Department of Pulmonary, Allergy, Critical Care, and Sleep Medicine, University of Miami Miller School of Medicine, Miami, FL 33136, USA.
Allergy Asthma Proc. 2013 May-Jun;34(3):255-60. doi: 10.2500/aap.2013.34.3651.
Rush immunotherapy (RIT) accelerates the build-up phase of traditional IT. The biggest potential benefit of using RIT is decreased time to symptomatic improvement. However, aeroallergen RIT carries an increased risk of systemic reaction (SR) compared with traditional IT. This study was designed to assess the safety of a modified 1-day multiple aeroallergen RIT protocol. A retrospective chart review was performed of 138 patients from an outpatient, university-based allergy practice who underwent RIT between November 2007 and February 2011. The RIT protocol consisted of eight injections over 5 hours, and stopped at one 10-fold dilution below the maintenance vial. All patients were premedicated on the same day of RIT with prednisone and histamine 1 and 2 receptor blockers. Primary end point observed was rate of SR. One hundred thirty-eight patients received a total of 2911 RIT injections. Thirty- eight patients (28%) had SRs. The SR rate per injection was 1.3%. Most of the reactions (82%) occurred after the last dose of the protocol. No patients with SR had severe anaphylaxis requiring emergency department support or hospitalization. The post-RIT SR rate was within the range seen with traditional IT. Well-controlled asthmatic patients were not at increased risk of SR compared with nonasthmatic patients. Modification of RIT to end at one 10-fold dilution below the maintenance vial for multiple aeroallergen RIT did not significantly decrease the SR rate compared with other protocols that end at the maintenance vial. Unlike hymenoptera RIT, aeroallergen RIT continues to be associated with a high risk of SR compared with traditional IT.
冲击免疫疗法(RIT)加速了传统免疫疗法的建立阶段。使用 RIT 的最大潜在益处是症状改善时间缩短。然而,与传统免疫疗法相比,过敏原 RIT 具有更高的全身反应(SR)风险。本研究旨在评估改良的 1 天多过敏原 RIT 方案的安全性。对 2007 年 11 月至 2011 年 2 月期间在一家大学过敏门诊接受 RIT 的 138 例患者的回顾性图表进行了回顾。RIT 方案由 5 小时内的 8 次注射组成,并且在维持瓶下方一个 10 倍稀释度处停止。所有患者均在 RIT 当天接受泼尼松和组胺 1 和 2 受体阻滞剂的预处理。观察的主要终点是 SR 率。138 例患者共接受 2911 次 RIT 注射。38 例(28%)患者发生 SR。每注射一次的 SR 发生率为 1.3%。大多数反应(82%)发生在方案的最后一次剂量后。没有发生 SR 的患者需要急诊室支持或住院治疗严重过敏反应。RIT 后 SR 率在传统 IT 范围内。与非哮喘患者相比,控制良好的哮喘患者发生 SR 的风险没有增加。与其他在维持瓶结束的方案相比,将 RIT 改为在维持瓶下方一个 10 倍稀释度结束,并不会显著降低多过敏原 RIT 的 SR 率。与膜翅目昆虫 RIT 不同,过敏原 RIT 与传统 IT 相比,继续与高 SR 风险相关。