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老年患者下肢人工关节置换或骨固定术后使用低分子量肝素克赛进行长期预防后静脉血栓栓塞的减少情况。

Reduction of venous thromboembolism following prolonged prophylaxis with the low molecular weight heparin Certoparin after endoprothetic joint replacement or osteosynthesis of the lower limb in elderly patients.

作者信息

Kolb Gerald, Bodamer Iris, Galster Heide, Seidlmayer Christoph, Grambach Konrad, Koudela Karel, Eisele Ralf R, Becker Clemens, Paal Valerie, Spannagel Uwe, Brom Joachim, Weidinger Gottfried

机构信息

Department of Internal Medicine, Division of Geriatric Medicine, St. Bonifatius-Hospital, Wilhelmstr. 13, 49809 Lingen, Germany.

出版信息

Thromb Haemost. 2003 Dec;90(6):1100-5. doi: 10.1160/TH03-01-0062.

Abstract

The peri- and postsurgical thromboembolic prophylaxis with low molecular weight heparins is a well established therapy regimen, but the optimum duration of prophylaxis after surgery still remains uncertain. A few studies have pointed to the fact that the thromboembolic risk of high-risk patients persists longer than the in-hospital period correlating with respective hypercoagulatory conditions. The aim of the present study was to test if a prolongation of thromboprophylaxis with the low molecular weight heparin Certoparin further reduces the rate of thromboembolism in high-risk patients after orthopedic surgery. The "Long-term Thromboprophylaxis"-Study was a multicenter, randomized, double-blind, placebo-controlled trial. 360 patients who underwent endoprothetic joint replacement or osteosynthesis of the lower limb were initially enrolled, all of them received prophylactically 3000 U anti-Xa of Certoparin once daily for 14 days followed by randomization to prolonged Certoparin application or to placebo up to day 42. Patients were screened for deep vein thrombosis by sonography every week. Coagulation markers (fibrin monomers and D-dimers) were determined during the course of the study. Venous thromboembolism during the prolongation period was observed in 18 patients receiving placebo versus 8 patients of the prolonged Certoparin group (12.1% versus 5.0%, intention-to-treat sample). The analysis revealed a statistically significant difference in favor of Certoparin (p=0.020), which was confirmed by per-protocol analysis (14.2% versus 5.5%, p=0.012). The differences remained significant, if analyses considered only clinically symptomatic thromboembolic events (p=0.040). Patients who developed a thrombosis showed a strong increase of coagulation markers as compared to patients without subsequent thrombosis. The respective differentiation started around 18 days before diagnosis of thrombosis. Only one minor bleeding complication was observed during prolonged Certoparin prophylaxis. The present study shows that patients after joint replacement or osteosynthesis of the lower extremities have a persisting risk to develop thromboembolic complications beyond the routine duration of thromboprophylaxis. Extended prophylaxis with Certoparin resulted in a significantly lower rate of thromboembolism and should be strongly recommended.

摘要

使用低分子量肝素进行围手术期和术后血栓栓塞预防是一种成熟的治疗方案,但术后预防的最佳持续时间仍不确定。一些研究指出,高危患者的血栓栓塞风险持续时间长于住院期,这与各自的高凝状态相关。本研究的目的是测试延长低分子量肝素Certoparin的血栓预防时间是否能进一步降低骨科手术后高危患者的血栓栓塞发生率。“长期血栓预防”研究是一项多中心、随机、双盲、安慰剂对照试验。最初纳入了360例行人工关节置换术或下肢骨固定术的患者,所有患者预防性使用3000 U Certoparin抗Xa因子,每日一次,共14天,随后随机分为延长使用Certoparin组或安慰剂组,直至第42天。每周通过超声检查患者是否有深静脉血栓形成。在研究过程中测定凝血标志物(纤维蛋白单体和D-二聚体)。在延长治疗期,接受安慰剂的18例患者与延长使用Certoparin组的8例患者发生静脉血栓栓塞(意向性治疗样本,分别为12.1%和5.0%)。分析显示,Certoparin组有统计学显著差异(p=0.020),按方案分析也证实了这一点(分别为14.2%和5.5%,p=0.012)。如果分析仅考虑临床症状性血栓栓塞事件,差异仍然显著(p=0.040)。与未发生血栓形成的患者相比,发生血栓形成的患者凝血标志物显著升高。各自的差异在血栓形成诊断前约18天开始出现。在延长使用Certoparin预防期间,仅观察到1例轻微出血并发症。本研究表明,行关节置换术或下肢骨固定术的患者在常规血栓预防期之后仍有发生血栓栓塞并发症的持续风险。延长使用Certoparin预防可显著降低血栓栓塞发生率,应强烈推荐。

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