Barriers to accessing palliative care for pediatric patients with cancer: A review of the literature

Author:

Haines Emily R.12ORCID,Frost A. Corey3,Kane Heather L.3,Rokoske Franziska S.2

Affiliation:

1. Department of Health Policy and Management, Gillings School of Global Public Health; The University of North Carolina at Chapel Hill; Chapel Hill North Carolina

2. End-of-Life, Hospice, and Palliative Care Program; RTI International; Research Triangle Park North Carolina

3. Child and Adolescent Research and Evaluation Program; RTI International; Research Triangle Park North Carolina

Publisher

Wiley

Subject

Cancer Research,Oncology

Reference70 articles.

1. Howlader N Noone AM Krapcho M SEER Cancer Statistics Review, 1975-2009 (Vintage 2009 Populations). Bethesda, MD: National Institutes of Health, National Cancer Institute, Surveillance, Epidemiology, and End Results (SEER) Program 2011

2. Symptoms and suffering at the end of life in children with cancer;Wolfe;N Engl J Med.,2000

3. Parents' perspective on symptoms, quality of life, characteristics of death and end-of-life decisions for children dying from cancer;Hechler;Klin Padiatr.,2008

4. Children dying from cancer: parents' perspectives on symptoms, quality of life, characteristics of death, and end-of-life decisions;Lutzau;J Palliat Care.,2012

5. Family perspectives on the quality of PPC;Contro;Arch Pediatr Adolesc Med.,2002

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