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澳大利亚维多利亚州学龄前儿童免疫接种后的潜在即刻过敏反应。

Potential immediate hypersensitivity reactions following immunization in preschool aged children in Victoria, Australia.

机构信息

a Department of General Medicine , The Royal Children's Hospital , Victoria , Australia.

b Surveillance of Adverse Events following Immunisation in Victoria (SAEFVIC), Murdoch Children's Research Institute , Victoria , Australia.

出版信息

Hum Vaccin Immunother. 2018;14(8):2088-2092. doi: 10.1080/21645515.2018.1460293. Epub 2018 May 10.

Abstract

Immediate hypersensitivity reactions (IHR) are rare but potentially serious adverse events following immunization (AEFI). Surveillance of Adverse Events following Vaccination in the Community (SAEFVIC) is an enhanced passive surveillance system that collects, analyses and reports information about AEFI in Victoria, Australia. We describe the incidence, timing and type of potential IHR following vaccination in preschool children reported over an 8-year period. A total of 2110 AEFI were reported in 1620 children, of which 23.5% (496) were classified as potential IHR. Of these, 37.1% (184) were suspected to be IgE-mediated, (including anaphylaxis, angioedema and/or urticaria) and 83.5% (414) occurred within 15 minutes of vaccination. The incidence of potential IHR was 5.4 per 100,000 doses, with that of suspected IgE-mediated IHR being 2.0 per 100,000 doses. The incidence of anaphylaxis was extremely low (0.13 per 100,000 doses) and is consistent with other published studies. Potential IHR following immunization should be reported to appropriate local pharmacovigilance systems and patients reviewed by specialists able to evaluate, investigate and manage future vaccinations.

摘要

立即型过敏反应(IHR)是疫苗接种后罕见但潜在严重的不良事件(AEFI)。社区疫苗接种不良事件监测(SAEFVIC)是一个强化的被动监测系统,用于收集、分析和报告澳大利亚维多利亚州 AEFI 的信息。我们描述了在 8 年期间报告的学前儿童接种疫苗后潜在 IHR 的发生率、时间和类型。在 1620 名儿童中报告了 2110 例 AEFI,其中 23.5%(496 例)被归类为潜在 IHR。其中,37.1%(184 例)疑似为 IgE 介导的(包括过敏反应、血管性水肿和/或荨麻疹),83.5%(414 例)发生在接种疫苗后 15 分钟内。潜在 IHR 的发生率为每 10 万剂 5.4 例,疑似 IgE 介导的 IHR 发生率为每 10 万剂 2.0 例。过敏反应的发生率极低(每 10 万剂 0.13 例),与其他已发表的研究一致。接种疫苗后应向适当的当地药物警戒系统报告潜在的 IHR,并由能够评估、调查和管理未来疫苗接种的专家对患者进行评估。

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