Division of Cardiothoracic Surgery, Washington University School of Medicine, St. Louis Children's Hospital, St. Louis, MO, USA.
Department of Perfusion, St. Louis Children's Hospital, St. Louis, MO, USA.
Artif Organs. 2021 Jan;45(1):15-21. doi: 10.1111/aor.13758. Epub 2020 Aug 5.
There is a paucity of data regarding the use of direct thrombin inhibitors such as bivalirudin for children on extracorporeal life support (ECLS). We sought to compare the outcomes of children on ECLS anticoagulated with bivalirudin versus heparin. Patients transitioned from heparin to bivalirudin were treated as a separate group. A single-institution, retrospective review of all consecutive children (neonate to 18 years) placed on ECLS in the cardiac or pediatric intensive care units was performed (June 2018-December 2019). Data collected included demographics, anticoagulation strategy, number of circuit interventions, blood product use on ECLS, survival to decannulation, and survival to discharge. Fifty-four children were placed on ECLS for a total of 56 runs. Demographics and venovenous versus venoarterial ECLS were similar. The bivalirudin group had longer median duration of support compared to the heparin group--11.0 days [IQR 6.2, 23.1] versus 3.3 days [2.1, 6.2], P < .001. Patients switched from heparin to bivalirudin had a similar duration of support (10.3 days [8.3, 18.3]) as those on bilvalirudin alone. However, there was no difference in red blood cell, fresh frozen plasma, or platelet transfusions. There was no difference in the number of circuit interventions, survival to decannulation or discharge. The freedom to first circuit intervention was longer with bivalirudin compared to heparin. Our data suggest that even with longer pediatric ECLS runs on bivalirudin, there were no differences in the outcomes between the heparin and bivalirudin groups, with longer freedom from first circuit intervention with bivalirudin. While this is the largest reported series comparing children on ECLS anticoagulated with heparin versus bivalirudin, larger studies are needed to determine the optimal anticoagulation strategy for this diverse and complicated group of children.
关于直接凝血酶抑制剂(如比伐卢定)在体外生命支持(ECLS)中的儿童使用的数据很少。我们旨在比较肝素和比伐卢定抗凝的 ECLS 患儿的结局。从肝素转换为比伐卢定的患儿作为单独一组进行治疗。对 2018 年 6 月至 2019 年 12 月在心脏或儿科重症监护病房接受 ECLS 的所有连续患儿(新生儿至 18 岁)进行了一项单中心回顾性研究。收集的数据包括人口统计学资料、抗凝策略、体外循环干预次数、ECLS 上的血液制品使用、脱机生存率和出院生存率。54 例患儿共进行了 56 次 ECLS。两组的人口统计学资料和静脉-静脉与静脉-动脉 ECLS 相似。与肝素组相比,比伐卢定组的中位支持时间更长,分别为 11.0 天(IQR 6.2,23.1)和 3.3 天(2.1,6.2),P < 0.001。从肝素转为比伐卢定的患儿的支持时间与单独使用比伐卢定的患儿相似(10.3 天[8.3,18.3])。然而,两组的红细胞、新鲜冷冻血浆和血小板输注无差异。两组的体外循环干预次数、脱机或出院生存率无差异。与肝素相比,比伐卢定的首次体外循环干预自由时间更长。我们的数据表明,即使比伐卢定治疗的儿科 ECLS 时间更长,肝素组和比伐卢定组的结局也没有差异,比伐卢定组的首次体外循环干预自由时间更长。虽然这是比较肝素和比伐卢定抗凝的 ECLS 患儿的最大系列报道,但仍需要更大的研究来确定这组复杂多样的患儿的最佳抗凝策略。