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The Development of a National Paediatric Psycho-Oncology Service
C Besani1,2,3, A Dunne1,2,3, S D'Arcy-Bewick2
1National Children's Cancer Service, Children's Health Ireland at Crumlin.
Insights
Psychological care for children with cancer in Ireland
Area of Science:
- Pediatric Oncology
- Psycho-oncology
- Healthcare Services Research
Background:
- The National Children's Cancer Service (NCCS) in Ireland aims to provide comprehensive care.
- International standards emphasize the importance of psychological support for pediatric cancer patients and families.
- Assessing current psychological service provision against these standards is crucial for identifying gaps.
Purpose of the Study:
- To evaluate the psychological care provided to children and adolescents with cancer and their families at the NCCS.
- To compare the NCCS's psychological services against national and international standards of care.
Main Methods:
- A retrospective audit of 316 referrals to the psychology service within malignant haematology and oncology at the NCCS.
- Data collected over a 32-month period (January 2013 to August 2016).
Main Results:
- An average of 189 (50%) urgently referred patients received psychological support annually.
- Only 22% of patients undergoing hematopoietic stem cell transplantation (HSCT) and 22% referred to palliative care received psychological input.
- 62% of teenage patients received psychological input during the audit period.
Conclusions:
- The current psychology service provision at the NCCS falls short of international standards of care.
- Secured funding for a principal psychologist post based on audit data and risk assessment.
- Further posts (HSCT, late-effects, neuropsychology) and model of care development are needed for equitable, evidence-based psychological care.
Abstract:
Aims To investigate the psychological care provided to children and young adolescents with cancer and their families within the National Children's Cancer Service (NCCS), Ireland, in respect of the national and international standards of care. Methods A retrospective audit of 316 referrals made over 32 months by the NCCS to the psychology service in malignant haematology and oncology was performed. Results The audit revealed that out of 316 patients, a yearly average of 189 (50%) of urgently referred patients received psychological support within the NCCS between January 2013 and August 2016. Furthermore only 20 (22%) undergoing haematopoietic stem cell transplantation (HSCT), 14 (22%) referred to the paediatric palliative care team, and 84 (62%) of teenage patients received psychological input during this timeframe. Conclusion The audit revealed that the current psychology service provision is failing to meet the international standards of care. Due to the data provided by this audit, in conjunction with a clinical risk assessment of the service, funds for the post of principal psychologist have been secured. Further psychology posts (HSCT, late-effects and neuropsychology), and development of the psycho-oncology model of care are required to ensure equality of access and evidence-based psychological care for all children with cancer.
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