Partsch H, Kechavarz B, Mostbeck A, Köhn H, Lipp C
Department of Dermatology, Ludwig Boltzmann Institute for Nuclear Medicine, Vienna, Austria.
J Vasc Surg. 1996 Nov;24(5):774-82. doi: 10.1016/s0741-5214(96)70012-5.
The purpose of this study was to compare the efficacy and safety of treating mobile iliofemoral patients with deep venous thrombosis (DVT) with subcutaneous low-molecular-weight heparin (dalteparin sodium) either 200 IU/kg once-daily (group 1) or 100 IU/kg twice-daily (group 2).
Consecutive patients with suspected iliofemoral DVT diagnosed by duplex ultrasonography and verified by radionuclide venography were randomized to one of the two low-molecular-weight heparin (LMWH) regimens. Perfusion and when necessary ventilation scans were performed for diagnosis of pulmonary emboli (PE) in all patients immediately after admission and were repeated after approximately 10 days, whereupon oral anticoagulation was started unless contraindicated. Minimal and maximal anti-factor Xa activity was measured after 2 to 3 days of therapy. All patients were kept mobile with compression bandages. The primary end point was reduction in frequency of PE as assessed on the second lung scan.
A total of 140 patients with confirmed DVT were randomized, 76 to group 1 and 64 to group 2. The two groups were comparable in their baseline clinical characteristics. In the initial lung scans 36 (47.4%) patients in group 1 and 29 (45.3%) patients in group 2 had objectively verified PE, but only 11 (14.5%) and 8 (12.5%) patients, respectively, had symptoms. After dalteparin treatment PE disappeared in two patients in group 1, but in two other cases new PEs occurred, (NS). In group 2 a resolution of PEs was observed in eight patients, whereas only one new PE could be detected. This change reflects the efficacy of therapy as defined by resolution of existing PEs and by the occurrence of new PEs and is statistically significant according to McNemar's chi-square test with the exact binomial method pair procedure (p < 0.05). Symptomatic PE was reduced from 14.5% to 5.3% in group 1 (96% to CI for the difference, -1.5% to +17.3%) and from 12.5% to 1.6% in group 2 (95% CI for the difference 0.7% to 18%, p < 0.05). There was one single fatal PE, one serious and three minor bleeding episodes in group 1, and one minor bleeding episode in group 2 (95% CI for the difference: -3.6% to +8.1%).
Treatment of ambulant iliofemoral patients with DVT with 100 IU/kg dalteparin twice-daily appears to be moe safe and effective than 200 IU/kg given once-daily. Bed rest is not necessary for treating mobile patients.
本研究旨在比较皮下注射低分子肝素(达肝素钠),每日一次200IU/kg(第1组)或每日两次100IU/kg(第2组)治疗伴有深静脉血栓形成(DVT)的可活动型髂股静脉患者的疗效和安全性。
经双功超声诊断并经放射性核素静脉造影证实为疑似髂股静脉DVT的连续患者被随机分为两种低分子肝素(LMWH)治疗方案之一。所有患者入院后立即进行灌注扫描,必要时进行通气扫描以诊断肺栓塞(PE),并在大约10天后重复进行,除非有禁忌,随后开始口服抗凝治疗。治疗2至3天后测量最小和最大抗Xa因子活性。所有患者均使用加压绷带并保持活动。主要终点是第二次肺部扫描评估的PE发生率降低。
共有140例确诊DVT患者被随机分组,76例入第1组,64例入第2组。两组的基线临床特征具有可比性。在初始肺部扫描中,第1组36例(47.4%)患者和第2组29例(45.3%)患者经客观证实有PE,但分别只有11例(14.5%)和8例(12.5%)患者有症状。达肝素治疗后,第1组有2例患者的PE消失,但另外2例出现了新的PE(无统计学差异)。在第2组中,观察到8例患者的PE得到缓解,而仅检测到1例新的PE。这种变化反映了治疗的疗效,即现有PE的缓解和新PE的发生,根据McNemar卡方检验和精确二项式方法配对程序,具有统计学意义(p<0.05)。第1组有症状的PE从14.5%降至5.3%(差异的96%CI为-1.5%至+17.3%),第2组从12.5%降至1.6%(差异的95%CI为0.7%至18%,p<0.05)。第1组有1例致命性PE、1例严重出血和3例轻微出血事件,第2组有1例轻微出血事件(差异的95%CI为:-3.6%至+8.1%)。
对于可活动型髂股静脉DVT患者,每日两次皮下注射100IU/kg达肝素似乎比每日一次注射200IU/kg更安全有效。对于可活动患者的治疗无需卧床休息。