Coping Strategies and Social Support for Transition Readiness Among Youth With Sickle Cell Disease

Category	Detail
Condition	Sickle Cell Disease
Key Mechanisms	Abnormal production of sickle hemoglobin leading to vaso-occlusion and associated complications.
Target Population	Adolescents and young adults with Sickle Cell Disease transitioning to adult care.
Care Setting	Pediatric and adult health care systems.

Sickle cell disease affects approximately 100,000 people in the US, primarily those of African descent.
Improved survival rates have led to a focus on transition from pediatric to adult care.
Barriers to transition include lack of timely care, negative perceptions, and socioeconomic factors.
Positive coping strategies are associated with higher transition readiness scores.
The study evaluates the impact of coping strategies and social support on transition readiness.

Conduct regular evaluations of health care-related quality of life and disease self-management.

Monitor for poorer disease outcomes and higher health care utilization during transition.

Young adults aged 17 to 28 years with Sickle Cell Disease.

Emphasize the importance of self-advocacy and coping strategies during the transition period.

Encourage strong relationships and clear communication between patients and health care providers.
Support the development of self-management skills in adolescents transitioning to adult care.
Address socioeconomic barriers to improve access to care.

Clinical Scorecard: Strategies for Managing Transition Readiness and the Role of Social Support in Youth with Sickle Cell Disease