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在英国一家三级中心确定低风险β-内酰胺类过敏患者。

Identifying Low-Risk Beta-Lactam Allergy Patients in a UK Tertiary Centre.

机构信息

Department of Adult Allergy, Guy's and St Thomas' NHS Foundation Trust, Guy's Hospital, London, UK; Peter Gorer Department of Immunobiology, Guy's Hospital, King's College London, London, UK.

Division of Rheumatology and Clinical Immunology, Department of Medicine, Queen Mary Hospital, University of Hong Kong, Hong Kong, China.

出版信息

J Allergy Clin Immunol Pract. 2019 Sep-Oct;7(7):2173-2181.e1. doi: 10.1016/j.jaip.2019.03.015. Epub 2019 Mar 25.

Abstract

BACKGROUND

There are marked geographical as well as temporal differences in patient sensitization profiles to β-lactams (BL).

OBJECTIVE

To determine the utility of skin test reagents and identify a cohort of patients where skin testing can be safely omitted in a cohort of patients referred to a UK tertiary referral center.

METHODS

A retrospective study of the clinical characteristics of 1092 patients referred for BL allergy testing was analyzed using multivariate regression analysis. The effectiveness of skin test reagents was also evaluated.

RESULTS

Multivariate logistic regression identified that a history of anaphylaxis (odds ratio [OR] 10.98, P = .001) and the patients' recall of the index drug (apart from ampicillin and meropenem, OR 3.51-12.43, P < .05) were independent predictors of type I BL allergic status and a time of less than 1 year elapsed since index reaction significantly increasing the odds of a patient with a history of anaphylaxis, having a type I BL allergy (OR 38.66, P = .003). An absence of anaphylactic severity, unknown name of the index drug and a reaction occurring more than 1 year before testing, has a negative predictive value (NPV) of 98.4%, which was similar to the NPV of skin testing of 98.9% for type I BL allergy. The NPV of skin testing with benzylpenicillin + amoxicillin ± index BL was similar with (98.9%) or without (98.1%) the use of benzylpenicillin polylysine and minor determinant for type I BL allergy.

CONCLUSION

We identified a "low risk" cohort of patients where the history is of similar reliability to skin testing in predicting nonallergic status for BL allergy.

摘要

背景

β-内酰胺类抗生素(BL)过敏患者的致敏谱存在明显的地域和时间差异。

目的

确定皮肤试验试剂的效用,并确定在英国三级转诊中心就诊的患者中,皮肤试验可安全省略的患者队列。

方法

使用多变量回归分析对 1092 例因 BL 过敏试验而转诊的患者的临床特征进行回顾性研究。还评估了皮肤试验试剂的有效性。

结果

多变量逻辑回归确定过敏反应史(比值比 [OR] 10.98,P=.001)和患者对索引药物的回忆(除氨苄西林和美罗培南外,OR 3.51-12.43,P<0.05)是 I 型 BL 过敏状态的独立预测因素,且自指数反应以来不到 1 年的时间显著增加了具有过敏反应史的患者发生 I 型 BL 过敏的可能性(OR 38.66,P=.003)。无过敏反应严重程度、未知索引药物名称和反应发生在测试前 1 年以上,其阴性预测值(NPV)为 98.4%,与 I 型 BL 过敏皮肤试验的 NPV(98.9%)相似。在不使用或使用苯唑西林多聚赖氨酸和主要决定因素的情况下,对青霉素+阿莫西林±索引 BL 进行皮肤试验的 NPV 相似,用于 I 型 BL 过敏。

结论

我们确定了一组“低风险”患者,其病史与皮肤试验在预测 BL 过敏的非过敏状态方面具有相似的可靠性。

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