Lung clearance index-triggered intervention in children with cystic fibrosis – A randomised pilot study

Research output: Contribution to journalJournal articleResearchpeer-review

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Lung clearance index-triggered intervention in children with cystic fibrosis – A randomised pilot study. / Voldby, Christian; Green, Kent; Kongstad, Thomas; Ring, Astrid Madsen; Sandvik, Rikke Mulvad; Skov, Marianne; Buchvald, Frederik; Pressler, Tacjana; Nielsen, Kim Gjerum.

In: Journal of Cystic Fibrosis, Vol. 19, No. 6, 2020, p. 934-941.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Voldby, C, Green, K, Kongstad, T, Ring, AM, Sandvik, RM, Skov, M, Buchvald, F, Pressler, T & Nielsen, KG 2020, 'Lung clearance index-triggered intervention in children with cystic fibrosis – A randomised pilot study', Journal of Cystic Fibrosis, vol. 19, no. 6, pp. 934-941. https://doi.org/10.1016/j.jcf.2020.06.010

APA

Voldby, C., Green, K., Kongstad, T., Ring, A. M., Sandvik, R. M., Skov, M., Buchvald, F., Pressler, T., & Nielsen, K. G. (2020). Lung clearance index-triggered intervention in children with cystic fibrosis – A randomised pilot study. Journal of Cystic Fibrosis, 19(6), 934-941. https://doi.org/10.1016/j.jcf.2020.06.010

Vancouver

Voldby C, Green K, Kongstad T, Ring AM, Sandvik RM, Skov M et al. Lung clearance index-triggered intervention in children with cystic fibrosis – A randomised pilot study. Journal of Cystic Fibrosis. 2020;19(6):934-941. https://doi.org/10.1016/j.jcf.2020.06.010

Author

Voldby, Christian ; Green, Kent ; Kongstad, Thomas ; Ring, Astrid Madsen ; Sandvik, Rikke Mulvad ; Skov, Marianne ; Buchvald, Frederik ; Pressler, Tacjana ; Nielsen, Kim Gjerum. / Lung clearance index-triggered intervention in children with cystic fibrosis – A randomised pilot study. In: Journal of Cystic Fibrosis. 2020 ; Vol. 19, No. 6. pp. 934-941.

Bibtex

@article{f0df91ad7ac4479095ec49dc7752e71f,
title = "Lung clearance index-triggered intervention in children with cystic fibrosis – A randomised pilot study",
abstract = "Hypothesis: Using increase in the lung clearance index (LCI) as a trigger for bronchoalveolar lavage (BAL) and associated antimicrobial treatment might benefit clinical outcomes in children with cystic fibrosis (CF). Methods: A 2-year, longitudinal, interventional, randomized, controlled pilot study with quarterly visits in 5–18 years old children with CF. LCI and z-scores for the forced expired volume in 1 s (zFEV1) and body mass index (zBMI) were obtained at every visit, CF Questionnaire-revised (CFQ-R) yearly and BAL and chest computed tomography at first and last visit. Children in the intervention group had BAL performed if LCI increased >1 unit from a fixed baseline value established at first visit. If the presence of a pathogen was documented in the BAL fluid, treatment was initiated/altered accordingly. Results: Twenty-nine children with CF were randomized to the control (n = 14) and intervention group (n = 15). The median (interquartile range) number of BAL procedures per child was 2.5 (2.0; 3.0) and 6.0 (4.0; 7.0) in the control and intervention group, respectively. There was no significant difference between groups in slope for the primary outcome LCI; difference was 0.21 (95% confidence interval: -0.45; 0.88) units/year. Likewise, there was no significant difference between groups in slope for the secondary outcomes zFEV1, zBMI, CFQ-R respiratory symptom score and the proportion of total disease and trapped air on chest computed tomography. Conclusions: LCI-triggered BAL and associated antimicrobial treatment did not benefit clinical outcomes in a small cohort of closely monitored school-age children with CF.",
keywords = "Bronchoalveolar lavage (BAL), Computed tomography, Cystic fibrosis, Multiple breath washout, Paediatric lung function testing",
author = "Christian Voldby and Kent Green and Thomas Kongstad and Ring, {Astrid Madsen} and Sandvik, {Rikke Mulvad} and Marianne Skov and Frederik Buchvald and Tacjana Pressler and Nielsen, {Kim Gjerum}",
year = "2020",
doi = "10.1016/j.jcf.2020.06.010",
language = "English",
volume = "19",
pages = "934--941",
journal = "Journal of Cystic Fibrosis",
issn = "1569-1993",
publisher = "Elsevier",
number = "6",

