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Optimising Palliative Care for Children with Metastatic Neuroblastoma and the Paediatrician's Role in a Shared Care
Manjusha Nair1, Priyakumari Thankamony1, Binitha Rajeswari1
1Department of Pediatric Oncology, Regional Cancer Centre, Thiruvananthapuram, Kerala, India.
Insights
Palliative care (PC) is crucial for children with metastatic neuroblastoma (NB), but access is limited. Early integration of PC services improves care quality for pediatric cancer patients.
Area of Science:
- Pediatric Oncology
- Palliative Care
- Cancer Epidemiology
Background:
- Metastatic cancer poses a significant burden on children in developing nations.
- Palliative care (PC) services for pediatric patients are often scarce and underutilized.
- Neuroblastoma (NB) is a common childhood cancer with advanced stages often requiring palliative support.
Purpose of the Study:
- To determine the palliative care needs of children diagnosed with metastatic neuroblastoma (NB).
- To assess the availability and utilization of palliative care services for these pediatric patients.
- To evaluate the timing and effectiveness of palliative care integration in NB management.
Main Methods:
- A retrospective analysis of medical records was conducted for children aged 1-14 years diagnosed with metastatic NB.
- Data were collected over a 10-year period (January 2008 - December 2017).
- Patient demographics, symptoms, PC consultation details, and outcomes were analyzed.
Main Results:
- Out of 119 patients with metastatic NB, 87 (73.1%) received PC consultation, with only 14.9% referred early.
- Pain was the most frequent symptom reported. Care shifted to PC at relapse (66.6%) or end-of-life (18.3%).
- Common end-of-life symptoms included nausea, vomiting, constipation, and abdominal distension. Median survival was 9 months from diagnosis.
Conclusions:
- Timely integration of PC services is essential for children with metastatic cancer.
- Shared care models involving oncology, PC teams, and pediatricians can improve care continuity.
- Enhanced palliative care provision can significantly improve the quality of life for pediatric cancer patients.
Objectives:
The burden of advanced and metastatic cancer is high among children in developing countries, and palliative care (PC) services for children are sparsely available and poorly accessed. To estimate the burden of PC requirements in children with metastatic neuroblastoma (NB), and to evaluate the PC services offered.
Materials And Methods:
Retrospective analysis of case records of children 1-14 years diagnosed with metastatic NB from 1 January 2008 to 31 December 2017.
Results:
One hundred and nineteen patients with metastatic NB were included, of which 87 patients received PC consultation. Early PC referral occurred only in 13 patients (14.9%), and pain was the most prominent symptom. Shifting of care from oncology to PC occurred at disease relapse in 58 patients (66.6%) and at end-of-life in 16 patients (18.3%). Nausea/vomiting, constipation and abdominal distension were the most common symptoms during end-of-life. Seventy-one patients (85%) died of disease, median time to death being 9 months from diagnosis and 4 months from relapse. The mean time from initiation of PC to death was 4.2 months.
Conclusion:
Timely integration of PC and shared care incorporating the oncology team, PC team and local paediatricians can ease out transition in care, ensure a continuum of care and improve the quality of treatment delivered to children with metastatic cancer.
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