Levine M N, Hirsh J, Gent M, Turpie A G, Leclerc J, Powers P J, Jay R M, Neemeh J
McMaster University, Hamilton, Ontario.
Ann Intern Med. 1991 Apr 1;114(7):545-51. doi: 10.7326/0003-4819-114-7-545.
To determine the relative efficacy and safety of low molecular weight (LMW) heparin (Enoxaparin) compared with standard calcium heparin for the prevention of postoperative deep vein thrombosis in patients undergoing elective hip surgery.
A double-blind, randomized, controlled trial.
Six hundred sixty-five consecutive patients undergoing hip replacement at five participating hospitals.
Patients received either fixed-dose LMW heparin, 30 mg subcutaneously twice daily, or fixed-dose standard calcium heparin, 7500 units subcutaneously twice daily; both regimens were started 12 to 24 hours after surgery and continued for 14 days or until discharge if sooner.
All patients had postoperative I-125-fibrinogen leg scanning and impedance plethysmography. If results of one or both tests were positive, then venography was done. Otherwise, venography was done between day 10 and day 14, or sooner if the patient was ready for discharge.
Evaluable venograms were obtained in 258 of the 333 patients randomly assigned to receive LMW heparin and in 263 of the 332 patients assigned to receive calcium heparin. For patients with evaluable venograms, thrombosis was detected in 50 patients (19.4%) who received LMW heparin compared with 61 patients (23.2%) who received standard heparin (difference, -3.8%; 95% CI, -11.1% to 3.6%) (P greater than 0.2). Proximal deep vein thrombosis was detected in 5.4% of the patients receiving LMW heparin and in 6.5% of the patients receiving standard heparin (difference, -1.1%; CI, - 5.2% to 3.3%) (P greater than 0.2). For the entire group of 665 patients, venous thrombosis occurred in 17.1% given LMW heparin and in 19.0% given standard heparin. Hemorrhagic complications occurred in 31 patients (9.3%) given standard heparin and in 17 patients (5.1%) given LMW heparin (difference, 4.2%; CI, 0.3% to 8.2%) (P = 0.035). The relative risk reduction was 45%. The rate of major bleeding in the standard heparin group was 5.7% compared with 3.3% in the LMW heparin group (difference, 2.4%; CI, -1.0% to 5.4%) (P = 0.13). The relative risk reduction was 42%.
Low molecular weight heparin is significantly less hemorrhagic than standard unfractionated heparin; the difference in the rate of deep vein thrombosis, although not statistically significant (P greater than 0.2), favors the use of LMW heparin.
确定低分子量(LMW)肝素(依诺肝素)与标准钙肝素相比,在接受择期髋关节手术患者中预防术后深静脉血栓形成的相对疗效和安全性。
一项双盲、随机、对照试验。
五家参与研究的医院中665例连续接受髋关节置换术的患者。
患者接受固定剂量的LMW肝素,皮下注射30mg,每日两次,或固定剂量的标准钙肝素,皮下注射7500单位,每日两次;两种方案均在术后12至24小时开始,持续14天,或如果患者提前出院则持续至出院。
所有患者均进行术后I-125-纤维蛋白原腿部扫描和阻抗体积描记法。如果一项或两项检查结果为阳性,则进行静脉造影。否则,在第10天至第14天之间进行静脉造影,如果患者准备好出院则提前进行。
随机分配接受LMW肝素的333例患者中有258例获得了可评估的静脉造影,分配接受钙肝素的332例患者中有263例获得了可评估的静脉造影。对于有可评估静脉造影的患者,接受LMW肝素的50例患者(19.4%)检测到血栓形成,而接受标准肝素的61例患者(23.2%)检测到血栓形成(差异为-3.8%;95%CI,-11.1%至3.6%)(P>0.2)。接受LMW肝素的患者中有5.4%检测到近端深静脉血栓形成,接受标准肝素的患者中有6.5%检测到近端深静脉血栓形成(差异为-1.1%;CI,-5.2%至3.3%)(P>0.2)。在665例患者的整个组中,接受LMW肝素的患者中有17.1%发生静脉血栓形成,接受标准肝素的患者中有19.0%发生静脉血栓形成。接受标准肝素的31例患者(9.3%)发生出血并发症,接受LMW肝素的17例患者(5.1%)发生出血并发症(差异为4.2%;CI,0.3%至8.2%)(P = 0.035)。相对风险降低45%。标准肝素组的大出血发生率为5.7%,而LMW肝素组为3.3%(差异为2.4%;CI,-1.0%至5.4%)(P = 0.13)。相对风险降低42%。
低分子量肝素的出血风险明显低于标准普通肝素;深静脉血栓形成率的差异虽然无统计学意义(P>0.2),但倾向于使用LMW肝素。