FXII decline during cardiopulmonary bypass and the limits of routine coagulation assays: a prospective observational analysis.

IF 2.5 3区 医学 Q2 ANESTHESIOLOGY
Sarah Thaler, Isabell Aster, Emmanuelle Patton, Charlotte Voigt, Sven Peterss, Matthias Feuerecker, Philipp Groene
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Abstract

Background: The contact activation system is triggered when blood comes into contact with artificial surfaces. Cardiopulmonary bypass (CPB) induces such activation, however the extent of factor XII (FXII) reduction and its reflection in routine coagulation assays remain unclear.

Methods: In this prospective observational study, 20 adult patients undergoing elective cardiac surgery with CPB (10 coronary artery bypass grafting (CABG), 10 aortic aneurysm repair) were analyzed. Blood samples were collected immediately prior to anesthesia induction (T1) and three minutes after protamine administration (T2). Laboratory analyses included FXII, factor VIII (FVIII), and factor V (FV) activities, activated partial thromboplastin time (aPTT), prothrombin time (Quick/INR), fibrinogen, and viscoelastic testing (ROTEM).

Results: FXII activity decreased significantly after CPB (whole cohort: 98% (79/122) vs. 62% (51/83); CABG: 108% (83/124) vs. 64% (47/85); aortic: 92% (75/119) vs. 61% (52/82), p < 0.001 each). FV declined, whereas FVIII tended to increase. aPTT prolongation was minimal and remained within the normal range. A strong correlation between FXII decline and aPTT change was observed only in CABG patients (ρ = - 0.835, p = 0.003). ROTEM clotting times were moderately prolonged after CPB but showed no correlation with FXII activity.

Conclusions: CPB induced a significant reduction in FXII activity. Global coagulation assays such as aPTT or ROTEM have limited sensitivity for contact factor deficiencies. Isolated prolongation of these parameters after CPB should be interpreted cautiously and, in the absence of clinical bleeding, should not routinely prompt hemostatic interventions. Future studies should address subgroup differences (CABG vs. aortic surgery) in larger cohorts.

Trial registration: The trial was registered in the German Clinical Trials Register (DRKS00034174).

体外循环期间FXII下降和常规凝血检测的局限性:一项前瞻性观察分析。
背景:当血液接触到人造表面时,接触激活系统就会被触发。体外循环(CPB)诱导这种激活,但因子XII (FXII)降低的程度及其在常规凝血试验中的反映尚不清楚。方法:本前瞻性观察研究对20例成人择期心脏手术合并CPB(10例冠状动脉旁路移植术(CABG), 10例主动脉瘤修复)患者进行分析。在麻醉诱导前立即(T1)和鱼精蛋白给药后3分钟(T2)采集血样。实验室分析包括FXII、因子VIII (FVIII)和因子V (FV)活性、活化部分凝血活素时间(aPTT)、凝血酶原时间(Quick/INR)、纤维蛋白原和粘弹性测试(ROTEM)。结果:CPB后FXII活性显著降低(全队列:98% (79/122)vs. 62% (51/83);CABG: 108% (83/124) vs. 64% (47/85);主动脉瓣:92% (75/119)vs 61% (52/82), p结论:CPB诱导FXII活性显著降低。整体凝血试验,如aPTT或ROTEM对接触因子缺乏的敏感性有限。CPB后这些参数的单独延长应谨慎解释,在没有临床出血的情况下,不应常规提示止血干预。未来的研究应该在更大的队列中解决亚组差异(CABG vs.主动脉手术)。试验注册:该试验已在德国临床试验注册(DRKS00034174)中注册。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
自引率
3.80%
发文量
55
审稿时长
10 weeks
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