对曾有β-内酰胺类抗生素低风险非即刻反应史的儿童进行初始单次治疗剂量挑战和 5 天延长药物激发试验的安全性。

IF 2.6 3区 医学 Q2 ALLERGY
Meltem Comert, Ozge Yilmaz Topal, Tugba Guler, Demet Tekcan, Hasibe Artac, Ilknur Kulhas Celik
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引用次数: 0

摘要

背景:虽然诊断β-内酰胺类抗生素(BLA)过敏的金标准是药物激发试验(DPT),但目前还没有针对儿童的标准化方案。目的:我们旨在评估临床特征和药物激发试验(DPT):我们的目的是评估对 BLA 有低风险非即刻反应 (NIR) 病史的儿童的临床特征和 DPT 结果,这些儿童接受了首次直接单治疗剂量挑战和为期 5 天的延长 DPT。方法:我们回顾性地评估了对 BLA 有低风险非即刻反应史的 0-18 岁儿童。在挑衅的第一天,我们在诊所实施了单剂量 DPT 方案,未进行任何皮试。治疗剂量经过调整,不超过年龄和体重的最大单剂量(MSUD)。白喉、百日咳、破伤风三联疫苗的剂量为 100%。为了找出有延迟反应的儿童,医生告诉家长或看护人继续在家给儿童用药 5 天。结果本研究共纳入 199 名儿童。患儿年龄的中位数(四分位数间距)为 62.5 个月(26.5-94 个月)。在可疑药物中,89 名儿童(81.7%)的主要罪魁祸首是阿莫西林-克拉维酸。85名儿童(78%)最常见的临床表现是斑丘疹性红斑,8名儿童(7.3%)的白喉、百日咳、破伤风三联疫苗(DPT)检测结果呈阳性。有 3 名儿童(2.8%)在服用第一剂 DPT 后出现反应。其余儿童继续在家中使用疑似 BLA。5名儿童(4.7%)在家中使用该药物时出现了反应。白喉、百日咳、破伤风三联疫苗检测结果呈阳性的所有儿童都出现了轻微的皮肤症状,并对阿莫西林-克拉维酸产生了反应。没有人出现全身或严重的皮肤反应。结论用为期 5 天的长效 DPT 进行初始直接单次治疗剂量挑战是评估儿童对 BLA 的低风险近红外反应的一种有用而安全的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The safety of initial single therapeutic dose challenge with a 5-day prolonged drug provocation test in children with a history of low-risk non-immediate reactions to beta-lactam antibiotics.

Background: Although the gold standard for diagnosing beta-lactam antibiotic (BLA) allergy is the drug provocation test (DPT), there is no standardized protocol for children. Objective: We aimed to evaluate the clinical features and DPT results of children with a history of low-risk non-immediate reactions (NIR) to BLA who underwent initial direct single therapeutic dose challenge with a 5-day prolonged DPT. Methods: We retrospectively evaluated children ages 0-18 years with a history of low-risk NIRs to BLAs. On the first day of provocation, a single-dose DPT protocol without any skin test was administered at the clinic. The therapeutic dose was adjusted to not exceed the maximum single-unit dose (MSUD) for age and weight. The DPT protocol was administered with 100% of MSUD. To identify children with delayed reactions, the parents or caregivers were told to continue giving the medication at home for 5 days. Results: One hundred and nine children were included in this study. The median (interquartile range) age of the children was 62.5 months (26.5-94 months). Of the suspected drugs, the main culprit drug was amoxicillin-clavulanic acid for 89 children (81.7%). The most common clinical manifestation was maculopapular exanthema, which occurred in 85 children (78%), and 8 (7.3%) had a positive DPT result. Three children (2.8%) developed a reaction after the first DPT dose. The remaining children continued to use the suspected BLA at home. Five children (4.7%) developed a reaction while using the drug at home. All the children with positive DPT results developed mild cutaneous signs and presented with a reaction to amoxicillin-clavulanic acid. None had a systemic or severe cutaneous reaction. Conclusion: Initial direct single therapeutic dose challenge with a 5-day prolonged DPT is a useful and safe way to assess low-risk NIRs to BLAs in children.

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来源期刊
CiteScore
5.70
自引率
35.70%
发文量
106
审稿时长
6-12 weeks
期刊介绍: Allergy & Asthma Proceedings is a peer reviewed publication dedicated to distributing timely scientific research regarding advancements in the knowledge and practice of allergy, asthma and immunology. Its primary readership consists of allergists and pulmonologists. The goal of the Proceedings is to publish articles with a predominantly clinical focus which directly impact quality of care for patients with allergic disease and asthma. Featured topics include asthma, rhinitis, sinusitis, food allergies, allergic skin diseases, diagnostic techniques, allergens, and treatment modalities. Published material includes peer-reviewed original research, clinical trials and review articles.
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