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门诊儿科人群青霉素过敏管理中的青霉素皮肤试验

Penicillin skin testing in the management of penicillin allergy in an outpatient pediatric population.

作者信息

Anterasian Christine M, Geng Bob

出版信息

Allergy Asthma Proc. 2018 Jul 1;39(4):305-310. doi: 10.2500/aap.2018.39.4138.

Abstract

BACKGROUND

Eight to ten percent of patients believe that they are allergic to penicillin, yet only 10% of those patients have evidence of an immunoglobulin E (IgE) mediated allergy upon penicillin skin testing (PST). In the adult population, a negative PST result is associated with a low risk of immediate reaction on oral challenge, but further studies are needed in the pediatric population.

OBJECTIVE

To calculate the negative predictive value (NPV) of the current skin testing regimen of penicillin, benzylpenicilloyl-polylysine (the major determinant), and ampicillin in a pediatric outpatient population to assess the utility of adding the minor determinant mixture to the skin testing regimen.

METHODS

A retrospective chart review was conducted of all pediatric patients seen in a single-center pediatric allergy/immunology outpatient clinic between January 1, 2010, and March 1, 2016, who underwent PST for presumed penicillin drug allergy.

RESULTS

Only 38% of patients who underwent PST had a drug reaction history consistent with an IgE-mediated reaction. 28.8% of the patients had a positive PST result. The addition of ampicillin to the standard PST regimen of penicillin and benzylpenicilloyl-polylysine identified an additional 4.1% of patients. Two patients (3.2%) reacted on oral challenge with a minor rash. The NPV of the PST regimen was 98%. No significant predictive variables for a positive PST result were identified.

CONCLUSION

Given the high NPV of the current PST regimen, we do not recommend additional testing with the minor determinant mixture. Despite this high NPV, the utility of PST in the low-risk, low-pretest probability outpatient pediatric population was limited, and select patients may be able to proceed directly to oral challenge.

摘要

背景

8%至10%的患者认为自己对青霉素过敏,但在这些患者中,只有10%在青霉素皮肤试验(PST)时有免疫球蛋白E(IgE)介导的过敏证据。在成人中,PST结果为阴性与口服激发试验时即刻反应的低风险相关,但儿科人群还需要进一步研究。

目的

计算青霉素、苄青霉素酰聚赖氨酸(主要决定簇)和氨苄西林当前皮肤试验方案在儿科门诊人群中的阴性预测值(NPV),以评估在皮肤试验方案中添加次要决定簇混合物的效用。

方法

对2010年1月1日至2016年3月1日在单中心儿科过敏/免疫门诊就诊且因疑似青霉素药物过敏接受PST的所有儿科患者进行回顾性病历审查。

结果

接受PST的患者中只有38%有与IgE介导反应一致的药物反应史。28.8%的患者PST结果为阳性。在青霉素和苄青霉素酰聚赖氨酸的标准PST方案中加入氨苄西林,又识别出4.1%的患者。两名患者(3.2%)在口服激发试验时出现轻微皮疹。PST方案的NPV为98%。未发现PST结果为阳性的显著预测变量。

结论

鉴于当前PST方案的NPV较高,我们不建议使用次要决定簇混合物进行额外检测。尽管NPV较高,但PST在低风险、预测试概率低的儿科门诊人群中的效用有限,部分患者可能可以直接进行口服激发试验。

相似文献

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Elective penicillin skin testing in a pediatric outpatient setting.儿科门诊环境中的选择性青霉素皮肤试验。
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