Telehealth spirometry for children with cystic fibrosis
Karla Logie1, Liam Welsh2, Sarath C Ranganathan1
1Respiratory Medicine, Royal Childrens Hospital Melbourne, Parkville, Victoria, Australia.
Insights
Telehealth spirometry is feasible for children with cystic fibrosis (CF) in regional areas. This remote monitoring approach supports CF care during home admissions and outpatient visits, saving significant travel time.
Area of Science:
- Pediatric Pulmonology
- Digital Health
- Respiratory Medicine
Background:
- Children with cystic fibrosis (CF) often require regular spirometry.
- Access to specialized respiratory care can be challenging for children in regional settings.
- Traditional spirometry necessitates frequent hospital visits, posing logistical and time burdens.
Purpose of the Study:
- To evaluate the feasibility of telehealth spirometry for pediatric patients with CF living in regional areas.
- To assess the effectiveness of remote spirometry in supporting ongoing CF care.
- To determine the impact of telehealth spirometry on reducing patient travel burden.
Main Methods:
- A feasibility study involving children aged 7-17 years with CF.
- Home-based spirometry assessments using SpiroUSB devices provided to families.
- Data transmission from home to a central pediatric hospital for analysis.
- Adherence to American Thoracic Society/European Respiratory Society spirometry criteria.
Main Results:
- High success rate (93%) in telehealth spirometry sessions.
- Successful implementation in children residing a median of 238 km from the hospital.
- Significant travel time savings averaging 5 hours and 34 minutes per hospital visit.
- Feasibility demonstrated across various home monitoring scenarios.
Conclusions:
- Home-based telehealth spirometry is a viable option for children with CF in remote locations.
- This technology can effectively support cystic fibrosis care teams during home admissions and outpatient monitoring.
- Telehealth spirometry enhances patient access to care and reduces the burden of travel for regional families.
Aim:
We assessed the feasibility of telehealth spirometry assessments for children with cystic fibrosis (CF) living in a regional setting.
Method:
Patients with acceptable computer hardware at home were provided with a SpiroUSB (Vyaire) spirometer. Spirometry was performed during 'home admissions' or for ongoing home monitoring in children living outside metropolitan Melbourne. At the end of the session, the family forwarded the data to the Royal Children's Hospital, Melbourne.
Results:
Twenty-two patients aged 7 to 17 years participated, with spirometry successful in 55 of 59 (93%) attempted sessions according to American Thoracic Society/European Respiratory Society criteria. The median distance between the subject's home and the hospital was 238 km (range 62-537 km) which equated to a travel time saving of 5 hours and 34 min per hospital visit.
Conclusion:
Home-based telehealth spirometry is feasible in children with CF and can support the CF team during home-based admissions and for ongoing outpatient monitoring.
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