Center for Pharmacoepidemiology Research and Training, Perelman School of Medicine, the University of Pennsylvania, Philadelphia, PA; Center for Clinical Epidemiology and Biostatistics, Perelman School of Medicine, the University of Pennsylvania, Philadelphia, PA; Department of Biostatistics, Epidemiology, and Informatics, Perelman School of Medicine, the University of Pennsylvania, Philadelphia, PA.
Department of Medicine, Perelman School of Medicine, the University of Pennsylvania, Philadelphia, PA; Department of Pathology and Laboratory Medicine, Perelman School of Medicine, the University of Pennsylvania, Philadelphia, PA.
Chest. 2018 Jan;153(1):133-142. doi: 10.1016/j.chest.2017.08.008. Epub 2017 Aug 18.
Enoxaparin 30 mg twice daily and dalteparin 5,000 units once daily are two common low-molecular-weight heparin (LMWH) thromboprophylaxis regimens used in the trauma population. Pharmacodynamic studies suggest that enoxaparin provides more potent anticoagulation than does dalteparin.
In 2009, our institution switched its formulary LMWH from enoxaparin to dalteparin followed by a switch back to enoxaparin in 2013. Using a difference in differences design, we contrasted the change in the VTE rate accompanying the LMWH switch with the change in a control group of trauma patients given unfractionated heparin (UFH) during the same period.
The study included 5,880 patients: enoxaparin period (enoxaparin, n = 2,371; UFH, n = 1,539) vs the dalteparin period (dalteparin, n = 1,046; UFH, n = 924). The VTE rate was unchanged in the LMWH group: 3.3/1000 days in the enoxaparin period vs 3.8/1000 days in the dalteparin period: rate ratio (RR), 1.16; 95% CI 0.74-1.81. The rate was also unchanged in the UFH control subjects: 5.7/1,000 days in the enoxaparin period vs 5.2/1,000 days in the dalteparin period: RR, 0.92; 95% CI, 0.61-1.38. After confounding adjustment, the ratio of the change in VTE rate between the LMWH and UFH groups was similar: RR, 1.06; 95% CI 0.71-2.00. A secondary analysis excluding patients with delayed or interrupted prophylaxis (or both) altered this estimate nonsignificantly in favor of enoxaparin: RR, 2.39; 95% CI, 0.80-7.09.
Our results suggest that dalteparin has an effectiveness similar to that of enoxaparin in real-world trauma patients. Future research should investigate how the timing and consistency of prophylaxis affects LMWH effectiveness.
依诺肝素 30mg,每日两次,达肝素 5000 单位,每日一次,是两种常用于创伤人群的低分子肝素(LMWH)预防血栓形成方案。药效学研究表明,依诺肝素比达肝素提供更有效的抗凝作用。
2009 年,我院的 LMWH 处方从依诺肝素转换到达肝素,随后于 2013 年又转换回依诺肝素。我们采用差异中的差异设计,对比 LMWH 转换时的静脉血栓栓塞(VTE)发生率变化,以及同期接受未分级肝素(UFH)治疗的创伤患者的对照组中的变化。
这项研究纳入了 5880 名患者:依诺肝素组(依诺肝素,n=2371;UFH,n=1539)与达肝素组(达肝素,n=1046;UFH,n=924)。LMWH 组的 VTE 发生率保持不变:依诺肝素期为 3.3/1000 天,达肝素期为 3.8/1000 天:比率(RR)为 1.16;95%CI 0.74-1.81。UFH 对照组的发生率也保持不变:依诺肝素期为 5.7/1000 天,达肝素期为 5.2/1000 天:RR 为 0.92;95%CI,0.61-1.38。经过混杂因素调整后,LMWH 和 UFH 组之间 VTE 发生率变化的比值相似:RR,1.06;95%CI,0.71-2.00。一项排除了延迟或中断预防治疗(或两者兼有)的患者的二次分析结果略微倾向于依诺肝素:RR,2.39;95%CI,0.80-7.09。
我们的结果表明,达肝素在真实世界的创伤患者中与依诺肝素具有相似的疗效。未来的研究应该调查预防治疗的时机和一致性如何影响 LMWH 的疗效。