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Feasibility of desensitizing children highly allergic to peanut by high-dose oral immunotherapy

Reier-Nilsen, Tonje (author)
Oslo Univ Hosp, Div Paediat & Adolescent Med, Oslo, Norway; Univ Oslo, Inst Clin Med, Oslo, Norway
Michelsen, Merethe Melbye (author)
Oslo Univ Hosp, Div Paediat & Adolescent Med, Oslo, Norway; Univ Oslo, Inst Clin Med, Oslo, Norway
Carlsen, Karin C. Lodrup (author)
Oslo Univ Hosp, Div Paediat & Adolescent Med, Oslo, Norway; Univ Oslo, Inst Clin Med, Oslo, Norway
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Carlsen, Kai-Hakon (author)
Oslo Univ Hosp, Div Paediat & Adolescent Med, Oslo, Norway; Univ Oslo, Inst Clin Med, Oslo, Norway
Mowinckel, Petter (author)
Oslo Univ Hosp, Div Paediat & Adolescent Med, Oslo, Norway
Nygaard, Unni C. (author)
Norwegian Inst Publ Hlth, Div Infect Control & Environm Hlth, Oslo, Norway
Namork, Ellen (author)
Norwegian Inst Publ Hlth, Div Infect Control & Environm Hlth, Oslo, Norway
Borres, Magnus P, 1956- (author)
Uppsala universitet,Pediatrisk inflammationsforskning,Thermo Fisher Sci, Uppsala, Sweden
Haland, Geir (author)
Oslo Univ Hosp, Div Paediat & Adolescent Med, Oslo, Norway; Univ Oslo, Inst Clin Med, Oslo, Norway
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 (creator_code:org_t)
2018-10-08
2019
English.
In: Allergy. European Journal of Allergy and Clinical Immunology. - : WILEY. - 0105-4538 .- 1398-9995. ; 74:2, s. 337-348
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Background: There are limited data on the feasibility, efficacy and safety of high‐dose oral immunotherapy (OIT) in children highly allergic to peanuts.Objective: In children highly allergic to peanut, we primarily aimed to determine the feasibility of reaching the maximum maintenance dose (MMD) of 5000 mg peanut protein or, alternatively, a lower individual maintenance dose (IMD), by OIT up‐dosing. Secondarily, we aimed to identify adverse events (AEs) and determine factors associated with reaching a maintenance dose.Methods: The TAKE‐AWAY peanut OIT trial enrolled 77 children 5‐15 years old, with a positive oral peanut challenge. Fifty‐seven were randomized to OIT with biweekly dose step‐up until reaching MMD or IMD and 20 to observation only. Demographic and biological characteristics, AEs, medication and protocol deviations were explored for associations with reaching maintenance dose.Results: All children had anaphylaxis defined by objective symptoms in minimum two organ systems during baseline challenge. The MMD was reached by 21.1%, while 54.4% reached an IMD of median (minimum, maximum) 2700 (250, 4000) mg peanut protein, whereas 24.5% discontinued OIT. During up‐dosing, 19.4% experienced anaphylaxis. Not reaching the MMD was caused by distaste for peanuts (66.7%), unacceptable AEs (26.7%) and social reasons (6.7%). Increased peanut s‐IgG4/s‐IgE ratio (OR [95% CI]: 1.02 [1.00, 1.04]) was associated with reaching MMD.Conclusion: Although 75.5% of children with peanut anaphylaxis reached a maintenance dose of 0.25‐5 g, only 21.1% reached the MMD. Distaste for peanuts and AEs, including high risk of anaphylaxis, limited the feasibility of reaching MMD.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Lungmedicin och allergi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Respiratory Medicine and Allergy (hsv//eng)

Keyword

adverse events
desensitization
feasibility
oral immunotherapy
peanut allergy

Publication and Content Type

ref (subject category)
art (subject category)

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