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新型改性壳聚糖海绵敷料在猪致死性动脉损伤模型中的疗效测定。

Determination of efficacy of novel modified chitosan sponge dressing in a lethal arterial injury model in swine.

机构信息

R Adams Cowley Shock Trauma Center, University of Maryland School of Medicine, Baltimore, Maryland 21201, USA.

出版信息

J Trauma Acute Care Surg. 2012 Apr;72(4):899-907. doi: 10.1097/TA.0b013e318248baa1.

Abstract

BACKGROUND

Chitosan is a functional biopolymer that has been widely used as a hemostat. Recently, its efficacy has been questioned due to clinical failures as a result of poor adhesiveness. The purpose of this study was to compare, in a severe groin injury model in swine, the hemostatic properties of an unmodified standard chitosan sponge with standard gauze dressing and a novel hydrophobically modified (hm) chitosan sponge. Previous studies have demonstrated that hm-chitosan provides greatly enhanced cellular adhesion and hemostatic effect via noncovalent insertion of hydrophobic pendant groups into cell membranes.

METHODS

Twenty-four Yorkshire swine were randomized to receive hm-chitosan (n = 8), unmodified chitosan (n = 8), or standard Accu-Sorb gauze dressing (n = 8) for hemostatic control. A complex groin injury involving arterial puncture (4.4-mm punch) of the femoral artery was made after splenectomy. After 30 seconds of uncontrolled hemorrhage, the randomized dressing was applied and compression was held for 3 minutes. Fluid resuscitation was initiated to achieve and maintain the baseline mean arterial pressure and the wound was inspected for bleeding. Failure of hemostasis was defined as pooling of blood outside the wound. Animals were then monitored for 180 minutes and surviving animals were killed.

RESULTS

Blood loss before treatment was similar between groups (p < 0.1). Compared with the hm-chitosan sponge group, which had no failures, the unmodified chitosan sponge group and the standard gauze group each had eight failures over the 180-minute observation period. For the unmodified chitosan sponge failures, six of which provided initial hemostasis, secondary rebleeding was observed 44 minutes ± 28 minutes after application. Standard gauze provided no initial hemostasis after the 3-minute compression interval.

CONCLUSIONS

Hm-chitosan is superior to unmodified chitosan sponges (p < 0.001) or standard gauze for controlling bleeding from a lethal arterial injury. The hm-chitosan technology may provide an advantage over native chitosan-based dressings for control of active hemorrhage.

摘要

背景

壳聚糖是一种功能生物聚合物,已被广泛用作止血剂。最近,由于其粘合性差导致临床失败,其功效受到质疑。本研究的目的是在猪严重腹股沟损伤模型中,比较未改性标准壳聚糖海绵与标准纱布敷料和新型疏水改性(hm)壳聚糖海绵的止血性能。先前的研究表明,hm-壳聚糖通过将疏水性侧链基团非共价插入细胞膜,提供了大大增强的细胞粘附和止血效果。

方法

24 头约克夏猪随机分为 hm-壳聚糖组(n = 8)、未改性壳聚糖组(n = 8)或标准 Accu-Sorb 纱布敷料组(n = 8)进行止血控制。脾切除后,进行涉及股动脉穿刺(4.4-mm 冲头)的复杂腹股沟损伤。在不受控制的出血 30 秒后,应用随机敷料并保持 3 分钟的压缩。启动液体复苏以达到并维持基础平均动脉压,并检查伤口是否有出血。止血失败定义为伤口外血液积聚。然后监测动物 180 分钟,存活动物被杀死。

结果

治疗前的失血量在各组之间相似(p < 0.1)。与未发生失败的 hm-壳聚糖海绵组相比,未改性壳聚糖海绵组和标准纱布组在 180 分钟观察期内各有 8 次失败。对于未改性壳聚糖海绵失败,其中 6 次提供了初始止血,在应用后 44 分钟±28 分钟观察到二次再出血。标准纱布在 3 分钟压缩间隔后没有提供初始止血。

结论

hm-壳聚糖在控制致死性动脉损伤出血方面优于未改性壳聚糖海绵(p < 0.001)或标准纱布。hm-壳聚糖技术可能为控制活动性出血提供优于天然壳聚糖敷料的优势。

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