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Paediatric type 1 diabetes in Ireland--results of the first national audit
Insights
This study assessed pediatric type 1 diabetes care in Ireland, finding significant variations in services and insulin pump use. A national strategy is recommended to standardize care and improve outcomes for children with diabetes.
Area of Science:
- Pediatric Endocrinology
- Public Health
- Diabetes Management
Background:
- Type 1 diabetes (T1D) management in children requires specialized, multidisciplinary care.
- Understanding current service provision is crucial for identifying areas for improvement in pediatric T1D care.
- The Republic of Ireland has 19 centers providing pediatric T1D care.
Purpose of the Study:
- To describe current services for children with type 1 diabetes in Ireland.
- To establish a baseline for future service and outcome improvements.
- To identify variations in care delivery across different centers.
Main Methods:
- A survey was sent to lead clinicians in 17 of 19 Irish pediatric T1D centers.
- Data collected in 2012 included demographics, patient numbers, diagnostics, management, resources, and policies.
- Information on insulin pump therapy and glycemic control (HbA1c) was gathered.
Main Results:
- 17 centers responded, covering 2518 pediatric patients with T1D.
- Insulin pump initiation occurred in 8 centers, with usage varying from 0% to 42%.
- Mean HbA1c levels ranged from 8.2% to 9.4%, indicating suboptimal glycemic control across centers. Significant variations in guidelines, appointment frequency, transition policies, and insulin types were noted.
Conclusions:
- There is considerable variation in the provision of pediatric type 1 diabetes care across the Republic of Ireland.
- Standardization of services, including insulin pump access and management protocols, is needed.
- A national approach is recommended to improve consistency and quality of care for children with T1D.
Abstract:
The aim of this study was to describe the services provided for children with type 1 diabetes in the Republic of Ireland, and to identify a baseline from which services and outcomes might be improved. Lead clinicians in 17 of the 19 centres providing paediatric type 1 diabetes care responded to requests for information from 2012 regarding demographics, patient numbers, diagnostics, outpatient management, multidisciplinary team resources, comorbidity screening, transition policy, clinical guidelines, and use of insulin pumps. The total number of patients attending these centres was 2518. Eight centres initiate insulin pump therapy. Insulin pump usage ranged from 0 to 42% of patients attending each centre. Self reported clinic mean haemoglobin A1c ranged from 8.2 to 9.4% (66.1 to 79.2 mmol/mol). Variation existed in guideline availability, frequency of clinic appointments, age of transition and insulin types used. We recommend a national approach to standardising and improving care for these patients.
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