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总血清IgE对过敏原特异性IgE结果呈阳性的预测价值。

The predictive value of total serum IgE for a positive allergen specific IgE result.

作者信息

Sinclair D, Peters S A

机构信息

Department of Clinical Biochemistry, Queen Alexandra Hospital, Portsmouth PO6 3LY, UK.

出版信息

J Clin Pathol. 2004 Sep;57(9):956-9. doi: 10.1136/jcp.2004.017681.

Abstract

BACKGROUND

Measurement of total serum IgE and allergen specific IgE is often requested to assess possible allergy. As public awareness increases, so do requests for allergy assessment; unless there is a clear "allergen suspect" in the history, several allergen specific IgE requests may be made. This increases the likelihood of detecting borderline increases in allergen specific IgE of uncertain relevance, and has important cost implications for the service.

AIMS

To provide an evidence base for this observation.

METHODS

In this retrospective observational study, results from 301 patients under 16 years of age from whom blood was taken for "allergy testing" from March 2001 to February 2003 were studied.

RESULTS

Allergen specific IgE testing in children with low total serum IgE concentrations (<10 IU/litre) yielded very few positive results (three of 73 children), except in those being investigated for an acute reaction to a single food; when IgE was 11-20 kU/litre, 13 of 73 children had positive allergen specific IgE; in the 21-40 kU/litre IgE group, 16 of 74 children had positive allergen specific IgE and in the 41-80 kU/litre group, 22 of 81 had positive allergen specific IgE.

CONCLUSIONS

Allergen specific IgE testing in children with low IgE concentrations (<10 kU/litre) produces few positive results in patients with non-specific symptoms. Laboratories should perform allergy testing for specific allergens regardless of total IgE concentration only when there are convincing clinical reasons to do so, and should not proceed with this if the total IgE is <10 kU/litre and the presenting symptoms are non-specific.

摘要

背景

总血清IgE和变应原特异性IgE的检测常用于评估可能的过敏情况。随着公众意识的提高,对过敏评估的需求也在增加;除非病史中有明确的“可疑变应原”,否则可能会进行多项变应原特异性IgE检测。这增加了检测到相关性不确定的边缘性变应原特异性IgE升高的可能性,并且对医疗服务有重要的成本影响。

目的

为这一观察结果提供证据基础。

方法

在这项回顾性观察研究中,对2001年3月至2003年2月期间因“过敏检测”而采血的301名16岁以下患者的结果进行了研究。

结果

总血清IgE浓度较低(<10 IU/升)的儿童进行变应原特异性IgE检测,阳性结果很少(73名儿童中有3名),但因单一食物急性反应而接受调查的儿童除外;当IgE为11 - 20 kU/升时,73名儿童中有13名变应原特异性IgE呈阳性;在IgE为21 - 40 kU/升的组中,74名儿童中有16名变应原特异性IgE呈阳性,在41 - 80 kU/升的组中,81名中有22名变应原特异性IgE呈阳性。

结论

IgE浓度较低(<10 kU/升)的儿童进行变应原特异性IgE检测,在非特异性症状患者中阳性结果很少。实验室仅在有令人信服的临床理由时,才应无论总IgE浓度如何对特定变应原进行过敏检测,而如果总IgE<10 kU/升且呈现的症状是非特异性的,则不应进行此项检测。

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