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2007年至2013年澳大利亚维多利亚州免疫接种后的儿童过敏性不良事件。

Pediatric anaphylactic adverse events following immunization in Victoria, Australia from 2007 to 2013.

作者信息

Cheng Daryl R, Perrett Kirsten P, Choo Sharon, Danchin Margie, Buttery Jim P, Crawford Nigel W

机构信息

Department of General Medicine, The Royal Children's Hospital, Melbourne, VIC, Australia; Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.

Department of General Medicine, The Royal Children's Hospital, Melbourne, VIC, Australia; Vaccine and Immunisation Research Group (VIRGo), Murdoch Childrens Research Institute and Melbourne School of Population and Global Health, The University of Melbourne, Melbourne, VIC, Australia; Department of Allergy and Immunology, Royal Children's Hospital, Melbourne, VIC, Australia.

出版信息

Vaccine. 2015 Mar 24;33(13):1602-7. doi: 10.1016/j.vaccine.2015.02.008. Epub 2015 Feb 16.

Abstract

BACKGROUND

Anaphylaxis is a rare life-threatening adverse event following immunization (AEFI). Variability in presentation can make differentiation between anaphylaxis and other AEFI difficult. This study summarizes pediatric anaphylaxis AEFI reported to an Australian state-based passive surveillance system.

METHODS

All suspected and reported pediatric (<18 years) anaphylaxis AEFI notified to SAEFVIC (Surveillance of Adverse Events Following Vaccination In the Community) Melbourne, Australia, between May 2007 to May 2013 were analyzed. Clinical descriptions of the AEFI, using the internationally recognized Brighton Collaboration case definition (BCCD) and final outcome were documented.

RESULTS

93% (25/27) of AEFI classified as anaphylaxis met BCCD criteria, with 36% (9/25), assessed as the highest level of diagnostic certainty (Level 1). Median age was 4.7 years (range 0.3-16.2); 48% of cases were male. The vaccine antigens administered included: diphtheria, tetanus, acellular pertussis (DTaP) alone or in combination vaccines containing other antigens in 11 of 25 cases (44%); and live attenuated measles mumps rubella (MMR) vaccine for six (five also had other vaccines concomitantly administered). The estimated incidence rate of anaphylaxis for DTaP vaccines was 0.36 cases per 100,000 doses, and 1.25 per 100,000 doses for MMR vaccines. The majority of cases had rapid onset, but in 24% (6/25) of cases, first symptoms of anaphylaxis developed ≥30 min after immunization. In 60% (15/25) of cases, symptoms resolved ≤60 min of presentation. Intramuscular adrenaline was administered in 90% (18/25) of cases. All cases made a full recovery with no sequelae identified.

CONCLUSION

This comprehensive case series of pediatric anaphylaxis as an AEFI identified that diagnostic criteria are useful when applied to a passive vaccine surveillance system when adequate clinical information is available. Anaphylaxis as an AEFI is rare and usually begins within 30 min of vaccination. However, healthcare professionals and vaccinees/parents should be aware that onset of anaphylaxis can be delayed beyond 30 min following immunization and that medical attention should be sought promptly if anaphylaxis is suspected.

摘要

背景

过敏反应是免疫接种后罕见的危及生命的不良事件(AEFI)。临床表现的差异可能使过敏反应与其他AEFI难以区分。本研究总结了向澳大利亚一个州的被动监测系统报告的儿童过敏反应AEFI。

方法

分析了2007年5月至2013年5月期间向澳大利亚墨尔本的SAEFVIC(社区疫苗接种后不良事件监测)报告的所有疑似和确诊的儿童(<18岁)过敏反应AEFI。使用国际认可的布莱顿协作病例定义(BCCD)记录AEFI的临床描述和最终结果。

结果

93%(25/27)被归类为过敏反应的AEFI符合BCCD标准,其中36%(9/25)被评估为最高诊断确定性水平(1级)。中位年龄为4.7岁(范围0.3 - 16.2岁);48%的病例为男性。接种的疫苗抗原包括:25例中的11例(44%)单独接种白喉、破伤风、无细胞百日咳(DTaP)或与含有其他抗原的联合疫苗;6例接种减毒活麻疹腮腺炎风疹(MMR)疫苗(其中5例同时接种了其他疫苗)。DTaP疫苗的过敏反应估计发病率为每100,000剂0.36例,MMR疫苗为每100,000剂1.25例。大多数病例起病迅速,但24%(6/25)的病例过敏反应的首发症状在免疫接种后≥30分钟出现。60%(15/25)的病例症状在就诊后≤60分钟缓解。90%(18/25)的病例使用了肌内注射肾上腺素。所有病例均完全康复,未发现后遗症。

结论

这个关于儿童过敏反应作为AEFI的综合病例系列表明,当有足够的临床信息时,诊断标准应用于被动疫苗监测系统是有用的。过敏反应作为AEFI很罕见,通常在接种后30分钟内开始。然而,医护人员以及疫苗接种者/家长应意识到过敏反应的发作可能在免疫接种后延迟超过30分钟,并且如果怀疑过敏反应应立即寻求医疗关注。

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