Remote monitoring of spirometry and oximetry in patients with connective tissue disease related interstitial lung disease: a prospective observational cohort study

Remote monitoring of forced vital capacity (FVC) and oximetry (SpO2) in patients with idiopathic pulmonary fibrosis (IPF) is emerging as an adjunct to routine in-person ambulatory care. Patients with connective tissue diseases (CTD) commonly have impaired hand function, diminished oral aperture and Raynaud's phenomenon, which can uniquely impair the user’s ability to use these devices. We aimed to assess the acceptability, usability and adherence to home monitoring in patients with CTD associated interstitial lung disease (CTD-ILD) compared to patients with IPF. Participants were recruited to a prospective observational cohort study (NCT06702228), provided with a portable handheld spirometer and finger pulse oximeter connected to a smart phone application (app), received training in their use, asked to use these at least once a week, and were reviewed at 6-months. Ninety-seven participants completed the 6-month study. Participants in the CTD-ILD group were slightly younger than those with IPF with a mean and standard deviation (SD) of 62.44 (15.25) compared to 70.21 (9.39) years (p = 0.005). The number of days the devices were used was lower in the CTD-ILD (69.2 versus 99.4, p = 0.028). In line with study instructions, there was no significant difference in weekly adherence with FVC or SpO2 measurement (71.5% versus 75%, p = 0.65). We found a strong correlation between home and hospital-based FVC (r = 0.76, p < 0.0001). Both groups reported finding the devices and app easy to use (77% versus 72%, p = 0.65), but more participants with CTD-ILD reported difficulty obtaining SpO2 readings compared to those with IPF (33.33% versus 12.77%, p = 0.02). Six (16.7%) participants from the CTD-ILD group experienced difficulty using the devices due to hand function impairment (p = 0.004), 3 (8.3%) were unable to use a finger probe at all and required an ear oximeter. We found no differences in the correlation of FVC adherence with age, ILD-GAP score, or participant reported symptom scores between the groups. While participants with CTD-ILD had lower device use than those with IPF, they did have high adherence, satisfaction and reported ease of use despite Raynaud's phenomenon and impaired hand function. Therefore, remote monitoring has potential as an adjunct to routine care in CTD-ILD.

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Publication Details

Journal
BMC Pulmonary Medicine
Published
2025-11-20
DOI
https://doi.org/10.1186/s12890-025-03966-6
Primary Topic
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
Type
article
Field-Weighted Citation Impact
0.00

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article

Remote monitoring of spirometry and oximetry in patients with connective tissue disease related interstitial lung disease: a prospective observational cohort study

Garrett Greene, Ross Morgan, Killian Hurley, Wan Lin Ng et al.
BMC Pulmonary Medicine
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
article

Remote monitoring of spirometry and oximetry in patients with connective tissue disease related interstitial lung disease: a prospective observational cohort study

Garrett Greene, Ross Morgan, Killian Hurley, Wan Lin Ng, Donough Howard, Imran Sulaiman, Laura Durcan, Aoife Carolan
article en

Abstract

Remote monitoring of forced vital capacity (FVC) and oximetry (SpO2) in patients with idiopathic pulmonary fibrosis (IPF) is emerging as an adjunct to routine in-person ambulatory care. Patients with connective tissue diseases (CTD) commonly have impaired hand function, diminished oral aperture and Raynaud's phenomenon, which can uniquely impair the user’s ability to use these devices. We aimed to assess the acceptability, usability and adherence to home monitoring in patients with CTD associated interstitial lung disease (CTD-ILD) compared to patients with IPF. Participants were recruited to a prospective observational cohort study (NCT06702228), provided with a portable handheld spirometer and finger pulse oximeter connected to a smart phone application (app), received training in their use, asked to use these at least once a week, and were reviewed at 6-months. Ninety-seven participants completed the 6-month study. Participants in the CTD-ILD group were slightly younger than those with IPF with a mean and standard deviation (SD) of 62.44 (15.25) compared to 70.21 (9.39) years (p = 0.005). The number of days the devices were used was lower in the CTD-ILD (69.2 versus 99.4, p = 0.028). In line with study instructions, there was no significant difference in weekly adherence with FVC or SpO2 measurement (71.5% versus 75%, p = 0.65). We found a strong correlation between home and hospital-based FVC (r = 0.76, p < 0.0001). Both groups reported finding the devices and app easy to use (77% versus 72%, p = 0.65), but more participants with CTD-ILD reported difficulty obtaining SpO2 readings compared to those with IPF (33.33% versus 12.77%, p = 0.02). Six (16.7%) participants from the CTD-ILD group experienced difficulty using the devices due to hand function impairment (p = 0.004), 3 (8.3%) were unable to use a finger probe at all and required an ear oximeter. We found no differences in the correlation of FVC adherence with age, ILD-GAP score, or participant reported symptom scores between the groups. While participants with CTD-ILD had lower device use than those with IPF, they did have high adherence, satisfaction and reported ease of use despite Raynaud's phenomenon and impaired hand function. Therefore, remote monitoring has potential as an adjunct to routine care in CTD-ILD.

BMC Pulmonary MedicineVol. 25(1)
University College Dublin (IE), Royal College of Surgeons in Ireland (IE), Beaumont Hospital (IE)
Health Research Board, Royal College of Surgeons in Ireland, European Commission
Openalex Percentile: Top 49%
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
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