From the Department of Pharmacy, NewYork-Presbyterian Hospital.
Department of Pediatrics, Columbia University Irving Medical Center, New York, New York.
ASAIO J. 2023 May 1;69(5):e205-e211. doi: 10.1097/MAT.0000000000001921. Epub 2023 Mar 20.
Bivalirudin has been used in increasing frequency as an alternative to unfractionated heparin (UFH) in pediatric recipients of Berlin Heart EXCOR ventricular assist devices (VAD). This single-center, retrospective review characterizes anticoagulant trends and outcomes in pediatric Berlin Heart VAD recipients implanted between September 1, 2013, and August 31, 2021, anticoagulated with either bivalirudin or UFH. Thirty-one patients were included; 65% who received bivalirudin and 35% who received UFH. The median age was 2.9 years, included 64.5% females, with 61.3% of patients diagnosed with dilated cardiomyopathy and 25.8% of patients with congenital heart disease. Therapeutic anticoagulation was achieved sooner in the bivalirudin group compared to UFH via anti-Xa monitoring (median 5.7 and 69.5 hours, respectively, p < 0.001). Bivalirudin had a greater number of therapeutic values comparatively to UFH (52% and 24%, respectively; p < 0.001) and a superior number of hours in the therapeutic range (67% and 32%, respectively; p < 0.001). Secondary outcomes were similar among the two groups, apart from greater chest tube output (UFH), more frequent events of elevated plasma-free hemoglobin (bivalirudin), and more frequent elevated inflammatory markers postimplant (bivalirudin). Prevalence of pump replacements secondary to significant clot burden and prevalence of stroke was comparable. In this patient cohort, bivalirudin demonstrated greater anticoagulation stability comparatively to UFH. Multicenter collaboration would be necessary to identify whether this further translates into improved patient outcomes.
比伐卢定在儿科柏林心脏 EXCOR 心室辅助装置(VAD)接受者中越来越多地替代未分级肝素(UFH)使用。这项单中心回顾性研究描述了 2013 年 9 月 1 日至 2021 年 8 月 31 日期间接受比伐卢定或 UFH 抗凝治疗的儿科柏林心脏 VAD 接受者的抗凝趋势和结果。31 例患者入选,65%接受比伐卢定,35%接受 UFH。中位年龄为 2.9 岁,包括 64.5%的女性,61.3%的患者诊断为扩张型心肌病,25.8%的患者患有先天性心脏病。通过抗 Xa 监测,与 UFH 相比,比伐卢定组更快达到治疗性抗凝(中位数分别为 5.7 和 69.5 小时,p<0.001)。与 UFH 相比,比伐卢定的治疗性值更多(分别为 52%和 24%,p<0.001),治疗范围内的时间更长(分别为 67%和 32%,p<0.001)。除了胸腔引流管引流量更大(UFH)、游离血红蛋白升高的事件更频繁(比伐卢定)以及植入后炎症标志物升高更频繁(比伐卢定)外,两组的次要结局相似。由于大量血栓负荷导致泵替换和中风的发生率相当。在这一患者队列中,比伐卢定与 UFH 相比表现出更强的抗凝稳定性。需要多中心合作来确定这是否进一步转化为改善患者结局。