Managed Reimbursement of Continuous Glucose Monitoring Sensors in Ireland: Year One Review
Author(s)
Alma Hanevy, BSc Pharm, Fiona McGahan, BSc Pharm, Stephen Doran, BSc Pharm MSc, Claire Gorry, BSc Pharm PhD, Michael Barry, MD PhD.
HSE Medicines Management Programme, Dublin, Ireland.
HSE Medicines Management Programme, Dublin, Ireland.
OBJECTIVES: Continuous glucose monitoring (CGM) systems provide an alternative approach to self-monitoring of blood glucose. From 2021 to 2023, Ireland’s payer, the Health Service Executive (HSE), experienced a significant increase in expenditure on CGM sensors, from €23.78 million in 2021 (6,000 patients) to €55.72 million in 2023 (16,900 patients). Following a rapid health technology assessment (HTA) on the use of CGM systems in adults with type 1 diabetes (T1DM), an online reimbursement application system (RAS) for CGM sensors was introduced on 1 December 2023. This study evaluates the impact of the RAS as a cost containment measure for CGM sensors during its first year of implementation.
METHODS: Data pertaining to individual reimbursement applications was extracted from the online RAS from 1 December 2023 and 30 November 2024. Utilisation and expenditure data were extracted from the national pharmacy claims database. Data was compiled and analysed in Microsoft Excel™.
RESULTS: A total of 4,552 applications were submitted for reimbursement approval. The overall approval rate was 65% (n=2,949), which represents an additional investment of approximately €9 million across the first full year of reimbursement support for eligible patients with T1DM. The avoided costs estimated from negative reimbursement recommendations amount to over €1.77 million. This estimate is based only on applications submitted via the RAS and the true avoided cost is likely much higher.
CONCLUSIONS: In its first year of implementation, the RAS has supported almost 3,000 additional patients with T1DM to access CGM sensor technology, whilst containing expenditure and providing budgetary oversight for the payer.
METHODS: Data pertaining to individual reimbursement applications was extracted from the online RAS from 1 December 2023 and 30 November 2024. Utilisation and expenditure data were extracted from the national pharmacy claims database. Data was compiled and analysed in Microsoft Excel™.
RESULTS: A total of 4,552 applications were submitted for reimbursement approval. The overall approval rate was 65% (n=2,949), which represents an additional investment of approximately €9 million across the first full year of reimbursement support for eligible patients with T1DM. The avoided costs estimated from negative reimbursement recommendations amount to over €1.77 million. This estimate is based only on applications submitted via the RAS and the true avoided cost is likely much higher.
CONCLUSIONS: In its first year of implementation, the RAS has supported almost 3,000 additional patients with T1DM to access CGM sensor technology, whilst containing expenditure and providing budgetary oversight for the payer.
Conference/Value in Health Info
2025-11, ISPOR Europe 2025, Glasgow, Scotland
Value in Health, Volume 28, Issue S2
Code
HPR135
Topic
Health Policy & Regulatory, Health Service Delivery & Process of Care
Topic Subcategory
Public Spending & National Health Expenditures, Reimbursement & Access Policy
Disease
Diabetes/Endocrine/Metabolic Disorders (including obesity), No Additional Disease & Conditions/Specialized Treatment Areas