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A retrospective study of peanut and tree nut allergy: Sensitization and correlations with clinical manifestations

机译:花生和坚果过敏的回顾性研究:致敏性及其与临床表现的关系

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摘要

Peanut (PN) and tree nut (TN) allergies are among the leading causes of fatal food-induced anaphylaxis and are increasing in prevalence, especially in children. Their cosensitization and concurrent clinical allergy have been understudied. This retrospective study investigated the correlation between PN and TN allergy, both in terms of in vitro sensitization (IVS) and clinical allergic manifestations. We conducted a retrospective medical record review at the Allergy Clinic at University Hospital of Brooklyn. Fourteen hundred six charts were reviewed, of which 76 (5.4%) had documented relevant clinical allergy: PN allergy but not TN allergy (n = 29) or TN allergy but not PN allergy (n = 11) or both (n = 30). Six patients with PN allergy but no TN exposure history were not included in the analysis. The majority of patients (67/76, 88.1%) had a concurrent history of asthma, rhinoconjunctivitis, or AD. Sensitivity of TN IVS predicting PN IVS was 38/39 (97%). Similarly, sensitivity of PN IVS predicting TN IVS was 38/42 (91%). Sensitivity of TN clinical allergy predicting PN allergy was 30/59 (51%). Sensitivity of PN clinical allergy predicting TN allergy was 30/41 (73%). The total number of organ systems involved in reported clinical reactions correlated with IVS to TN (p = 0.004) but not IVS to PN (p = 0.983). In summary, we found PN sensitization predicts TN sensitization in vitro , with lower predictability for clinical reactions.
机译:花生(PN)和树坚果(TN)过敏是致命的食物诱发过敏反应的主要原因,并且患病率呈上升趋势,尤其是在儿童中。他们的增敏作用和并发的临床过敏已经被研究不足。这项回顾性研究从体外致敏(IVS)和临床过敏表现两个方面研究了PN和TN过敏之间的相关性。我们在布鲁克林大学医院过敏诊所进行了回顾性病历审查。审查了146张图表,其中76张(5.4%)已记录相关的临床过敏:PN过敏但不TN过敏(n = 29)或TN过敏但PN过敏(n = 11)或两者(n = 30) 。分析中不包括6名PN过敏但无TN暴露史的患者。大多数患者(67 / 76,88.1%)同时患有哮喘,鼻结膜炎或AD。 TN IVS预测PN IVS的敏感性为38/39(97%)。同样,预测PN IVS的PN IVS的敏感性为38/42(91%)。预测PN过敏的TN临床过敏的敏感性为30/59(51%)。预测TN过敏的PN临床过敏的敏感性为30/41(73%)。所报告的临床反应中涉及的器官系统总数与IVS与TN相关(p = 0.004),而不与IVS与PN相关(p = 0.983)。总之,我们发现PN致敏作用可预测体外TN致敏作用,对临床反应的可预测性较低。

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