首页> 外文期刊>Journal of endovascular therapy: an official journal of the International Society of Endovascular Specialists >Continuous Tenecteplase Infusion Combined With Peri/Postprocedural Platelet Glycoprotein IIb/IIIa Inhibition in Peripheral Arterial Thrombolysis: Initial Safety and Feasibility Experience.
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Continuous Tenecteplase Infusion Combined With Peri/Postprocedural Platelet Glycoprotein IIb/IIIa Inhibition in Peripheral Arterial Thrombolysis: Initial Safety and Feasibility Experience.

机译:连续性替奈普酶输注结合外周/溶栓后血小板糖蛋白IIb / IIIa抑制在外周动脉溶栓中的初步安全性和可行性经验。

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Purpose: To evaluate a continuous-infusion protocol for peripheral arterial thrombolysis using tenecteplase (TNK), with regard to the technique, dosing, infusion times, and clinical outcomes.Methods: Between November 1999 and July 2002, 48 patients (30 men; mean age 68.5+/-11.9 years) presented with acute limb ischemia (ALI) owing to iliofemoral arterial thrombosis, which was treated with continuous TNK infusion (either 0.50 mg/h [n=22, group A] or 0.25 mg/h [n=26, group B]). All patients received periprocedural heparin (500 U/h) and peri and postprocedural tirofiban for 6 to 12 hours. Follow-up included ankle-brachial index and duplex ultrasound at baseline, 1 month, and 6 months. The variables retrospectively analyzed included total infusion time, total TNK dose, fibrinogen analysis, clinical and thrombolysis outcomes, and complications.Results: The overall clinical procedural success was 95.8%. Complete (>95%) lysis was observed in 35 (73%) patients; overall mean infusion time was 7.5 hours, and overall mean TNK dose was 4.8 mg. No deaths, intracranial bleeding, or embolic events occurred in either group. Of the 8 (16.7%) complications, 5 (10.4%) were major: 1 femoral repair (group A), 2 >5-cm nonsurgical hematomas (1 in each group), and 2 gastrointestinal hemorrhages (1 in each group). The 3 (6.3%) minor complications were minor hematomas (2 in group A and 1 in group B). The 30-day and 14-month mean limb salvage rates were 95.8% (46/ 48) and 89.6% (43/48), respectively.Conclusions: Continuous TNK infusion (0.25-0.50 mg/h) is a safe and feasible treatment for continuous pharmacological thrombolysis in ALI, potentially offering decreased infusion times and bleeding complications, as well as improved outcomes.
机译:目的:从技术,剂量,输注时间和临床效果等方面,评估使用替奈普酶(TNK)连续输注治疗外周动脉血栓溶解的方法。方法:1999年11月至2002年7月,48例患者(30名男性;平均股动脉血栓形成导致急性肢体缺血(ALI),年龄为68.5 +/- 11.9岁,并接受连续TNK输注(0.50 mg / h [n = 22,A组]或0.25 mg / h [n] = 26,B组])。所有患者接受围手术期肝素(500 U / h)以及围手术期和围手术期替罗非班治疗6至12小时。随访包括在基线,1个月和6个月时的踝臂指数和双工超声。回顾性分析的变量包括总输注时间,总TNK剂量,纤维蛋白原分析,临床和溶栓结果以及并发症。结果:总体临床程序成功率为95.8%。 35名(73%)患者观察到完全(> 95%)裂解;总平均输注时间为7.5小时,总平均TNK剂量为4.8 mg。两组均未发生死亡,颅内出血或栓塞事件。在8例并发症中(16.7%),其中5例(10.4%)为严重并发症:1例股骨修补术(A组),2例> 5-cm非手术性血肿(每组1例)和2胃肠道出血(每组1例)。 3例(6.3%)轻度并发症为轻度血肿(A组2例,B组1例)。 30天和14个月的平均肢体抢救率分别为95.8%(46/48)和89.6%(43/48)。结论:连续TNK输注(0.25-0.50 mg / h)是一种安全可行的治疗方法用于ALI中持续的药理溶栓治疗,可能减少输注时间和出血并发症,并改善结果。

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