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非β-内酰胺类抗生素过敏反应。

Non-β-Lactam Antibiotic Hypersensitivity Reactions.

机构信息

Departments of General Medicine and.

Monash Health, Clayton, Victoria, Australia.

出版信息

Pediatrics. 2020 Jan;145(1). doi: 10.1542/peds.2019-2256. Epub 2019 Dec 3.

Abstract

OBJECTIVES

Antibiotics are among the most common prescriptions in children, and non-β-lactam antibiotics (NBLAs) account for almost half of those prescribed in Australian pediatric hospitals. Despite this, data on NBLA hypersensitivity in children are limited. This study describes reported hypersensitivity reactions to NBLAs in children and the results of allergy evaluation.

METHODS

Children with a suspected NBLA allergy who had skin testing and/or an intravenous or oral challenge test (OCT) between May 2011 and June 2018 were included. Patients were excluded if they were >18 years old or did not complete the allergy evaluation for any reason other than allergic reaction.

RESULTS

Over the 7-year study period, 141 children had 150 allergy evaluations of 15 different NBLAs. The median time from the initial reported reaction to allergy evaluation was 1.9 (range 0.1-14.9) years. Overall, 27 of the 150 (18.0%) challenge tests to NBLAs had positive results, with the rate of positive OCT results being highest for trimethoprim-sulfamethoxazole (15 of 46; 32.6%) and macrolides (8 of 77; 10.4%). Although 4 children reported initial anaphylactic reactions, no patients had severe symptoms on rechallenge or required adrenaline. Of the challenges that had positive results, the majority of children (23 of 27; 85.2%) had symptoms on repeat challenge similar to those that were initially reported.

CONCLUSIONS

Overall, 8 of 10 children with NBLA allergy could be delabeled. On average, patients waited 1.9 years to be rechallenged. Timely access to allergy evaluation to delabel these patients is needed to preserve first-line antibiotics.

摘要

目的

抗生素是儿童最常用的处方之一,而非β-内酰胺类抗生素(NBLAs)约占澳大利亚儿科医院处方的一半。尽管如此,儿童对 NBLAs 过敏的数据仍然有限。本研究描述了儿童对 NBLAs 过敏的报告过敏反应和过敏评估的结果。

方法

纳入 2011 年 5 月至 2018 年 6 月期间接受皮肤试验和/或静脉或口服挑战试验(OCT)的疑似 NBLAs 过敏的儿童。如果患者年龄大于 18 岁或因过敏反应以外的任何原因未完成过敏评估,则将其排除在外。

结果

在 7 年的研究期间,共有 141 名儿童对 15 种不同的 NBLAs 进行了 150 次过敏评估。从首次报告过敏反应到过敏评估的中位时间为 1.9 年(范围 0.1-14.9 年)。总体而言,150 次 NBLAs 挑战测试中有 27 次(18.0%)结果阳性,其中甲氧苄啶-磺胺甲恶唑(15/46;32.6%)和大环内酯类药物(8/77;10.4%)的 OCT 阳性结果率最高。尽管有 4 名儿童报告了初始过敏反应,但在重新挑战时没有患者出现严重症状或需要肾上腺素。在阳性结果的挑战中,大多数儿童(23/27;85.2%)在重复挑战时出现与最初报告相似的症状。

结论

总体而言,10 名 NBLAs 过敏儿童中有 8 名可以被重新标记。平均而言,患者需要等待 1.9 年才能再次接受挑战。需要及时进行过敏评估以重新标记这些患者,以保留一线抗生素。

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