Parents of Pediatric Solid Organ Transplant Recipients: Transition to Home and Chronic Illness Care

Parents of children that have received a heart, kidney, liver or lung transplant will be invited to participate in this protocol.

Involvement in this study entails completion of questionnaires at 4 separate time points. Parents will first complete questionnaires regarding discharge teaching, care coordination and readiness for hospital discharge on the day of discharge from the hospital. Parents will subsequently complete questionnaires at 3 weeks, 3 months and 6 months after discharge. The post discharge questionnaires assess coping, family management, adherence and utilization of healthcare resources.

Currently, no research has been conducted related to readiness for hospital discharge of a parent as the primary caregiver for a child with solid organ transplant or the sequential relationships between hospitalization care and the trajectory of post-discharge outcomes. This research will fill the gap in knowledge needed for care of solid organ transplant children and parents.

The ability to identify factors in the first year after transplant that are predictive of decreased coping and non-adherence affords an opportunity to develop nursing and health interventions that have significant implications for care decisions, as well as disease activity and health care costs.

Inclusion criteria

• the parent's child has undergone a heart, kidney, liver, lung or multivisceral transplant and is being discharged home from the hospital
• the parent is English speaking (tools being used have been validated for English participants only)
• the parent is 18 years of age or older

Exclusion criteria

• presence of significant communication or cognitive impairment on the part of the parent that would preclude completion of questionnaires based on self-report
• the child has already experienced the discharge to home transition after a previous transplant.