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低分子量肝素用于有症状静脉血栓栓塞症的长期治疗:与口服抗凝剂随机对照比较的荟萃分析

Low-molecular-weight heparin for the long-term treatment of symptomatic venous thromboembolism: meta-analysis of the randomized comparisons with oral anticoagulants.

作者信息

Iorio A, Guercini F, Pini M

机构信息

Sezione de Medicina Interna e Cardiovasculare, Università di Perugia, Perugia, Italy.

出版信息

J Thromb Haemost. 2003 Sep;1(9):1906-13. doi: 10.1046/j.1538-7836.2003.00364.x.

Abstract

BACKGROUND

The management of venous thromboembolism (VTE) requires an initial treatment with unfractionated heparin (UFH) or low-molecular-weight heparin (LMWH), followed by oral anticoagulants (OA) for at least 3 months. OA treatment however, requires laboratory monitoring of anticoagulation, carries a definite risk of bleeding, and may be contraindicated in some patients. As an alternative to vitamin K antagonists, subcutaneous LMWH has been proposed and evaluated in randomized clinical trials, but they are all small studies that lack the power to establish if these two treatment modalities are equivalent in efficacy or safety.

OBJECTIVES

The objective of this review was to evaluate the efficacy (VTE recurrence) and safety (bleeds and deaths) of long-term treatment of VTE with LMWH compared with OA. A secondary endpoint was to evaluate the effect of LMWH on cancer mortality.

METHODS

Computerized searches of MedLine and EmBase were performed. In addition, randomized clinical trials were located through personal communication with colleagues, and through the manual scanning of meeting proceedings and reference lists of relevant studies. When necessary, the authors of the selected papers were called to obtain additional information. Two reviewers (AI and FG) reviewed and extracted data independently using a standard form. The primary analysis was performed for efficacy and safety endpoints on an intention-to-treat basis for the study period of randomized treatment. A meta-regression analysis was used to investigate the relationship between daily dose and clinical outcome.

RESULTS

Seven studies that fulfillled our predefined criteria were identified, for a total of 1379 patients. When all studies were combined, a statistically non-significant reduction in the risk of VTE (OR 0.66; 95% confidence interval [CI] 0.41, 1.07) and in the risk of major bleeding (OR 0.45; 95% CI 0.18, 1.11) in favor of LMWH treatment was found. No difference in total mortality (OR 1.19; 95% CI 0.78, 1.83) or in cancer-related mortality was observed between the LMWH and the OA treatment.

CONCLUSIONS

The results of this meta-analysis indicate that a 3-month course of LMWH is as effective and safe as a corresponding period of OA treatment, and may thus be considered as a valuable alternative option for patients in whom OA treatment appears contraindicated or problematic.

摘要

背景

静脉血栓栓塞症(VTE)的治疗需要先用普通肝素(UFH)或低分子肝素(LMWH)进行初始治疗,随后口服抗凝剂(OA)至少3个月。然而,OA治疗需要进行抗凝的实验室监测,有明确的出血风险,并且在某些患者中可能是禁忌的。作为维生素K拮抗剂的替代方案,皮下注射LMWH已在随机临床试验中被提出并评估,但这些都是小型研究,缺乏确定这两种治疗方式在疗效或安全性上是否等效的能力。

目的

本综述的目的是评估与OA相比,LMWH长期治疗VTE的疗效(VTE复发)和安全性(出血和死亡)。次要终点是评估LMWH对癌症死亡率的影响。

方法

对MedLine和EmBase进行计算机检索。此外,通过与同事的个人交流、手动扫描会议记录和相关研究的参考文献列表来查找随机临床试验。必要时,联系所选论文的作者以获取更多信息。两名审稿人(AI和FG)使用标准表格独立审查和提取数据。对随机治疗研究期间的疗效和安全性终点进行意向性分析。使用meta回归分析来研究每日剂量与临床结局之间的关系。

结果

确定了7项符合我们预定义标准的研究,共1379例患者。当所有研究合并时,发现LMWH治疗在VTE风险(OR 0.66;95%置信区间[CI] 0.41,1.07)和大出血风险(OR 0.45;95% CI 0.18,1.11)方面有统计学上无显著意义的降低。在LMWH和OA治疗之间,总死亡率(OR 1.19;95% CI 0.78,1.83)或癌症相关死亡率没有差异。

结论

这项meta分析的结果表明,3个月疗程的LMWH与相应时间段的OA治疗一样有效和安全,因此对于OA治疗似乎禁忌或有问题的患者,可被视为一种有价值的替代选择。

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