心脏移植心肺旁路术中阿哌沙班的 CytoSorb 血液吸收

Anouk Frering MD , Antoine Abi Lutfallah MD , Aude Carillion MD, PhD , Daniel Wendt MD , Pascal Leprince MD, PhD , Adrien Bougle MD, PhD , Guillaume Lebreton MD, PhD
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引用次数: 0

摘要

背景心脏移植是一种需要心肺旁路(CPB)的急诊手术,手术时间难以预测。等待移植的患者通常有多种抗凝原因。使用 CytoSorb 在术中去除阿哌沙班似乎是一种有趣的解决方案,适用于需要紧急 CPB 干预的使用 DOACs 的患者。本短文旨在描述一名心脏移植患者在紧急 CPB 期间使用 CytoSorb 血液吸附装置的围手术期效果。这名患者患有终末期心力衰竭,在过去一年中多次出现失代偿。由于心房颤动,他曾使用维生素 K 拮抗剂 (VKA) 抗凝,后改用阿哌沙班。在整个 CPB 过程中,使用 CytoSorb 血盒进行了血液吸附。术前、术中和术后均检测抗因子Xa活性(AFXaA)水平,以监测抗凝情况。麻醉诱导时和服用 UFH 后,AFXaA 水平分别为 330ng/mL 和 317ng/mL。此后,AFXaA在CPB期间降至137ng/mL,在CPB结束和使用原胺后降至57ng/mL。手术后,AFXaA水平在接下来的14小时内稳定在50ng/mL以上。没有观察到原发性移植物功能障碍,在术后 72 小时内,患者没有发生任何需要再次介入或输血的出血事件。我们观察到,CytoSorb 可以作为术中去除阿哌沙班的潜在解决方案,如果这一疗效在更大规模的试验中得到证实,那么移植候选者就可以使用 DOACs 治疗,而无需改用 VKAs。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
CytoSorb hemoadsorption of apixaban during cardio-pulmonary bypass for heart transplantation

Background

Heart transplantation is an emergency surgery requiring cardio-pulmonary bypass (CPB) and its timing is unpredictable. Patients on the transplant waiting list often have multiple reasons for being anticoagulated. Intraoperative removal of apixaban using CytoSorb seems to be an interesting solution for patients on DOACs requiring an emergency CPB intervention. The aim of this short communication is to describe the perioperative effects of the use of the CytoSorb hemoadsorption device during emergency CPB for a heart transplant patient.

Methods

A 61-year-old male patient wait-listed for heart transplantation was admitted to our hospital to benefit from a heart transplantation. This patient, has an end-stage heart failure with multiple episodes of decompensation over the previous year. He was anticoagulated with a Vitamin K antagonist (VKA) due to atrial fibrillation and was switched to apixaban. Hemoadsorption by a CytoSorb cartridge was performed during the entire CPB duration. Anti-Factor Xa Activity (AFXaA) levels were taken before, during and after surgery in order to monitor anticoagulation.

Results

Surgery consisted of an orthotopic heart transplantation with bi-caval anastomoses. At the time of anesthesia induction and after UFH administration, AFXaA levels were 330ng/mL and 317ng/mL, respectively. Thereafter, AFXaA decreased to 137ng/mL during CPB and to 57ng/mL after the end of CPB and protamine administration. After surgery, AFXaA levels stabilized over 50ng/mL over the next 14 hours. No primary graft dysfunction was observed, and during the post-operative period of 72 hours, the patient did not have any bleeding events requiring reintervention or transfusion.

Conclusion

We observed that CytoSorb could be a potential solution to remove apixaban intraoperatively. If this efficacy is confirmed in larger trials, it would allow transplant candidates to be treated with DOACs without requiring a switch to VKAs.
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