首页> 美国卫生研究院文献>Cardiovascular Diseases >ULTRASTRUCTURAL ANALYSES OF BLOOD-INTERFACING LININGS FORMED WITHIN PARTIAL ARTIFICIAL HEARTS OR ABDOMINAL LEFT VENTRICULAR ASSIST DEVICES: A QUALITATIVE SCHEME FOR HUMAN PSEUDONEOINTIMAL ACCRETION KINETICS
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ULTRASTRUCTURAL ANALYSES OF BLOOD-INTERFACING LININGS FORMED WITHIN PARTIAL ARTIFICIAL HEARTS OR ABDOMINAL LEFT VENTRICULAR ASSIST DEVICES: A QUALITATIVE SCHEME FOR HUMAN PSEUDONEOINTIMAL ACCRETION KINETICS

机译:部分人工心脏或腹侧左心室辅助装置形成的血液界面衬里的超微结构分析:人伪神经内分泌增生动力学的定性方案

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摘要

Following each of 21 clinical trials with the partial artificial heart or abdominal left ventricular assist device (ALVAD), we have examined the blood-interfacing human pseudoneointimal (PNI) linings formed on the fibril-flocked pumping surface by scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The salient results of these ultrastructural analyses can be summarized: (1) early PNI accretion kinetics (< 24 hrs) involve plasma protein adsorption, entrapment of erythrocytes, platelets, lymphocytes, numerous neutrophils and macrophages, and the deposition of fibrin within fibril flock interstices (TEM); (2) the surface (< 24 hrs) consists of interconnected fibrin strands (SEM); (3) later PNI accretion kinetics (1-6 days) involve the formation of alternating cellular and fibrin layers (TEM); (4) the surface (1-6 days) consists of cellular aggregates (inter-membrane distances of 340 Å) simulating an endothelial interface (SEM, TEM).Based on these analyses, a plausible sequence of events for human PNI accretion kinetics can be advanced, i.e., 0-24 hrs: (a) maximal foreign body response of blood in contact with Dacron fibrils, (b) cellular lysis and fibrin compaction; 1-6 days: (c) accretion and lysis of cellular aggregates (neutrophils, macrophages) 3-4μ thick, (d) accretion of linear fibrin aggregates, 8-10μ thick, and (e) cyclic replication (up to six) of phases c and d.
机译:在使用部分人工心脏或腹部左心室辅助装置(ALVAD)进行的21项临床试验中的每项试验之后,我们已经通过扫描电子显微镜(SEM)和扫描电镜观察了在原纤维聚集的泵浦表面形成的与血液连接的人假神经内膜(PNI)衬里。透射电子显微镜(TEM)。这些超微结构分析的主要结果可以归纳为:(1)早期PNI吸收动力学(<24小时)涉及血浆蛋白吸附,红细胞,血小板,淋巴细胞,大量嗜中性粒细胞和巨噬细胞的包埋,以及纤维蛋白在原纤维群间的沉积。 (TEM); (2)表面(<24小时)由相互连接的纤维蛋白链(SEM)组成; (3)以后的PNI吸收动力学(1-6天)涉及交替的细胞层和纤维蛋白层(TEM)的形成; (4)表面(1-6天)由模拟内皮界面(SEM,TEM)的细胞聚集体(膜间距离为340Å)组成。基于这些分析,可能的人类PNI吸收动力学事件序列可以提前,即0-24小时:(a)与涤纶纤维接触的血液的最大异物反应,(b)细胞裂解和纤维蛋白压紧; 1-6天:(c)3-4μ厚的细胞聚集体(嗜中性粒细胞,巨噬细胞)的积聚和裂解,(d)8-10μ厚的线性纤维蛋白聚集体的积聚和(e)环状复制(最多六个)阶段c和d。

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