| Autor: |
Bogetz, Jori F., Revette, Anna, Partin, Lindsay, DeCourcey, Danielle D. |
| Zdroj: |
Hospital Pediatrics; September 2022, Vol. 12 Issue: 9 p832-842, 11p |
| Abstrakt: |
Children with complex chronic conditions (CCCs) and their parents benefit from supportive serious illness care when their conditions are severe and impact their quality of life and stress. This includes not only expert medical care but also effective relationships with the clinical team. Existing data suggest that there are opportunities for improvement. This study’s aim was to explore important aspects of the relationships and resources that facilitate supportive serious illness care among children with CCCs and their parents.We conducted semistructured interviews with adolescents and young adults (AYAs) with CCCs (aged 13–35 years), and parents of children with CCCs across 2 academic pediatric centers in the United States from December 2018 to April 2019. Transcripts were iteratively coded and analyzed by a team that included a sociologist, pediatric intensivist, and palliative care researcher by using inductive and deductive thematic analysis.Seven AYAs with CCCs and 9 parents participated (16 total; 1 AYA–parent dyad). Two key categories were identified around relationships with the clinical team: trust and fostering collaboration. Three key categories related to resources are information needs, making sense of life with illness, and supportive community. Many of the key categories and themes identified by participants had both tangible and intangible components and revealed the distinct yet interconnected nature of these aspects of care.Awareness and cultivation of relationship and resource support through innovative interventions and attention to those with increased needs in these areas may improve the serious illness care provided to children with CCCs and their parents. |
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