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蛋白水解酶作为污染伤口抗菌预防的辅助手段。

Proteolytic enzymes as adjuncts to antimicrobial prophylaxis of contaminated wounds.

作者信息

Rodeheaver G, Marsh D, Edgerton M T, Edlich R F

出版信息

Am J Surg. 1975 May;129(5):537-44. doi: 10.1016/0002-9610(75)90313-x.

Abstract

When a tissue is injured, its vessels exhibit a marked increase in vascular permeability. Blood proteins, including fibrinogen, traverse the vessel walls and lead to the development of a surface coagulum. This inflammatory response continues until primary closure of the wound edges is accomplished. The thickness of the surface coagulum is roughly proportional to the time interval between wounding and closure. This coagulum encompasses the surface contaminants, preventing contact with either topical or systemic antibiotics. The presence of this surface coagulum limits the time in which antibiotic prophylaxis is effective. At three hours after injury, antimicrobial prophylaxis of contaminated wounds has no therapeutic value. Hydrolysis of the protein coagulum by proteolytic enzymes enhances the activity of the antibiotic in experimental wounds. The success of proteolytic enzymes as adjuncts to delayed antibiotic treatment can be correlated with the clot lysis activity of the enzymes in vitro. Travase, the most potent fibrinolytic enzyme, is the most effective adjunct to delayed antibiotic therapy of contaminated wounds. In contrast, the active enzymes found in Elase, which exhibit no significant clot lysis activity in vitro, do not potentiate the activity of antibiotics in wounds subjected to a delay in treatment. Travase prolongs the period of effective topical antibiotic action for at least eight hours in experimental contaminated wounds. The therapeutic merit of Travase is also apparent when the antibiotic is administered systemically. Travase shows promise as an adjunct to a variety of antibiotics that are effective against both gram-positive and gram-negative organisms. The results of these experimental studies support our belief that clinical studies support our belief that clinical studies should now be initiated to test the therapeutic value of Travase as an adjunct to antibiotics in heavily contaminated wounds subjected to an unavoidable delay in treatment.

摘要

当组织受到损伤时,其血管的通透性会显著增加。包括纤维蛋白原在内的血液蛋白会穿过血管壁,导致表面凝块的形成。这种炎症反应会持续到伤口边缘初步闭合。表面凝块的厚度大致与受伤和闭合之间的时间间隔成正比。这种凝块包裹着表面污染物,阻止其与局部或全身使用的抗生素接触。这种表面凝块的存在限制了抗生素预防有效的时间。受伤三小时后,对污染伤口进行抗菌预防没有治疗价值。蛋白水解酶对蛋白凝块的水解可增强实验性伤口中抗生素的活性。蛋白水解酶作为延迟抗生素治疗辅助剂的成功与否与酶在体外的凝块溶解活性相关。曲伐沙星(Travase)是最有效的纤维蛋白溶解酶,是污染伤口延迟抗生素治疗最有效的辅助剂。相比之下,弹性酶(Elase)中发现的活性酶在体外没有显著的凝块溶解活性,在延迟治疗的伤口中不会增强抗生素的活性。在实验性污染伤口中,曲伐沙星可将局部抗生素有效作用时间延长至少八小时。当全身使用抗生素时,曲伐沙星的治疗价值也很明显。曲伐沙星有望作为多种对革兰氏阳性和革兰氏阴性菌均有效的抗生素的辅助剂。这些实验研究结果支持我们的观点,即现在应该开展临床研究,以测试曲伐沙星作为在不可避免延迟治疗的严重污染伤口中抗生素辅助剂的治疗价值。

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