Kovaltchouk Uliana, Jeimy Samira, Soller Lianne, Robertson Kara, Abrams Elissa M, Cameron Scott B, Kim Harold, Chan Edmond S
Division of Clinical Immunology and Allergy, Department of Medicine, Western University, London, Ontario, Canada.
Department of Pediatrics, Division of Allergy and Immunology, University of British Columbia, Vancouver, British Columbia, Canada.
J Allergy Clin Immunol Glob. 2023 Feb 8;2(2):100080. doi: 10.1016/j.jacig.2023.100080. eCollection 2023 May.
The safety of pediatric food oral immunotherapy (Ped-OIT) has been depicted by some as less favorable than subcutaneous immunotherapy (SCIT) owing to the increased number of serious adverse events requiring epinephrine. A review of real-world data comparing Ped-OIT and SCIT safety is necessary to guide shared decision making.
Our aim was to compare the safety and adverse event profiles of peanut Ped-OIT and SCIT using Canadian real-word literature.
We performed a retrospective review of recent Canadian real-world literature on peanut Ped-OIT and SCIT safety and adverse events.
The incidences of systemic reactions requiring epinephrine were 11 in 270 patients (4.07%) and 12 in 41,020 doses (0.029%) in a multicenter study in British Columbia, Alberta, Manitoba, and Nova Scotia studying 270 preschool-age children treated with peanut OIT. Similarly, a multicenter study in South-Western Ontario examining 160 patients between the ages of 1 and 17 years who were treated with peanut OIT showed that the incidences of systemic reactions requiring epinephrine were 5 in 160 patients (3.1%) and 8 in 52,751 doses (0.015%). A single-center retrospective review of 380 patients receiving aeroallergen SCIT showed that the incidences of systemic reactions requiring epinephrine were 28 in 380 patients (7.4%) and 1 in 1047 injection visits (0.095%). These findings are comparable to those of a review of 860 patients in Ontario who received either aeroallergen or venom SCIT, in which the incidence of systemic reaction requiring epinephrine was 10 in 4242 injections (0.24%).
Despite differences in the OIT protocols used and age groups studied, recent real-world data suggest that the safety of preschool peanut OIT or peanut OIT using a slower buildup schedule is comparable to that of SCIT.
由于需要使用肾上腺素治疗的严重不良事件数量增加,一些人认为儿童食物口服免疫疗法(Ped - OIT)的安全性不如皮下免疫疗法(SCIT)。有必要回顾比较Ped - OIT和SCIT安全性的真实世界数据,以指导共同决策。
我们的目的是利用加拿大的真实世界文献,比较花生Ped - OIT和SCIT的安全性及不良事件情况。
我们对加拿大近期关于花生Ped - OIT和SCIT安全性及不良事件的真实世界文献进行了回顾性研究。
在不列颠哥伦比亚省、艾伯塔省、曼尼托巴省和新斯科舍省开展的一项多中心研究中,对270名接受花生口服免疫疗法的学龄前儿童进行研究,结果显示,需要使用肾上腺素治疗的全身反应发生率在270名患者中为11例(4.07%),在41,020次剂量中为12例(0.029%)。同样,安大略省西南部的一项多中心研究对160名年龄在1至17岁之间接受花生口服免疫疗法的患者进行了检查,结果显示,需要使用肾上腺素治疗的全身反应发生率在160名患者中为5例(3.1%),在52,751次剂量中为8例(0.015%)。一项对380名接受气传变应原皮下免疫疗法患者的单中心回顾性研究显示,需要使用肾上腺素治疗的全身反应发生率在380名患者中为28例(7.4%),在1047次注射就诊中为1例(0.095%)。这些结果与安大略省一项对860名接受气传变应原或毒液皮下免疫疗法患者的回顾性研究结果相当,在该研究中,需要使用肾上腺素治疗的全身反应发生率在4242次注射中为10例(0.24%)。
尽管所使用的口服免疫疗法方案和研究的年龄组有所不同,但近期的真实世界数据表明,学龄前花生口服免疫疗法或采用较慢递增方案的花生口服免疫疗法的安全性与皮下免疫疗法相当。