Sánchez-Borges Mario, Caballero-Fonseca Fernan, Capriles-Hulett Arnaldo
Allergy-Immunology Service, Centro Médico-Docente La Trinidad, Caracas, Venezuela.
Ann Allergy Asthma Immunol. 2005 Jan;94(1):34-8. doi: 10.1016/S1081-1206(10)61282-3.
Selective inhibitors of cyclooxygenase 2 (COX-2) are generally tolerated by patients sensitive to nonsteroidal anti-inflammatory drugs (NSAIDs) that inhibit COX-1. Valdecoxib is a new sulfonamide-containing COX-2-specific inhibitor indicated for the treatment of acute pain, osteoarthritis, and rheumatoid arthritis.
To compare the clinical tolerance to rofecoxib and valdecoxib in patients who previously developed urticaria and angioedema while taking classic NSAIDs.
Patients with challenge-proven NSAID cutaneous sensitivity were submitted to single-blinded controlled oral challenges with rofecoxib, 50 mg, and valdecoxib, 40 mg.
Twenty-eight patients (19 females and 9 males; mean +/- SD age, 28.6 +/- 15.0 years; age range, 10-61 years) participated in this study. Twenty-two (85%) of 26 patients who underwent skin tests were atopic, as demonstrated by a clinical history of rhinitis and/or asthma plus positive immediate-type skin hypersensitivity test results. A previous exclusive cutaneous reaction pattern (urticaria and/or angioedema) had occurred in 10 patients (36%), whereas a mixed pattern of skin and respiratory symptoms had occurred in 18 patients (64%). Twenty patients (71%) were multiple reactors, and 8 patients (28%) were single reactors. In this current study, 2 patients (7%) taking rofecoxib experienced angioedema, and 1 patient (4%) taking valdecoxib experienced urticaria.
Rofecoxib and valdecoxib can be safely used by most NSAID-sensitive patients with cutaneous reactions. Our findings suggest that isolated cross-reactions may occur in these patients, and for this reason, controlled oral provocation may be prudent when prescribing valdecoxib or rofecoxib for patients who have previously had urticaria or angioedema triggered by NSAIDs.
环氧化酶2(COX - 2)选择性抑制剂通常为对抑制COX - 1的非甾体抗炎药(NSAIDs)敏感的患者所耐受。伐地昔布是一种新型含磺酰胺的COX - 2特异性抑制剂,用于治疗急性疼痛、骨关节炎和类风湿关节炎。
比较既往服用经典NSAIDs时出现荨麻疹和血管性水肿的患者对罗非昔布和伐地昔布的临床耐受性。
经激发试验证实对NSAIDs皮肤敏感的患者接受单盲对照口服罗非昔布(50毫克)和伐地昔布(40毫克)激发试验。
28例患者(19例女性和9例男性;平均±标准差年龄,28.6±15.0岁;年龄范围,10 - 61岁)参与了本研究。26例接受皮肤试验的患者中有22例(85%)为特应性,有鼻炎和/或哮喘的临床病史以及即刻型皮肤过敏试验结果阳性可证明。既往有10例患者(36%)出现过单纯皮肤反应模式(荨麻疹和/或血管性水肿),而18例患者(64%)出现过皮肤和呼吸道症状的混合模式。20例患者(71%)为多重反应者,8例患者(28%)为单一反应者。在本研究中,服用罗非昔布的2例患者(7%)出现血管性水肿,服用伐地昔布的1例患者(4%)出现荨麻疹。
大多数有皮肤反应的NSAIDs敏感患者可安全使用罗非昔布和伐地昔布。我们的研究结果表明这些患者可能会出现孤立的交叉反应,因此,对于既往有NSAIDs引发的荨麻疹或血管性水肿的患者,在开具伐地昔布或罗非昔布处方时进行口服激发试验可能较为谨慎。