Ponec D, Irwin D, Haire W D, Hill P A, Li X, McCluskey E R
Division of Radiology, Tri-City Medical Center, Oceanside, California, USA.
J Vasc Interv Radiol. 2001 Aug;12(8):951-5. doi: 10.1016/s1051-0443(07)61575-9.
Central venous access devices (CVADs) are a mainstay of current medical therapy but often become occluded by thrombus. Tissue plasminogen activator (alteplase), at a dose of 2 mg per 2 mL, has been shown to be effective in restoring flow to catheters proven by radiographic contrast injection to be occluded by thrombus. The purpose of this double-blind placebo-controlled multicenter trial was to determine the efficacy of alteplase in occluded catheters without earlier contrast injections or radiographic examinations.
Patients were eligible for inclusion if blood could not be withdrawn from their catheter after a period of normal function of at least 48 hours. Single or multiple catheters, peripherally inserted central catheters, catheters with valves, and implanted ports were eligible; catheters used for hemodialysis were not included. Patients were randomly assigned to one of two groups. In one group, patients received a first dose of 2 mg alteplase followed, if needed, by a second dose of 2 mg alteplase and a third dose of placebo. The other group received placebo first followed by one 2-mg dose of alteplase and then a second, if needed. Each dose was allowed to dwell for 2 hours and ability to withdraw blood from the catheter was reassessed. The endpoint was restoration of the ability to withdraw and infuse through the catheter. One hundred forty-nine patients were randomized: 74 received placebo first, 75 received alteplase first.
After the first 2-hour treatment, function was restored to 74% in the alteplase arm and 17% in the placebo arm (P <.0001 compared to placebo). After one or two treatments, function was restored in 90% of patients. There were no serious study-drug-related adverse events, no intracranial hemorrhage, no major hemorrhage, and no embolic events.
Infusion of alteplase appeared to be safe and effective in restoring flow to occluded catheters without need for pretreatment radiographic evaluation.
中心静脉通路装置(CVADs)是当前医学治疗的主要手段,但常因血栓形成而堵塞。组织纤溶酶原激活剂(阿替普酶),剂量为每2毫升2毫克,已被证明可有效恢复经放射造影剂注射证实因血栓堵塞的导管的血流。这项双盲安慰剂对照多中心试验的目的是确定在不进行早期造影剂注射或放射学检查的情况下,阿替普酶对堵塞导管的疗效。
如果导管在至少48小时的正常功能期后无法抽出血液,则患者符合纳入标准。单根或多根导管、外周静脉穿刺中心静脉导管、带瓣膜的导管和植入式端口均符合条件;用于血液透析的导管不包括在内。患者被随机分为两组。一组患者先接受2毫克阿替普酶的首剂治疗,如有需要,随后接受第二剂2毫克阿替普酶和第三剂安慰剂治疗。另一组患者先接受安慰剂治疗,随后接受一剂2毫克阿替普酶治疗,如有需要再接受第二剂治疗。每剂药物保留2小时,然后重新评估从导管中抽出血液的能力。终点指标是恢复通过导管进行抽血和输液的能力。149名患者被随机分组:74名患者先接受安慰剂治疗,75名患者先接受阿替普酶治疗。
在首次2小时治疗后,阿替普酶组74%的患者导管功能恢复,安慰剂组为17%(与安慰剂组相比,P<.0001)。经过一或两次治疗后,90%的患者导管功能恢复。没有与研究药物相关的严重不良事件,没有颅内出血,没有大出血,也没有栓塞事件。
在不进行预处理放射学评估的情况下,输注阿替普酶似乎对恢复堵塞导管的血流是安全有效的。