Augusta University Medical Center, Augusta, Georgia, USA.
Department of Clinical and Administrative Pharmacy, The University of Georgia College of Pharmacy, Athens, Georgia, USA.
Pharmacotherapy. 2021 Jun;41(6):508-514. doi: 10.1002/phar.2526. Epub 2021 May 7.
The purpose of this study was to evaluate the utility of routine anti-Xa peak monitoring for trauma patients initiated on weight-based enoxaparin for venous thromboembolism (VTE) prophylaxis and identify patient populations where monitoring is necessary.
Retrospective study.
Augusta University (AU) Medical Center in Augusta, Georgia, a level 1 trauma center.
Adult patients admitted to the trauma surgery service requiring chemical VTE prophylaxis.
At least three consecutive doses of enoxaparin 0.5 mg/kg subcutaneously every 12 hour for VTE prophylaxis prior to an anti-Xa peak as the initial chemical VTE prophylaxis strategy.
The primary end point was the percentage of patients who achieved goal anti-Xa peak of 0.2-0.6 unit/ml. The incidence of newly diagnosed VTE and clinically significant bleeding were assessed as secondary end points.
From January 1, 2018, through February 28, 2019, 300 patients met inclusion criteria. Anti-Xa peaks were within goal in 91% of all patients, 7.7% were below goal, and 1.3% were above goal. For patients who did not meet the goal, dose adjustments were made in 70.4% of patients. New levels were obtained in 73.7% of those patients, and all repeat levels was within goal. Clinically significant bleeding occurred in 5.3% of patients. Newly diagnosed VTE occurred in 1.7% of patients.
The use of initial weight-based enoxaparin dosing in trauma patients routinely achieved the prespecified target anti-Xa goal. In conclusion, anti-Xa levels are not necessary for routine monitoring of weight-based enoxaparin for VTE prophylaxis in trauma patients. Incidence of clinically significant bleeding and newly diagnosed VTE were similar to previous studies.
本研究旨在评估对接受依诺肝素体重剂量预防静脉血栓栓塞症(VTE)的创伤患者进行常规抗 Xa 峰值监测的效果,并确定需要监测的患者人群。
回顾性研究。
佐治亚州奥古斯塔大学(AU)医疗中心,一个 1 级创伤中心。
需要化学 VTE 预防的入住创伤外科服务的成年患者。
至少连续 3 次皮下给予依诺肝素 0.5mg/kg,每 12 小时 1 次,然后进行抗 Xa 峰值检测,作为初始化学 VTE 预防策略。
主要终点是达到 0.2-0.6 单位/ml 目标抗 Xa 峰值的患者百分比。新发 VTE 和临床显著出血的发生率被评估为次要终点。
2018 年 1 月 1 日至 2019 年 2 月 28 日,300 名患者符合纳入标准。所有患者中有 91%的抗 Xa 峰值在目标范围内,7.7%低于目标,1.3%高于目标。对于未达到目标的患者,70.4%的患者调整了剂量。在这些患者中,73.7%的患者获得了新的水平,所有重复水平均在目标范围内。5.3%的患者发生了临床显著出血。1.7%的患者新发 VTE。
在创伤患者中,初始使用依诺肝素体重剂量通常可达到规定的目标抗 Xa 水平。总之,对于创伤患者依诺肝素体重剂量预防 VTE,抗 Xa 水平不需要常规监测。临床显著出血和新发 VTE 的发生率与既往研究相似。