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皮肤试验诊断克拉霉素过敏的敏感性和特异性。

Sensitivity and specificity of skin tests in the diagnosis of clarithromycin allergy.

机构信息

Paediatric Allergy and Immunology Unit, A. Meyer Children's Hospital, Department of Paediatric, University of Florence, Florence, Italy.

出版信息

Ann Allergy Asthma Immunol. 2010 May;104(5):417-9. doi: 10.1016/j.anai.2010.03.010.

Abstract

BACKGROUND

Clarithromycin is one of the most frequently prescribed oral macrolidic antibiotics in the pediatric population. Suspected adverse reactions to clarithromycin have been frequently described by parents of children examined in pediatric allergy units, but there is a lack of reliable methods available in detecting the presence of specific IgE antibodies.

OBJECTIVE

To investigate the prevalence of a clarithromycin allergy in children seen in a pediatric allergy unit using standardized skin tests and oral provocation tests (OPTs).

METHODS

Sixty-four children were referred with a history of a clarithromycin-associated adverse drug reaction. All these children underwent skin tests and OPTs. The nonirritating intradermal skin test concentration for clarithromycin was determined in a control group of 18 children who had tolerated clarithromycin in the previous month.

RESULTS

The threshold nonirritating intradermal concentration was established at the 10:2 dilution (0.5 mg/mL). Nine of the 64 children had an immediately positive intradermal response to the 10:2 dilution and only 1 child to the 10:3 dilution (0.05 mg/mL). None had positive skin prick test results or delayed skin responses to intradermal tests. Four of 64 children (6%) with previously described adverse reactions due to clarithromycin intake had a positive OPT reaction. When we correlated the intradermal skin test results to the OPT results, intradermal test sensitivity and specificity were 75% and 90%, respectively.

CONCLUSION

Intradermal tests seem to be useful in allergologic workup in children with suspected clarithromycin hypersensitivity and may help reduce the need for OPTs.

摘要

背景

克拉霉素是儿科人群中最常开的口服大环内酯类抗生素之一。在儿科过敏科就诊的儿童的家长经常会报告怀疑对克拉霉素的不良反应,但目前缺乏可靠的方法来检测特异性 IgE 抗体。

目的

使用标准化皮肤试验和口服激发试验(OPT)来调查儿科过敏科就诊的儿童对克拉霉素过敏的发生率。

方法

有 64 名儿童因与克拉霉素相关的药物不良反应而被转介。所有这些儿童都接受了皮肤试验和 OPT。在过去一个月内耐受克拉霉素的 18 名儿童的对照组中,确定了克拉霉素非刺激性皮内试验浓度。

结果

非刺激性皮内试验的阈值浓度定为 10:2 稀释度(0.5mg/ml)。64 名儿童中有 9 名对 10:2 稀释度有即刻阳性皮内反应,只有 1 名对 10:3 稀释度(0.05mg/ml)有阳性反应。没有儿童的皮肤点刺试验结果或皮内试验延迟反应呈阳性。在因摄入克拉霉素而出现先前描述的不良反应的 64 名儿童中,有 4 名(6%)的 OPT 反应呈阳性。当我们将皮内试验结果与 OPT 结果相关联时,皮内试验的敏感性和特异性分别为 75%和 90%。

结论

皮内试验似乎可用于对疑似克拉霉素过敏的儿童进行过敏检测,并可能有助于减少 OPT 的需要。

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