Unsupervised home spirometry is not equivalent to supervised clinic spirometry in children and young people with cystic fibrosis: Results from the CLIMB-CF study

Claire Edmondson (Lead / Corresponding author), Nicole Westrupp, Christopher Short, Paul Seddon, Catherine Olden, Colin Wallis, Malcolm Brodlie, Francis Baxter, Jonathan McCormick, Susan MacFarlane, Richard Brooker, Margaret Connon, Salim Ghayyda, Lesley Blaikie, Rebecca Thursfield, Lynsey Brown, April Price, Erin Fleischer, Daniel Hughes, Christine DonnellyMark Rosenthal, John Wallenburg, Keith Brownlee, Eric W. F. W. Alton, Andrew Bush, Jane C. Davies

Research output: Contribution to journalArticlepeer-review

3 Citations (Scopus)
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Abstract

Background: Handheld spirometry allows monitoring of lung function at home, of particular importance during the COVID-19 pandemic. Pediatric studies are unclear on whether values are interchangeable with traditional, clinic-based spirometry. We aimed to assess differences between contemporaneous, home (unsupervised) and clinic (supervised) spirometry and the variability of the former. The accuracy of the commercially available spirometer used in the study was also tested.

Methods: Data from participants in the Clinical Monitoring and Biomarkers to stratify severity and predict outcomes in children with cystic fibrosisc (CLIMB-CF) Study aged ≥ 6 years who had paired (±1 day) clinic and home forced expiratory volume in 1 s (FEV1 ) readings were analyzed. Variability during clinical stability over 6-months was assessed. Four devices from Vitalograph were tested using 1 and 3 L calibration syringes.

Results: Sixty-seven participants (median [interquartile range] age 10.7 [7.6-13.9] years) provided home and clinic FEV1 data pairs. The mean (SD) FEV1 % bias was 6.5% [±8.2%]) with wide limits of agreement (-9.6% to +22.7%); 76.2% of participants recorded lower results at home. Coefficient of variation of home FEV1 % during stable periods was 9.9%. Data from the testing of the handheld device used in CLIMB-CF showed a potential underread.

Conclusion: In children and adolescents, home spirometry using hand-held equipment cannot be used interchangeably with clinic spirometry. Home spirometry is moderately variable during clinical stability. New handheld devices underread, particularly at lower volumes of potential clinical significance for smaller patients; this suggests that supervision does not account fully for the discrepancy. Opportunities should be taken to obtain dual device measurements in clinic, so that trend data from home can be utilized more accurately.

Original languageEnglish
Pages (from-to)2871-2880
Number of pages10
JournalPediatric Pulmonology
Volume58
Issue number10
Early online date28 Jul 2023
DOIs
Publication statusPublished - Oct 2023

Keywords

  • cystic fibrosis
  • remote monitoring
  • remote spirometry
  • unsupervised spirometry

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