Perez Ortiz Alba, Dempfle Carl E, Jung Toni, Doniga Thalia, Weiß Christel, Hetjens Svetlana, Schaible Thomas, Rafat Neysan
Department of Neonatology, University Children's Hospital Mannheim, University of Heidelberg, Mannheim, Germany.
IMD Coagulation Center Mannheim, Mannheim, Germany.
Front Pediatr. 2021 Sep 17;9:685906. doi: 10.3389/fped.2021.685906. eCollection 2021.
The optimal management of anticoagulation in neonatal/pediatric patients during extracorporeal membrane oxygenation (ECMO) has not been established yet and varies greatly among ECMO centers worldwide. Therefore, we aimed to assess whether the use of anti-factor Xa assay and/or thromboelastometry correlate better than activated clotting time with heparin dose in newborns with congenital diaphragmatic hernia during ECMO. We also examined whether these coagulation assays correlate with thrombotic and/or hemorrhagic complications, when the management of anticoagulation is based only on activated clotting time values. A prospective observational study in a neonatal ECMO center was conducted. We included all neonates with congenital diaphragmatic hernia born in our institution between March 2018 and January 2019 and requiring support with venoarterial ECMO. A total of 26 ECMO runs were analyzed. During the study, the heparin dose was still adjusted according to activated clotting time values. Measurements of anti-factor Xa assay, activated partial thromboplastin time, and a thromboelastometry from the same blood specimen were performed twice a day. Anti-factor Xa levels showed a moderate correlation with heparin dose, whereas the other tests showed a weak correlation. Four patients (17.4%) had thrombotic complications, 2 patients (8.7%) experienced life-threatening bleeding, and in 11 patients (47.8%) disseminated intravascular coagulation (DIC) occurred. Anti-factor Xa levels were lower in the group with thrombotic complications (0.23 vs. 0.27 IU/ml; = 0.002), while activated partial thromboplastin time was higher in the group with hemorrhagic complications (69.4 s vs. 59.8 s; = 0.01). In patients experiencing DIC, heparin dose and anti-factor Xa levels were lower, while no difference in activated clotting time and clotting time in INTEM and INTEM-HEPTEM were shown. Anti-factor Xa levels correlate better to heparin dose than activated clotting time. The use of anti-factor Xa assay instead of activated clotting time for dosing of unfractionated heparin could reduce thrombotic complications in neonates with congenital diaphragmatic hernia on ECMO support. The thromboelastometry showed no additional benefit for this purpose.
体外膜肺氧合(ECMO)期间新生儿/儿科患者抗凝的最佳管理方案尚未确定,全球各ECMO中心的做法差异很大。因此,我们旨在评估在先天性膈疝新生儿接受ECMO治疗期间,抗Xa因子检测和/或血栓弹力图检测与肝素剂量的相关性是否优于活化凝血时间。我们还研究了在仅根据活化凝血时间值进行抗凝管理时,这些凝血检测与血栓形成和/或出血并发症之间是否存在相关性。我们在一家新生儿ECMO中心进行了一项前瞻性观察研究。我们纳入了2018年3月至2019年1月在我们机构出生且需要静脉-动脉ECMO支持的所有先天性膈疝新生儿。共分析了26次ECMO运行情况。在研究期间,肝素剂量仍根据活化凝血时间值进行调整。每天对同一血样进行两次抗Xa因子检测、活化部分凝血活酶时间检测和血栓弹力图检测。抗Xa因子水平与肝素剂量呈中度相关,而其他检测显示相关性较弱。4例患者(17.4%)出现血栓形成并发症,2例患者(8.7%)发生危及生命的出血,11例患者(47.8%)发生弥散性血管内凝血(DIC)。发生血栓形成并发症的组中抗Xa因子水平较低(0.23 vs. 0.27 IU/ml;P = 0.002),而发生出血并发症的组中活化部分凝血活酶时间较高(69.4秒 vs. 59.8秒;P = 0.01)。在发生DIC的患者中,肝素剂量和抗Xa因子水平较低,而活化凝血时间以及INTEM和INTEM-HEPTEM中的凝血时间无差异。抗Xa因子水平与肝素剂量的相关性优于活化凝血时间。在接受ECMO支持的先天性膈疝新生儿中,使用抗Xa因子检测而非活化凝血时间来调整普通肝素剂量可减少血栓形成并发症。血栓弹力图检测在这方面未显示出额外益处。