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提高青霉素过敏标签去除的有效性。

Improving the Effectiveness of Penicillin Allergy De-labeling.

作者信息

Bourke Jack, Pavlos Rebecca, James Ian, Phillips Elizabeth

机构信息

Department of Clinical Immunology, Sir Charles Gairdner Hospital, Perth, Western Australia, Australia; Department of Clinical Immunology, Royal Perth Hospital, Perth, Western Australia, Australia.

Institute for Immunology & Infectious Diseases, Murdoch University, Perth, Western Australia, Australia.

出版信息

J Allergy Clin Immunol Pract. 2015 May-Jun;3(3):365-34.e1. doi: 10.1016/j.jaip.2014.11.002. Epub 2015 Jan 13.

Abstract

BACKGROUND

Approximately 10-20% of hospitalized patients are labeled as penicillin allergic, and this is associated with significant health and economic costs.

OBJECTIVES

We looked at the effectiveness of penicillin allergy de-labeling in clinical practice with the aim of deriving risk stratification models to guide testing strategies.

METHODS

Consecutive patients aged 15 years or more, referred to a Western Australian public hospital drug allergy service between 2008 and 2013 for beta-lactam allergy, were included. Follow-up surveys were conducted. Results of skin prick testing and intradermal testing (SPT/IDT) and oral challenge (OC), and follow-up of post testing antibiotic usage were the main outcomes.

RESULTS

SPT/IDT was performed in 401 consecutive patients with immediate (IMM) (≤ 1 hour) (n = 151) and nonimmediate (NIM) (>1 hour) (n = 250) reactions. Of 341 patients, 42 (12.3%) were SPT/IDT+ to ≥ 1 penicillin reagents, including 35/114 (30.4%) in the IMM group and 7/227 (3.1%) in the NIM group (P < .0001). Of 355 SPT/IDT patients, 3 (0.8%), all in the IMM group, had nonserious positive OC reactions to single dose penicillin VK (SPT/IDT negative predictive value [NPV] 99.2%). Selective or unrestricted beta-lactam was recommended in almost 90% overall, including 238/250 (95.2%) in the NIM group and 126/151 (83.4%) in the IMM group (P = .0001). Of 182 patients, 137 (75.3%) were following the allergy label modifications (ALM) at the time of follow-up.

CONCLUSIONS

Penicillin SPT/IDT/OC safely de-labels penicillin-allergic patients and identifies selective beta-lactam allergies; however, incomplete adherence to ALM recommendations impairs effectiveness. Infrequent SPT/IDT+ and absent OC reactions in patients with NIM reactions suggest OC alone to be a safe and cost-effective de-labeling strategy that could improve the coverage of penicillin allergy de-labeling in lower risk populations.

摘要

背景

约10%-20%的住院患者被标记为对青霉素过敏,这与巨大的健康和经济成本相关。

目的

我们研究了青霉素过敏重新标记在临床实践中的有效性,旨在推导风险分层模型以指导检测策略。

方法

纳入2008年至2013年间转诊至西澳大利亚一家公立医院药物过敏服务部门的15岁及以上因β-内酰胺过敏的连续患者。进行随访调查。主要结局包括皮肤点刺试验和皮内试验(SPT/IDT)结果、口服激发试验(OC)结果以及试验后抗生素使用情况的随访。

结果

对401例有即刻(IMM)(≤1小时)(n = 151)和非即刻(NIM)(>1小时)(n = 250)反应的连续患者进行了SPT/IDT。在341例患者中,42例(12.3%)对≥1种青霉素试剂的SPT/IDT呈阳性,其中IMM组35/114例(30.4%),NIM组7/227例(3.1%)(P <.0001)。在355例接受SPT/IDT的患者中,3例(0.8%)均在IMM组,对单剂量青霉素V钾有非严重的阳性OC反应(SPT/IDT阴性预测值[NPV]为99.2%)。总体上近90%的患者被建议使用选择性或非限制性β-内酰胺类药物,其中NIM组238/250例(95.2%),IMM组126/151例(83.4%)(P =.0001)。在182例患者中,137例(75.3%)在随访时遵循了过敏标签修改(ALM)建议。

结论

青霉素SPT/IDT/OC能安全地对青霉素过敏患者进行重新标记,并识别出选择性β-内酰胺过敏;然而,对ALM建议的不完全遵循会削弱其有效性。NIM反应患者中SPT/IDT阳性少见且无OC反应,这表明单独使用OC是一种安全且具有成本效益的重新标记策略,可提高低风险人群中青霉素过敏重新标记的覆盖率。

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