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对神经肌肉阻滞剂、硫喷妥钠和阿片类药物的IgE依赖性过敏反应的诊断。

Diagnosis of IgE-dependent anaphylaxis to neuromuscular blocking drugs, thiopentone and opioids.

作者信息

Baldo B A, Fisher M M

机构信息

Kolling Institute of Medical Research, Royal North Shore Hospital of Sydney, St Leonards NSW, Australia.

出版信息

Ann Fr Anesth Reanim. 1993;12(2):173-81. doi: 10.1016/S0750-7658(05)81027-5.

Abstract

Although allergenic cross-reactivity of neuromuscular blocking drugs (NMBDs) is recognised clinically and has been firmly established at the serological and immunochemical levels, interpretation of in vitro inhibition findings for clinical purposes is not always straightforward. Points to be taken into account when considering serum IgE direct binding and inhibition results and when determining which NMBDs a patient may be sensitive to, include the relationship between in vitro potencies and clinical findings and the nature of the drug solid phase used for testing. It should also be remembered that the stimulating antigenic source for the patients' NMBD-reactive IgE antibodies is almost always unknown. A comparison of skin and IgE radioimmunoassay (RIA) tests for NMBDs in 29 patients is presented and difficulties involved in interpreting the results of both tests are discussed. Methods for increasing the detection of NMBD-reactive IgE antibodies are outlined. In screening sera of patients for IgE antibodies to thiopentone and morphine as well as NMBDs, multiple drug reactivities have been detected in a few subjects. Attention is drawn to defects in the existing thiopentone RIA although it is clear that the test is specific in patients who react to the drug. Addition of the serum tryptase assay to skin tests and IgE RIAs for NMBDs, thiopentone and morphine provides a powerful combination of diagnostic tests for the investigation of anaphylactoid reactions to anaesthetic drugs.

摘要

尽管神经肌肉阻滞药物(NMBDs)的变应原交叉反应在临床上已得到认可,并且在血清学和免疫化学水平上也已得到确证,但出于临床目的对体外抑制试验结果的解读并非总是那么简单直接。在考虑血清IgE直接结合和抑制试验结果以及确定患者可能对哪些NMBDs敏感时,需要考虑的要点包括体外效价与临床结果之间的关系以及用于检测的药物固相的性质。还应记住,患者的NMBD反应性IgE抗体的刺激抗原来源几乎总是未知的。本文介绍了对29例患者进行的NMBDs皮肤试验和IgE放射免疫测定(RIA)的比较,并讨论了两种试验结果解读中存在的困难。概述了增加检测NMBD反应性IgE抗体的方法。在筛查患者血清中针对硫喷妥钠、吗啡以及NMBDs的IgE抗体时,在少数受试者中检测到了多种药物反应性。尽管很明显硫喷妥钠RIA在对该药物有反应的患者中具有特异性,但文中也指出了现有硫喷妥钠RIA存在的缺陷。将血清类胰蛋白酶测定法与NMBDs、硫喷妥钠和吗啡的皮肤试验及IgE RIA相结合,为调查麻醉药物过敏样反应提供了强大的诊断试验组合。

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