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Unusual clinical course in a child with cystic fibrosis treated with fat emulsion
Insights
Essential fatty acid deficiency in cystic fibrosis (CF) patients may be corrected with parenteral soya oil emulsion. This treatment improved sweat tests and pancreatic function, keeping the child healthy and suggesting a preventative role for CF manifestations.
Area of Science:
- Pediatrics
- Nutritional Science
- Genetics
Background:
- Cystic Fibrosis (CF) is a genetic disorder affecting multiple organs.
- Essential fatty acid (EFA) deficiency is a known complication in CF patients.
- Parenteral nutrition is crucial for managing severe cases.
Purpose of the Study:
- To investigate the therapeutic potential of soya oil emulsion in a child with cystic fibrosis.
- To assess the impact of correcting essential fatty acid deficiency on CF symptoms.
- To evaluate the long-term health outcomes of this intervention.
Main Methods:
- A child diagnosed with cystic fibrosis received regular parenteral soya oil emulsion from infancy.
- Clinical monitoring included sweat tests and assessment of pancreatic function.
- Overall health status and disease manifestations were regularly evaluated.
Main Results:
- Significant improvement in sweat test results was observed.
- Relief from pancreatic achylia (a digestive disorder) was achieved.
- The child remained in excellent health without apparent CF-related complications.
Conclusions:
- Parenteral soya oil emulsion can effectively correct essential fatty acid deficiency in cystic fibrosis.
- This intervention may alleviate key symptoms such as impaired sweat chloride excretion and pancreatic insufficiency.
- Correcting EFA deficiency shows promise in preventing or mitigating manifestations of cystic fibrosis.
Abstract:
A child diagnosed as having cystic fibrosis by customary criteria has been given regular parenteral soya oil emulsion from near birht. Sweat tests have improved, pancreatic achylia was relieved, and the child at present remains entirely well. Correction of the essential fatty acid deficiency found in cystic fibrosis may prevent some of the manifestations of the disease.
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