Université de Lyon, Université Jean Monnet, Saint-Etienne, France.
J Thromb Haemost. 2011 Mar;9(3):464-72. doi: 10.1111/j.1538-7836.2011.04182.x.
Unfractionated heparin (UFH) and low-molecular-weight heparin (LMWH) are both recommended for venous thromboembolism (VTE) prophylaxis in hospitalized medical patients.
To perform an individual patient data meta-analysis to evaluate the relative efficacy and safety of the LMWH enoxaparin and UFH in preventing VTE in hospitalized medical patients.
Randomized clinical trials comparing subcutaneous enoxaparin (4000 IU once-daily) and UFH (5000 IU subcutaneous two- or three-times daily) for VTE prevention were identified by a systematic search. Individual patient data were obtained from each eligible trial.
Overall, four trials were eligible, including 3600 patients randomized to receive enoxaparin (n = 1799) or UFH (n = 1801). Median patient age was 71 years, and 49.3% were female. Compared with UFH, enoxaparin was associated with risk reductions of 37% for total VTE [relative risk (RR) 0.63, 95% confidence interval (CI) 0.51-0.77] and 62% for symptomatic VTE (RR 0.38, 95% CI 0.17-0.85) at day 15. RR for total VTE in stroke and non-stroke patients was 0.59 (95% CI 0.47-0.74) and 0.87 (95% CI 0.51-1.50), respectively. Major bleeding rates were consistently low and similar between treatment groups at day 15 (RR 1.13, 95% CI 0.53-2.44). There was a trend towards reduced risk for mortality in patients receiving enoxaparin (RR 0.83, 95% CI 0.64-1.08), compared with UFH.
Enoxaparin significantly reduces VTE in hospitalized medical patients, compared with UFH, without increasing the risk for major bleeding, and was associated with a trend towards reduced all-cause mortality.
普通肝素(UFH)和低分子肝素(LMWH)均被推荐用于预防住院内科患者静脉血栓栓塞症(VTE)。
进行一项个体患者数据荟萃分析,以评估 LMWH 依诺肝素和 UFH 在预防住院内科患者 VTE 中的相对疗效和安全性。
通过系统搜索,确定了比较皮下依诺肝素(4000IU 每日一次)和 UFH(5000IU 皮下每日 2 或 3 次)预防 VTE 的随机临床试验。从每个合格试验中获得个体患者数据。
共有四项试验符合条件,包括 3600 名患者随机分配接受依诺肝素(n=1799)或 UFH(n=1801)。中位患者年龄为 71 岁,49.3%为女性。与 UFH 相比,依诺肝素可降低 37%的总 VTE 风险[相对风险(RR)0.63,95%置信区间(CI)0.51-0.77]和 62%的有症状 VTE 风险(RR 0.38,95% CI 0.17-0.85)在第 15 天。在卒中患者和非卒中患者中,总 VTE 的 RR 为 0.59(95% CI 0.47-0.74)和 0.87(95% CI 0.51-1.50)。第 15 天,两组之间的大出血发生率始终较低且相似(RR 1.13,95% CI 0.53-2.44)。与 UFH 相比,接受依诺肝素的患者死亡率降低的趋势(RR 0.83,95% CI 0.64-1.08)。
与 UFH 相比,依诺肝素可显著降低住院内科患者的 VTE,且不增加大出血风险,并与全因死亡率降低的趋势相关。