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磺达肝癸钠在血液透析期间作为抗凝剂的应用:一项初步研究。

Use of fondaparinux as an anticoagulant during hemodialysis: a preliminary study.

作者信息

Sombolos K I, Fragia T K, Gionanlis L C, Veneti P E, Bamichas G I, Fragidis S K, Georgoulis I E, Natse T A

机构信息

Renal Unit, G.H. G. Papanikolaou, Vas. Olgas 82, Thessaloniki, Greece.

出版信息

Int J Clin Pharmacol Ther. 2008 Apr;46(4):198-203. doi: 10.5414/cpp46198.

Abstract

OBJECTIVE

To study the effect of fondaparinux, a new antithrombotic agent, as an anticoagulant during a 4-hour conventional hemodialysis session. materials and methods: Fondaparinux was administered as an anticoagulant to 16 chronic hemodialysis patients during a single 4-hour hemodialysis session at an intravenous bolus dose of 2.5 mg. Eight patients were using high-flux polyester polymer alloy (PEPA) dialyzers (Group A) and the remainder low-flux polysulfone dialyzers (Group B), whilst all had received conventional doses of tinzaparin sodium as an anticoagulant during the previous month. The dialyzers were primed with 1 l of normal saline containing 5,000 IU of unfractionated heparin. Blood samples for the measurement of INR, APTT (activated partial thromboplastin time) and anti-Xa levels were taken before the study dialysis session (pre), 5 min postdialysis (post), and before the next dialysis session (next). Mean fibrin/clot formation in the extracorporeal circuit and dialyzer was assessed macroscopically by visual inspection and was graded using a 4-point scale.

RESULTS

Predialysis anti-Xa levels were 0.04 A+/- 0.03 IU/ml in Group A, and 0.025 A+/- 0.025 IU/ml in Group B (p = NS). Postdialysis anti-Xa levels were significantly higher than predialysis levels in both groups (Group A = 0.16 A+/- 0.04 IU/ml, Group B = 0.46 A+/- 0.12 IU/ml, p < 0.02 for both) and significantly higher in Group B compared to Group A (p < 0.025). Anti-Xa levels before the next dialysis session were 0.06 A+/- 0.04 IU/ml in Group A and 0.25 A+/- 0.06 IU/ml in Group B (p < 0.0001 between Groups A and B). APTT values were significantly higher in postdialysis than predialysis samples for both groups (higher by 27.0 A+/- 26.0% in Group A and 24.3 A+/- 31.9% in Group B). No significant differences were found when comparing APTT values in pre, post and next samples between Groups A and B. No differences were also found between pre, post and next samples for INR values, either within or between groups. Mean fibrin/ clot formation score in the extracorporeal circuit at the end of the study dialysis session was significantly higher in patients of Group A than those of Group B (p < 0.05). Dialysis had to be terminated before the completion of 4 hours in 2 patients of Group A because of the presence of extensive fibrin/clots in the circuit and dialyzer.

CONCLUSIONS

Our findings indicate that fondaparinux sodium at an intravenous dose of 2.5 mg can be used successfully as an anticoagulant during a 4-hour conventional hemodialysis session in patients dialyzed with low-flux polysulfone dialyzers, but not in those dialyzed with high-flux dialyzers. However, anti-Xa levels in the former patients were still increased before the next dialysis session, potentially exposing the patients to an increased risk of bleeding.

摘要

目的

研究新型抗血栓药物磺达肝癸钠在4小时常规血液透析过程中作为抗凝剂的效果。材料与方法:16例慢性血液透析患者在单次4小时血液透析过程中接受磺达肝癸钠作为抗凝剂,静脉推注剂量为2.5mg。8例患者使用高通量聚酯聚合物合金(PEPA)透析器(A组),其余患者使用低通量聚砜透析器(B组),同时所有患者在上个月均接受常规剂量的那屈肝素钙作为抗凝剂。透析器用含5000IU普通肝素的1L生理盐水预充。在研究透析 session 前(pre)、透析后5分钟(post)和下次透析 session 前(next)采集血样,用于测定INR、活化部分凝血活酶时间(APTT)和抗Xa水平。通过肉眼观察对体外循环和透析器中的平均纤维蛋白/凝块形成进行宏观评估,并使用4分制进行分级。

结果

A组透析前抗Xa水平为0.04±0.03IU/ml,B组为0.025±0.025IU/ml(p=无统计学意义)。两组透析后抗Xa水平均显著高于透析前水平(A组=0.16±0.04IU/ml,B组=0.46±0.12IU/ml,两组p均<0.02),且B组显著高于A组(p<0.025)。下次透析 session 前A组抗Xa水平为0.06±0.04IU/ml,B组为0.25±0.06IU/ml(A组和B组之间p<0.0001)。两组透析后APTT值均显著高于透析前样本(A组升高27.0±26.0%,B组升高24.3±31.9%)。A组和B组在pre、post和next样本中的APTT值比较无显著差异。组内和组间INR值在pre、post和next样本中也无差异。研究透析 session 结束时,A组患者体外循环中的平均纤维蛋白/凝块形成评分显著高于B组患者(p<0.05)。A组有2例患者因体外循环和透析器中出现大量纤维蛋白/凝块,在透析4小时结束前不得不终止透析。

结论

我们的数据表明,静脉注射剂量为2.5mg的磺达肝癸钠可成功用于使用低通量聚砜透析器进行透析的患者在4小时常规血液透析过程中的抗凝,但不适用于使用高通量透析器的患者。然而,前一组患者在下一次透析 session 前抗Xa水平仍会升高,这可能使患者面临出血风险增加的问题。

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