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局部抗凝和抗聚集治疗危重症患者 CVVH:一项前瞻性、随机、对照的初步研究。

Regional anticoagulation and antiaggregation for CVVH in critically ill patients: a prospective, randomized, controlled pilot study.

机构信息

Department of Medical and Surgical Critical Care, Florence University, Florence, Italy.

出版信息

Acta Anaesthesiol Scand. 2010 Jan;54(1):92-7. doi: 10.1111/j.1399-6576.2009.02031.x. Epub 2009 Jul 24.

DOI:10.1111/j.1399-6576.2009.02031.x
PMID:19650808
Abstract

BACKGROUND

The aim of this study is to assess the efficacy and clinical safety of regional anticoagulation (heparin pre-filter plus post-filter protamine) plus antiaggregation (pre-filter prostacyclin) [Group 1 (G1)] vs. only systemic heparin anticoagulation without antiaggregation [Group 2 (G2)] in critically ill patients with acute renal failure undergoing continuous veno-venous haemofiltration (CVVH).

METHODS

One hundred and ten patients were randomized in a prospective, controlled pilot study. G1 patients received 1000 U/h pre-filter heparin, 10 mg/h post-filter protamine sulphate and 4 ng/kg/min pre-filter prostacyclin, while G2 patients received 1000 U/h pre-filter heparin. The haemofilter transmembrane pressure (TMP) and lifespan, as well as the platelet count were observed 1 h before, and at 6, 12, 18, 24 and 36 h from the beginning of CVVH.

RESULTS

Haemofilter TMP remained unchanged in G1 while it increased up to three times in G2 (P=0.0002). The median filter lifespan was 68 h in G1 and 19 h in G2. The rate of spontaneous circuit failure was 24% in G1 and 93% in G2 (P=0.0001). The platelet count was stable over the treatment period in G1 while in G2 it decreased progressively (P=0.0073).

CONCLUSION

In critically ill patients suffering from acute renal failure, regional anticoagulation with pre-filter heparin and post-filter protamine plus antiaggregation during CVVH is a simple and safe procedure that prevents increases in filter TMP and increases circuit life time compared with systemic anticoagulation with pre-filter heparin only.

摘要

背景

本研究旨在评估局部抗凝(肝素预滤器加后滤器鱼精蛋白)加抗聚集(预滤器前列环素)[第 1 组(G1)]与仅全身肝素抗凝而不抗聚集[第 2 组(G2)]在接受连续静脉-静脉血液滤过(CVVH)的急性肾衰竭危重症患者中的疗效和临床安全性。

方法

110 例患者前瞻性随机对照试验。G1 组患者接受 1000 U/h 预滤器肝素、10 mg/h 后滤器硫酸鱼精蛋白和 4 ng/kg/min 预滤器前列环素,而 G2 组患者接受 1000 U/h 预滤器肝素。观察 CVVH 开始前 1 小时、开始后 6、12、18、24 和 36 小时的血液滤器跨膜压(TMP)和寿命以及血小板计数。

结果

G1 组血液滤器 TMP 保持不变,而 G2 组则增加至三倍(P=0.0002)。G1 组滤器中位寿命为 68 小时,G2 组为 19 小时。G1 组自发性回路故障发生率为 24%,G2 组为 93%(P=0.0001)。G1 组血小板计数在整个治疗期间保持稳定,而 G2 组则逐渐下降(P=0.0073)。

结论

在急性肾衰竭的危重症患者中,与仅用预滤器肝素全身抗凝相比,CVVH 期间使用预滤器肝素和后滤器鱼精蛋白加抗聚集进行局部抗凝是一种简单且安全的方法,可防止滤器 TMP 升高并延长回路寿命。

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