Division of Immunology, Boston Children's Hospital, Department of Pediatrics Harvard Medical School, Boston, Mass.
Department of Pharmacy, Boston Children's Hospital, Boston, Mass.
J Allergy Clin Immunol Pract. 2018 Sep-Oct;6(5):1711-1716.e4. doi: 10.1016/j.jaip.2017.11.040. Epub 2018 Jan 12.
The 2003 Joint Task Force on Practice Parameters recommended standardizing allergen subcutaneous immunotherapy (SCIT). Data from longitudinal surveillance survey in North America reported a systemic reaction (SR) rate of 0.1% to 0.2% of injection visits. The rate of SR to standardized SCIT in pediatric patients has not been well evaluated.
The objective of this study was to evaluate the rate of SRs to standardized SCIT in pediatric patients aged 5 to 18 years in a single tertiary care center in the United States.
A retrospective chart review was conducted in 2 groups: group 1 started SCIT within a period extending from January 2009 to June 2012, whereas group 2 started SCIT within a period extending from January 2013 to June 2016. The protocol was modified in group 2 such that updosing and maintenance doses were adjusted in the spring for tree and grass pollen and in the fall for weed pollen.
There were a total of 128 patients in group 1 and 118 patients in group 2. The rate of SR was 0.429% in group 1 and 0.364% in group 2, which was not significant. There was no difference in the severity of SR in the 2 groups with no-fatal or near-fatal SR noted. Asthma was a significant risk factor in the younger age subgroup aged 5 to 11 years.
Standardized SCIT appears to be associated with an SR rate of 0.429% to 0.364% of visits in pediatric patients. Protocol modification did not lead to a significant drop in SR. Larger multicenter studies are required to further evaluate the rate of SRs from standardized SCIT.
2003 年联合实践参数工作组建议标准化变应原皮下免疫疗法(SCIT)。来自北美纵向监测调查的数据报告注射就诊时的全身性反应(SR)发生率为 0.1%至 0.2%。标准化 SCIT 在儿科患者中的 SR 发生率尚未得到很好的评估。
本研究的目的是评估美国一家三级保健中心的 5 至 18 岁儿科患者接受标准化 SCIT 的 SR 发生率。
对两组进行回顾性图表审查:第 1 组在 2009 年 1 月至 2012 年 6 月期间开始接受 SCIT,第 2 组在 2013 年 1 月至 2016 年 6 月期间开始接受 SCIT。第 2 组的方案进行了修改,即春季调整树木和草花粉的增量剂量和维持剂量,秋季调整杂草花粉的增量剂量和维持剂量。
第 1 组共有 128 例患者,第 2 组共有 118 例患者。第 1 组的 SR 发生率为 0.429%,第 2 组为 0.364%,差异无统计学意义。两组的 SR 严重程度无差异,均未出现致命或接近致命的 SR。哮喘是 5 至 11 岁年龄较小亚组的一个显著危险因素。
标准化 SCIT 似乎与儿科患者就诊时 0.429%至 0.364%的 SR 发生率相关。方案修改并未导致 SR 发生率显著下降。需要更大规模的多中心研究进一步评估标准化 SCIT 的 SR 发生率。