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单次延长药物激发试验,无需皮试,用于诊断儿童对β-内酰胺类药物轻度非即刻过敏反应是安全的。

Single-dose prolonged drug provocation test, without previous skin testing, is safe for diagnosing children with mild non-immediate reactions to beta-lactams.

机构信息

Paediatrics Unit, Hospital Regional Universitario de Malaga, Málaga, Spain.

Allergy Research Group, Instituto de Investigación Biomédica de Málaga-IBIMA-ARADyAL, Málaga, Spain.

出版信息

Allergy. 2021 Aug;76(8):2544-2554. doi: 10.1111/all.14800. Epub 2021 Mar 24.

DOI:10.1111/all.14800
PMID:33650109
Abstract

INTRODUCTION

Mild non-immediate reactions (NIRs) to beta-lactams (BLs) are the most frequent manifestation of drug allergy in children. The diagnostic approach is complex as the utility of skin tests (STs) and lymphocyte transformation tests (LTTs) is controversial. Drug provocation test (DPT) is the gold standard, although no standardized protocols exist. We aimed to investigate the utility of DPT in a unique dose without previous STs, and LTTs in the diagnosis of NIRs to BLs in children.

METHODS

We prospectively evaluated children 0-14 years old referred to the Regional University Hospital of Málaga during 2017-2020 reporting NIRs to BLs. We performed a DPT with a unique dose followed by regular treatment at home. If positive, STs and LTTs were done after the reaction had disappeared.

RESULTS

We included 194 children, having 24 (12.4%) a positive DPT. The main culprit was AX (70.1%) followed by AX-clavulanic acid (CLV) (26.8%) and the main symptoms maculopapular exanthema (MPE) (49.5%) and delayed-urticaria (48.5%). A decrease (p = 0.013) in the interval of days between drug administration and onset of symptoms was observed in positive DPT compared with the original reaction (3.5 vs 6 days), with no differences in the overall percentage of MPE and delayed-appearing urticaria (p = 0.551). No severe reactions occurred during DPT. Moreover, STs were positive in 13.33% and LTTs in 52.9%.

CONCLUSIONS

Single-dose DPT without previous STs is a safe and useful way to assess NIRs to BLs in children. LTT has shown to be useful, confirming a T-cell mechanism involved in these reactions.

摘要

介绍

β-内酰胺类药物(BLs)的轻度非即刻反应(NIRs)是儿童药物过敏最常见的表现。由于皮肤试验(STs)和淋巴细胞转化试验(LTTs)的实用性存在争议,因此诊断方法较为复杂。药物激发试验(DPT)是金标准,尽管目前尚无标准化方案。我们旨在研究在未进行 STs 和 LTTs 的情况下,采用独特剂量的 DPT 诊断儿童 BL 类药物 NIRs 的效果。

方法

我们前瞻性评估了 2017 年至 2020 年期间因 BL 类药物 NIR 而转至马拉加区域大学医院的 0-14 岁儿童。我们进行了一次 DPT 试验,采用独特剂量,随后在家中进行常规治疗。如果阳性,则在反应消退后进行 STs 和 LTTs。

结果

我们纳入了 194 名儿童,其中 24 名(12.4%)的 DPT 阳性。主要的罪魁祸首是 AX(70.1%),其次是 AX-克拉维酸(CLV)(26.8%),主要症状是斑丘疹性皮疹(MPE)(49.5%)和迟发性荨麻疹(48.5%)。与原始反应相比,阳性 DPT 组的药物给药与症状发作之间的天数间隔有所减少(p=0.013),MPE 和迟发性荨麻疹的总发生率无差异(p=0.551)。在 DPT 期间未发生严重反应。此外,13.33%的儿童 STs 阳性,52.9%的儿童 LTTs 阳性。

结论

无需进行先前的 STs 即可进行单次剂量 DPT,这是一种安全且有用的评估儿童 BL 类药物 NIRs 的方法。LTT 表明有用,证实了 T 细胞机制在这些反应中起作用。

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