From the Carilion Clinic, Virginia Tech Carilion School of Medicine, Roanoke, Virginia.
J Trauma Acute Care Surg. 2022 Jan 1;92(1):93-97. doi: 10.1097/TA.0000000000003418.
Trauma is a major risk factor for the development of a venous thromboembolism (VTE). After observing higher than expected VTE rates within our center's Trauma Quality Improvement Program data, we instituted a change in our VTE prophylaxis protocol, moving to enoxaparin dosing titrated by anti-Xa levels. We hypothesized that this intervention would lower our symptomatic VTE rates.
Adult trauma patients at a single institution meeting National Trauma Data Standard criteria from April 2015 to September 2019 were examined with regards to VTE chemoprophylaxis regimen and VTE incidence. Two groups of patients were identified based on VTE protocol-those who received enoxaparin 30 mg twice daily without routine anti-Xa levels ("pre") versus those who received enoxaparin 40 mg twice daily with dose titrated by serial anti-Xa levels ("post"). Univariate and multivariate analyses were performed to define statistically significant differences in VTE incidence between the two cohorts.
There were 1698 patients within the "pre" group and 1406 patients within the "post" group. The two groups were essentially the same in terms of demographics and risk factors for bleeding or thrombosis. There was a statistically significant reduction in VTE rate (p = 0.01) and deep vein thrombosis rate (p = 0.01) but no significant reduction in pulmonary embolism rate (p = 0.21) after implementation of the anti-Xa titration protocol. Risk-adjusted Trauma Quality Improvement Program data showed an improvement in rate of symptomatic pulmonary embolism from fifth decile to first decile.
A protocol titrating prophylactic enoxaparin dose based on anti-Xa levels reduced VTE rates. Implementation of this type of protocol requires diligence from the physician and pharmacist team. Further research will investigate the impact of protocol compliance and time to appropriate anti-Xa level on incidence of VTE.
Therapeutic/care management, Level IV.
创伤是发生静脉血栓栓塞症(VTE)的主要危险因素。在观察到我们中心创伤质量改进计划数据中的 VTE 发生率高于预期后,我们改变了 VTE 预防方案,将依诺肝素的剂量调整为抗 Xa 水平。我们假设这种干预措施会降低我们的症状性 VTE 发生率。
对符合国家创伤数据标准标准的单中心成年创伤患者进行 VTE 化学预防方案和 VTE 发生率检查。根据 VTE 方案将患者分为两组-接受依诺肝素 30mg 每日两次且无常规抗 Xa 水平(“前”)与接受依诺肝素 40mg 每日两次且剂量根据连续抗 Xa 水平滴定(“后”)。进行单变量和多变量分析以确定两组之间 VTE 发生率的统计学差异。
“前”组有 1698 例患者,“后”组有 1406 例患者。两组在出血或血栓形成的危险因素方面基本相同。在实施抗 Xa 滴定方案后,VTE 发生率(p=0.01)和深静脉血栓形成率(p=0.01)均显著降低,但肺栓塞率(p=0.21)无显著降低。风险调整后的创伤质量改进计划数据显示,症状性肺栓塞发生率从第五个十分位数降至第一个十分位数。
基于抗 Xa 水平滴定预防性依诺肝素剂量的方案降低了 VTE 发生率。实施这种方案需要医生和药剂师团队的努力。进一步的研究将调查方案依从性和达到适当抗 Xa 水平的时间对 VTE 发生率的影响。
治疗/护理管理,IV 级。