[实验动物主动脉重建手术局部止血液的疗效和安全性(一项实验研究)]。

R E Kalinin, I A Suchkov, A A Krylov, S B Bazaev, A A Gerasimov
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引用次数: 0

摘要

背景:大多数血管外科开放手术是在全身性低凝的情况下进行的,从而使止血的实现复杂化。重建区的可靠止血水平是以观察一系列因素为代价的。通常,当传统的止血方法不足以达到目的时,使用局部止血剂就成为绝对必要的。目的:通过动物实验,探讨在主动脉重建手术中使用止血剂Hemoblock与合成材料联合止血的有效性和安全性。材料与方法:选用80只杂交猫,采用盲随机法随机分为4组:2个实验组和2个对照组。在全身麻醉的情况下,这些动物在体内接受了腹主动脉异体成形术的手术。同种异体成形术的材料分别为涤纶纤维(n=40)和聚四氟乙烯(n=40)织造和针织的涤纶补片。结果与讨论:2A组(涤纶)和1A组(涤纶+止血剂)的平均失血量分别为15.69 ml和14.6 ml,两组间差异无统计学意义(p=0.24)。使用聚四氟乙烯作为塑料材料的2B组失血量为20.12 ml,而使用聚四氟乙烯+ Hemoblock的1B组失血量为14.2 ml。统计分析表明,额外使用Hemoblock获得的数值明显更好(p=0.03)。2A组(涤纶组)的平均出血时间为265.8 s, 1A组(涤纶组+血阻剂组)的平均出血时间为240.6 s,两组止血时间差异有统计学意义(p)。止血溶液Hemoblock的应用使手术干预的结果在使用PTFE时减少29.4%的出血量,使用涤纶时减少6.9%,使用PTFE贴片时减少9%的出血时间,使用涤纶贴片时减少9.5%的出血时间等参数上有了明显的改善。在实验期间,没有出现与使用局部止血溶液Hemoblock相关的并发症。
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[Efficacy and safety of local hemostatic solution in reconstructive operations on the aorta in laboratory animals (an experimental study)].

Background: Most open operative interventions in vascular surgery are performed in conditions of systemic hypocoagulation, thus additionally complicating the achievement of hemostasis. A reliable level of hemostasis in the reconstruction zone is achieved at the expense of observing a series of factors. Frequently, when the traditional methods of hemostasis are not enough for the purpose, the use of local hemostatic agents becomes absolutely necessary.

Objective: Our study was aimed at investigating the efficacy and safety of using the hemostatic agent 'Hemoblock' to achieve hemostasis during reconstructive operations on the aorta in combination with synthetic materials in a laboratory experiment on animals.

Materials and methods: The study included 80 mongrel cats divided into 4 equal groups by blind randomization: 2 experimental groups and 2 control groups. In the vivarium under general anesthesia, the animals underwent surgery - alloplasty of the abdominal aorta. Dacron patches, being woven and knitted prosthetic grafts made of polyester fiber (n=40), and PTFE patches (n=40) were used as the material for alloplasty.

Results and discussion: The mean volume of blood loss volume in group 2A (Dacron) and in group 1A (Dacron + Hemoblock) amounted to 15.69 ml and 14.6 ml, respectively, with no significant difference between the groups (p=0.24). The volume of blood loss in group 2B, using PTFE as a plastic material, was 20.12 ml, and in group 1B (PTFE + Hemoblock) it was 14.2 ml. Statistical analysis demonstrated significantly better values obtained with the additional use of Hemoblock (p=0.03). The mean bleeding time in group 2A (Dacron) was 265.8 s and in group 1A (Dacron + Hemoblock) it was 240.6 s, which was a statistically better time to achieve hemostasis (p<0.001). In group 2B (PTFE), the bleeding time was 285 s and in group 1B (PTFE + Hemoblock) it was 259.2 s, with a statistically significant between-group difference in favor of the additional use of Hemoblock (p<0.001).

Conclusion: Applying the hemostatic solution Hemoblock made it possible to significantly improve the results of surgical interventions in terms of such parameters as reducing blood loss by 29.4% when using PTFE and by 6.9% when using Dacron, as well as to decrease the bleeding time by 9% when using PTFE patches and by 9.5% when using Dacron patches. During the experiment, there were no complications associated with the use of the local hemostatic solution Hemoblock.

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