Delivering Pediatric Palliative Care: From Denial, Palliphobia, Pallilalia to Palliactive
Stefan J Friedrichsdorf1,2, Eduardo Bruera3
1Children's Hospitals and Clinics of Minnesota, 2525 Chicago Ave S, Minneapolis, MN 55403, USA. stefan.friedrichsdorf@childrensMN.org.
Insights
Pediatric palliative care (PPC) is crucial for children with life-limiting conditions, yet barriers like lack of education and funding hinder its delivery. Addressing myths can improve symptom management and quality of life.
Area of Science:
- Pediatric Palliative Care (PPC)
- Child Health
- End-of-Life Care
Background:
- Over 21 million children worldwide need pediatric palliative care (PPC) annually, with over 8 million requiring specialized services.
- In the US, over 42,000 children die yearly, highlighting the need for advanced interdisciplinary PPC.
- Despite being a standard of pediatric medicine, significant barriers impede optimal PPC delivery.
Discussion:
- Barriers include lack of formal education, reimbursement issues, emotional impact on caregivers, and insufficient staffing/funding for PPC teams.
- Distressing symptoms like pain and nausea are often unaddressed or ineffectively treated during the end-of-life period.
- Myths and misconceptions contribute to inadequate symptom control in children with life-limiting diseases.
Key Insights:
- PPC integrates comfort care and symptom management with disease-directed treatments, allowing families to pursue both.
- Access to interdisciplinary care is vital for optimizing children's physical, psychological, and spiritual wellbeing.
- Every children's hospital is expected to offer interdisciplinary palliative care services as standard of care.
Outlook:
- Addressing common myths and misconceptions can overcome clinical obstacles to effective PPC.
- Understanding the four typical stages of PPC program implementation is key for widespread adoption.
- Focus on concurrent disease-directed treatments and palliative care maximizes quality of life for children with serious illnesses.
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.
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