代理

J. Finlay, A. Dix
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摘要

先生,我饶有兴趣地阅读了Seyednejad等人关于局部止血剂的综述。作者已经作出了巨大的努力,给所有可用的凝血剂及其优点和缺点的概述。然而,我想指出评论图5中的一个错误。该图描述了不同的局部药物和凝血级联的组成部分之间的关系,如内在和外在途径。5年前,关于凝血途径功能成分的概念观念发生了变化。60年代,梯级和瀑布假说提出了接触因子引发凝血的内在途径。外源性组织因子途径被认为在凝血激活中起辅助作用。将凝血系统分为内在途径和外在途径并不能准确反映凝血。目前的观点是,凝血主要通过组织因子/因子- viia途径进行。凝血酶是在F via暴露于TF和随后激活因子X进入Xa后产生的。TF/F- viia复合物和fxa均被组织因子通路抑制剂抑制。辅因子分子因子V与因子Xa的相互作用导致凝血酶生成增加。凝血酶的产生被抗凝血酶和活化蛋白c下调。因此,目前人们对凝血的激活及其扩增和抑制回路的看法比两种分别以凝血酶形成为终点的途径更为全面。M. A. Boermeester外科,学术医学中心,Meibergdreef 9, 1105AZ阿姆斯特丹,荷兰DOI: 10.1002/bjs.6602作者回复:局部止血剂(Br J surgery; 2008;95: 1197 - 1225)
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Agents
Sir I read with interest the review by Seyednejad et al. on topical haemostatic agents. The authors have made a tremendous effort to give an overview of all available clotting agents and their advantages and disadvantages. Nevertheless, I would like to point out an error in figure 5 of the review. This figure depicts the relationship between different topical agents and components of the clotting cascade such as the intrinsic and extrinsic pathways. More than 5 years ago, the conceptual thoughts about the functional components of the coagulation pathway changed. In the sixties, the cascade and waterfall hypotheses proposed an intrinsic pathway of coagulation initiated by contact factors. The extrinsic tissue factor pathway was thought to play an ancillary role in activation of coagulation. The segregation of the coagulation system into the intrinsic and extrinsic pathways fails to reflect coagulation accurately. The current view is that coagulation predominantly proceeds by the tissue factor/factor-VIIa pathway. Thrombin is generated after exposure of F VIIa to TF and subsequent activation of factor X into Xa. Both TF/F-VIIa complex and F Xa are inhibited by tissue factor pathway inhibitor. Interaction of the cofactor molecule factor V with factor Xa results in increased thrombin generation. The TF/F-VIIa pathway has several amplification loops, which maintain Xa generation via positive feedback mechanisms involving factors VIII, IX and XI. Thrombin generation is downregulated by antithrombin and activated protein C. Thus, currently a more holistic view is held on activation of coagulation and its amplification and inhibition loops than two pathways that both separately end in thrombin formation. M. A. Boermeester Department of Surgery, Academic Medical Center, Meibergdreef 9, 1105AZ Amsterdam, The Netherlands DOI: 10.1002/bjs.6602 Authors’ reply: Topical haemostatic agents (Br J Surg 2008; 95: 1197–1225)
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