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美国国立过敏与传染病研究所协作临床试验的结果,该试验旨在测试在住院成人中使用主要和次要青霉素衍生物进行皮肤试验的预测价值。

Results of the National Institute of Allergy and Infectious Diseases Collaborative Clinical Trial to test the predictive value of skin testing with major and minor penicillin derivatives in hospitalized adults.

作者信息

Sogn D D, Evans R, Shepherd G M, Casale T B, Condemi J, Greenberger P A, Kohler P F, Saxon A, Summers R J, VanArsdel P P

机构信息

National Institute of Allergy and Infectious Diseases, Bethesda, MD.

出版信息

Arch Intern Med. 1992 May;152(5):1025-32.

PMID:1580706
Abstract

BACKGROUND

A history (or lack thereof) of penicillin allergy is known to be unreliable in predicting reactions on subsequent administration of the drug. This study tests the usefulness of four penicillin allergen skin tests in the prediction of IgE-mediated reactions subsequent to administration of penicillin.

METHODS

Eight centers cooperated in the National Institute of Allergy and Infectious Diseases trial of the predictive value of skin testing with major and minor penicillin derivatives. Hospitalized adults were tested with a major determinant (octa-benzylpenicilloyl-ocytalysine) and a minor determinant mixture and its components (potassium benzylpenicillin, benzylpenicilloate, and benzylpenicilloyl-N-propylamine). Patients then received a therapeutic course of penicillin and were observed, for 48 hours, for adverse reactions compatible with an IgE-mediated immediate or accelerated allergy.

RESULTS

Among 726 history-positive patients, 566 with negative skin tests received penicillin and only seven (1.2%) had possibly IgE-mediated reactions. Among 600 history-negative patients, 568 with negative skin tests received penicillin and none had a reaction. Only nine of the 167 positive skin test reactors received a penicillin agent and then usually by cautious incremental dosing. Two (22%) of these nine patients had reactions compatible with IgE-mediated immediate or accelerated penicillin allergy; both were positive to the two determinants.

CONCLUSIONS

These data corroborate previous data about the negative predictive value of negative skin tests to these materials. The reaction rate in skin test-positive patients was significantly higher than in those with negative skin tests, demonstrating the positive predictive value of positive tests to both major and minor determinants. The number of patients positive only to the major determinant or only to the minor determinant mix was too small to draw conclusions about the positive predictive value of either reagent alone.

摘要

背景

已知青霉素过敏史(或无过敏史)在预测后续用药反应方面并不可靠。本研究测试了四种青霉素过敏原皮肤试验在预测青霉素给药后IgE介导反应中的效用。

方法

八个中心合作参与了美国国立过敏和传染病研究所关于主要和次要青霉素衍生物皮肤试验预测价值的试验。对住院成人用主要决定簇(八苄基青霉素酰-卵清蛋白)、次要决定簇混合物及其成分(苄青霉素钾、苄青霉素酯和苄青霉素酰-N-丙胺)进行检测。然后患者接受一个疗程的青霉素治疗,并观察48小时,以观察是否有与IgE介导的速发型或速发加剧型过敏反应相符的不良反应。

结果

在726例有过敏史阳性的患者中,566例皮肤试验阴性的患者接受了青霉素治疗,只有7例(1.2%)可能发生了IgE介导的反应。在600例无过敏史的患者中,568例皮肤试验阴性的患者接受了青霉素治疗,无一例出现反应。167例皮肤试验阳性者中只有9例接受了青霉素制剂,且通常是通过谨慎的递增剂量给药。这9例患者中有2例(22%)出现了与IgE介导的速发型或速发加剧型青霉素过敏反应相符的反应;二者对两种决定簇均呈阳性。

结论

这些数据证实了先前关于这些物质皮肤试验阴性预测价值的数据。皮肤试验阳性患者的反应率显著高于皮肤试验阴性患者,表明对主要和次要决定簇检测呈阳性的预测价值。仅对主要决定簇或仅对次要决定簇混合物呈阳性的患者数量过少,无法得出关于任何一种试剂单独阳性预测价值的结论。

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