体外补充纤维蛋白原增加凝块硬度,与血小板减少症患者输注血小板相当

B. Schenk, A. K. Lindner, Benjamin Treichl, M. Bachler, M. Hermann, O. Larsen, C. Fenger-Eriksen, D. Wally, H. Tauber, C. Velik-Salchner, D. Fries
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引用次数: 4

摘要

本研究探讨了在血小板减少患者(血小板计数< 15010 L−1)中,体外使用浓缩纤维蛋白原与体内血小板输注(PT)如何改善凝块硬度。虽然PT目前是临床显著性血小板减少症患者预防出血的一线治疗方法,但PT具有显著的风险,包括病毒或细菌感染、发热性和非发热性输血反应以及输血相关肺损伤。此外,PT的有效性也各不相同。鉴于其在血小板活化和凝块形成中的作用,纤维蛋白原浓缩物的使用可能是降低PT的有用工具。动物模型实验数据表明,纤维蛋白原浓缩物比PT更能改善凝块硬度。本研究纳入了100例年龄在18 - 35岁之间需要PT治疗的患者。在纳入的患者中,88%的患者血小板减少,65%的患者接受了抗血小板药物治疗。ptr的适应症多种多样,但最常见的适应症是弥漫性(微血管)出血倾向。入组患者的血液样本在PT前立即采集,PT后1小时和24小时采集。使用ROTEM(旋转血栓弹性测定法),用纤维蛋白原浓缩物在浓度为50、100、200和400mg kg−1时分析血液样本的最大凝块硬度(MCF)。ROTEM是一种预测、管理和纠正凝血参数的工具。结果发现,纤维蛋白原在PT前后显著增加mcf,且呈剂量依赖性。100和200 mg kg - 1纤维蛋白原浓缩物在体外的效果与PT在体内的效果相当。与PT相比,400 mg kg - 1组MCF明显改善(P < 0.001)。该研究表明,纤维蛋白原浓缩物在体外补偿凝块硬度的程度与体内PT相似,可以在适当的情况下作为替代治疗方法。这些结果需要在临床试验中得到证实。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fibrinogen Supplementation Ex Vivo Increases Clot Firmness Comparable to Platelet Transfusion in Thrombocytopenia
This study investigates how the use of fibrinogen concentrate ex vivo compares to the use of in vivo platelet transfusion (PT) to improve clot firmness in patients with thrombocytopenia (platelet count <150 10 L−1). While PT is currently first-line treatment to prevent bleeding in patients with clinically significant thrombocytopenia, PT carries significant risks, including viral or bacterial infection, febrile and nonfebrile transfusion reactions, and transfusion-related lung injury. Furthermore, the effectiveness of PT varies. The use of fibrinogen concentrate might be a useful tool to reduce PT, given its role in platelets activation and clot formation. Experimental data in animal models have indicated that fibrinogen concentrate can improve clot firmness better than PT. For this investigation, 100 patients aged between 18 and 35 years in need of PT were enrolled. Of the patients included, 88% were thrombocytopenic, and 65% had received antiplatelet medication. Indications for PTwere variable, but the most common indication was diffuse (microvascular) bleeding tendency. The enrolled patients’ blood samples were collected immediately before PT and 1 and 24 hours after PT. Using ROTEM (rotational thromboelastometry), the blood samples citrated with fibrinogen concentrate were analyzed at concentrations of 50, 100, 200, and 400mg kg−1 for the maximum clot firmness (MCF). ROTEM is a tool to predict, manage, and correct coagulation parameters. It was found that fibrinogen supplementation increasedMCF significantly and dose-dependently before and after PT. The effect of equivalent doses of 100 and 200 mg kg−1of fibrinogen concentrate ex vivo was comparable to that of PT in vivo. It was also noted that MCF improved markedly with 400 mg kg−1 compared with PT (P < 0.001). This study suggests that fibrinogen concentrate ex vivo compensates clot firmness to a similar degree as PT in vivo and could serve as an alternative treatment in appropriate situation. These results need to be confirmed in clinical trials.
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