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在一家二级儿科转诊中心,分子过敏诊断作为传统诊断的辅助手段

Molecular Allergy Diagnostics as an Adjunct to Conventional Diagnostics in a Secondary Pediatric Referral Center.

作者信息

Wolthers Ole D

机构信息

Asthma and Allergy Clinic, Children's Clinic Randers, Randers, Denmark.

出版信息

Recent Pat Inflamm Allergy Drug Discov. 2019;13(1):73-76. doi: 10.2174/1872213X13666190610143439.

Abstract

BACKGROUND

Several compositions for determination of specific molecular components in allergens have recently been patented. The role of Molecular Allergy (MA) diagnostics in suspected IgE mediated allergic conditions is currently debated. Guideline reports have concluded that population- based studies involving evaluation of the usefulness of MA diagnostics are needed.

OBJECTIVE

To evaluate the usefulness of MA diagnostics in a secondary pediatric referral center.

METHODS

A total of 961 children and adolescents aged 0.2-18.8 (mean 7.0) years was included in a prospective observational survey. Inclusion criterion was a suspected diagnosis of an IgE mediated condition based on history and clinical symptoms and signs. If a specific diagnosis could not be reached from conventional investigations suspected peanut allergy, birch pollen allergy and associated crossreactivity, insect allergy and triggering allergens for specific immunotherapy were assessed by MA diagnostics.

RESULTS

Based on conventional work-up a diagnostic conclusion was established in 946 patients (98.4%). MA diagnostics were performed in 15 individuals (1.6%), 7 girls and 8 boys aged 3.2 to 17.8 (mean 10.6) years. In 8 cases a specific diagnosis was established based on MA diagnostics; in 7 cases MA diagnostics could not improve diagnosis. MA were most frequently (N = 7 (14%)) used in children with peanut allergy (N = 50).

CONCLUSION

Most patients in a secondary pediatric referral center with suspected IgE mediated allergy can be managed by conventional diagnostic methods. MA diagnostics may be useful in small and selected subgroups as in patients with suspected peanut allergy, however, may not be helpful in all cases.

摘要

背景

最近已有多项用于测定过敏原中特定分子成分的组合物获得专利。目前,分子过敏(MA)诊断在疑似IgE介导的过敏病症中的作用存在争议。指南报告得出结论,需要开展基于人群的研究来评估MA诊断的效用。

目的

评估MA诊断在二级儿科转诊中心的效用。

方法

一项前瞻性观察性调查纳入了961名年龄在0.2至18.8岁(平均7.0岁)的儿童和青少年。纳入标准为基于病史、临床症状和体征疑似诊断为IgE介导的病症。如果通过传统检查无法得出明确诊断,对于疑似花生过敏、桦树花粉过敏及相关交叉反应、昆虫过敏以及特异性免疫治疗的触发过敏原,则通过MA诊断进行评估。

结果

基于传统检查,946名患者(98.4%)得出了诊断结论。对15名个体(1.6%)进行了MA诊断,其中7名女孩和8名男孩,年龄在3.2至17.8岁(平均10.6岁)。8例基于MA诊断得出了明确诊断;7例中MA诊断未能改善诊断。MA诊断最常用于花生过敏儿童(n = 50)中的7例(14%)。

结论

在二级儿科转诊中心,大多数疑似IgE介导过敏的患者可通过传统诊断方法进行处理。MA诊断可能对小部分特定亚组患者有用,如疑似花生过敏的患者,但并非对所有病例都有帮助。

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