Karunakaran Duva, Chan Edmond S, Zhang Qian, Bone Jeffrey N, Carr Stuart, Kapur Sandeep, Rex Gregory A, McHenry Mary, Cameron Scott B, Cook Victoria E, Leo Sara, Wong Tiffany, Gerstner Thomas V, Yeung Joanne, Abrams Elissa M, Mak Raymond, Erdle Stephanie C, Soller Lianne
British Columbia Children's Hospital, Vancouver, British Columbia.
Department of Medicine, Queen's University, Kingston, Ontario.
J Allergy Clin Immunol Glob. 2023 Mar 21;2(2):100094. doi: 10.1016/j.jacig.2023.100094. eCollection 2023 May.
An understanding of how patient characteristics such as age, baseline peanut-specific IgE, and atopic comorbidities may influence potential safety outcomes during peanut oral immunotherapy (P-OIT) could aid in shared decision making between clinicians and patient families.
This study explored the relationship between baseline patient characteristics and reactions during P-OIT using a large sample size to better understand potential risk factors influencing P-OIT safety.
Data were obtained from the Food Allergy Immunotherapy (FAIT) registry, which collects real-world OIT data from community and academic allergy clinics across Canada. Multivariable logistic regression modeling was performed to examine the relationship between baseline patient characteristics and reactions during P-OIT. Multiple imputation was applied to reduce potential bias caused by missingness and to maximize the use of available information to preserve statistical power.
Between April 2017 and June 2021, a total of 653 eligible patients initiated P-OIT. Multivariable regression analysis showed pre-OIT grade 2+ initial reaction (odds ratio [OR] = 1.33, 95% confidence interval [CI] 1.10, 1.61), allergic rhinitis (OR = 1.60, 95% CI 1.08, 2.38), older age (OR = 1.01, 95% CI 1.00, 1.02), and higher baseline peanut-specific IgE (OR = 1.02, 95% CI 1.02, 1.03) were associated with grade 2+ reaction during P-OIT after adjusting for potential risk factors.
Our study identified several clinically important risk factors for grade 2+ reactions during P-OIT: pre-OIT grade 2+ initial reaction, allergic rhinitis, older age, and higher baseline peanut-specific IgE. These results highlight the need for individualized risk stratification for OIT.
了解年龄、基线花生特异性IgE和特应性合并症等患者特征如何影响花生口服免疫疗法(P-OIT)期间的潜在安全结果,有助于临床医生和患者家属共同做出决策。
本研究使用大样本量探讨了基线患者特征与P-OIT期间反应之间的关系,以更好地了解影响P-OIT安全性的潜在风险因素。
数据来自食物过敏免疫疗法(FAIT)登记处,该登记处收集了加拿大各地社区和学术过敏诊所的真实世界OIT数据。进行多变量逻辑回归建模,以检查基线患者特征与P-OIT期间反应之间的关系。应用多重填补法来减少因数据缺失导致的潜在偏差,并最大限度地利用可用信息以保持统计效力。
在2017年4月至2021年6月期间,共有653名符合条件的患者开始接受P-OIT。多变量回归分析显示,在调整潜在风险因素后,OIT前2级以上初始反应(比值比[OR]=1.33,95%置信区间[CI]1.10,1.61)、过敏性鼻炎(OR=1.60,95%CI 1.08,2.38)、年龄较大(OR=1.01,95%CI 1.00,1.02)和较高的基线花生特异性IgE(OR=1.02,95%CI 1.02,1.03)与P-OIT期间2级以上反应相关。
我们的研究确定了P-OIT期间2级以上反应的几个临床重要风险因素:OIT前2级以上初始反应、过敏性鼻炎、年龄较大和较高的基线花生特异性IgE。这些结果凸显了对OIT进行个体化风险分层的必要性。