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组织型纤溶酶原激活剂与肝素用于封管透析导管:一项系统评价。

Tissue plasminogen activator versus heparin for locking dialysis catheters: A systematic review.

作者信息

Firwana Belal M, Hasan Rim, Ferwana Mazen, Varon Joseph, Stern Aaron, Gidwani Umesh

机构信息

Department of Medicine, University of Damascus, Damascus, Syria.

出版信息

Avicenna J Med. 2011 Oct;1(2):29-34. doi: 10.4103/2231-0770.90913.

Abstract

BACKGROUND AND OBJECTIVES

Hemodialysis catheters are commonly used when renal replacement therapy is initiated. These catheters have significant complications. Among "locking" solutions used in an attempt to decrease these complications is recombinant tissue plasminogen activator (rt-PA). This systematic review is to determine the efficacy of rt-PA versus heparin, the standard of care.

MATERIALS AND METHODS

A systematic review of randomized controlled trials studying rt-PA alone or rt-PA plus heparin versus heparin alone as locking agents for hemodialysis catheters, which included patients needed a temporary hemodialysis catheter for hemodialysis. We identified relevant trials through electronic databases and correspondence with experts. Two investigators independently reviewed potentially eligible trials and extracted data.

RESULTS

Three trials met the inclusion criteria. One trial reported an improved catheter malfunctioning in patients using rt-PA plus heparin to lock catheters (20.0%) versus heparin alone (34.8%). Another trial reported higher blood flow rate in hemodialysis catheters in patients who received rt-PA (231.6 ± 12.4 mL/min) compared with those who received heparin (206.9 mL/min). The third trial reported formation and weight of clots which were decreased by half in rt-PA group versus heparin group.

CONCLUSIONS

In the few randomized trials that met our inclusion criteria, the use of rt-PA as a locking solution for hemodialysis catheters seems to be associated with fewer adverse events and catheter malfunctioning as compared with heparin. Our systematic review is limited by the few randomized trials addressing our question and the wide variety of outcome measures. Further prospective randomized trials are needed to confirm this conclusion.

摘要

背景与目的

在开始肾脏替代治疗时,血液透析导管被广泛使用。这些导管存在严重并发症。在尝试减少这些并发症的“封管”溶液中,重组组织型纤溶酶原激活剂(rt-PA)是其中一种。本系统评价旨在确定rt-PA与作为护理标准的肝素相比的疗效。

材料与方法

对随机对照试验进行系统评价,这些试验研究单独使用rt-PA或rt-PA加肝素与单独使用肝素作为血液透析导管封管剂的情况,纳入需要临时血液透析导管进行血液透析的患者。我们通过电子数据库和与专家通信来识别相关试验。两名研究者独立审查潜在符合条件的试验并提取数据。

结果

三项试验符合纳入标准。一项试验报告,使用rt-PA加肝素封管的患者导管功能障碍发生率(20.0%)低于单独使用肝素的患者(34.8%)。另一项试验报告,接受rt-PA的患者血液透析导管的血流速度(231.6±12.4 mL/分钟)高于接受肝素的患者(206.9 mL/分钟)。第三项试验报告,rt-PA组的血栓形成和重量较肝素组减少了一半。

结论

在符合我们纳入标准的少数随机试验中,与肝素相比,使用rt-PA作为血液透析导管的封管溶液似乎与较少的不良事件和导管功能障碍相关。我们的系统评价受到针对我们问题的随机试验数量较少以及结局指标种类繁多的限制。需要进一步的前瞻性随机试验来证实这一结论。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9657/3507063/9b1bc2423d51/AJM-1-29-g001.jpg

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