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一项关于贝米肝素有效性和安全性的前瞻性观察性研究,首次给药于膝关节或髋关节置换手术后6小时。

A prospective observational study on the effectiveness and safety of bemiparin, first dose administered 6 h after knee or hip replacement surgery.

作者信息

Abad J Ignacio, Gómez-Outes Antonio, Martínez-González Javier, Rocha Eduardo

机构信息

Department of Orthopaedic Surgery and Trauma, Carlos Haya Hospital, Avda. Carlos Haya, s/n, Malaga 29010, Spain.

出版信息

Arch Orthop Trauma Surg. 2007 Oct;127(8):665-70. doi: 10.1007/s00402-006-0239-x. Epub 2006 Nov 7.

Abstract

INTRODUCTION

Bemiparin has shown to be effective and safe in clinical trials in total knee or hip replacement.

MATERIALS AND METHODS

We conducted a prospective, open, multicentre, uncontrolled study to audit the utilisation patterns of bemiparin 3,500 IU/day, first dose administered 6 h after surgery, in 1,009 patients undergoing total hip or knee replacement surgery in standard clinical practice. We analysed rates of documented symptomatic venous thromboembolism (VTE) [deep-vein thrombosis (DVT) and pulmonary embolism (PE)] confirmed by objective methods, major bleeding, death, thrombocytopaenia and other adverse events up to 6 weeks.

RESULTS

Rate of documented symptomatic DVT was 0.3% (95% CI, 0.1-0.9%). No cases of documented PE were reported. There were 14 (1.4%) major bleedings (95% CI, 0.8-2.3%). Neuraxial anaesthesia was used in 937 (92.9%) patients. There were no cases of spinal haematoma, fatal bleeding or bleeding in critical organs. There were 6 (0.6%) cases of mild thrombocytopaenia, which did not require treatment discontinuation. No cases of severe type II heparin-induced thrombocytopaenia were observed. There were no deaths during bemiparin prophylaxis. The median length of hospitalisation was 9 days and 92.5% of patients continued prophylaxis post-hospitalisation for a total median time of 38 days. There were no thromboembolic or bleeding complications during post-hospitalisation prophylaxis. Postoperative start of prophylaxis with bemiparin permitted that 29.3% of patients could be admitted to hospital the same day of the intervention.

CONCLUSION

Bemiparin prophylaxis, started 6 h after surgery and given for 5-6 weeks after total hip or knee replacement, was associated with low rates of VTE, major bleeding and other adverse events in normal clinical practice. Bemiparin thromboprophylaxis started 6 h after surgery makes neuraxial anaesthesia/analgesia procedures easier, without compromising efficacy.

摘要

引言

在全膝关节或髋关节置换的临床试验中,贝米肝素已显示出有效且安全。

材料与方法

我们开展了一项前瞻性、开放性、多中心、非对照研究,以审核在标准临床实践中接受全髋关节或膝关节置换手术的1009例患者使用贝米肝素3500国际单位/天(首剂在术后6小时给药)的使用模式。我们分析了通过客观方法确诊的有症状静脉血栓栓塞(VTE)[深静脉血栓形成(DVT)和肺栓塞(PE)]、大出血、死亡、血小板减少症及其他不良事件直至6周时的发生率。

结果

有症状DVT的记录发生率为0.3%(95%可信区间,0.1 - 0.9%)。未报告有记录的PE病例。有14例(1.4%)大出血(95%可信区间,0.8 - 2.3%)。937例(92.9%)患者使用了椎管内麻醉。未发生脊髓血肿、致命性出血或重要器官出血的病例。有6例(0.6%)轻度血小板减少症,无需停药治疗。未观察到严重的II型肝素诱导的血小板减少症病例。在贝米肝素预防期间无死亡病例。中位住院时间为9天,92.5%的患者在出院后继续预防,总中位时间为38天。出院后预防期间无血栓栓塞或出血并发症。术后开始使用贝米肝素预防使29.3%的患者可在干预当天入院。

结论

在全髋关节或膝关节置换术后6小时开始并在术后5 - 6周给予贝米肝素预防,在正常临床实践中与VTE、大出血及其他不良事件的低发生率相关。术后6小时开始的贝米肝素血栓预防使椎管内麻醉/镇痛操作更容易,且不影响疗效。

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