Hauch O, Jørgensen L N, Kølle T R, Nerstrøm H, Schebye O, Wille-Jørgensen P, Ostergaard P
Department of Surgery, Copenhagen Municipal Hospital, Denmark.
Acta Chir Scand Suppl. 1988;543:90-5.
The efficacy and safety of a new not yet registered low molecular weight heparin (LMWH) (Logiparin) as thromboprophylactic agent was assessed in 51 patients undergoing major elective surgery. The patients were divided into three groups receiving either 2,500 anti-Xa international units (IU) (group 1), 50 IU per kg body weight (group 2) or 3,500 IU (group 3) subcutaneously once daily. All patients were screened with the 125I-fibrinogen uptake test, and whenever a FUT was abnormal or when clinical signs were present ascending phlebography was performed. Thrombosis occurred in 12.5% of the patients in group 1 and 0% of the patients in groups 2 and 3 (p greater than 0.05). In groups 1 and 2 only minor bleeding complications were recorded. In group 3 there was one haemorrhagic episode requiring interruption of the LMWH treatment. The optimal doses of this new LMWH seems to be in the range 2,500 IU-3,500 IU once daily. The final dose recommendation has to be established in large scale clinical trials.
一种尚未注册的新型低分子量肝素(LMWH)(洛吉肝素)作为血栓预防剂的疗效和安全性,在51例接受择期大手术的患者中进行了评估。患者被分为三组,分别每日皮下注射2500抗Xa国际单位(IU)(第1组)、每公斤体重50 IU(第2组)或3500 IU(第3组)。所有患者均采用125I-纤维蛋白原摄取试验进行筛查,当纤维蛋白原摄取试验异常或出现临床症状时,进行上行静脉造影。第1组12.5%的患者发生血栓形成,第2组和第3组患者血栓形成率为0%(p>0.05)。第1组和第2组仅记录到轻微出血并发症。第3组有1例出血事件,需要中断低分子量肝素治疗。这种新型低分子量肝素的最佳剂量似乎在每日2500 IU-3500 IU范围内。最终的剂量建议必须在大规模临床试验中确定。