Literature DB >> 22888105

Practicability of nitrogen multiple-breath washout measurements in a pediatric cystic fibrosis outpatient setting.

Florian Singer1, Elisabeth Kieninger, Chiara Abbas, Sophie Yammine, Oliver Fuchs, Elena Proietti, Nicolas Regamey, Carmen Casaulta, Urs Frey, Philipp Latzin.   

Abstract

BACKGROUND: Although lung clearance index (LCI) is a sensitive indicator of mild cystic fibrosis (CF) lung disease, it is rarely measured due to lengthy protocols and the commercial unavailability of multiple-breath washout (MBW) setups and tracer gases. We used a newly validated, commercially available nitrogen (N2 ) MBW setup to assess success rate, duration, and variability of LCI within a 20 min timeframe, during clinical routine. We also evaluated the relationship between LCI and other clinical markers of CF lung disease.
METHODS: One hundred thirty six children (83 with CF) between 4 and 16 years were studied in a pediatric CF outpatient setting. One hundred eighteen out of 136 children were naïve to MBW. Within 20 min, each child was trained, N2 MBW was performed, and LCI was analyzed. We assessed intra- and between-test reproducibility in a subgroup of children.
RESULTS: At least one LCI was feasible in 123 (90%) children, with a mean (range) of 3.3 (1.2-6.4) min per test. Two or more measurements were feasible in 56 (41%) children. Comparing LCI in CF versus controls, LCI mean (SD) was 12.0 (3.9) versus 6.1 (0.9), and the intra- and inter-test coefficient of repeatability was 1.00 versus 0.81 and 0.96 versus 0.62, respectively. LCI was correlated with spirometry, blood gases, and Pseudomonas aeruginosa infection.
CONCLUSIONS: Using available N2 MBW equipment, LCI measurements are practical and fast in children. LCI is correlated with markers of CF lung disease. Longer timeframes would be required for triplicate N2 MBW tests in inexperienced children.
Copyright © 2012 Wiley Periodicals, Inc.

Entities:  

Keywords:  children; cystic fibrosis; efficiency; reproducibility; respiratory function test

Mesh:

Substances:

Year:  2012        PMID: 22888105     DOI: 10.1002/ppul.22651

Source DB:  PubMed          Journal:  Pediatr Pulmonol        ISSN: 1099-0496


  21 in total

1.  A simple method to reconstruct the molar mass signal of respiratory gas to assess small airways with a double-tracer gas single-breath washout.

Authors:  Johannes Port; Ziran Tao; Annika Junger; Christoph Joppek; Philipp Tempel; Kim Husemann; Florian Singer; Philipp Latzin; Sophie Yammine; Joachim H Nagel; Martin Kohlhäufl
Journal:  Med Biol Eng Comput       Date:  2017-03-29       Impact factor: 2.602

2.  Multiple-Breath Washout as a Lung Function Test in Cystic Fibrosis. A Cystic Fibrosis Foundation Workshop Report.

Authors:  Padmaja Subbarao; Carlos Milla; Paul Aurora; Jane C Davies; Stephanie D Davis; Graham L Hall; Sonya Heltshe; Philipp Latzin; Anders Lindblad; Jessica E Pittman; Paul D Robinson; Margaret Rosenfeld; Florian Singer; Tim D Starner; Felix Ratjen; Wayne Morgan
Journal:  Ann Am Thorac Soc       Date:  2015-06

3.  Lung clearance index as an outcome measure for clinical trials in young children with cystic fibrosis. A pilot study using inhaled hypertonic saline.

Authors:  Padmaja Subbarao; Sanja Stanojevic; Meghan Brown; Renee Jensen; Margaret Rosenfeld; Stephanie Davis; Lyndia Brumback; Per Gustafsson; Felix Ratjen
Journal:  Am J Respir Crit Care Med       Date:  2013-08-15       Impact factor: 21.405

4.  Lumacaftor/Ivacaftor in Patients Aged 6-11 Years with Cystic Fibrosis and Homozygous for F508del-CFTR.

Authors:  Carlos E Milla; Felix Ratjen; Gautham Marigowda; Fang Liu; David Waltz; Margaret Rosenfeld
Journal:  Am J Respir Crit Care Med       Date:  2017-04-01       Impact factor: 21.405

5.  Impact of Software Settings on Multiple-Breath Washout Outcomes.

Authors:  Selina Summermatter; Florian Singer; Philipp Latzin; Sophie Yammine
Journal:  PLoS One       Date:  2015-07-13       Impact factor: 3.240

6.  Ivacaftor in a young boy with the rare gating mutation S549R--use of lung clearance index to track progress: a case report.

Authors:  Nina Lenherr; Marco Lurà; Daniel Trachsel; Philipp Latzin; Juerg Hammer
Journal:  BMC Pulm Med       Date:  2015-10-16       Impact factor: 3.317

7.  The effect of time-of-day and chest physiotherapy on multiple breath washout measures in children with clinically stable cystic fibrosis.

Authors:  Christian Voldby; Kent Green; Susanne Rosthøj; Thomas Kongstad; Lue Philipsen; Frederik Buchvald; Marianne Skov; Tania Pressler; Per Gustafsson; Kim G Nielsen
Journal:  PLoS One       Date:  2018-01-10       Impact factor: 3.240

8.  Closed circuit rebreathing to achieve inert gas wash-in for multiple breath wash-out.

Authors:  Alex R Horsley; Katherine O'Neill; Damian G Downey; J Stuart Elborn; Nicholas J Bell; Jaclyn Smith; John Owers-Bradley
Journal:  ERJ Open Res       Date:  2016-01-22

Review 9.  Quantification of Phenotypic Variability of Lung Disease in Children with Cystic Fibrosis.

Authors:  Mirjam Stahl; Eva Steinke; Marcus A Mall
Journal:  Genes (Basel)       Date:  2021-05-25       Impact factor: 4.096

10.  Multiple breath nitrogen washout: a feasible alternative to mass spectrometry.

Authors:  Renee Jensen; Sanja Stanojevic; Karyn Gibney; Juliana Giraldo Salazar; Per Gustafsson; Padmaja Subbarao; Felix Ratjen
Journal:  PLoS One       Date:  2013-02-15       Impact factor: 3.240

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