Dünser Martin W, Fries Dietmar R, Schobersberger Wolfgang, Ulmer Hanno, Wenzel Volker, Friesenecker Barbara, Hasibeder Walter R, Mayr Andreas J
*Division of General and Surgical Intensive Care Medicine, Department of Anesthesiology and Critical Care Medicine, and the †Institute of Medical Biostatistics, The University of Innsbruck, Innsbruck, Austria.
Anesth Analg. 2004 Jul;99(1):201-206. doi: 10.1213/01.ANE.0000118105.85933.8A.
Arginine vasopressin (AVP) is a potent supplementary vasopressor in advanced vasodilatory shock, but decreases in platelet count have been reported during AVP therapy. In this study we evaluated the effects of AVP infusion on the coagulation system in advanced vasodilatory shock when compared to norepinephrine (NE) infusion alone. Forty-two patients with advanced vasodilatory shock (NE requirements >0.5 microg x kg(-1) x min(-1), mean arterial blood pressure <70 mm Hg) were prospectively randomized to receive an additional AVP infusion (4 U/h) or NE infusion alone. Most patients received coagulation active treatment (fresh-frozen plasma, thrombocyte concentrates, coagulation factors, and continuous veno-venous hemofiltration with heparin). At baseline and 1, 24, and 48 h after randomization, coagulation laboratory variables and a modified thrombelastography were measured. There were no differences between groups in plasmatic coagulation variables. Although there was no significant difference between groups, platelet count significantly decreased in AVP patients (P = 0.036). There were no differences in results of modified thrombelastography analyses between groups. AVP infusion in advanced vasodilatory shock with severe multiorgan dysfunction syndrome does not increase plasma concentrations of Factor VIII, von Willebrand Factor antigen, and ristocetin Co-Factor but may stimulate platelet aggregation and induce thrombocytopenia. Global coagulation, assessed by modified thrombelastography, is not different from patients receiving NE infusion alone.
精氨酸加压素(AVP)是晚期血管舒张性休克中一种有效的补充血管升压药,但有报道称在AVP治疗期间血小板计数会下降。在本研究中,我们评估了与单独输注去甲肾上腺素(NE)相比,输注AVP对晚期血管舒张性休克患者凝血系统的影响。42例晚期血管舒张性休克患者(NE需求量>0.5μg·kg⁻¹·min⁻¹,平均动脉血压<70mmHg)被前瞻性随机分组,分别接受额外的AVP输注(4U/h)或单独的NE输注。大多数患者接受了凝血活性治疗(新鲜冷冻血浆、血小板浓缩物、凝血因子以及肝素持续静脉-静脉血液滤过)。在随机分组后的基线、1小时、24小时和48小时,测量凝血实验室指标和改良血栓弹力图。两组间血浆凝血指标无差异。虽然两组间无显著差异,但AVP组患者的血小板计数显著下降(P = 0.036)。两组间改良血栓弹力图分析结果无差异。在伴有严重多器官功能障碍综合征的晚期血管舒张性休克中,输注AVP不会增加血浆VIII因子、血管性血友病因子抗原和瑞斯托霉素辅因子的浓度,但可能刺激血小板聚集并导致血小板减少。通过改良血栓弹力图评估的整体凝血情况与单独接受NE输注的患者无差异。