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Published on: June 20, 2020
[Transition in health care from youth to adulthood for disabled people]
V Tiffreau1, A Schill, S Popielarz
1Service de médecine physique et de réadaptation, hôpital Swynghedauw, CHRU de Lille, 59037 Lille cedex, France. v-tiffreau@chru-lille.fr
Insights
Transitioning young patients with chronic health conditions from pediatric to adult care is challenging due to poor collaboration. Improved coordination between pediatricians and adult services is essential for specialized follow-up and competent care.
Area of Science:
- Pediatric Healthcare
- Healthcare Transition
- Chronic Illness Management
Context:
- Children with chronic health conditions often require specialized care beyond age 18.
- The transition from pediatric to adult healthcare systems presents significant challenges for patients and families.
- Poor collaboration between pediatric and adult medical specialists can lead to gaps in care and patient anxiety.
Purpose:
- To examine U.S. and English models for healthcare transition in young people with chronic conditions.
- To highlight the difficulties faced during the transition to adult healthcare.
- To emphasize the need for improved coordination between pediatric and adult healthcare services.
Summary:
- Most children with chronic health conditions survive into adulthood, necessitating a seamless transition to adult care.
- Current transition processes are hindered by inadequate collaboration between specialists and families, raising concerns about adult specialist competence.
- The report analyzes healthcare transition models in the U.S. and England, using a neuromuscular disorders clinic as a case study.
Impact:
- Improved healthcare transition models can ensure continuity of specialized care for young adults with chronic conditions.
- Enhanced collaboration between pediatric and adult healthcare providers is crucial for successful patient outcomes.
- Addressing transition challenges can alleviate family concerns regarding the competence of adult specialists and the quality of ongoing care.
Abstract:
Most children born with a chronic health condition or disability are expected to live more than 20 years. Health care is provided for these children in paediatric units until they are 18 years old, and the transition to the adult health care system is difficult because of poor collaboration between specialists and families who sometimes wonder if the adult specialist will be competent, although young disabled people need specialised follow-up. This report discusses U.S. and English models in the transition in health care. Coordination between paediatricians and adult services is necessary. The neuromuscular disorders clinic is cited as an example.
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