Beijing Institute of Respiratory Medicine, Beijing Chao-Yang Hospital, Capital Medical University, Beijing, PR China.
Respir Res. 2009 Dec 29;10(1):128. doi: 10.1186/1465-9921-10-128.
Urokinase (UK) 2 200 U/kg.h for 12 hours infusion(UK-12 h)is an ACCP recommended regimen in treating acute pulmonary embolism (PE). It is unclear whether this dose and time can be reduced further. We compared the efficacy and safety of 20, 000 U/kg for 2 hours (UK-2 h) with the UK-12 h regime in selected PE patients.
A randomized trial involving 129 patients was conducted. Patients with acute PE were randomly assigned to receive either UK-12 h (n = 70), or UK-2 h (n = 59). The efficacy was determined by the improvement of right heart dysfunction and perfusion defect at 24 h and 14 d post UK treatment. The bleeding incidence, death rate and PE recurrence were also evaluated.
Similarly significant improvements in right heart dysfunction and lung perfusion defects were observed in both groups. Overall bleeding incidents were low in both groups. Major bleeding directly associated with UK infusion occurred in one patient in the UK-2 h group and one in the UK-12 h group. Mortality rates were low, with one reported fatal recurrent in the UK-12 h group and none in the UK-2 h group. When the rate of bleeding, death and PE recurrence were compared separately in the hemodynamic instability and the massive anatomic obstruction subgroups, no significant difference was found.
The UK-2 h regimen exhibits similar efficacy and safety as the UK-12 h regimen for acute PE.
尿激酶(UK)2200U/kg.h 持续输注 12 小时(UK-12 h)是 ACCP 推荐的急性肺栓塞(PE)治疗方案。目前尚不清楚该剂量和时间是否可以进一步减少。我们比较了 20000U/kg 持续输注 2 小时(UK-2 h)与 UK-12 h 方案在选择的 PE 患者中的疗效和安全性。
一项涉及 129 例患者的随机试验。将急性 PE 患者随机分为 UK-12 h 组(n=70)或 UK-2 h 组(n=59)。通过 UK 治疗后 24 小时和 14 天右心功能障碍和灌注缺陷的改善来确定疗效。还评估了出血发生率、死亡率和 PE 复发率。
两组患者右心功能障碍和肺灌注缺陷均有明显改善。两组出血事件均较低。与 UK 输注直接相关的主要出血事件发生在 UK-2 h 组的 1 例患者和 UK-12 h 组的 1 例患者。死亡率较低,UK-12 h 组报告 1 例复发性致命病例,UK-2 h 组无死亡病例。当分别比较血流动力学不稳定和大解剖阻塞亚组的出血、死亡和 PE 复发率时,未发现显著差异。
UK-2 h 方案与 UK-12 h 方案治疗急性 PE 的疗效和安全性相似。