosis (CF) bronchiectasis; (2) to provide guidelines on management based on published studies where possible or a consensus view; and (3) to identify gaps in our knowledge and identify areas for future study.The diagnosis, investigation and particularly management of bronchiectasis has been largely empirical and the subject of relatively few controlled clinical trials. There are no clear guidelines, although an Australian position statement has been published concerning bronchiectasis in children. The purposes of these guidelines were therefore threefold: (1) to identify relevant studies in non-cystic fibrosis (CF) bronchiectasis; (2) to provide guidelines on management based on published studies where possible or a consensus view; and (3) to identify gaps in our knowledge and identify areas for future study.
Author Bilton, D
Hill, A T
Pasteur, M C
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/20627931$$D View this record in MEDLINE/PubMed
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Stockley, Robert A
Bush, Andrew
Sonnappa, Samantha
Hill, Adam T
Herriot, Richard
Emmanue, Xavier
Carr, Siobhán
Wilson, Robert
Greenstone, Mike
Elborn, Stuart
Cole, Bridget
Kalima, Pota
Sinfield, Frances
French, Jane
Wallis, Colin
Spencer, David A
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Cornford, Charles
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Pasteur, Mark C
Bott, Julia
Parry, G Wyn
Bilton, Diana
Pryor, Jennifer
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SubjectTerms Administration, Inhalation
Adult
Anti-Bacterial Agents - administration & dosage
Anti-Bacterial Agents - therapeutic use
Bronchiectasis - diagnosis
Bronchiectasis - etiology
Bronchiectasis - therapy
Child
Cystic Fibrosis - complications
Diagnostic Techniques, Respiratory System
Evidence-Based Medicine
Humans
Infusions, Intravenous
Nebulizers and Vaporizers
Physical Therapy Modalities
Respiratory Function Tests
Respiratory System Agents - therapeutic use
Tomography, X-Ray Computed
Title British Thoracic Society guideline for non-CF bronchiectasis
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