Clinic for Angiology, Inselspital-University Hospital and University of Bern, Bern, Switzerland.
Clinic for Cardiology, Swiss Cardiovascular Center, Inselspital-University Hospital and University of Bern, Bern, Switzerland.
Eur Heart J. 2015 Mar 7;36(10):597-604. doi: 10.1093/eurheartj/eht531. Epub 2013 Dec 13.
No standardized local thrombolysis regimen exists for the treatment of pulmonary embolism (PE). We retrospectively investigated efficacy and safety of fixed low-dose ultrasound-assisted catheter-directed thrombolysis (USAT) for intermediate- and high-risk PE.
Fifty-two patients (65 ± 14 years) of whom 14 had high-risk PE (troponin positive in all) and 38 intermediate-risk PE (troponin positive in 91%) were treated with intravenous unfractionated heparin and USAT using 10 mg of recombinant tissue plasminogen activator per device over the course of 15 h. Bilateral USAT was performed in 83% of patients. During 3-month follow-up, two [3.8%; 95% confidence interval (CI) 0.5-13%] patients died (one from cardiogenic shock and one from recurrent PE). Major non-fatal bleeding occurred in two (3.8%; 95% CI, 0.5-13%) patients: one intrathoracic bleeding after cardiopulmonary resuscitation requiring transfusion, one intrapulmonary bleeding requiring lobectomy. Mean pulmonary artery pressure decreased from 37 ± 9 mmHg at baseline to 25 ± 8 mmHg at 15 h (P < 0.001) and cardiac index increased from 2.0 ± 0.7 to 2.7 ± 0.9 L/min/m(2) (P < 0.001). Echocardiographic right-to-left ventricular end-diastolic dimension ratio decreased from 1.42 ± 0.21 at baseline to 1.06 ± 0.23 at 24 h (n = 21; P < 0.001). The greatest haemodynamic benefit from USAT was found in patients with high-risk PE and in those with symptom duration < 14 days.
A standardized catheter intervention approach using fixed low-dose USAT for the treatment of intermediate- and high-risk PE was associated with rapid improvement in haemodynamic parameters and low rates of bleeding complications and mortality.
目前针对肺栓塞(PE)的治疗尚未形成标准化的局部溶栓方案。本研究回顾性分析了固定低剂量超声辅助导管溶栓(USAT)治疗中高危 PE 的疗效和安全性。
52 名患者(65±14 岁)接受了静脉注射普通肝素和 USAT 治疗,其中 14 名患者为高危 PE(所有患者的肌钙蛋白均呈阳性),38 名患者为中危 PE(91%的患者肌钙蛋白呈阳性),每个装置使用 10mg 重组组织型纤溶酶原激活剂,共使用 15 小时。83%的患者进行了双侧 USAT。在 3 个月的随访期间,有 2 例患者(3.8%;95%置信区间 [CI]:0.5-13%)死亡(1 例心源性休克,1 例复发性 PE)。2 例(3.8%;95%CI:0.5-13%)患者发生严重非致命性出血:1 例心肺复苏后出现胸腔内出血,需输血治疗,1 例肺内出血,需行肺叶切除术。肺动脉平均压从基线时的 37±9mmHg 降至 15 小时时的 25±8mmHg(P<0.001),心指数从 2.0±0.7L/min/m2升至 2.7±0.9L/min/m2(P<0.001)。超声心动图右心室舒张末期与左心室舒张末期内径比从基线时的 1.42±0.21降至 24 小时时的 1.06±0.23(n=21;P<0.001)。USAT 治疗中高危 PE 患者和症状持续时间<14 天的患者的血流动力学获益最大。
采用固定低剂量 USAT 治疗中高危 PE 的标准化导管介入方法可快速改善血流动力学参数,出血并发症和死亡率低。