Alström T, Gräsbeck R, Lindblad B, Solberg H E, Winkel P, Viinikka L
Scand J Clin Lab Invest. 1993 Oct;53(6):649-52.
The concentrations of blood components are influenced by a number of preanalytical factors, the importance of which varies [1]. Therefore it is necessary to standardize the specimen collection, as was done by the Committee on Reference Values of the Scandinavian Society for Clinical Chemistry and Clinical Physiology, which in 1975 published its recommendation on the production of reference values in clinical chemistry [2]. It was the very first recommendation of its kind. Since then, new information has accumulated, and it has become necessary to revise the part concerning the preparation of subjects for blood collection, the collection procedure itself, and the subsequent handling of the specimen. Also, The International Federation of Clinical Chemistry (Expert Panel on Theory of Reference Values) has produced its own recommendation [3]. The recommendation described below replaces pp. 39-44 of the former Scandinavian recommendation [2]. The procedure described below is designed for the collection of specimens for the measurement of the majority of components in blood and specimen collection from the cubital vein is described. It can be easily adapted for the collection of blood from other vessels [4]. Certain laboratory investigations require a special protocol. In that case, the preparation of the subject prior to and during specimen collection as well as the procedure itself should be described in sufficient detail to permit reproduction by adequately trained personnel. In any project designed to produce reference values the same protocol for the preparation of individuals and specimen collection should be used throughout the project. The protocol should be described in detail. Thus, it is not satisfactory to state only that the present recommendation was followed. Each section of the recommendation is followed by a check list for points which should be taken into account.
血液成分的浓度受多种分析前因素的影响,其重要性各不相同[1]。因此,有必要对样本采集进行标准化,正如斯堪的纳维亚临床化学与临床生理学学会参考值委员会所做的那样,该委员会于1975年发布了关于临床化学参考值制定的建议[2]。这是此类建议中的首个。自那时以来,新信息不断积累,因此有必要修订有关采血前受试者准备、采血程序本身以及样本后续处理的部分。此外,国际临床化学联合会(参考值理论专家小组)也制定了自己的建议[3]。以下所述建议取代了之前斯堪的纳维亚建议[2]中的第39 - 44页。以下所述程序旨在采集用于检测血液中大多数成分的样本,并描述了从肘静脉采集样本的方法。它可以很容易地适用于从其他血管采集血液[4]。某些实验室检查需要特殊方案。在这种情况下,应详细描述受试者在样本采集前和采集过程中的准备情况以及程序本身,以便经过充分培训的人员能够重复操作。在任何旨在制定参考值的项目中,整个项目应使用相同的个体准备和样本采集方案。该方案应详细描述。因此,仅说明遵循了本建议是不令人满意的。建议的每个部分后面都附有一个应考虑要点的检查表。