通过直接激发试验对疑似对β-内酰胺类抗生素有迟发性反应的儿童和青少年进行 "去标签化 "治疗:德国皮肤变态反应与健康医学协会 (GPAU)、德国变态反应与临床免疫学协会 (DGAKI) 和德国变态反应学家协会 (ÄDA)的共识文件。

Allergologie select Pub Date : 2024-05-31 eCollection Date: 2024-01-01 DOI:10.5414/ALX02480E
Irena Neustädter, Sophie Blatt, Gerda Wurpts, Heinrich Dickel, Christian Walter, Werner Aberer, Sebastian Bode, Timo Buhl, Sunhild Gernert, Susanne Harner, Guido Heine, Sebastian Kerzel, Meike Köhler, Lars Lange, Joachim List, Hans F Merk, Thomas Nüßlein, Hagen Ott, Franziska Sattler, Antje Schuster, Helen Straube, Bettina Wedi, Torsten Zuberbier, Knut Brockow
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引用次数: 0

摘要

背景:约有 10% 的欧洲儿童被归类为对药物过敏。在这些儿童中,大多数都没有发现对β-内酰胺类抗生素(BLA)过敏。在大多数情况下,红斑是由感染引起的:本文旨在描述药物过敏误诊的原因和后果。我们提出了一种在使用 BLA 治疗期间出现延迟反应病史的情况下确定正确诊断的方法。为此,我们通过电子邮件交流的方式讨论了这一建议,并在参与医学会的药物过敏工作组成员之间达成了共识:结果:仅凭病史怀疑对 BLA 过敏会对今后的抗生素治疗产生负面影响。与用药无关的发热感染引起的红斑是儿童的常见病。因此,为疑似超敏反应的儿童和青少年推荐一个标准化的澄清程序就显得尤为重要。病史应作为诊断药物过敏或其他可能鉴别诊断的依据。轻度斑丘疹性红斑(MPE)可能是药物过敏或非特异性病毒性红斑的表现。无并发症的 MPE 不伴有明显的全身受累,也没有粘膜受累或皮肤水疱。只有少数无并发症的 MPE 患儿的皮肤测试呈阳性,只有 ~ 7 - 16% 的疑似 BLA 诊断可通过激发试验得到证实。因此,对于无并发症的 MPE 患儿,即使事先未进行皮试,也可在门诊环境中进行药物激发试验。本文介绍了一种为期 3 天的门诊直接激发方案,用于对无并发症的 MPE 儿童进行 BLA 脱标:结论:许多儿童和青少年在发生无并发症的 MPE 后,在接受 BLA 治疗的同时却被不必要地拒绝接受 BLA 治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
"Delabeling" by direct provocation testing in children and adolescents with a suspected history of a delayed reaction to β-lactam antibiotics: Consensus paper of Gesellschaft für pädiatrische Allergologie und Umweltmedizin (GPAU), Deutsche Gesellschaft für Allergologie und klinische Immunologie (DGAKI), and Ärzteverband deutscher Allergologen (ÄDA).

Background: Approximately 10% of European children are classified as allergic to drugs. In the majority of these children, no allergy to β-lactam antibiotics (BLA) can be found. In most cases, the exanthema is caused by the infection.

Materials and methods: The objective of this paper is to describe the causes and consequences of a misdiagnosis of drug allergy. We propose a method for establishing a correct diagnosis in the case of a history of a delayed reaction during treatment with a BLA. For this purpose, a proposal was discussed via e-mail communication, and consensus was reached among the members of the drug allergy working groups of the participating medical societies.

Results: The suspicion of a BLA allergy based on the medical history alone can have a negative impact on future antibiotic treatment. Exanthema associated with febrile infections not related to drug administration is a frequent finding in children. This makes it all the more important to be able to recommend a standardized procedure for clarification in children and adolescents with suspected hypersensitivity reactions. The medical history should be the basis on which to diagnose either a drug allergy or another possible differential diagnosis. A mild maculopapular exanthema (MPE) can be an expression of a drug allergy or a nonspecific viral exanthema. Uncomplicated MPE is not associated with significant systemic involvement, and there is no involvement of the mucous membranes or cutaneous blistering. Only a small number of children with uncomplicated MPE show positive skin tests and only ~ 7 - 16% of suspected BLA diagnoses can be confirmed by provocation tests. Thus, in children with uncomplicated MPE, drug provocation can be performed in an outpatient setting even without prior skin testing. This paper presents a 3-day outpatient direct provocation scheme for BLA delabeling in children with uncomplicated MPE.

Conclusion: Many children and adolescents are unnecessarily denied treatment with BLA after an uncomplicated MPE while being treated with a BLA.

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