Oral food challenge outcomes in children and adolescents in a tertiary centre: A 5-year experience
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Updated: Aug 4, 2025

A Treatment Package without Escape Extinction to Address Food Selectivity
Published on: August 21, 2015
Joshua G Jacob1,2, Suran L Fernando1,2, Claire Nickolls1
1Department of Clinical Immunology and Allergy, Royal North Shore Hospital, Sydney, New South Wales, Australia.
Insights
Factors like atopic dermatitis, prior anaphylaxis, and larger skin prick test (SPT) wheal sizes increase the risk of reactions during oral food challenges (OFC) in children. A low-risk group for home-based OFC was identified.
Area of Science:
- Allergy and Immunology
- Pediatric Allergy
- Clinical Research
Background:
- Oral food challenges (OFC) are crucial for diagnosing food allergies in children.
- Identifying predictive factors for OFC outcomes can optimize patient management.
Purpose of the Study:
- To determine factors present at initial assessment associated with successful oral food challenge (OFC) or challenge failure in Australian pediatric patients.
- To identify a low-risk group suitable for domiciliary OFC.
Main Methods:
- Retrospective review of 456 pediatric OFCs over 5 years.
- Collected data included demographics, comorbidities, skin prick test (SPT) results, reaction history, and OFC outcomes.
- Statistical analysis to identify factors correlating with OFC reactions.
Main Results:
- 12.3% of OFCs resulted in a reaction.
- Atopic dermatitis, increasing SPT wheal size, and a history of anaphylaxis were significantly associated with OFC reactions.
- A low-risk group was identified with no clear prior reaction history and SPT results <3 mm.
Conclusions:
- Atopic dermatitis, prior anaphylaxis history, and larger SPT wheal size are key predictors of OFC reactions in children.
- Domiciliary OFC may be a safe option for a select low-risk pediatric group.
- Further large-scale, multicenter studies are needed to validate findings in the Australian population.
Aim:
Oral food challenges (OFC) are an important tool in the assessment of food allergy. We sought to identify factors available at initial assessment visit which were associated with successful outcome or challenge failure in Australian children.
Methods:
We conducted a retrospective review of all paediatric patients who underwent OFC in our allergy service over a 5-year period. Clinical data comprising patient demographics, co-morbidities, skin prick test (SPT) results, nature of previous reactions, elapsed time since previous reactions and outcome at OFC were recorded.
Results:
Four hundred and fifty-six OFCs were conducted, with 56 cases (12.3%) resulting in a reaction. Likelihood of reaction at OFC was significantly increased for patients with atopic dermatitis (odds ratio 1.99). When stratified by food substance, atopic dermatitis had the strongest association with reaction within the peanut group (odds ratio 3.2), and no association was demonstrated for soy or prawn. Increasing SPT wheal size (P < 0.001) and previous history of anaphylaxis to the challenge food (P < 0.001) correlated with failure at OFC. A low-risk group was identified, of patients with no clear history of prior reaction to the challenge food, and SPT result <3 mm.
Conclusions:
Factors identified at assessment visit which correlated with reaction at OFC are atopic dermatitis, prior history of anaphylaxis, and increasing SPT wheal size. Domiciliary OFC could be considered in a select low-risk group of patients undergoing food challenge. This study was performed at a single centre with limited sample size, further large-scale and multicentre study verification of our data will provide more accurate representation of the Australian demographic.
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