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.

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