Utility of In Vitro Heparin and Protamine Titration for Dosing During Cardiopulmonary Bypass Surgery

PhD M.L. Zucker, MS C.L. Barrett, BA K. Bennett, PhD F.M. LaDuca
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引用次数: 1

Abstract

Methods used to maintain a hemostatic balance during cardiopulmonary bypass surgery include the optimization of heparin and protamine dosing. Higher heparin doses have been associated with increased bleeding, while other studies have attributed reduced blood loss and transfusion requirements to lower protamine doses. We have evaluated the use of an in vitro heparin and protamine titration system and compared it to standard dosing in patients undergoing surgery requiring cardiopulmonary bypass. Based upon the principle of the Hemochron® RxDx® system, Heparin Response Tests (HRT) and Protamine Response Tests (PRT) were performed for 40 patients undergoing cardiac surgery at three hospital centers. The Activated Clotting Time (ACT) was used to monitor adequate heparin dosing prior to placing the patient on bypass, and to monitor heparin reversal after protamine dosing. The efficacy of heparin reversal was determined using the Protamine Dose Assay (PDA-O) test. All centers used standard hospital pharmaceutical preparations of heparin and protamine. Heparin and protamine RxDx dosing was compared to standard hospital practice for each site. Based on the HRT, the average heparin dose was not different from empirical dosing; however, individual differences were as high as 11,000 units. Only a single patient required a second heparin bolus prior to initiation of bypass. On average, the protamine dose predicted by the PRT was only 67% of the empirical protamine dose. The PDA-O test identified the need for additional protamine in 13% of patients. Patients administered additional protamine at the request of the surgical team, despite the presence of a normal PDA-O test, had no further decrease in ACT. In summary, the in vitro HRT and PRT system did not alter the initial heparin dose yet significantly decreased the protamine doses administered. Based on prior clinical outcome studies, this reduction is expected to have a beneficial effect on postoperative bleeding and transfusion requirements.
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体外肝素和鱼精蛋白滴定在体外循环手术中给药的应用
体外循环手术中维持止血平衡的方法包括肝素和鱼精蛋白剂量的优化。较高的肝素剂量与出血增加有关,而其他研究将减少失血量和输血需求归因于较低的鱼精蛋白剂量。我们评估了体外肝素和鱼精蛋白滴定系统的使用,并将其与需要体外循环手术的患者的标准剂量进行了比较。基于hemchron®RxDx®系统的原理,对三家医院中心的40例接受心脏手术的患者进行了肝素反应试验(HRT)和鱼精蛋白反应试验(PRT)。激活凝血时间(ACT)用于监测患者搭桥前肝素的充足剂量,并监测鱼精蛋白给药后肝素的逆转。采用鱼精蛋白剂量测定法(PDA-O)检测肝素逆转的疗效。所有中心都使用标准的医院药物制剂肝素和鱼精蛋白。肝素和鱼精蛋白RxDx的剂量比较标准医院做法的每个地点。基于HRT,平均肝素剂量与经验剂量无差异;然而,个体差异高达11000个单位。只有一个病人需要第二次肝素丸在搭桥开始之前。平均而言,PRT预测的鱼精蛋白剂量仅为经验鱼精蛋白剂量的67%。PDA-O检测发现13%的患者需要额外的鱼精蛋白。患者在手术小组的要求下给予额外的鱼精蛋白,尽管存在正常的PDA-O测试,ACT没有进一步下降。总之,体外HRT和PRT系统没有改变初始肝素剂量,但显著降低了给予的鱼精蛋白剂量。根据先前的临床结果研究,这种减少有望对术后出血和输血需求产生有益的影响。
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