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

Author:

Edmondson Claire12ORCID,Westrupp Nicole12,Short Christopher12,Seddon Paul3,Olden Catherine3,Wallis Colin4,Brodlie Malcolm56,Baxter Francis6,McCormick Jonathan7,MacFarlane Susan7,Brooker Richard8,Connon Margaret8,Ghayyda Salim9,Blaikie Lesley9,Thursfield Rebecca10ORCID,Brown Lynsey10,Price April11,Fleischer Erin11,Hughes Daniel12,Donnelly Christine12,Rosenthal Mark12,Wallenburg John13ORCID,Brownlee Keith14,Alton Eric W. F. W.12,Bush Andrew12,Davies Jane C.12ORCID

Affiliation:

1. NHLI, Imperial College London UK

2. Royal Brompton Hospital Part of Guy's & St Thomas' NHS Trust London UK

3. Royal Alexandra Children's Hospital Brighton UK

4. Great Ormond Street Hospital CF Unit London UK

5. Translational and Clinical Research Institute, Faculty of Medical Sciences Newcastle University Newcastle upon Tyne UK

6. Great North Children's Hospital Newcastle upon Tyne Hospitals NHS Foundation Trust Newcastle upon Tyne UK

7. Ninewells Hospital Dundee UK

8. Royal Aberdeen Children's Hospital Aberdeen UK

9. Raigmore Hospital, Inverness UK

10. Alder Hey Children's NHS Foundation Trust Liverpool UK

11. Dept of Pediatrics London Health Sciences Centre London Ontario Canada

12. IWK Health Centre Halifax Nova Scotia Canada

13. Cystic Fibrosis Canada Toronto Ontario Canada

14. Cystic Fibrosis Trust UK London UK

Abstract

AbstractBackgroundHandheld 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.MethodsData 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.ResultsSixty‐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.ConclusionIn 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.

Funder

Cystic Fibrosis Trust

Cystic Fibrosis Canada

Publisher

Wiley

Subject

Pulmonary and Respiratory Medicine,Pediatrics, Perinatology and Child Health

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