Anti-Xa-guided enoxaparin thromboprophylaxis reduces rate of deep venous thromboembolism in high-risk trauma patients.

IF 2.9 2区 医学 Q2 CRITICAL CARE MEDICINE Journal of Trauma and Acute Care Surgery Pub Date : 2016-12-01 DOI:10.1097/TA.0000000000001193
George A Singer, Gina Riggi, Charles A Karcutskie, Tanaz M Vaghaiwalla, Howard M Lieberman, Enrique Ginzburg, Nicholas Namias, Edward B Lineen
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引用次数: 51

Abstract

Background: Appropriate prophylaxis against venous thromboembolism (VTE) remains undefined. This study evaluated an anti-Xa-guided enoxaparin thromboprophylaxis (TPX) protocol on the incidence of VTE in high-risk trauma patients based on Greenfield's Risk Assessment Profile (RAP) score.

Methods: This is a retrospective observational study of patients admitted to a trauma intensive care unit over a 12-month period. Patients were included if they received anti-Xa-guided enoxaparin TPX. Dosage was adjusted to a prophylactic peak anti-Xa level of 0.2 to 0.4 IU/mL. Subgroup analysis was performed on high-risk patients (RAP score ≥10) who received lower-extremity duplex ultrasound surveillance for deep vein thrombosis (DVT). Data are expressed as mean ± SD. Significance was assessed at p < 0.05.

Results: One hundred thirty-one patients received anti-Xa-guided enoxaparin TPX. Four patients were excluded for age or acute VTE on admission. Fifty-six patients with RAP score of ≥10 and surveillance duplex evaluations were included in the subgroup analysis with mean age 43 ± 20 years, Injury Severity Score of 25 ± 10, and RAP score of 16 ± 4. Prophylactic anti-Xa levels were initially achieved in 34.6% of patients. An additional 25.2% required 40 to 60 mg twice daily to reach prophylactic levels; 39.4% never reached prophylactic levels. Weight, body mass index, ISS, and RAP score were significantly higher with subprophylactic anti-Xa levels. One patient developed bleeding complications (0.8%). No patient developed intracerebral bleeding or heparin-induced thrombocytopenia.Nine VTE events occurred in the high-risk subgroup, including four DVT (7.1%), all asymptomatic, and five pulmonary emboli (8.9%). The historical rate of DVT in similar patients (ISS 31 ± 12 and RAP score 16 ± 5) was 20.5%, a significant decrease (p = 0.031). Mean chest Abbreviated Injury Scale scores were significantly higher for patients developing pulmonary emboli than DVT, 3.0 ± 1.1 vs. 0.0 (p < 0.001).

Conclusions: Mean chest Abbreviated Injury Scale score was higher in patients developing pulmonary embolism. Increased weight, body mass index, ISS, and RAP score are associated with subprophylactic anti-Xa levels. Anti-Xa-guided enoxaparin dosing reduced the rate of DVT from 20.5% to 7.1% in high-risk trauma patients.

Level of evidence: Therapeutic study, level IV.

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抗xa引导依诺肝素血栓预防可降低高危创伤患者深静脉血栓栓塞率。
背景:静脉血栓栓塞(VTE)的适当预防仍未明确。本研究基于Greenfield风险评估量表(RAP)评分,评估了抗xa引导的依诺肝素血栓预防(TPX)方案对高危创伤患者静脉血栓栓塞发生率的影响。方法:这是一项回顾性观察性研究,研究对象是在创伤重症监护室住院12个月以上的患者。如果患者接受了抗xa引导的依诺肝素TPX,则纳入其中。剂量调整到预防性峰值抗xa水平为0.2 ~ 0.4 IU/mL。对RAP评分≥10分接受下肢双工超声监测深静脉血栓形成(DVT)的高危患者进行亚组分析。数据以mean±SD表示。p < 0.05。结果:131例患者接受了抗xa引导的依诺肝素TPX治疗。4例患者因年龄或入院时急性静脉血栓栓塞被排除。纳入56例RAP评分≥10分并伴有监测双重评价的患者进行亚组分析,平均年龄43±20岁,损伤严重程度评分25±10分,RAP评分16±4分。预防性抗xa水平最初在34.6%的患者中达到。另外25.2%的人需要每天两次40至60毫克才能达到预防水平;39.4%从未达到预防水平。亚预防抗xa水平升高,体重、体质指数、ISS和RAP评分显著升高。1例出现出血并发症(0.8%)。没有患者发生脑出血或肝素诱导的血小板减少症。高危亚组发生9例静脉血栓栓塞事件,包括4例深静脉血栓栓塞(7.1%),全部无症状,5例肺栓塞(8.9%)。相似患者历史DVT发生率(ISS 31±12分,RAP 16±5分)为20.5%,差异有统计学意义(p = 0.031)。肺栓塞患者的平均胸部缩短损伤评分明显高于DVT患者,分别为3.0±1.1分和0.0分(p < 0.001)。结论:肺栓塞患者的平均胸部短缩损伤评分较高。体重增加、体重指数、ISS和RAP评分与亚预防抗xa水平相关。在高危创伤患者中,抗xa引导的依诺肝素剂量使DVT发生率从20.5%降低到7.1%。证据等级:治疗性研究,四级。
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来源期刊
CiteScore
6.00
自引率
11.80%
发文量
637
审稿时长
2.7 months
期刊介绍: The Journal of Trauma and Acute Care Surgery® is designed to provide the scientific basis to optimize care of the severely injured and critically ill surgical patient. Thus, the Journal has a high priority for basic and translation research to fulfill this objectives. Additionally, the Journal is enthusiastic to publish randomized prospective clinical studies to establish care predicated on a mechanistic foundation. Finally, the Journal is seeking systematic reviews, guidelines and algorithms that incorporate the best evidence available.
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