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[麻醉受试者类过敏反应中的血浆组胺测定。采集方法和血浆制备对组胺测量值的影响]

[Plasma histamine assay in anaphylactoid reactions of the anesthetized subject. Effects of collection methods and plasma preparation on measured histamine].

作者信息

Lorenz W, Neugebauer E, Schmal A

出版信息

Ann Fr Anesth Reanim. 1982;1(3):271-6. doi: 10.1016/s0750-7658(82)80040-3.

Abstract

Plasma histamine assay in man is indicated for the diagnosis of histamine release, as well as the elucidation of the mechanisms of adverse drug reactions, and the identification of clinical situations in anaesthesia and surgery where a pathological plasma histamine level may occur. Normal and pathological plasma histamine levels vary considerably in the literature. Data from various studies, especially one involving 300 patients in Heidelberg (G.F.R.), allow us to define the normal range for human plasma histamine as 0-1.0 ng . ml-1 . Values greater than 1 ng . ml-1 have to be considered as pathological. The problems related to blood collection and plasma preparation are considered here. Any judgement concerning the method described in the test must take into consideration our long experience of 15 years with it, its reliability in clinical conditions, its practicability, its relatively low cost, and finally, the absence of radioisotopes.

摘要

人体血浆组胺检测可用于诊断组胺释放,阐明药物不良反应机制,以及识别麻醉和手术中可能出现病理性血浆组胺水平的临床情况。文献中正常和病理性血浆组胺水平差异很大。来自各种研究的数据,尤其是一项涉及德国海德堡300名患者的研究,使我们能够将人体血浆组胺的正常范围定义为0 - 1.0 ng·ml⁻¹。大于1 ng·ml⁻¹的值必须被视为病理性的。这里考虑了与采血和血浆制备相关的问题。关于该检测中描述方法的任何判断都必须考虑到我们15年的长期经验、其在临床条件下的可靠性、实用性、相对较低的成本,以及最后没有放射性同位素这一点。

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