PMID- 28380495 OWN - NLM STAT- MEDLINE DCOM- 20170829 LR - 20220409 IS - 1423-0097 (Electronic) IS - 1018-2438 (Print) IS - 1018-2438 (Linking) VI - 172 IP - 3 DP - 2017 TI - Risk Factors for Severe Reactions during Double-Blind Placebo-Controlled Food Challenges. PG - 173-182 LID - 10.1159/000458724 [doi] AB - BACKGROUND: Severe anaphylactic symptoms can occur during oral food challenges (OFCs). Thus, high-risk patients (e.g., patients with a history of anaphylaxis or high antigen-specific immunoglobulin E [IgE] levels) must carefully undergo OFCs in hospitals. We attempted to identify the risk factors for severe symptoms during OFC testing among high-risk patients. METHODS: We retrospectively evaluated patients' characteristics and severe symptoms that were experienced during a double-blind placebo-controlled food challenge test performed before the patients underwent oral immunotherapy between June 2008 and June 2012. Patients were >/=5 years old and had an anaphylactic history or antigen-specific IgE (>30 kUA/L). Severe symptoms were defined using the grading of the Japanese Anaphylaxis Guidelines, which are modified from the European Academy of Allergology and Clinical Immunology Guidelines. RESULTS: We evaluated 393 cases with positive test results, including 98 cases with severe symptoms. The most frequent severe symptoms were respiratory (77%), gastrointestinal (28%), cardiovascular (27%), and neurological (13%) symptoms. Multivariate analysis revealed that the significant factors for a severe reaction were a history of anaphylaxis to the causative food (adjusted odds ratio [OR]: 2.147, p = 0.003), older age (per 1 year increase, adjusted OR: 1.102, p = 0.044), and an egg OFC (adjusted OR: 0.433, p = 0.003). CONCLUSIONS: The risk factors for a severe reaction to OFCs were a history of an anaphylactic reaction and older age. An egg OFC was associated with low risk of severe symptoms during OFC. Therefore, OFCs for patients with these risk factors should only be performed under specialist supervision with access to rapid treatment and full resuscitation equipment. CI - (c) 2017 The Author(s) Published by S. Karger AG, Basel. FAU - Yanagida, Noriyuki AU - Yanagida N AD - Department of Pediatrics, Sagamihara National Hospital, Sagamihara, Japan. FAU - Sato, Sakura AU - Sato S FAU - Asaumi, Tomoyuki AU - Asaumi T FAU - Ogura, Kiyotake AU - Ogura K FAU - Ebisawa, Motohiro AU - Ebisawa M LA - eng PT - Controlled Clinical Trial PT - Journal Article DEP - 20170406 PL - Switzerland TA - Int Arch Allergy Immunol JT - International archives of allergy and immunology JID - 9211652 RN - 0 (Allergens) RN - 37341-29-0 (Immunoglobulin E) RN - YKH834O4BH (Epinephrine) SB - IM MH - Administration, Oral MH - Allergens/administration & dosage/*adverse effects/immunology MH - Anaphylaxis/drug therapy/etiology MH - Animals MH - Arachis/adverse effects/immunology MH - Child MH - Desensitization, Immunologic/*adverse effects MH - Double-Blind Method MH - Eggs/adverse effects MH - Epinephrine/therapeutic use MH - Female MH - Food Hypersensitivity/immunology/*therapy MH - Humans MH - Immunoglobulin E/blood/immunology MH - Male MH - Milk/adverse effects/immunology MH - Odds Ratio MH - Triticum/adverse effects/immunology PMC - PMC5475236 OTO - NOTNLM OT - Anaphylaxis OT - Children OT - Food hypersensitivity OT - Oral food challenge OT - Pediatric patients EDAT- 2017/04/06 06:00 MHDA- 2017/08/30 06:00 PMCR- 2017/04/06 CRDT- 2017/04/06 06:00 PHST- 2016/02/22 00:00 [received] PHST- 2017/01/31 00:00 [accepted] PHST- 2017/04/06 06:00 [pubmed] PHST- 2017/08/30 06:00 [medline] PHST- 2017/04/06 06:00 [entrez] PHST- 2017/04/06 00:00 [pmc-release] AID - 000458724 [pii] AID - iaa-0172-0173 [pii] AID - 10.1159/000458724 [doi] PST - ppublish SO - Int Arch Allergy Immunol. 2017;172(3):173-182. doi: 10.1159/000458724. Epub 2017 Apr 6.