baked milk allergy

  • 文章类型: Journal Article
    背景:牛奶和鸡蛋过敏影响约1.9%和0.9%的儿童,分别。饮食进步疗法(DAT),包括牛奶(ML)和鸡蛋(EL)梯子,烤牛奶(BM-OIT)和烤鸡蛋(BE-OIT)口服免疫疗法是这些患者的潜在治疗选择。
    目的:对IgE介导的牛奶或鸡蛋过敏儿童DAT的安全性和有效性进行系统评价和荟萃分析。
    方法:进行了系统的文献综述,探索22种潜在结果,进行荟萃分析,其中>3项研究报告数据。等级方法用于确定每个结果的证据的确定性,以及JohannaBriggs研究所用于确定偏差风险的工具。
    结果:在筛选的9946项研究中,有29项研究符合纳入标准。公差发生在69%的EL,58%的ML,49%的BE-OIT和29%的BM-OIT患者。所有严重的过敏反应发生在21%的EL,25%的ML,20%的BE-OIT和61%的BM-OIT患者,在3%的EL中使用肾上腺素,2%的ML,和9%的BM-OIT患者。19%的BE-OIT患者和10%的BM-OIT患者发生家庭反应。停药发生在14%的EL,17%的ML,17%的BE-OIT和20%的BM-OIT患者。产卵和BE-OIT耐受性的平均时间为13.25个月(4项研究)和19.1个月(3项研究)。证据的确定性很低,偏见的风险很高。研究异质性高,可归因于多种因素。
    结论:支持DAT安全性和有效性的证据的确定性非常低。我们不能得出DAT加速耐受性发展的结论。
    BACKGROUND: Cow\'s milk and egg allergy affect approximately 1.9% and 0.9% of children, respectively. Dietary advancement therapies (DATs), including milk (ML) and egg (EL) ladders, and baked milk (BM-OIT) and baked egg (BE-OIT) oral immunotherapy, are potential therapeutic options for these patients.
    OBJECTIVE: To perform systematic review and meta-analysis of the safety and efficacy of DATs in children with IgE-mediated milk or egg allergy.
    METHODS: A systematic literature review was conducted, exploring 22 potential outcomes, with meta-analysis performed where ≥3 studies reported data. The GRADE approach was used to determine the certainty of evidence for each outcome, and the Johanna Briggs Institute tools were used for determining risk of bias.
    RESULTS: Twenty-nine studies met inclusion criteria among 9946 titles screened. Tolerance occurred in 69% of EL, 58% of ML, 49% of BE-OIT, and 29% of BM-OIT patients. All-severity allergic reactions occurred in 21% of EL, 25% of ML, 20% of BE-OIT, and 61% of BM-OIT patients, with epinephrine use in 3% of EL, 2% of ML, and 9% of BM-OIT patients. At-home reactions occurred in 19% of BE-OIT and 10% of BM-OIT patients. Discontinuation occurred in 14% of EL, 17% of ML, 17% of BE-OIT, and 20% of BM-OIT patients. The mean time to BE egg and BE-OIT tolerance was 13.25 months (4 studies) and 19.1 months (3 studies). Certainty of evidence was very low, and risk of bias high. Study heterogeneity was high, attributable to multiple factors.
    CONCLUSIONS: There is very low certainty of evidence supporting DAT safety and efficacy. We cannot conclude that DAT accelerates tolerance development.
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  • 文章类型: Journal Article
    饮食进步疗法(DAT)构成了一个跨越广泛加热物品摄入的连续体,渐进式牛奶/蛋梯,口服免疫疗法(OIT)。这些代表了食物过敏管理从严格避免到可以调节免疫系统以发展对特定形式的过敏原的耐受性的积极疗法的演变。许多鸡蛋或牛奶个体在基线时对烤鸡蛋/牛奶有耐受性,经常食用(在家摄取)烤牛奶或鸡蛋是一个安全的过程,具有潜在的生活质量和免疫益处。牛奶和蛋梯,开发用于非IgE介导的过敏,越来越多地适应IgE介导的变态反应,作为一种潜在安全的家庭选择,可以逐步改善饮食。然而,关于这些方法的安全性和有效性的数据有限,或者哪个患者最适合哪个DAT。还不清楚广泛加热的过敏原消耗和梯子是否容易受到影响OIT的日常耐受性和安全性的相同患者特异性因素的影响。最近几起涉及对牛奶或蛋制品的近乎致命或致命反应的事件(均为哮喘患者)突出表明,DAT并非无风险,医生在这些治疗中的指导是必不可少的。此类指导可能包括在开始任何DAT之前获得知情同意,并在任何形式的DAT中为OIT制定相同的安全给药规则。这个讲台讨论了有关DAT安全性的实际问题,并考虑临床医生如何最大限度地保护患者,同时定义这些概念的实际实施的安全性和有效性。
    Dietary advancement therapies (DATs) constitute a continuum spanning extensively heated item ingestion, progressive milk or egg ladders, and oral immunotherapy (OIT). These represent an evolution in food allergy management from strict avoidance to an active therapy that may modulate the immune system to develop tolerance to particular forms of the allergen. Many egg or milk individuals are tolerant to baked egg or milk at baseline, and regular consumption (at home ingestion) of baked milk or egg is a safe process with potential quality of life and immunologic benefit. Milk and egg ladders, developed for non-IgE mediated allergy, are increasingly being adapted to IgE-mediated allergy as a potentially safe at-home option for gradual dietary advancement. However, data are limited regarding how safe and effective these approaches are or what patient is best suited for which DAT. It is also unclear whether extensively heated allergen consumption and ladders are susceptible to the same patient-specific factors that affect day-to-day tolerance and safety in OIT. Several recent events involving near-fatal or fatal reactions to milk or egg products (all among patients with asthma) have highlighted that DATs are not risk-free, and that physician guidance in these therapies is essential. Such guidance may include obtaining informed consent before starting any DAT and instituting the same safe dosing rules for OIT across any form of DAT. This rostrum discusses practical concerns about the safety of DAT, and considerations regarding how clinicians can maximize patient protection while defining the safety and efficacy of real-world implementation of these concepts.
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