Continuity of care and caring: what matters to parents of children with life-threatening conditions

J Pediatr Nurs. 2005 Oct;20(5):335-46. doi: 10.1016/j.pedn.2005.03.005.

Abstract

This 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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Attitude to Health*
  • Child
  • Child, Hospitalized / psychology
  • Child, Preschool
  • Continuity of Patient Care / standards*
  • Empathy*
  • Female
  • Frustration
  • Health Services Needs and Demand
  • Hospitals, Pediatric
  • Hospitals, Teaching
  • Humans
  • Infant
  • Male
  • Middle Aged
  • Nursing Methodology Research
  • Palliative Care / psychology
  • Palliative Care / standards*
  • Parents / psychology*
  • Patient-Centered Care / standards
  • Professional-Family Relations
  • Qualitative Research
  • Quality of Health Care / standards
  • Surveys and Questionnaires
  • Total Quality Management / organization & administration
  • Trust
  • United States