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首页> 外文期刊>Current medical research and opinion >Economic and clinical evaluation of fondaparinux vs. enoxaparin for thromboprophylaxis following general surgery.
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Economic and clinical evaluation of fondaparinux vs. enoxaparin for thromboprophylaxis following general surgery.

机译:磺达肝癸钠与依诺肝素对普外科手术后血栓预防的经济和临床评价。

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摘要

PURPOSE: Patients undergoing general surgical procedures are at increased risk for venous thromboembolism (VTE). Compliance rates with established guidelines for VTE thromboprophylaxis in patients at moderate-to-high risk are notably low. Recent literature has demonstrated that fondaparinux is associated with lower costs and fewer VTEs than enoxaparin in patients undergoing major orthopedic surgery (MOS), but data are limited in patients undergoing general surgery. This study was conducted to evaluate the cost implications and relative real-world effectiveness of fondaparinux vs. enoxaparin in general surgery patients. METHODS: Data were obtained from inpatient billing records from over 500 hospitals using Premier's Perspective Comparative Database. Patients hospitalized for general surgery between July 1, 2003 and January 31, 2006 were eligible for inclusion. Eligible patients were included if they received fondaparinux or enoxaparin after their general surgery date. Patients were excluded if they received both anticoagulants on their first day of therapy, were <18 years of age on the surgery date, or did not have data 6 months prior and 1 month post hospitalization. Included patients were stratified into two cohorts based on their first anticoagulant, fondaparinux or enoxaparin. Patients were matched in each group on 1:1 case-control matching based on propensity scores. RESULTS: A total of 5364 patients were included (n = 2682 for each cohort) from 326 unique hospitals. Average total costs per patient for the fondaparinux group were significantly lower than the enoxaparin group (Dollars 15 156 vs. 17 741, p < 0.0001). Patients receiving fondaparinux were significantly less likely to experience a VTE (2.80 vs. 3.77%, p = 0.046, a 35% relative risk reduction). No significant differences in bleeding events between the cohorts were observed (p = 0.6047), and no significant differences in all-cause inpatient death were noted (p = 0.3673). CONCLUSION: Fondaparinux was associated with significantly lower costs and fewer VTEs compared to enoxaparin without an increase in bleed rates or all-cause inpatient mortality. The findings from this study are limited by the retrospective study design and should only be generalized to a similar patient population.
机译:目的:接受一般外科手术的患者发生静脉血栓栓塞(VTE)的风险增加。中高风险患者对既定的VTE预防血栓栓塞指南的依从率很低。最近的文献表明,与大剂量骨科手术(MOS)的患者相比,磺达肝癸钠与依诺肝素相比具有更低的成本和更少的VTE,但在接受普外科手术的患者中数据有限。这项研究的目的是评估磺达肝癸钠与依诺肝素在普通外科手术患者中的成本影响和相对实际效果。方法:使用Premier的Perspective比较数据库从500多家医院的住院计费记录中获取数据。在2003年7月1日至2006年1月31日期间住院接受普外科手术的患者符合入选条件。如果在一般手术日期之后接受了磺达肝癸钠或依诺肝素治疗,则纳入了符合条件的患者。如果患者在治疗的第一天同时接受了两种抗凝剂,在手术日期时年龄小于18岁,或者在住院前6个月和住院后1个月没有数据,则将其排除在外。根据他们的第一种抗凝药,磺达肝素或依诺肝素,将患者分为两组。根据倾向评分,在各组中按1:1病例对照匹配对患者进行匹配。结果:总共纳入了326家独特医院的5364名患者(每组n = 2682)。磺达肝癸钠组每位患者的平均总费用显着低于依诺肝素组(Dollars 15 156 vs. 17 741,p <0.0001)。接受磺达肝癸钠的患者发生VTE的可能性显着降低(2.80 vs. 3.77%,p = 0.046,相对危险度降低35%)。队列之间的出血事件无显着差异(p = 0.6047),全因住院死亡无显着差异(p = 0.3673)。结论:与依诺肝素相比,Fondaparinux的成本显着降低,VTE减少,而出血率或全因住院死亡率均未增加。这项研究的结果受到回顾性研究设计的限制,只能推广到相似的患者人群。

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