Jensen Eva, Andréasson Svenerik, Bengtsson Anders, Berggren Håkan, Ekroth Rolf, Larsson Lars E, Ouchterlony John
Department of Pediatric Anesthesiology and Intensive Care, Sahlgrenska University Hospital, Gothenburg, Sweden.
Ann Thorac Surg. 2004 Mar;77(3):962-7. doi: 10.1016/j.athoracsur.2003.09.028.
This study describes the response in hemostasis during open-heart surgery with cardiopulmonary bypass (CPB) in children (<== 10 kg) and tests the hypothesis that the use of a biocompatible perfusion system, in comparison with a conventional system, causes less hemostatic activation.
Prospective, randomized, controlled clinical study. Forty consecutive children <== 10 kg were included and divided into two groups: group bioc. (n = 19) treated with a fully heparin-coated system, centrifugal pump, and a closed circuit, and group conv. (n = 21) treated with an uncoated system, roller pump, and a hard shell venous reservoir. Concentrations of plasma thrombin-antithrombin (TAT), D-dimer, tissue plasminogen activator antigen (t-PA ag), and the complex consisting of tissue plasminogen activator and its inhibitor plasminogen activator inhibitor-1 (t-PA-PAI-1) were measured.
The biochemical variables measured increased significantly in both groups during the study period. There was less activation of fibrinolysis during cardiopulmonary bypass (t-PA ag: p = 0.009) in patients treated with the biocompatible perfusion system than in patients treated with the conventional system. A trend in favor of the biocompatible system based on the D-dimer and TAT data (p = 0.07 for both measurements) was observed but no significant intergroup differences regarding these variables or t-PA-PAI-1 were found.
Open-heart surgery with cardiopulmonary bypass in children (<== 10 kg) causes transient activation of the coagulation and fibrinolytic systems. This study demonstrates that the use of a biocompatible perfusion system results in a lower extent of activation of fibrinolysis during CPB than the use of a conventional system.
本研究描述了体重小于10千克儿童在体外循环(CPB)心脏直视手术中的止血反应,并检验了以下假设:与传统系统相比,使用生物相容性灌注系统引起的止血激活更少。
前瞻性、随机、对照临床研究。连续纳入40名体重小于10千克的儿童,分为两组:生物相容性组(n = 19),使用完全肝素涂层系统、离心泵和闭合回路进行治疗;传统组(n = 21),使用未涂层系统、滚压泵和硬壳静脉储血器进行治疗。测量血浆凝血酶 - 抗凝血酶(TAT)、D - 二聚体、组织纤溶酶原激活物抗原(t - PA ag)以及由组织纤溶酶原激活物及其抑制剂纤溶酶原激活物抑制剂 - 1组成的复合物(t - PA - PAI - 1)的浓度。
在研究期间,两组测量的生化变量均显著增加。与使用传统系统治疗的患者相比,使用生物相容性灌注系统治疗的患者在体外循环期间纤维蛋白溶解的激活较少(t - PA ag:p = 0.009)。基于D - 二聚体和TAT数据观察到有利于生物相容性系统的趋势(两项测量的p值均为0.07),但在这些变量或t - PA - PAI - 1方面未发现显著的组间差异。
体重小于10千克儿童的体外循环心脏直视手术会导致凝血和纤维蛋白溶解系统的短暂激活。本研究表明,与使用传统系统相比,使用生物相容性灌注系统在体外循环期间纤维蛋白溶解的激活程度更低。