Care Coordination in the Spina Bifida Clinic Setting: Current Practice and Future Directions
Abstract
Introduction
Although the potential benefits of care coordination are widely recognized, little is known about care coordination in the multidisciplinary spina bifida clinic setting. This study examined several aspects of care coordination in this environment.
Method
We conducted semi-structured interviews with clinic staff (N = 43) and focus groups with caregivers (N = 38) at seven spina bifida clinics in the United States.
Results
Clinic staff described several primary goals of care coordination, including coordinating multiple services during one visit to ease the burden on families. Although the structure of care coordination varied across the clinics, several clinics had a dedicated care coordinator. Barriers and facilitators to care coordination included staffing issues, clinic day logistics, community resources, and family-related concerns. Despite challenges associated with care coordination processes, clinic staff and caregivers alike believed that care coordination is beneficial.
Discussion
Study findings suggest ways that care might be coordinated optimally in spina bifida clinics. A synthesis of these findings for clinics interested in implementing care coordination or improving the care coordination services they currently offer is provided.
Key Words: Spina bifida, care coordination
Funding for this study was provided by the Centers for Disease Control and Prevention, Office of Strategy and Innovation.
Conflicts of interest: None to report.
PII: S0891-5245(10)00143-4
doi:10.1016/j.pedhc.2010.06.003
© 2012 National Association of Pediatric Nurse Practitioners. All rights reserved.
