止血前分析阶段:主要异常及纠正方法

Khayati Siham, Mouayche Ikhlas, Bahri Raihane, Ait Si Ali Zineb, Yahyaoui Hicham, A. A. Mustapha, C. Mohammed
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引用次数: 2

摘要

分析前错误仍然占实验室发生的所有错误的近70%,对患者构成危险、浪费时间和额外费用。前分析步骤中各组分的控制对止血探查试验的有效性具有重要意义。我们的工作的目的是确定在止血前分析阶段的主要异常,并提出纠正的方法。我们对分析前阶段的止血进行了前瞻性和描述性研究。它是以一项调查的形式,确定与这一阶段有关的主要错误。检查是在马拉喀什阿维森纳军事医院血液学实验室进行的,为期4周。我们的调查是在止血室进行的,止血室接收来自医院各部门的收集管和抽血室(非住院患者)。止血室收到400张处方卡和相应的管子。所有收到的卡片上都有提及处方文件的相关参数:患者的全名和性别,且与相应试管上的标注一致。患者的年龄以及他们的临床和治疗信息分别在73%和13%的检查请求中被提及。与采血相关的分析前止血参数:63%的样本在实验室抽血室采集,37%来自医院各部门。卡片或试管的标签上没有提到样品的实现时间。所有样品使用的抗凝剂为浓度为3.8%的柠檬酸钠。22.25%的患者充填不合规。管道系统的登记和分类是手动的。离心速度为5000 G,温度为22℃,离心5分钟。溶血样本占3%。
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Pre-analytical Phase in Hemostasis: The Main Anomalies and Means to Correct Them
Pre-analytical errors still represent nearly 70% of all errors occurring in the laboratory, constituting a danger, a waste of time and an additional cost to the patient. The control of the different components of the pre-analytical step is important for the validity of the hemostasis exploration tests. The purpose of our work is to identify the main anomalies of the pre-analytical phase in hemostasis and to propose the means to correct them. We conducted a prospective and descriptive study on the pre-analytical phase of hemostasis. It was in the form of a survey, identifying the main errors related to this phase. It was performed at the Hematology laboratory of the Avicenna Military Hospital of Marrakech and spread over a period of 4 weeks. Our investigation took place at the hemostasis room, which received the collection tubes from the various hospital departments and the blood drawing room (for non-hospitalized patients). The hemostasis room received 400 prescription cards and their corresponding tubes. The parameters related to the prescription file: full name and gender of the patients, were mentioned on all the cards received and they were in conformity with those marked on the corresponding tube. The age of the patients and their clinical and therapeutic informations were mentioned in 73% and 13% of the exam requests, respectively. For the pre-analytical hemostasis parameters related to the blood collection: 63% of samples were taken at the laboratory's blood drawing room, while 37% came from the various hospital departments. Time of the realization of the samples was not mentioned on the cards or on the labels of the tubes. The anticoagulant used for all samples was sodium citrate at a concentration of 3.8%. The filling of the tubes was noncompliant in 22.25%. Registration and triage of the tubes systems were manual. Centrifugation was carried out at a rotation speed of 5000 G for 5 minutes and at a temperature set at 22°C. Hemolyzed samples accounted for 3% of the tubes.
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