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Updated: Aug 3, 2025

A Treatment Package without Escape Extinction to Address Food Selectivity
Published on: August 21, 2015
Intractable Feeding Intolerance in Children With Severe Neurological Impairment: A Retrospective Case Review of Nine
Naomi T Katz1,2,3, Monica S Cooper2,4,5, Aeshan Kularatne1
1Victorian Paediatric Palliative Care Program, Royal Children's Hospital, Parkville, VIC, Australia.
Insights
Intractable feeding intolerance in children with severe neurological impairment (SNI) is a critical issue. This study highlights its role in patient decline and emphasizes the need for prognostic conversations and goal-concordant care.
Area of Science:
- Pediatric Gastroenterology
- Palliative Care
- Neurology
Background:
- Severe neurological impairment (SNI) in children often presents with poorly understood intractable feeding intolerance.
- This condition can contribute to patient deterioration and mortality.
Purpose of the Study:
- To describe nine children with SNI experiencing intractable feeding intolerance.
- To propose terminology for severe feeding difficulties in children with SNI.
Main Methods:
- Retrospective case series analysis of nine children with SNI.
- Review of clinical data, including feeding interventions, symptom management, and outcomes.
Main Results:
- Children died at a mean age of 10.3 years, with a median of 3.1 months from palliative care referral to death.
- Gastrointestinal dysfunction was documented in seven children, with a median of 3.9 months between documentation and death.
- All children required gastrostomy tubes, and seven also required jejunal tubes, with limited survival post-jejunal tube insertion.
Conclusions:
- 'Intractable feeding intolerance' signifies a critical juncture for reassessing medical interventions.
- Further research is needed to identify predictors and understand the contribution of feeding intolerance to mortality.
- Clinician-family prognostic discussions and goal-concordant care are vital during life and in the terminal phase.
Background:
Intractable feeding intolerance in children with severe neurological impairment (SNI) is poorly defined and understood.
Objectives:
(1) To describe 9 children with SNI, where intractable feeding intolerance was thought to be a contributor to their deterioration or death. (2) To consider terminology to describe the severe end of the spectrum of feeding difficulties in children with SNI.
Results:
Mean age at death was 10.3 years (range: 5 - 15.6), and median time from palliative care referral to death was 3.1 months. Location of death was home (n = 3), hospice (n = 1), and hospital (n = 5) with 1 death in intensive care. Gastrointestinal "failure" or "dysfunction" were documented for 7 children, (median time between documentation and death was 3.9 months (range: .1 to 13.1)). All children were fed via a gastrostomy tube during their life (median age of insertion 2.5 years (range: 1.2 to 6.8 years)), and 7 via the jejunal route (median age of insertion 9.2 years (range 2.4 to 14.7 years)). Children lived a median of 9 percent of their lives after jejunal tube feeding was commenced. No child had home-based parenteral nutrition. Multiple symptom management medications were required.
Conclusion:
'Intractable feeding intolerance' describes a clinical crossroads in a child's life where there is an opportunity to consider the appropriateness of further interventions. Further work should explore predictors of intractable feeding intolerance and the delicate balance between cause or contributor to death. The importance of clinician-family prognostic conversations and goal-concordant care both during life and in the terminal phase is highlighted.
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