Multiple-breath washout as a lung function test in cystic fibrosis: A cystic fibrosis foundation workshop report

QR Code

Multiple-breath washout as a lung function test in cystic fibrosis: A cystic fibrosis foundation workshop report

The lung clearance index (LCI) is a lung function parameter derived from the multiple-breath washout (MBW) test. Although first developed 60 years ago, the technique was not widely used for many years. Recent technological advances in equipment design have produced gains in popularity for this test...

Full description

Bibliographic Details
Main Authors:	Subbarao, P., Milla, C., Aurora, P., Davies, J., Davis, S., Hall, Graham, Heltshe, S., Latzin, P., Lindblad, A., Pittman, J., Robinson, P., Rosenfeld, M., Singer, F., Starner, T., Ratjen, F., Morgan, W.
Format:	Journal Article
Published:	2015
Online Access:	http://hdl.handle.net/20.500.11937/54367

Similar Items

Multiple-breath washout outcomes are sensitive to inflammation and infection in children with cystic fibrosis
by: Ramsey, K., et al.
Published: (2017)

Preschool multiple-breath washout testing an official American Thoracic Society technical statement
by: Robinson, P., et al.
Published: (2018)

US Cystic Fibrosis Foundation and European Cystic Fibrosis Society consensus recommendations for the management of non-tuberculous mycobacteria in individuals with cystic fibrosis
by: Floto, R. Andres, et al.
Published: (2016)

The clinical utility of lung clearance index in early cystic fibrosis lung disease is not impacted by the number of multiple-breath washout trials
by: Foong, Rachel, et al.
Published: (2018)

Airway infection and Pseudomonas aeruginosa in bronchiectasis (cystic fibrosis and non-cystic fibrosis bronchiectasis)
by: Webb, Karmel
Published: (2022)

Delayed publications of clinical trials in cystic fibrosis
by: Hurley, M.N., et al.
Published: (2011)

Intravenous antibiotics for pulmonary exacerbations in people with cystic fibrosis
by: Hurley, M., et al.
Published: (2015)

Perceptions of Population Cystic Fibrosis Prenatal and Preconception Carrier Screening Among Individuals with Cystic Fibrosis and Their Family Members
by: Maxwell, Susannah, et al.
Published: (2011)

Association of Antibiotics, Airway Microbiome and Inflammation in Infants with Cystic Fibrosis.
by: Pittman, J., et al.
Published: (2017)

Identifying peroxidases and their oxidants in the early pathology of cystic fibrosis.
by: Thomson, E., et al.
Published: (2010)

Infection, inflammation,and lung function decline in infants with cystic fibrosis
by: Pillarisetti, N., et al.
Published: (2011)

METABOLOMIC RESPONSE OF HEALTHY AND CYSTIC FIBROSIS EPITHELIUM TO RHINOVIRUS
by: Agudelo-Romero, P., et al.
Published: (2019)

Cystic fibrosis microbiology: advances in antimicrobial therapy
by: Waters, Valerie, et al.
Published: (2015)

Prophylactic anti-staphylococcal antibiotics for cystic fibrosis
by: Smyth, Alan R., et al.
Published: (2014)

Cost-Effectiveness of Carrier Screening for Cystic Fibrosis in Australia
by: Norman, Richard, et al.
Published: (2012)

Respiratory viral infections in Western Australians with cystic fibrosis
by: Brestovac, Brian, et al.
Published: (2020)

Exhaled breath hydrogen cyanide as a marker of early Pseudomonas aeruginosa infection in children with cystic fibrosis
by: Gilchrist, Francis J., et al.
Published: (2015)

Early respiratory infection is associated with reduced spirometry in children with cystic fibrosis
by: Ramsey, K., et al.
Published: (2014)

Xbox Kinect™ represents high intensity exercise for adults with cystic fibrosis
by: Holmes, H., et al.
Published: (2013)

Impact of lung disease on respiratory impedance in young children with cystic fibrosis
by: Ramsey, K., et al.
Published: (2015)

The association between Staphylococcus aureus and subsequent bronchiectasis in children with cystic fibrosis
by: Caudri, D., et al.
Published: (2018)

Prevention of treatment related adverse effects in cystic fibrosis
by: Jain, Kamini
Published: (2018)

Mitigating the harm caused by Pseudomonas aeruginosa in Cystic Fibrosis
by: Palser, Sally C.
Published: (2024)

POLYMICROBIAL INFECTION AND NEUTROPHILIC DISEASE IN CYSTIC FIBROSIS AIRWAYS
by: Laucirica, D.R., et al.
Published: (2019)

European Cystic Fibrosis Society standards of care: best practice guidelines
by: Smyth, Alan R., et al.
Published: (2014)

Understanding chronic inflammatory diseases in the human lung: the cystic fibrosis and idiopathic pulmonary fibrosis paradigms
by: Liu, Yi-Chia
Published: (2014)

Airway surface liquid pH is not acidic in children with cystic fibrosis
by: Schultz, A., et al.
Published: (2017)

Early detection of lung function abnormalities in young children with cystic fibrosis
by: Gangell, C., et al.
Published: (2012)

Inducible NO synthase expression is low in airway epithelium from young children with cystic fibrosis
by: Moeller, A., et al.
Published: (2006)

Height and Weight fail to detect early signs of malnutrition in children with cystic fibrosis
by: Stapleton, Denise, et al.
Published: (2001)

Understanding the Costs of Care for Cystic Fibrosis: an Analysis by Age and Health State
by: Van Gool, K., et al.
Published: (2013)

Novel approaches to the treatment of Pseudomonas aeruginosa infections in cystic fibrosis
by: Hurley, M.N., et al.
Published: (2012)

Antibiotic strategies for eradicating Pseudomonas aeruginosa in people with cystic fibrosis
by: Langton Hewer, Simon C., et al.
Published: (2014)

sTREM-1 is elevated in cystic fibrosis and correlates with proteases
by: Forrester, D.L., et al.
Published: (2017)

Cost Effectiveness of Screening Individuals With Cystic Fibrosis for Colorectal Cancer
by: Gini, A., et al.
Published: (2018)

Exploring Approaches to Exercise Testing and Training in Adults with Cystic Fibrosis
by: Sawyer, Abbey
Published: (2020)

Cystic fibrosis diagnosis: Impact on mothers of affected Australian children
by: Priddis, Lynn, et al.
Published: (2009)

Pancreatic cystosis: A rare pancreatic manifestation in cystic fibrosis
by: Mohammad A. Wazzan,
Published: (2015)

MINIATURISATION OF AN IN VITRO TRANSMIGRATION MODEL OF NEUTROPHIL RECRUITMENT TO CYSTIC FIBROSIS AIRWAYS
by: Laucirica, D., et al.
Published: (2019)

An official American Thoracic Society workshop report: Optimal lung function tests for monitoring cystic fibrosis, bronchopulmonary dysplasia, and recurrent wheezing in children less than 6 years of age
by: Rosenfeld, M., et al.
Published: (2013)