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VALIDA项目:过敏诊断检测的验证(过敏诊断中检测评估的工具与建议)

VALIDA project: Validation of allergy diagnostics assays (Tools and recommendations for the assessment of tests in the diagnosis of allergy).

作者信息

Casas María L, Esteban Ángel, González-Muñoz Miguel, Labrador-Horrillo Moisés, Pascal Mariona, Teniente-Serra Aina

机构信息

Clinical Analysis Service, Fundación Alcorcón University Hospital, Alcorcón, Madrid, Spain.

Spanish Society of Laboratory Medicine (SEQC-ML), Barcelona, Spain.

出版信息

Adv Lab Med. 2020 Aug 21;1(4):20200051. doi: 10.1515/almed-2020-0051. eCollection 2020 Dec.

Abstract

allergen-specific immunoglobulin E (IgE) detection and quantification tests are routinely performed in clinical laboratories to diagnose patients with a suspected allergy. Numerous commercial assays are available to test for allergies, but the results can vary widely, thereby influencing both diagnosis and treatment. Given the challenges posed by differences in the various assays for determination of specific IgE, a group of experts has compiled in a document a series of recommendations on the implications that the use of a certain technique may have and the impact on the management of the allergic patient that the differences between the various techniques represent. The reading and analysis of this consensus document will help to understand the implications of the change of diagnostic method in the management of the patient with allergy, in the quality of life and in the socioeconomic costs associated with the disease.

摘要

变应原特异性免疫球蛋白E(IgE)检测和定量试验在临床实验室中常规进行,以诊断疑似过敏患者。有许多商业检测方法可用于检测过敏,但结果可能差异很大,从而影响诊断和治疗。鉴于各种检测方法在测定特异性IgE方面存在差异带来的挑战,一组专家在一份文件中汇编了一系列建议,内容涉及使用某种技术可能产生的影响以及各种技术之间的差异对过敏患者管理的影响。阅读和分析这份共识文件将有助于理解诊断方法的改变对过敏患者管理、生活质量以及与该疾病相关的社会经济成本的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6413/10197418/9df257b94fc6/j_almed-2020-0051_fig_001.jpg

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