}

RIS

TY - JOUR

T1 - Lung clearance index-triggered intervention in children with cystic fibrosis – A randomised pilot study

AU - Voldby, Christian

AU - Green, Kent

AU - Kongstad, Thomas

AU - Ring, Astrid Madsen

AU - Sandvik, Rikke Mulvad

AU - Skov, Marianne

AU - Buchvald, Frederik

AU - Pressler, Tacjana

AU - Nielsen, Kim Gjerum

PY - 2020

Y1 - 2020

N2 - Hypothesis: Using increase in the lung clearance index (LCI) as a trigger for bronchoalveolar lavage (BAL) and associated antimicrobial treatment might benefit clinical outcomes in children with cystic fibrosis (CF). Methods: A 2-year, longitudinal, interventional, randomized, controlled pilot study with quarterly visits in 5–18 years old children with CF. LCI and z-scores for the forced expired volume in 1 s (zFEV1) and body mass index (zBMI) were obtained at every visit, CF Questionnaire-revised (CFQ-R) yearly and BAL and chest computed tomography at first and last visit. Children in the intervention group had BAL performed if LCI increased >1 unit from a fixed baseline value established at first visit. If the presence of a pathogen was documented in the BAL fluid, treatment was initiated/altered accordingly. Results: Twenty-nine children with CF were randomized to the control (n = 14) and intervention group (n = 15). The median (interquartile range) number of BAL procedures per child was 2.5 (2.0; 3.0) and 6.0 (4.0; 7.0) in the control and intervention group, respectively. There was no significant difference between groups in slope for the primary outcome LCI; difference was 0.21 (95% confidence interval: -0.45; 0.88) units/year. Likewise, there was no significant difference between groups in slope for the secondary outcomes zFEV1, zBMI, CFQ-R respiratory symptom score and the proportion of total disease and trapped air on chest computed tomography. Conclusions: LCI-triggered BAL and associated antimicrobial treatment did not benefit clinical outcomes in a small cohort of closely monitored school-age children with CF.

AB - Hypothesis: Using increase in the lung clearance index (LCI) as a trigger for bronchoalveolar lavage (BAL) and associated antimicrobial treatment might benefit clinical outcomes in children with cystic fibrosis (CF). Methods: A 2-year, longitudinal, interventional, randomized, controlled pilot study with quarterly visits in 5–18 years old children with CF. LCI and z-scores for the forced expired volume in 1 s (zFEV1) and body mass index (zBMI) were obtained at every visit, CF Questionnaire-revised (CFQ-R) yearly and BAL and chest computed tomography at first and last visit. Children in the intervention group had BAL performed if LCI increased >1 unit from a fixed baseline value established at first visit. If the presence of a pathogen was documented in the BAL fluid, treatment was initiated/altered accordingly. Results: Twenty-nine children with CF were randomized to the control (n = 14) and intervention group (n = 15). The median (interquartile range) number of BAL procedures per child was 2.5 (2.0; 3.0) and 6.0 (4.0; 7.0) in the control and intervention group, respectively. There was no significant difference between groups in slope for the primary outcome LCI; difference was 0.21 (95% confidence interval: -0.45; 0.88) units/year. Likewise, there was no significant difference between groups in slope for the secondary outcomes zFEV1, zBMI, CFQ-R respiratory symptom score and the proportion of total disease and trapped air on chest computed tomography. Conclusions: LCI-triggered BAL and associated antimicrobial treatment did not benefit clinical outcomes in a small cohort of closely monitored school-age children with CF.

KW - Bronchoalveolar lavage (BAL)

KW - Computed tomography

KW - Cystic fibrosis

KW - Multiple breath washout

KW - Paediatric lung function testing

U2 - 10.1016/j.jcf.2020.06.010

DO - 10.1016/j.jcf.2020.06.010

M3 - Journal article

C2 - 32576447

AN - SCOPUS:85086744942

VL - 19

SP - 934

EP - 941

JO - Journal of Cystic Fibrosis

JF - Journal of Cystic Fibrosis

SN - 1569-1993

IS - 6

ER -

ID: 260252862