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使用酮洛芬口服激发试验来检测有阿司匹林诱发荨麻疹病史患者中的交叉反应者。

Use of ketoprofen oral challenges to detect cross-reactors among patients with a history of aspirin-induced urticaria.

作者信息

Asero Riccardo

机构信息

Ambulatorio di Allergologia, Clinica San Carlo, Paderno Dugnano (MI), Italy.

出版信息

Ann Allergy Asthma Immunol. 2006 Aug;97(2):187-9. doi: 10.1016/S1081-1206(10)60011-7.

Abstract

BACKGROUND

In patients with a history of urticaria induced by a single nonsteroidal anti-inflammatory drug (NSAID), advising elimination of all drugs that inhibit cyclooxygenase 1 (COX-1) can lead to unnecessary avoidance of useful NSAIDs.

OBJECTIVE

To classify patients with a history of aspirin-induced urticaria as cross-reactors or single-drug reactors by oral challenges with another strong COX-1 inhibitor, namely, ketoprofen.

METHODS

Forty otherwise healthy patients with a history of acute urticaria after the ingestion of aspirin underwent single-blind, placebo-controlled oral challenges with ketoprofen. In patients who did not tolerate ketoprofen, tolerance tests with drugs exerting either COX-1 inhibition at high doses (acetaminophen and nimesulide) or no COX-1 inhibition at therapeutic doses (rofecoxib and tramadol) were performed.

RESULTS

In 24 patients (60%), ketoprofen induced urticaria that was controlled by an intravenous antihistamine; 18 (75%) of the 24 patients reacted after the first provocative dose. On subsequent challenges, 3 (38%) of 8 ketoprofen reactors did not tolerate nimesulide, whereas acetaminophen tramadol and rofecoxib were tolerated by 18 of 18, 14 of 14, and 16 of 16 ketoprofen reactors, respectively. Three ketoprofen reactors reported the onset of spontaneous recurrent urticaria 1 to 3 years after the challenge tests.

CONCLUSION

In patients with a history of urticaria induced by a single NSAID, oral challenges with alternative COX-1 inhibitors are helpful in detecting whether they are true single-NSAID reactors; weak COX-1 inhibitors should be challenged subsequently only in those who show multiple-NSAID intolerance.

摘要

背景

对于有单一非甾体抗炎药(NSAID)诱发荨麻疹病史的患者,建议停用所有抑制环氧化酶1(COX - 1)的药物可能会导致不必要地避免使用有用的NSAID。

目的

通过用另一种强效COX - 1抑制剂酮洛芬进行口服激发试验,将有阿司匹林诱发荨麻疹病史的患者分类为交叉反应者或单一药物反应者。

方法

40名既往有服用阿司匹林后发生急性荨麻疹病史的健康患者接受了酮洛芬的单盲、安慰剂对照口服激发试验。对于不能耐受酮洛芬的患者,进行了高剂量时具有COX - 1抑制作用(对乙酰氨基酚和尼美舒利)或治疗剂量时无COX - 1抑制作用(罗非昔布和曲马多)的药物耐受性试验。

结果

24名患者(60%)出现了由酮洛芬诱发的荨麻疹,可通过静脉注射抗组胺药控制;24名患者中有18名(75%)在首次激发剂量后出现反应。在随后的激发试验中,8名酮洛芬反应者中有3名(38%)不能耐受尼美舒利,而18名酮洛芬反应者中分别有18名、14名和16名耐受对乙酰氨基酚、曲马多和罗非昔布。3名酮洛芬反应者在激发试验后1至3年报告出现自发性复发性荨麻疹。

结论

对于有单一NSAID诱发荨麻疹病史的患者,用其他COX - 1抑制剂进行口服激发试验有助于检测他们是否为真正的单一NSAID反应者;随后仅应在那些表现出多种NSAID不耐受的患者中对弱COX - 1抑制剂进行激发试验。

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