Kopelman Tammy R, Walters Jarvis W, Bogert James N, Basharat Usmaan, Pieri Paola G, Davis Karole M, Quan Asia N, Vail Sydney J, Pressman Melissa A
Department of Surgery, Maricopa Medical Center, 2601 East Roosevelt, Phoenix, AZ 85008, United States.
Injury. 2017 May;48(5):1088-1092. doi: 10.1016/j.injury.2016.10.039. Epub 2016 Nov 3.
Optimal enoxaparin dosing for deep venous thrombosis (DVT) prophylaxis remains elusive. Prior research demonstrated that trauma patients at increased risk for DVT based upon Greenfield's risk assessment profile (RAP) have DVT rates of 10.8% despite prophylaxis. The aim of this study was to determine if goal directed prophylactic enoxaparin dosing to achieve anti-Xa levels of 0.3-0.5IU/ml would decrease DVT rates without increased complications.
Retrospective review of trauma patients having received prophylactic enoxaparin and appropriately timed anti-Xa levels was performed. Dosage was adjusted to maintain an anti-Xa level of 0.3-0.5IU/ml. RAP was determined on each patient. A score of ≥5 was considered high risk for DVT. Sub-analysis was performed on patients who received duplex examinations subsequent to initiation of enoxaparin therapy to determine the incidence of DVT.
306 patients met inclusion criteria. Goal anti-Xa levels were met initially in only 46% of patients despite dosing of >40mg twice daily in 81% of patients; however, with titration, goal anti-Xa levels were achieved in an additional 109 patients (36%). An average enoxaparin dosage of 0.55mg/kg twice daily was required for adequacy. Bleeding complications were identified in five patients (1.6%) with three requiring intervention. There were no documented episodes of HIT. Subsequent duplex data was available in 197 patients with 90% having a RAP score >5. Overall, five DVTs (2.5%) were identified and all occurred in the high-risk group. All patients were asymptomatic at the time of diagnosis.
An increased anti-Xa range of 0.3-0.5IU/ml was attainable but frequently required titration of enoxaparin dosage. This produced a lower rate of DVT than previously published without increased complications.
用于预防深静脉血栓形成(DVT)的依诺肝素最佳剂量仍不明确。先前的研究表明,根据格林菲尔德风险评估量表(RAP),有DVT高风险的创伤患者尽管接受了预防措施,其DVT发生率仍为10.8%。本研究的目的是确定目标导向的预防性依诺肝素给药以达到0.3 - 0.5IU/ml的抗Xa水平是否会降低DVT发生率且不增加并发症。
对接受预防性依诺肝素治疗且抗Xa水平检测时间合适的创伤患者进行回顾性分析。调整剂量以维持抗Xa水平在0.3 - 0.5IU/ml。确定每位患者的RAP。评分≥5被认为是DVT高风险。对依诺肝素治疗开始后接受双功超声检查的患者进行亚组分析,以确定DVT的发生率。
306例患者符合纳入标准。尽管81%的患者每日两次给药剂量>40mg,但最初只有46%的患者达到目标抗Xa水平;然而,通过滴定,另外109例患者(36%)达到了目标抗Xa水平。充分抗凝平均需要每日两次给予0.55mg/kg的依诺肝素剂量。5例患者(1.6%)出现出血并发症,其中3例需要干预。没有记录到肝素诱导的血小板减少症(HIT)发作。197例患者有后续双功超声检查数据,其中90%的患者RAP评分>5。总体而言,发现5例DVT(2.5%),均发生在高风险组。所有患者在诊断时均无症状。
可达到0.3 - 至0.5IU/ml的更高抗Xa范围,但经常需要滴定依诺肝素剂量。这使得DVT发生率低于先前公布的数据,且未增加并发症。