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Children (Basel). 2018 Aug 31;5(9). pii: E120. doi: 10.3390/children5090120.

Delivering Pediatric Palliative Care: From Denial, Palliphobia, Pallilalia to Palliactive.

Author information

1
Children's Hospitals and Clinics of Minnesota, 2525 Chicago Ave S, Minneapolis, MN 55403, USA. stefan.friedrichsdorf@childrensMN.org.
2
University of Minnesota Medical School, 420 Delaware Street SE, Minneapolis, MN 55455, USA. stefan.friedrichsdorf@childrensMN.org.
3
Department of Palliative Care and Rehabilitation Medicine, The University of Texas, MD Anderson Cancer Center, 1515 Holcombe Blvd., Houston, TX 77030, USA. ebruera@mdanderson.org.

Abstract

Among the over 21 million children with life-limiting conditions worldwide that would benefit annually from a pediatric palliative care (PPC) approach, more than eight million would need specialized PPC services. In the United States alone, more than 42,000 children die every year, half of them infants younger than one year. Advanced interdisciplinary pediatric palliative care for children with serious illnesses is now an expected standard of pediatric medicine. Unfortunately, in many institutions there remain significant barriers to achieving optimal care related to lack of formal education, reimbursement issues, the emotional impact of caring for a dying child, and most importantly, the lack of interdisciplinary PPC teams with sufficient staffing and funding. Data reveals the majority of distressing symptoms in children with serious illness (such as pain, dyspnea and nausea/vomiting) were not addressed during their end-of-life period, and when treated, therapy was commonly ineffective. Whenever possible, treatment should focus on continued efforts to control the underlying illness. At the same time, children and their families should have access to interdisciplinary care aimed at promoting optimal physical, psychological and spiritual wellbeing. Persistent myths and misconceptions have led to inadequate symptom control in children with life-limiting diseases. Pediatric Palliative Care advocates the provision of comfort care, pain, and symptom management concurrently with disease-directed treatments. Families no longer have to opt for one over the other. They can pursue both, and include integrative care to maximize the child's quality of life. Since most of the sickest children with serious illness are being taken care of in a hospital, every children's hospital is now expected to offer an interdisciplinary palliative care service as the standard of care. This article addresses common myths and misconceptions which may pose clinical obstacles to effective PPC delivery and discusses the four typical stages of pediatric palliative care program implementation.

KEYWORDS:

barriers; hospice; myths; pediatric palliative care; program development; program implementation

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