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评价美国国立过敏和传染病研究所/食物过敏和过敏反应网络标准用于急诊科患者过敏反应诊断的价值。

Evaluation of national institute of allergy and infectious diseases/food allergy and anaphylaxis network criteria for the diagnosis of anaphylaxis in emergency department patients.

机构信息

Department of Emergency Medicine, Mayo Clinic, Rochester, MN 55905, USA.

出版信息

J Allergy Clin Immunol. 2012 Mar;129(3):748-52. doi: 10.1016/j.jaci.2011.09.030. Epub 2011 Nov 1.

Abstract

BACKGROUND

Diagnostic criteria were proposed at the Second Symposium on the Definition and Management of Anaphylaxis convened by the National Institute of Allergy and Infectious Diseases/Food Allergy and Anaphylaxis Network (NIAID/FAAN). Validation is needed before these criteria can be widely adapted into clinical practice.

OBJECTIVE

Our aim was to retrospectively assess the diagnostic accuracy of the NIAID/FAAN criteria for the diagnosis of anaphylaxis in emergency department (ED) patients.

METHODS

A retrospective cohort study of ED patients presenting from April to October 2008 was conducted. Patients given a diagnosis of an allergic reaction or anaphylaxis and a subset of patients with related diagnoses were included. Electronic medical records were reviewed and data were abstracted to determine whether the NIAID/FAAN criteria were met. Records were also independently reviewed in a blinded fashion by 2 experienced attending allergists. Final diagnosis by allergists was considered the reference standard.

RESULTS

Of 214 patients, 86 (40.2%) met the NIAID/FAAN criteria for anaphylaxis. Allergists gave 61 (28.5%) patients diagnoses of anaphylaxis, 59 (96.7%) of whom satisfied the NIAID/FAAN criteria. The interrater agreement between allergists was substantial (κ = 0.77). The test characteristics of the NIAID/FAAN criteria were as follows: sensitivity, 96.7% (95% CI, 88.8% to 99.1%); specificity, 82.4% (95% CI, 75.5% to 87.6%); positive predictive value, 68.6% (95% CI, 58.2% to 77.4%); negative predictive value, 98.4% (95% CI, 94.5% to 99.6%); positive likelihood ratio, 5.48; and negative likelihood ratio, 0.04.

CONCLUSIONS

These results suggest that the NIAID/FAAN criteria are highly sensitive but less specific and are likely to be useful in the ED for the diagnosis of anaphylaxis.

摘要

背景

过敏反应和过敏性休克诊断标准是由美国国立过敏和传染病研究所/食物过敏和过敏性休克网络(NIAID/FAAN)第二次定义和管理过敏反应研讨会提出的。在这些标准被广泛应用于临床实践之前,需要对其进行验证。

目的

本研究旨在回顾性评估 NIAID/FAAN 标准在急诊科(ED)患者诊断过敏反应中的诊断准确性。

方法

对 2008 年 4 月至 10 月期间就诊于 ED 的患者进行回顾性队列研究。入组患者被诊断为过敏反应或过敏反应,以及具有相关诊断的亚组患者。审查电子病历并提取数据以确定是否符合 NIAID/FAAN 标准。病历还由 2 位经验丰富的主治过敏症医生进行独立盲法审查。过敏症医生的最终诊断被视为参考标准。

结果

在 214 例患者中,86 例(40.2%)符合 NIAID/FAAN 诊断过敏反应的标准。过敏症医生诊断 61 例(28.5%)患者为过敏反应,其中 59 例(96.7%)符合 NIAID/FAAN 标准。过敏症医生之间的一致性很高(κ=0.77)。NIAID/FAAN 标准的测试特征如下:敏感性为 96.7%(95%CI,88.8%至 99.1%);特异性为 82.4%(95%CI,75.5%至 87.6%);阳性预测值为 68.6%(95%CI,58.2%至 77.4%);阴性预测值为 98.4%(95%CI,94.5%至 99.6%);阳性似然比为 5.48;阴性似然比为 0.04。

结论

这些结果表明,NIAID/FAAN 标准具有很高的敏感性,但特异性较低,可能有助于急诊科诊断过敏反应。

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