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Updated: Sep 30, 2025

Home-Based Prescribed Pulmonary Exercise in Patients with Stable Chronic Obstructive Pulmonary Disease
Published on: August 24, 2019
Telehealth application of an ultrasonic home spirometer
Michael Doumit1,2, Rianna Ledwos3, Leanne Plush3
1Department of Health Sciences, Macquarie University, Sydney, New South Wales, Australia michael.doumit@mq.edu.au.
Insights
This study validated a personal ultrasonic spirometer for home use, finding it reliable for telehealth sessions but advising caution when comparing results with lab equipment.
Area of Science:
- Pulmonary Function Testing
- Medical Device Validation
- Pediatric Respiratory Health
Background:
- Spirometry is crucial for diagnosing and monitoring respiratory conditions.
- Home-based spirometry can improve patient access and adherence.
- Personal ultrasonic spirometers offer a portable solution for remote monitoring.
Purpose of the Study:
- To assess the validity and home usability of a personal ultrasonic spirometer.
- To evaluate the performance of children using the device during telehealth appointments.
Main Methods:
- Children performed spirometry using both laboratory equipment and a personal ultrasonic spirometer.
- Supervised telehealth sessions were conducted to assess home use.
- Intraclass correlation coefficient (ICC) and Bland-Altman analysis were used for validity assessment.
Main Results:
- High ICC values (0.991 for FEV1, 0.989 for FVC) indicated excellent between-device reliability.
- Bland-Altman analysis showed wide limits of agreement, suggesting caution for interchangeable use with lab equipment.
- 89% of supervised telehealth spirometry sessions were deemed acceptable.
Conclusions:
- The personal ultrasonic spirometer demonstrates excellent reliability for between-device measurements.
- While suitable for telehealth applications, caution is advised when comparing its results directly with traditional laboratory spirometry.
- The device shows promise for remote monitoring of pediatric respiratory health.
Objective:
To investigate the validity and home use of a personal ultrasonic spirometer.
Methods:
Supervised spirometry was performed using laboratory equipment and a personal ultrasonic spirometer. In addition, the ability of children to perform acceptable spirometry during supervised telehealth appointments at home was assessed.
Results:
59 children completed spirometry on both devices. There was high between-device intraclass correlation coefficient (ICC) for forced expiratory volume in 1 s (FEV1) and forced vital capacity (FVC): ICC 0.991 (95% CI 0.985 to 0.995) and 0.989 (95% CI 0.981 to 0.993), respectively. Bland-Altman analysis revealed mean bias and limits of agreement of -0.01 (-0.22 to 0.24) L for FEV1 and -0.02 (-0.30 to 0.33) L for FVC. 125 of 140 (89%) supervised telehealth spirometry sessions were acceptable.
Conclusion:
There was excellent reliability in between-device measurements; however, the limits of agreement were wide. Therefore, caution is needed if the device is used interchangeably with laboratory equipment. High success rates of telehealth spirometry sessions indicate the device is suitable for this application.
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