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The Feasibility and Validity of Home Spirometry for People with Cystic Fibrosis

Is It Comparable to Spirometry in the Clinic

Bibliographic Data

ID15713433
AuthorsAthina Sopiadou (Aristotle University of Thessaloniki), Maria Gioulvanidou (Aristotle University of Thessaloniki), Christos Kogias (0000-0002-0864-9985, Aristotle University of Thessaloniki), Elissavet-Anna Chrysochoou (Aristotle University of Thessaloniki), Ioustini Kalaitzopoulou (0009-0001-7614-038X, Aristotle University of Thessaloniki), Elpis Hatziagorou (0000-0001-9505-2054, Aristotle University of Thessaloniki, corresponding author)
Year2025
Volume12
Issue3
Pages277-277
Publication date2025-02-25
Open AccessYes
TypeARTICLE
VenueChildren (JOURNAL)
Journal identifiersISSN: 2227-9067 • E-ISSN: 2227-9067
PublisherMultidisciplinary Digital Publishing Institute (PUBLISHER • CH)
DOI10.3390/children12030277
PMID40150559
OpenAlexW4407922573
LanguageEN
References cited35

Background/Objectives : Home spirometry allows people with cystic fibrosis (CF) to monitor their lung function from home. However, there are concerns about its feasibility and validity compared to traditional clinic spirometry. The aim of this study was to evaluate the feasibility and validity of telehealth spirometry for patients with CF living in a regional setting. Methods : This retrospective study included forty-eight people with cystic fibrosis (pwCF) aged 6-33 years. Participants performed home spirometry using a portable flow sensor spirometer over a one-year period, without supervision. Spirometry readings from portable spirometers were compared with the nearest in-clinic spirometry using the intra-correlation coefficient (ICC) and Bland-Altman plots. Data were collected over a period of one year, with regular intervals of measurements. Results : In 427 of the 877 (48.6%) attempted sessions, successful spirometry at home was recorded. Although we showed good reliability between at-home and in-clinic measurements using the Bland-Altman plots and intraclass correlation co-efficient (ICC) (values ranged from 0.76 to 0.88), analysis of the 117 pairs of at-home and in-clinic spirometries showed that mean differences of forced expiratory volume in the 1st sec (FEV1) and forced vital capacity (FVC) obtained at home (both in liter and z-score) had, on average, lower values than the corresponding values at the clinic. Conclusions : Home-based telehealth spirometry is feasible among pwCF and provides advantages, especially for those from remote or secluded areas. However, lower values in FVC and FEV1 obtained through home spirometry should not be used interchangeably with clinic values

Asthma · Cystic fibrosis · Diffusing capacity · Intraclass correlation · Lung · Lung function · Physical therapy · Psychometrics · Spirometer · Spirometry · Vital capacity · Chronic Obstructive Pulmonary Disease (COPD) Research · Cystic Fibrosis Research Advances · Medicine · Neonatal Respiratory Health Research · Internal Medicine

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  • Standardisation of spirometry

    Martin R Miller, J Hankinson et al.•European Respiratory Journal•2005

  • Statistical Methods for Assessing Agreement Between Two Methods of Clinical Measurement

    Open Access•J Martin Bland, DouglasG Altman•The Lancet•1986

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