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Transition in chronic illness: Who is going where?
Katharine S Steinbeck1, Lynne Brodie, Susan J Towns
1Endocrinology and Adolescent Medicine, Royal Prince Alfred Hospital and the University of Sydney, New South Wales, Australia. kss@email.cs.nsw.gov.au
Insights
Effective transition from pediatric to adult care is crucial for young people with chronic illnesses. This study highlights the need for better data collection and management to support this critical process.
Area of Science:
- Pediatric healthcare transition
- Chronic illness management
- Healthcare systems research
Background:
- Increasing survival rates for childhood chronic illnesses necessitate a focus on transitioning care to adult services.
- Strategic planning and optimal patient management require accurate data on patient numbers.
- The New South Wales Greater Metropolitan Clinical Taskforce Transition Program initiated a data collection exercise.
Purpose of the Study:
- To assess the current state of patient data collection for chronic illness transition care.
- To identify the prevalence of different clinical groups requiring transition to adult care.
- To inform strategic planning for improving the transition process.
Main Methods:
- Face-to-face interviews with over 200 clinicians across 68 clinical services in tertiary pediatric hospitals.
- Data collected between August 2004 and October 2005.
- Information gathered on approximately 4200 patients.
Main Results:
- Sixty-eight services maintained chronic illness patient databases, with less than half being electronic.
- Only 12% of services could specifically identify patients actively transitioning.
- Top clinical groups needing transition included diabetes, endocrinology, neurology, spina bifida, and gastroenterology.
Conclusions:
- A significant number of young individuals with chronic illness and disability require effective transition to adult care.
- The study identified key pediatric aspects of the transition process needing improvement.
- Enhanced data management is essential for successful healthcare transitions.
Aim:
With increasing survival rates for chronic childhood illness, there has been an increasing focus on the transition of clinical care from paediatric to adult services. Data regarding patient numbers are essential for strategic planning and for optimal management. We report on a data collection exercise from the New South Wales Greater Metropolitan Clinical Taskforce Transition Program.
Methods:
Data were collected between August 2004 and October 2005 through face-to-face interviews with over 200 clinicians in 68 clinical services in tertiary paediatric hospitals in New South Wales, providing information on approximately 4200 patients.
Results:
Sixty-eight services kept a database on patients with chronic illness but less than half were electronic. Eight services (12%) could specifically identify patients in the active phase of transition on their databases. The five most prevalent clinical groups requiring transition to adult specialist health care (excluding cerebral palsy and developmental disability) were diabetes, other endocrinology, neurology, spina bifida and gastroenterology.
Conclusions:
There are large numbers of young people with chronic illness and disability who need effective transition to long-term adult care. This study has enabled the identification of paediatric aspects of the transition process that require attention.
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