Langenecker S A, Felfernig M, Werba A, Mueller C M, Chiari A, Zimpfer M
Department of Anesthesia and General Intensive Care, University of Vienna, Austria.
Crit Care Med. 1994 Nov;22(11):1774-81.
To investigate anticoagulation with prostacyclin (prostaglandin I2 [PGI2]) and/or heparin during continuous venovenous hemofiltration, and the role of in vitro tests of primary hemostasis in controlling anticoagulation.
Prospective, randomized, controlled trial.
Intensive care unit.
Forty-six consecutive, critically ill, mechanically ventilated patients with postoperative acute renal failure.
Anticoagulation of the patient's blood was accomplished using heparin (6.0 +/- 0.3 IU/kg/hr for group 1), PGI2 (7.7 +/- 0.7 ng/kg/min for group 2), or both PGI2 and heparin (6.4 +/- 0.3 ng/kg/min, 5.0 +/- 0.4 IU/kg/hr, respectively, for group 3), administered into the extracorporeal line before the hemofilter during continuous venovenous hemofiltration.
After Ethics Committee approval and informed consent were obtained, tests of primary and secondary hemostasis, plasma concentrations of 6-ketoprostaglandin F1 alpha (by radioimmunoassay), and hemodynamic measurements were performed before hemofiltration and 24 hrs after hemofiltration. In groups 1 and 3, hemodynamic parameters remained stable, whereas in group 2 (the PGI2 group), there were significant reductions in systemic and pulmonary vascular resistances and mean arterial pressure. Platelet function was unchanged in group 1, and was inhibited in groups 2 and 3. Corresponding with the prolongation of in vitro bleeding time, the 6-ketoprostaglandin F1 alpha concentration was increased, indicating an effective inhibition of platelet aggregation within the hemofilter. Platelet counts remained stable in all patients. Plasma coagulation tests were stable in groups 2 and 3, and were prolonged in group 1. In all patients, no major bleeding complications were observed and there was no clinically important bleeding. Mean hemofilter duration lasted longest in group 3. Blood urea nitrogen and circulating creatinine concentrations decreased significantly in groups 2 and 3 within the study period.
Patients receiving both PGI2 and heparin showed better hemodynamic profiles and enhanced hemofilter duration compared with the other groups and no bleeding complications were observed. Therefore, we recommend anticoagulation with PGI2 and heparin during continuous venovenous hemofiltration with close monitoring of platelet function, coagulation profile, and overall hemodynamics.
探讨在持续静静脉血液滤过期间使用前列环素(前列腺素I2 [PGI2])和/或肝素进行抗凝,以及体外初级止血试验在控制抗凝中的作用。
前瞻性、随机、对照试验。
重症监护病房。
46例连续的、重症、机械通气的术后急性肾衰竭患者。
在持续静静脉血液滤过期间,于血液滤过器前将肝素(第1组6.0±0.3 IU/kg/小时)、PGI2(第2组7.7±0.7 ng/kg/分钟)或PGI2与肝素(第3组分别为6.4±0.3 ng/kg/分钟、5.0±0.4 IU/kg/小时)注入体外循环管路,对患者血液进行抗凝。
在获得伦理委员会批准并取得知情同意后,于血液滤过前及血液滤过24小时后进行初级和次级止血试验、通过放射免疫测定法测定血浆6-酮前列腺素F1α浓度以及血流动力学测量。在第1组和第3组中,血流动力学参数保持稳定,而在第2组(PGI2组)中,全身和肺血管阻力以及平均动脉压显著降低。第1组血小板功能未改变,第2组和第3组血小板功能受到抑制。与体外出血时间延长相对应,6-酮前列腺素F1α浓度升高,表明血液滤过器内血小板聚集受到有效抑制。所有患者血小板计数保持稳定。第2组和第3组血浆凝血试验稳定,第1组血浆凝血试验延长。所有患者均未观察到严重出血并发症,也无临床重要出血情况。第3组平均血液滤过持续时间最长。在研究期间,第2组和第3组血尿素氮和循环肌酐浓度显著降低。
与其他组相比,同时接受PGI2和肝素治疗的患者血流动力学状况更好,血液滤过持续时间延长,且未观察到出血并发症。因此,我们建议在持续静静脉血液滤过期间使用PGI2和肝素进行抗凝,并密切监测血小板功能、凝血情况和整体血流动力学。