Ethylene oxide allergy in children with spina bifida
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Published on: August 20, 2018
T Pittman1, J Kiburz, G Steinhardt
1Division of Neurological Surgery, Cardinal Glennon Children's Hospital, St. Louis, Missouri 63104, USA.
Insights
Ethylene oxide (EtO) exposure may cause allergic reactions in children with myelomeningoceles. This study found EtO-specific IgE in 23% of these children, often linked to latex allergy and shunt use.
Area of Science:
- Immunology
- Pediatrics
- Medical Devices
Background:
- Allergic reactions to ethylene oxide (EtO) sterilized medical products have been reported in children with myelomeningoceles.
- Understanding the prevalence and clinical significance of EtO-specific IgE is crucial for patient safety.
Purpose of the Study:
- To determine the prevalence of EtO-specific IgE in children with myelomeningoceles.
- To assess the significance of EtO-specific IgE in this patient population.
Main Methods:
- Serum samples were collected from children with myelomeningoceles, chronically ill controls, and well-child controls.
- Enzyme-linked immunosorbent assay (ELISA) was used to detect IgE antibodies against EtO and latex.
Main Results:
- 23% of children with myelomeningoceles (17/75) had EtO-specific IgE, compared to 4% of chronically ill controls (1/26) and 0% of well controls.
- Children with EtO-specific IgE were more likely to be atopic, have a shunt, and possess latex-specific IgE.
- These children had undergone more surgical procedures, including shunt revisions.
Conclusions:
- While EtO-specific IgE was detected, no cases of anaphylaxis attributed to EtO exposure occurred during the study period.
- The findings highlight a potential link between EtO exposure, myelomeningocele management (shunts), and allergic sensitization.
Background:
Allergic reactions to ethylene oxide (EtO-treated products have occurred in several children with myelomeningoceles.
Objective:
The object of this study was to define the prevalence and significance of EtO-specific IgE among the children in our myelomeningocele clinic.
Methods:
The study population comprised three groups: children clinic.
Methods:
The study population comprised three groups: children with myelomeningoceles, chronically ill controls (defined as children who had undergone at least three major operations), and well-child controls. Serum specimens were collected from each child, and a commercially available ELISA designed to identify IgE directed against both EtO and latex was performed on the specimens.
Results:
Seventeen of 75 (23%) children with myelomeningoceles had antibodies directed against EtO, as did 1 of 26 (4%) chronically ill controls. None of the 25 well controls had detectable levels of anti-EtO IgE. Children with antibodies directed against EtO were more likely to be atopic (p = 0.007) and to have a shunt (p = 0.021) and were markedly more likely to have antibodies directed against latex (p = 0.001). On average they had undergone more shunt revisions and other operations than had children without anti-EtO antibodies.
Conclusion:
During the period of study no child had anaphylaxis thought to have been due to EtO exposure.
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