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Initiating Palliative Care Referrals in Pediatric Oncology
Andrea Cuviello1, Jessica C Raisanen2, Pamela K Donohue3
1St Jude Children's Research Hospital, Memphis, Tennessee, USA.
Insights
Pediatric oncologists recognize the need for early palliative care (PC) but face inconsistent referral practices. A standardized screening tool could improve PC integration for children with cancer.
Area of Science:
- Pediatric Oncology
- Palliative Care
- Healthcare Systems Research
Background:
- Early palliative care (PC) improves quality of life for pediatric cancer patients.
- Referral practices for PC by pediatric oncologists are inconsistent.
- Few children with cancer receive formal PC consultations.
Purpose of the Study:
- Describe patient characteristics influencing PC referrals by oncologists.
- Identify strategies to enhance PC integration in pediatric cancer care.
Main Methods:
- Mixed-methods study utilizing semistructured interviews with pediatric oncology providers.
- Conventional content analysis of audiotaped interview transcripts.
Main Results:
- Over 75% of 77 interviewed providers felt PC was consulted too late, citing communication and system barriers.
- Poor prognosis, symptom management, comorbidities, and psychosocial needs were common referral triggers, yet inconsistently applied.
- 85% of providers believed a screening tool would standardize PC referrals; 50% reported limited formal PC training.
Conclusions:
- Pediatric oncologists are committed to improving PC integration for children with cancer.
- Standardized referral practices, potentially via a screening tool, are beneficial.
- Additional PC education may enhance provider recognition of referral triggers.
Context:
Early palliative care (PC) has been shown to improve the quality of life of children with cancer, yet referral practices by pediatric oncology providers remains inconsistent and few patients receive a formal PC consult.
Objectives:
We sought to describe patient characteristics used by oncologists for PC referral and identify ways to improve PC integration into the care for children with cancer.
Methods:
This mixed-methods study used semistructured audiotaped interviews to explore the patient or disease characteristics used by pediatric oncology providers to trigger PC referral. Conventional content analysis was applied to interview transcripts.
Results:
About 77 participants with diverse experience were interviewed. More than 75% of participants reported that PC was consulted too late and cited communication and systems issues as the top barriers. Most participants (85%) stated that a screening tool would be helpful to standardize referral practices to PC. Characteristics such as poor prognosis (88%), symptom management (86%), comorbidities (65%), and psychosocial needs (65%) were commonly reported triggers that should initiate PC consultation. However, when presented with case scenarios that included these characteristics, participants did not consistently identify the PC triggers. Nearly 50% of participants stated they had received some formalized PC training; however, only one-third of these participants noted completing a PC rotation.
Conclusion:
Our findings suggest that pediatric oncologists are committed to improving the integration of PC for their patients and that standardization of referral practices, through the use of a screening tool, would be of benefit. Additional PC education might reinforce pediatric oncologists' recognition of PC triggers.
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