Schobesberger Silvia, Thumfart Helena, Selinger Florian, Schlimp Christoph J, Zipperle Johannes, Ertl Peter
Faculty of Technical Chemistry, TU Wien, Getreidemarkt 9, 1060 Vienna, Austria.
Ludwig-Boltzmann-Institute for Traumatology, The Research Center in Cooperation with AUVA, Donaueschingenstraße 13, 1200 Vienna, Austria.
ACS Omega. 2024 Feb 5;9(7):8533-8542. doi: 10.1021/acsomega.3c10045. eCollection 2024 Feb 20.
Fibrinogen is a coagulation factor in human blood and the first one to reach critical levels in major bleeding. Hypofibrinogenemia (a too low fibrinogen concentration in blood) poses great challenges to first responders, clinicians, and healthcare providers since it represents a risk factor for exsanguination and massive transfusion requirements. Thus, the rapid assessment of the fibrinogen concentration at the point of care has gained considerable importance in preventing and managing major blood loss. However, in whole blood measurements, hematocrit variations affect the amount (volume fraction) of plasma that passes the detection zone. In an attempt to accurately determine realistic critical levels of fibrinogen (<1.5 mg/mL) in patients needing immediate treatment and medical interventions, we have developed novel diagnostic systems capable of estimating hematocrit and critical fibrinogen concentrations. A lateral flow assay (LFA) for the detection of fibrinogen has been developed by establishing a workflow employing rapid characterization methods to streamline LFA development. The integration of two detection lines enables (i) the identification of fibrinogen (first line) present in the sample and (ii) the determination of the clinically critical fibrinogen concentrations below 1.5 mg/mL (second line). Furthermore, the paper-based separation of blood cells from plasma provides a semiquantitative estimate of the hematocrit by analyzing the fractions. Initial validation of the point-of-care (PoC) hematocrit test revealed good comparability to a standard laboratory method. The developed diagnostic systems have the ability to accelerate decision-making in cases with major bleeding.
纤维蛋白原是人体血液中的一种凝血因子,也是大出血时第一个达到临界水平的因子。低纤维蛋白原血症(血液中纤维蛋白原浓度过低)给急救人员、临床医生和医疗服务提供者带来了巨大挑战,因为它是失血和大量输血需求的一个风险因素。因此,在护理点快速评估纤维蛋白原浓度对于预防和处理大出血至关重要。然而,在全血测量中,血细胞比容的变化会影响通过检测区域的血浆量(体积分数)。为了准确确定需要立即治疗和医疗干预的患者体内纤维蛋白原的实际临界水平(<1.5 mg/mL),我们开发了能够估计血细胞比容和临界纤维蛋白原浓度的新型诊断系统。通过建立一种采用快速表征方法的工作流程来简化侧向流动分析(LFA)的开发,从而开发出了一种用于检测纤维蛋白原的LFA。两条检测线的整合实现了:(i)识别样品中存在的纤维蛋白原(第一条线),以及(ii)确定临床临界纤维蛋白原浓度低于1.5 mg/mL(第二条线)。此外,基于纸张的血细胞与血浆分离通过分析各部分提供了血细胞比容的半定量估计。护理点(PoC)血细胞比容测试的初步验证显示与标准实验室方法具有良好的可比性。所开发的诊断系统有能力在大出血病例中加快决策制定。