• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

标准化变应原皮下免疫治疗儿童患者的全身反应,包括和不包括季节性剂量调整。

Systemic Reactions in Pediatric Patients Receiving Standardized Allergen Subcutaneous Immunotherapy with and without Seasonal Dose Adjustment.

机构信息

Division of Immunology, Boston Children's Hospital, Department of Pediatrics Harvard Medical School, Boston, Mass.

Department of Pharmacy, Boston Children's Hospital, Boston, Mass.

出版信息

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.

DOI:10.1016/j.jaip.2017.11.040
PMID:29339129
Abstract

BACKGROUND

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.

OBJECTIVE

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.

METHODS

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.

RESULTS

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.

CONCLUSIONS

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.

摘要

背景

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。

目的

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。

方法

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。

结果

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。

结论

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。

相似文献

1
Systemic Reactions in Pediatric Patients Receiving Standardized Allergen Subcutaneous Immunotherapy with and without Seasonal Dose Adjustment.标准化变应原皮下免疫治疗儿童患者的全身反应,包括和不包括季节性剂量调整。
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.
2
Risk factors for fatal and nonfatal reactions to subcutaneous immunotherapy: National surveillance study on allergen immunotherapy (2008-2013).皮下免疫疗法致死和非致死反应的危险因素:变应原免疫疗法国家监测研究(2008 - 2013年)
Ann Allergy Asthma Immunol. 2016 Apr;116(4):354-359.e2. doi: 10.1016/j.anai.2016.02.001. Epub 2016 Mar 3.
3
Detection of risk factors for systemic adverse reactions to SCIT with natural depot allergen extracts: a retrospective study.天然长效变应原提取物皮下免疫治疗全身不良反应危险因素的检测:一项回顾性研究
Eur Ann Allergy Clin Immunol. 2015 Nov;47(6):211-7.
4
Systemic reactions to subcutaneous immunotherapy: Effects of dosing and aeroallergen content.皮下免疫治疗的全身反应:剂量和变应原含量的影响。
Ann Allergy Asthma Immunol. 2019 Sep;123(3):284-287. doi: 10.1016/j.anai.2019.06.021. Epub 2019 Jul 2.
5
Immunologic effect and tolerability of intra-seasonal subcutaneous immunotherapy with an 8-day up-dosing schedule to 10,000 standardized quality-units: a double-blind, randomized, placebo-controlled trial.免疫效果和耐受性的季节性皮下免疫治疗与 8 天增毒方案到 10000 标准化质量单位:一项双盲、随机、安慰剂对照试验。
Clin Ther. 2012 Oct;34(10):2072-81. doi: 10.1016/j.clinthera.2012.09.006.
6
Systemic tolerability of specific subcutaneous immunotherapy with index-of-reactivity-standardized allergen extracts administered using clustered regimens: a retrospective, observational, multicenter study.采用聚类方案给予反应指数标准化变应原提取物进行特异性皮下免疫治疗的全身耐受性:一项回顾性、观察性、多中心研究。
Ann Allergy Asthma Immunol. 2009 Mar;102(3):247-52. doi: 10.1016/S1081-1206(10)60088-9.
7
The safety profile of subcutaneous allergen immunotherapy in children with asthma in Hangzhou, East China.中国东部杭州地区哮喘儿童皮下变应原免疫治疗的安全性概况
Allergol Immunopathol (Madr). 2017 Nov-Dec;45(6):541-548. doi: 10.1016/j.aller.2017.04.002. Epub 2017 Jun 17.
8
Short-term subcutaneous grass pollen immunotherapy under the umbrella of anti-IL-4: A randomized controlled trial.短期皮下草花粉免疫治疗在抗 IL-4 保护伞下:一项随机对照试验。
J Allergy Clin Immunol. 2016 Feb;137(2):452-461.e9. doi: 10.1016/j.jaci.2015.08.046. Epub 2015 Oct 31.
9
[Analysis of adverse reactions induced by subcutaneous immunotherapy against dust mite allergy in 234 cases with allergic rhinitis and asthma].[234例变应性鼻炎和哮喘患者尘螨变应原皮下免疫治疗不良反应分析]
Zhonghua Er Ke Za Zhi. 2012 Oct;50(10):726-31.
10
Subcutaneous Immunotherapy for Allergic Asthma in a Single Center of Korea: Efficacy, Safety, and Clinical Response Predictors.韩国单中心过敏性哮喘皮下免疫疗法:疗效、安全性及临床反应预测因素
J Korean Med Sci. 2017 Jul;32(7):1124-1130. doi: 10.3346/jkms.2017.32.7.1124.

引用本文的文献

1
Focused allergic rhinitis practice parameter for Canada.加拿大变应性鼻炎针对性诊疗规范
Allergy Asthma Clin Immunol. 2024 Aug 8;20(1):45. doi: 10.1186/s13223-024-00899-3.
2
Safety of subcutaneous immunotherapy with Novo-Helisen-Depot in the children: a retrospective analysis from a single center in Northern China.诺和海利生长效剂型皮下免疫疗法在儿童中的安全性:来自中国北方单中心的回顾性分析
Front Pediatr. 2024 Apr 25;12:1370224. doi: 10.3389/fped.2024.1370224. eCollection 2024.