Division of Trauma and Surgical Critical Care, LAC + USC Medical Center, University of Southern California, 2051 Marengo Street, Inpatient Tower C5L100, Los Angeles, CA, 90033, USA.
World J Surg. 2019 Nov;43(11):2797-2803. doi: 10.1007/s00268-019-05096-7.
The optimal timing of VTE prophylaxis initiation after blunt solid organ injury is controversial. Retrospective studies suggest initiation ≤48 h is safe. This prospective study examined the safety and efficacy of early VTE prophylaxis initiation after nonoperative blunt solid organ injury.
All patients >15 years of age presenting after blunt trauma (12/01/16-11/30/17) were prospectively screened. Patients were included if solid organ injury (liver, spleen, kidney) was diagnosed on admission CT scan and nonoperative management was planned. ED deaths, transfers, patients with pre-existing bleeding disorders or home antiplatelet/anticoagulant medications, and those who did not receive VTE prophylaxis were excluded. Demographics, injury/clinical data, type/timing of VTE prophylaxis initiation, and outcomes were collected. Patients were dichotomized into study groups based on VTE prophylaxis initiation time: Early (≤48 h) vs Late (>48 h after admission). Prophylaxis initiation was at the discretion of the attending trauma surgeon. The primary study outcome was VTE event rate. Secondary outcomes included hospital length of stay (LOS), intensive care unit (ICU) LOS, need for and volume of post-prophylaxis blood transfusion, need for delayed (post-prophylaxis) interventional radiology (IR) or operative intervention, failure of nonoperative management, and mortality. Outcomes were compared with univariate analysis. Multivariate analysis with logistic regression determined independent predictors of late VTE prophylaxis initiation.
After exclusions, 118 patients were identified. Median ISS was 22 [IQR 14-26]. Median AAST grade of injury was 2 [IQR 2-3] for liver, 2 [IQR 1-3] for spleen, and 3 [IQR 2-3] for kidney. Compared to late prophylaxis patients (n = 57, 48%), early prophylaxis patients (n = 61, 52%) had significantly fewer DVTs (n = 0, 0% vs n = 5, 9%, p = 0.024) but similar rates of PE (n = 2, 3% vs n = 3, 5%, p = 0.672). TBI was the only significant risk factor for late prophylaxis (OR 0.22, p = 0.015). No patient in either group required delayed intervention (operative or IR) for bleeding. There was no difference in volume of post-prophylaxis blood transfusion.
In this prospective study of patients with nonoperative blunt solid organ injuries, early (≤48 h) initiation of VTE prophylaxis resulted in a lower incidence of DVTs without an associated increase in bleeding or need for intervention. Early initiation of VTE prophylaxis is likely to be safe and beneficial for patients with blunt solid organ injury.
关于开始静脉血栓栓塞症(venous thromboembolism,VTE)预防的最佳时机,一直存在争议。回顾性研究表明,在受伤后 48 小时内开始预防是安全的。本前瞻性研究旨在探讨非手术治疗的钝性实质性器官损伤患者早期开始 VTE 预防的安全性和有效性。
对 2016 年 12 月 1 日至 2017 年 11 月 30 日期间因钝性创伤就诊的所有年龄大于 15 岁的患者进行前瞻性筛选。纳入标准为入院 CT 扫描诊断为实质性器官损伤(肝、脾、肾),并计划非手术治疗。排除标准为急诊死亡、转院、有预先存在的出血性疾病或家庭抗血小板/抗凝药物治疗的患者,以及未接受 VTE 预防的患者。收集患者的人口统计学、损伤/临床数据、VTE 预防开始的类型和时间,以及结局等信息。根据 VTE 预防开始时间将患者分为两组:早期(≤48 小时)与晚期(入院后>48 小时)。预防开始的时间由主治创伤外科医生决定。主要研究结局为 VTE 事件发生率。次要结局包括住院时间(length of stay,LOS)、重症监护病房(intensive care unit,ICU)LOS、预防后输血的需求和量、预防后需要延迟(介入放射学或手术干预)、非手术管理失败以及死亡率。通过单变量分析比较结局。使用逻辑回归的多变量分析确定晚期 VTE 预防开始的独立预测因素。
排除后,共纳入 118 例患者。中位创伤严重程度评分(injury severity score,ISS)为 22 分[四分位距(interquartile range,IQR)为 14-26]。中位美国创伤外科学会(American Association for the Surgery of Trauma,AAST)器官损伤分级为 2 级(IQR 2-3)的肝损伤,2 级(IQR 1-3)的脾损伤和 3 级(IQR 2-3)的肾损伤。与晚期预防组(n=57,48%)相比,早期预防组(n=61,52%)的深静脉血栓(DVT)发生率明显较低(n=0,0%比 n=5,9%,p=0.024),但肺栓塞(pulmonary embolism,PE)发生率相似(n=2,3%比 n=3,5%,p=0.672)。创伤性脑损伤(traumatic brain injury,TBI)是晚期预防的唯一显著危险因素(比值比 0.22,p=0.015)。两组均无患者因出血而需要延迟干预(手术或介入放射学)。预防后输血的量无差异。
在这项对非手术治疗的钝性实质性器官损伤患者的前瞻性研究中,早期(≤48 小时)开始 VTE 预防可降低 DVT 的发生率,而不会增加出血或干预的需求。对于钝性实质性器官损伤患者,早期开始 VTE 预防可能是安全且有益的。