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用于恢复血液透析中心静脉导管通畅的溶栓治疗:一项系统评价

Thrombolysis for restoration of patency to haemodialysis central venous catheters: a systematic review.

作者信息

Clase C M, Crowther M A, Ingram A J, Cinà C S

机构信息

Division of Nephrology, Dalhousie University, Halifax, Nova Scotia, Canada.

出版信息

J Thromb Thrombolysis. 2001 Apr;11(2):127-36. doi: 10.1023/a:1011272632286.

Abstract

Urokinase, previously used to restore patency to thrombosed haemodialysis catheters, is now unavailable in North America. We performed systematic reviews of four questions related to the safety and efficacy of alternative agents for catheter thrombolysis, searching Medline and the Cochrane Controlled Clinical Trials Register. In dialysis patients, large case series have documented that urokinase is safe and effective (>70 % efficacy for catheter instillation, and >80 % for systemic lysis). Experience with streptokinase is limited and allergic complications develop with repeated use. Studies of catheter instillation with 1--2 mg of tPA per lumen reported short-term success in 83--98 % of uses. One non-peer-reviewed study described 44--59 % success using systemic tissue plasminogen activator (tPA), 2.5 mg through each of 2 lumens, over 1 h. Meta-analysis of randomized comparisons of urokinase and tPA as full-dose thrombolytic agents suggested that 1 mg tPA was likely equivalent in thrombolytic potency to 36,000 units urokinase. In nondialysis populations, four case series suggested that catheter instillation with 0.5--2 mg tPA was effective and safe in reestablishing patency, and a randomized controlled trial found 2--4 mg tPA more effective than 5,000--10,000 units urokinase. No complications have been reported in any patient treated with systemic or local tPA for catheter thrombolysis. In studies of fistula thrombolysis with 5--50 mg tPA major complications occurred in one episode in 130 patients treated. This review suggests that 1--2 mg/lumen tPA is a suitable dose for catheter instillation and likely to be more effective than 5000 units/lumen urokinase. Systemic lysis with 5--10 mg tPA is likely to be safe and effective in suitably selected patients. Further studies are needed.

摘要

尿激酶曾用于恢复血栓形成的血液透析导管的通畅性,如今在北美已无法获得。我们通过检索Medline和Cochrane对照临床试验注册库,对与替代药物用于导管溶栓的安全性和有效性相关的四个问题进行了系统评价。在透析患者中,大量病例系列记录显示尿激酶安全有效(导管内注入的有效率>70%,全身溶栓的有效率>80%)。链激酶的使用经验有限,且重复使用会出现过敏并发症。关于每管腔注入1 - 2毫克组织型纤溶酶原激活剂(tPA)进行导管内溶栓的研究报告称,短期成功率为83% - 98%。一项未经同行评审的研究描述了通过两个管腔各注入2.5毫克全身组织型纤溶酶原激活剂(tPA),历时1小时,成功率为44% - 59%。对尿激酶和tPA作为全剂量溶栓剂的随机对照比较进行的荟萃分析表明,1毫克tPA的溶栓效力可能等同于36,000单位尿激酶。在非透析人群中,四个病例系列表明,每管腔注入0.5 - 2毫克tPA在恢复通畅方面有效且安全,一项随机对照试验发现2 - 4毫克tPA比5,000 - 10,000单位尿激酶更有效。在接受全身或局部tPA进行导管溶栓治疗的任何患者中均未报告并发症。在使用5 - 50毫克tPA进行动静脉内瘘溶栓的研究中,130例接受治疗的患者中有1例出现了严重并发症。本综述表明,每管腔1 - 2毫克tPA是适合导管内注入的剂量,可能比每管腔5000单位尿激酶更有效。对于经过适当选择的患者,5 - 10毫克tPA进行全身溶栓可能安全有效。仍需进一步研究。

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