Nielsen J D, Landorph A
Hjertemedicinsk afdeling Y., Bispebjerg Hospital, København.
Ugeskr Laeger. 1994 Oct 3;156(40):5844-9.
A review based on 17 randomised studies on low molecular weight heparin (LMWH) versus unfractionated heparin (UFH) in the treatment of objectively verified deep venous thrombosis (DVT) is presented. Long-term treatment with LMWH was compared with long-term UFH in two studies and with warfarin in one study. In the rest of the studies LMWH and UFH were used during initiation of oral anticoagulant therapy, and these studies were included in a meta-analysis. The relative risk of progression of DVT during LMWH treatment compared with UFH was 0.63 (95% confidence interval: 0.39-1.00) and the relative risk of major bleeding was 0.41 (95% confidence interval: 0.24-0.70). There was no significant difference in the reduction of Marder score during treatment (LMWH 5.0 versus UFH 3.8) or in the frequency of new symptomatic, scintigraphically or angiographically verified pulmonary embolism (LMWH 0.6% versus UFH 1.1%). The frequency of complications seemed independent of whether LMWH was administered once or twice daily. Monitoring of LMWH treatment is not considered necessary but determination of anti-factor Xa in plasma is recommended if bleeding occurs during treatment with LMWH.
本文呈现了一项基于17项随机研究的综述,这些研究比较了低分子量肝素(LMWH)与普通肝素(UFH)在治疗经客观证实的深静脉血栓形成(DVT)中的效果。在两项研究中,将LMWH的长期治疗与UFH的长期治疗进行了比较,在一项研究中则与华法林进行了比较。在其余研究中,LMWH和UFH在口服抗凝治疗起始阶段使用,这些研究被纳入了一项荟萃分析。与UFH相比,LMWH治疗期间DVT进展的相对风险为0.63(95%置信区间:0.39 - 1.00),大出血的相对风险为0.41(95%置信区间:0.24 - 0.70)。治疗期间Marder评分的降低(LMWH为5.0,UFH为3.8)或新的有症状的、经闪烁扫描或血管造影证实的肺栓塞发生频率(LMWH为0.6%,UFH为1.1%)没有显著差异。并发症的发生频率似乎与LMWH是每日给药一次还是两次无关。LMWH治疗无需进行监测,但如果在LMWH治疗期间发生出血,建议测定血浆中的抗Xa因子。