Division of Allergy, Asthma and Immunology, Scripps Clinic, San Diego, California 92130, USA.
Ann Allergy Asthma Immunol. 2010 Aug;105(2):130-5. doi: 10.1016/j.anai.2010.05.020. Epub 2010 Jul 1.
Intranasal ketorolac challenges can induce respiratory reactions in patients with aspirin-exacerbated respiratory disease (AERD).
To determine whether intranasal ketorolac challenges might be used for aspirin desensitization.
One hundred patients with suspected AERD who were referred to Scripps Clinic from May 1, 2007 to December 31, 2009 were challenged with 4 increasing doses of ketorolac intranasally at 30-minute intervals. Symptoms, objective changes in the results of their nasal examination, peak nasal inspiratory flow rates, and forced expiratory volume in 1 second (FEV(1)) values were recorded. After nasal ketorolac dosing, patients were given oral aspirin as part of the challenge and desensitization. A control group consisted of 100 patients who had previously undergone our standard oral aspirin challenges and desensitization. Both groups were consecutively enrolled and had similar clinical characteristics.
Compared with the standard oral aspirin challenge and desensitization, intranasal ketorolac and modified aspirin challenge significantly attenuated the mean percentage decrease in FEV(1) values (8.5% vs 13.4%; P = .01) and decreased the percentage of extrapulmonary reactions (23% vs 45%; P = .002), particularly laryngospasm (7% vs19%; P = .02) and gastrointestinal reactions (12% vs 33%; P = .001). This new protocol was significantly shorter, lasting an average of 1.9 vs 2.6 days (P = <.001). In fact, 83% of the patients completed the new protocol in less than 48 hours compared with only 20% in the oral challenge control group (P < .001).
Intranasal ketorolac challenge and desensitization followed by rapid oral aspirin challenges is effective, safe, and less time-consuming than our standard oral aspirin desensitization protocol.
鼻内给予酮咯酸可诱发阿司匹林加重性呼吸系统疾病(AERD)患者的呼吸反应。
确定鼻内给予酮咯酸是否可用于阿司匹林脱敏。
2007 年 5 月 1 日至 2009 年 12 月 31 日,将 100 例疑似 AERD 的患者转诊至 Scripps 诊所,每 30 分钟鼻内给予 4 个递增剂量的酮咯酸。记录症状、鼻检查结果的客观变化、峰鼻吸气流量(PNIF)值和 1 秒用力呼气量(FEV1)值。鼻内给予酮咯酸后,患者接受口服阿司匹林作为挑战和脱敏的一部分。对照组由 100 例先前接受我们标准口服阿司匹林挑战和脱敏的患者组成。两组均连续入组且具有相似的临床特征。
与标准口服阿司匹林挑战和脱敏相比,鼻内酮咯酸和改良阿司匹林挑战显著减轻 FEV1 值的平均百分比下降(8.5%比 13.4%;P =.01),并减少了肺外反应的百分比(23%比 45%;P =.002),尤其是喉痉挛(7%比 19%;P =.02)和胃肠道反应(12%比 33%;P =.001)。新方案明显更短,平均持续时间为 1.9 天比 2.6 天(P = <.001)。实际上,83%的患者在不到 48 小时内完成了新方案,而对照组中只有 20%的患者(P <.001)。
鼻内给予酮咯酸挑战和脱敏后快速给予口服阿司匹林挑战有效、安全且耗时更短,优于我们的标准口服阿司匹林脱敏方案。