Palliative Care as a Standard of Care in Pediatric Oncology

Meaghann S Weaver1,2, Katherine E Heinze3, Katherine P Kelly4

  • 1Department of Oncology, Children's National Health System, Washington, DC.

Pediatric Blood & Cancer
|December 25, 2015
PubMed

Insights

This study reviewed pediatric palliative cancer care literature to develop a psychosocial standard. Key areas include symptom management, communication, and shared decision-making for improved care.

Area of Science:

  • Palliative Care
  • Pediatric Oncology
  • Psychosocial Support

Background:

  • Pediatric and adolescent cancer patients require specialized palliative care.
  • Existing literature on psychosocial aspects of pediatric palliative cancer care is extensive but requires synthesis.
  • A standardized approach is needed to improve care quality.

Purpose of the Study:

  • To systematically review pediatric and adolescent palliative cancer care literature.
  • To inform the development of a psychosocial standard for pediatric palliative cancer care.
  • To identify key areas for improving psychosocial support in pediatric oncology.

Main Methods:

  • Systematic literature review of four databases (1995-2015).
  • Inclusion of 73 papers from an initial review of 209 papers.
  • Synthesis of findings to identify critical themes.

Main Results:

  • Urgent considerations include symptom assessment and intervention.
  • Direct patient report is crucial for understanding needs.
  • Effective communication and shared decision-making are vital components.
  • Identified themes highlight the need for standardized assessments and interventions.

Conclusions:

  • Standardizing palliative care assessments and interventions can enhance care quality.
  • Improved psychosocial standards benefit children and adolescents with cancer.
  • Family members also benefit from standardized, high-quality palliative care.
  • This review provides a foundation for developing evidence-based psychosocial standards in pediatric oncology.

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