Volume 55, Issue 3 pp. 649-653
ORIGINAL ARTICLE

The utility of moment ratios and abbreviated endpoints of the multiple breath washout test in preschool children with cystic fibrosis

Michelle Shaw MSc

Michelle Shaw MSc

Translational Medicine Program, Research Institute, Hospital for Sick Children, Toronto, Ontario, Canada

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Martinus C. Oppelaar BSc

Martinus C. Oppelaar BSc

Translational Medicine Program, Research Institute, Hospital for Sick Children, Toronto, Ontario, Canada

Department of Paediatric Pulmonology, Radboud University Medical Center, Amalia Children's Hospital, Nijmegen, The Netherlands

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Renee Jensen RRT

Renee Jensen RRT

Translational Medicine Program, Research Institute, Hospital for Sick Children, Toronto, Ontario, Canada

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Sanja Stanojevic PhD

Sanja Stanojevic PhD

Translational Medicine Program, Research Institute, Hospital for Sick Children, Toronto, Ontario, Canada

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Stephanie D. Davis MD

Stephanie D. Davis MD

Division of Pediatric Pulmonology, Department of Pediatrics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina

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George Retsch-Bogart MD

George Retsch-Bogart MD

Division of Pediatric Pulmonology, Department of Pediatrics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina

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Felix A. Ratjen MD

Corresponding Author

Felix A. Ratjen MD

Division of Respiratory Medicine, Department of Pediatrics, Hospital for Sick Children, Toronto, Ontario, Canada

Correspondence Felix A. Ratjen, Research Institute, Hospital for Sick Children; Division of Respiratory Medicine, Department of Pediatrics, Hospital for Sick Children, 555 University Avenue, Toronto, ON M5G 1X8, Canada.

Email: [email protected]

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First published: 03 January 2020
Citations: 10

Abstract

Background

The multiple breath washout (MBW) test may be most useful in tracking disease progression over time to inform treatment decisions. In the clinical setting, alternative outcomes, which can be obtained quickly and easily, may facilitate interpretation of clinically relevant changes in lung function.

Methods

In this secondary analysis of data from 78 cystic fibrosis (CF) and 72 healthy control (HC) subjects between the ages of 2.6 and 5.9 years, MBW was performed at enrollment, 1, 3, 6, 9, and 12 months, as well as during symptomatic visits using the Exhalyzer D (EcoMedics AG, Duernten, Switzerland). The lung clearance index, LCI2.5, was compared to moment ratios (M1/M0 and M2/M0) at the standard cutoff (1/40th of starting tracer gas concentration) as well as LCI5 and moment ratios at 1/20th of the starting concentration (M1/M0 at LCI5, and M2/M0 at LCI5).

Results

All outcomes were able to distinguish between health and disease. LCI5 reduced testing time by 40% and increased feasibility by more than 10%. The limits of biological reproducibility in healthy children were similar between LCI2.5 (15%), LCI5 (12%), M1/M0 at LCI2.5 (14%), and M1/M0 at LCI5 (12%), but markedly larger for M2/M0 at LCI2.5 (30%) and M2/M0 at LCI5 (25%). Each outcome deteriorated significantly with worsening pulmonary symptoms, the magnitude of deterioration was greatest for M2/M0.

Conclusions

In preschool children with CF, LCI5 was more feasible to obtain and track disease progression. The second moment ratio was most sensitive to pulmonary symptoms, but had the greatest variability both within and between subjects.

CONFLICT OF INTERESTS

The authors declare that there are no conflict of interests.

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