The pediatric palliative and hospice care landscape shows important variations in coverage options across communities.
Community-based organizations provide essential services, but many children still lack adequate access to care.
Further evaluations are needed to enhance awareness and improve pediatric community-based palliative care.
Addressing these coverage issues could significantly improve the care experiences for pediatric patients.
Abstract
Background: The pediatric literature describes reliance on community-based palliative and hospice organizations in extending the reach of care for children.