King Faisal Specialist Hospital & Research Center, Riyadh, Kingdom of Saudi Arabia.
Ann Pharmacother. 2021 May;55(5):592-604. doi: 10.1177/1060028020960409. Epub 2020 Sep 22.
The use of extracorporeal membrane oxygenator (ECMO) support devices are associated with complications, including bleeding and thrombosis. Unfractionated heparin (UFH) is the gold standard anticoagulant in ECMO patients. Clinically, UFH is monitored through activated clotting time (ACT), activated partial thromboplastin time (aPTT), and anti-factor Xa assay. It is unknown which assay best predicts anticoagulation effects in adults.
To assess the correlation of UFH dosing and monitoring using an established protocol.
A pilot, prospective cohort, historically controlled study was conducted at a tertiary care hospital. Patients ≥18 years-old who received ECMO on the multifaceted anticoagulation protocol were included and compared with those on the conventional method of anticoagulation. The primary end point was to assess the correlation between UFH dose and different monitoring methods throughout 72 hours using the new protocol guided by ACT and anti-factor Xa assay.
In each arm, 20 patients were enrolled. The study revealed that anti-factor Xa assay had the largest number of "strong" correlations 11/20 (55%), followed by both aPTT and aPTT ratio 10/20 (50%), and, finally, ACT 2/20 (10%). Concordance between anti-factor Xa assay and the other monitoring parameters in the prospective arm was generally low: 31% with aPTT ratio, 26% with ACT, and 23% with aPTT.
The adaption of a multifaceted anticoagulation protocol using anti-factor Xa assay may provide a better prediction of heparin dosing in adults ECMO patients compared with the conventional ACT-based protocol. Further studies are needed to assess the safety and different monitoring modalities.
体外膜肺氧合(ECMO)支持设备的使用与并发症相关,包括出血和血栓形成。未分馏肝素(UFH)是 ECMO 患者的金标准抗凝剂。临床上,通过激活凝血时间(ACT)、部分激活凝血活酶时间(aPTT)和抗因子 Xa 测定来监测 UFH。尚不清楚哪种检测方法最能预测成人的抗凝效果。
评估使用既定方案的 UFH 给药和监测的相关性。
在一家三级保健医院进行了一项试点前瞻性队列历史对照研究。纳入了接受多方面抗凝方案 ECMO 的≥18 岁患者,并与接受传统抗凝方法的患者进行比较。主要终点是评估新方案指导下 ACT 和抗因子 Xa 测定的 UFH 剂量与 72 小时内不同监测方法之间的相关性。
在每个组中,都纳入了 20 名患者。研究表明,抗因子 Xa 测定具有最大数量的“强”相关性 11/20(55%),其次是 aPTT 和 aPTT 比值 10/20(50%),最后是 ACT 2/20(10%)。前瞻性组中抗因子 Xa 测定与其他监测参数之间的一致性通常较低:与 aPTT 比值的一致性为 31%,与 ACT 的一致性为 26%,与 aPTT 的一致性为 23%。
与基于常规 ACT 的方案相比,使用抗因子 Xa 测定的多方面抗凝方案的适应可能为成人 ECMO 患者的肝素给药提供更好的预测。需要进一步研究来评估安全性和不同的监测模式。