• Karen S Heller, Mildred Z Solomon, and Initiative for Pediatric Palliative Care (IPPC) Investigator Team.
• Education Development Center, Inc., Newton, MA 02458, USA.
• J Pediatr Nurs. 2005 Oct 1; 20 (5): 335-46.

AbstractThis article presents parents' perceptions regarding continuity and coordination of care of children with life-threatening conditions as revealed through qualitative analysis of interviews with 36 bereaved parents of children who died after receiving care at three geographically dispersed teaching hospitals in the United States. Parental concerns about and experience of continuity of care were framed primarily in terms of the quality and continuity of relationships with healthcare providers throughout a child's illness and death and the continuity and consistency of information that they received about their child's condition and care. Continuity in relationships was perceived as key in ensuring that clinicians knew and cared about the child and parents, which in turn contributed to parents' confidence that their child would receive the best possible care. In the absence of continuous, caring relationships with staff, parents reported frustration, hypervigilance, and mistrust about the quality of care that their child received.

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