Clot formation risk in the clearing fluid after arterial catheter blood sampling: coagulation factors consumption over time - a prospective pilot study.

IF 2 3区 医学 Q2 ANESTHESIOLOGY Journal of Clinical Monitoring and Computing Pub Date : 2024-12-12 DOI:10.1007/s10877-024-01252-0
Jerome E Dauvergne, Elodie Boissier, Bertrand Rozec, Karim Lakhal, Damien Muller
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Abstract

After blood sampling from an arterial catheter, the reinjection of the clearing fluid (a mixture of saline solution and blood) is proposed to limit blood loss. However, reinjecting clots may cause embolic complications. The primary objective was to assess fibrinogen consumption in the clearing fluid as an indicator of clot formation over time. Additionally, we searched for macroscopic clots, evaluated changes in prothrombin time, factors II and V. In this prospective observational pilot study, we enrolled adult patients in an intensive care unit with a radial artery catheter who required measurements of hemostasis parameters. We used a locally developed closed blood sampling system. Hemostasis parameters were measured in patients' pure blood (reference) and in the clearing fluid, at 2, 3, and 5 min after the complete filling of the reservoir. Thirty patients were included and 120 samples were analyzed. Fibrinogen levels decreased over time: median [interquartile range (IQR)] of 4.3 [IQR:3.1;5.9] as reference level, 3.6 [IQR:2.7;4.7] at 2 min (p < 0.001), 3.4 [IQR:2.1;4.3] at 3 min (p < 0.001) and 3.0 [IQR:1.7;4.1] g/L at 5 min (p < 0.001). No clot was macroscopically detected in any samples. An antiplatelet agent was administered in 11 (37%) patients. Unfractionated heparin anti-Xa activity was higher than 0.10 UI/ml in 17 (57%). Although no macroscopic clots were observed in the clearing fluid, its coagulation factors decreased over the 5 min following reservoir filling, indicating potential initiation of clot formation. Our findings stress the need for further studies assessing the safety of reinjecting clearing fluid as part of patient blood management.

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动脉导管采血后清液中的血栓形成风险:凝血因子随时间的消耗-一项前瞻性先导研究。
在动脉导管采血后,建议重新注射清除液(生理盐水和血液的混合物)以限制失血。然而,再注射血块可能导致栓塞并发症。主要目的是评估清除液中纤维蛋白原的消耗作为血块形成的指标。此外,我们寻找宏观凝块,评估凝血酶原时间、因子II和v的变化。在这项前瞻性观察性先导研究中,我们招募了在重症监护病房使用桡动脉导管需要测量止血参数的成年患者。我们使用了当地开发的封闭血液采样系统。在储血器完全填充后2、3、5分钟,分别测量患者纯血(参考)和清液的止血参数。纳入30例患者,分析120份样本。纤维蛋白原水平随着时间的推移而下降:参考水平中位数[四分位数范围(IQR)]为4.3 [IQR:3.1;5.9], 2分钟时为3.6 [IQR:2.7;4.7]
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来源期刊
CiteScore
4.30
自引率
13.60%
发文量
144
审稿时长
6-12 weeks
期刊介绍: The Journal of Clinical Monitoring and Computing is a clinical journal publishing papers related to technology in the fields of anaesthesia, intensive care medicine, emergency medicine, and peri-operative medicine. The journal has links with numerous specialist societies, including editorial board representatives from the European Society for Computing and Technology in Anaesthesia and Intensive Care (ESCTAIC), the Society for Technology in Anesthesia (STA), the Society for Complex Acute Illness (SCAI) and the NAVAt (NAVigating towards your Anaestheisa Targets) group. The journal publishes original papers, narrative and systematic reviews, technological notes, letters to the editor, editorial or commentary papers, and policy statements or guidelines from national or international societies. The journal encourages debate on published papers and technology, including letters commenting on previous publications or technological concerns. The journal occasionally publishes special issues with technological or clinical themes, or reports and abstracts from scientificmeetings. Special issues proposals should be sent to the Editor-in-Chief. Specific details of types of papers, and the clinical and technological content of papers considered within scope can be found in instructions for authors.
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