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特异性环氧化酶-2抑制剂依托考昔在阿司匹林诱发的呼吸道疾病哮喘患者中的安全性。

Safety of etoricoxib, a specific cyclooxygenase-2 inhibitor, in asthmatic patients with aspirin-exacerbated respiratory disease.

作者信息

El Miedany Yasser, Youssef Sally, Ahmed Ihab, El Gaafary Maha

机构信息

Department of Rheumatology and Rehabilitation, Faculty of Medicine, Ain Shams University, Cairo, Egypt.

出版信息

Ann Allergy Asthma Immunol. 2006 Jul;97(1):105-9. doi: 10.1016/S1081-1206(10)61378-6.

Abstract

BACKGROUND

Treatment of rheumatic conditions is limited in patients with asthma owing to concerns of nonsteroidal anti-inflammatory drugs potentially provoking asthma. Cross-sensitivity to all anti-inflammatory drugs that inhibit cyclooxygenase enzymes occurs in these individuals.

OBJECTIVES

To study the safety of etoricoxib, a specific cyclooxygenase-2 inhibitor, and to determine whether it cross-reacts with asthma in patients with aspirin-exacerbated respiratory disease (AERD).

METHODS

This study included 77 patients who had experienced asthma induced by aspirin and at least 1 other nonsteroidal anti-inflammatory drug. Baseline evaluation included blood pressure measurement, nasal examination, spirometry, and peak expiratory flow rate measurement. Patients were given placebo the first day and then were challenged with once-daily etoricoxib in 3 different doses: 60 mg on day 2, 90 mg on day 3, and 120 mg on day 4. If no evidence of intolerance was seen, each patient was rechallenged with 60 or 90 mg of etoricoxib once daily (according to the rheumatic condition) 7 days later. Reassessment of the baseline measurements was performed daily from day 1 to day 4 after the initial challenge, on day 7 after rechallenge, and after 1 month of drug intake. If the patient developed any mucosal or skin reaction, hypotension, upper or lower airway obstruction, conjunctival reaction, or laryngeal edema during the challenge test, it was considered a positive response.

RESULTS

Etoricoxib was well tolerated, without any signs of immediate or delayed hypersensitivity in aspirin- and nonsteroidal anti-inflammatory drug-induced asthmatic patients. None of 77 study patients experienced any symptoms or developed dyspnea, change in nasal examination, significant variation in peak expiratory flow rate greater than 20%, or decline in forced expiratory volume in 1 second greater than 15% during etoricoxib challenge. The exact 1-sided confidence interval for the probability of etoricoxib inducing cross-reactions in patients with AERD was 0% to 2%.

CONCLUSIONS

These results confirm the lack of cross-reactivity between specific cyclooxygenase-2 inhibitors and aspirin in AERD. Etoricoxib was safe for treating inflammation in patients with AERD.

摘要

背景

由于担心非甾体抗炎药可能诱发哮喘,哮喘患者的风湿性疾病治疗受到限制。这些个体对所有抑制环氧化酶的抗炎药存在交叉敏感性。

目的

研究特异性环氧化酶-2抑制剂依托考昔的安全性,并确定其在阿司匹林诱发的呼吸道疾病(AERD)患者中是否与哮喘发生交叉反应。

方法

本研究纳入77例曾因阿司匹林及至少1种其他非甾体抗炎药诱发哮喘的患者。基线评估包括血压测量、鼻腔检查、肺功能测定和呼气峰值流速测量。患者第1天服用安慰剂,然后在第2天、第3天和第4天分别接受3种不同剂量的依托考昔每日1次的激发试验,剂量分别为60mg、90mg和120mg。如果未观察到不耐受证据,7天后根据风湿性疾病情况,每名患者再次每日接受60mg或90mg依托考昔激发试验。在初始激发试验后的第1天至第4天、再次激发试验后的第7天以及服药1个月后,每天对基线测量指标进行重新评估。如果患者在激发试验期间出现任何黏膜或皮肤反应、低血压、上呼吸道或下呼吸道梗阻、结膜反应或喉水肿,则视为阳性反应。

结果

依托考昔耐受性良好,在阿司匹林和非甾体抗炎药诱发哮喘的患者中未出现任何即刻或延迟过敏反应迹象。77例研究患者在依托考昔激发试验期间均未出现任何症状或发生呼吸困难、鼻腔检查改变、呼气峰值流速显著变化超过20%或第1秒用力呼气容积下降超过15%。依托考昔在AERD患者中诱发交叉反应概率的确切单侧置信区间为0%至2%。

结论

这些结果证实特异性环氧化酶-2抑制剂与阿司匹林在AERD中不存在交叉反应。依托考昔治疗AERD患者的炎症是安全的。

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