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电动液压全人工心脏的慢性体内评估

Chronic in vivo evaluation of an electrohydraulic total artificial heart.

作者信息

Parnis S M, Yu L S, Ochs B D, Macris M P, Frazier O H, Kung R T

机构信息

Cullen Cardiovascular Research Laboratories, Texas Heart Institute, Houston 77225-0345, USA.

出版信息

ASAIO J. 1994 Jul-Sep;40(3):M489-93. doi: 10.1097/00002480-199407000-00048.

DOI:10.1097/00002480-199407000-00048
PMID:8555564
Abstract

Development of the Abiomed total artificial heart (TAH) designed for human use is progressing. Implant durations of longer than 60 days have been achieved in calves. The device consists of blood pumps, valves, and a hydraulic atrial flow balancing chamber fabricated from polyetherurethane. The energy converter, a centrifugal hydraulic pump with a rotary fluid switching valve, is positioned between the blood pumps. In two consecutive chronic in vivo studies (47 days and longer than 60 days), cardiac output was maintained in excess of 8 l/min. The atrial flow balancing chamber maintained a mean right-to-left pressure gradient of 7.5 and -1.4 mmHg in each respective study. There were no pulmonary complications. Platelet counts, fibrinogen concentrations, and hematocrit values returned to baseline levels within 20 days, whereas bilirubin, serum glutamic-oxaloacetic transaminase, blood urea nitrogen, and creatinine levels returned to normal within 1 week of implant. After the first post-operative day, plasma free hemoglobin levels of less than 10 mg/dl indicated no device-related hemolysis throughout the duration of the studies. At explant (47 day study), pathologic analysis showed no renal infarcts, no tissue necrosis, and no thermal damage. The device was fully encapsulated by 2-4 mm thick fibrous connective tissue. A newly designed textured-to-smooth surface inflow showed no signs of pannus ingrowth or thrombotic complications. These studies demonstrate that this TAH is suitable for long-term implantation.

摘要

用于人类的Abiomed全人工心脏(TAH)的研发正在取得进展。在小牛身上已实现植入时间超过60天。该装置由血泵、瓣膜和一个由聚醚聚氨酯制成的液压心房血流平衡腔组成。能量转换器是一个带有旋转流体切换阀的离心液压泵,位于血泵之间。在两项连续的慢性体内研究(47天和超过60天)中,心输出量维持在每分钟8升以上。在各自的研究中,心房血流平衡腔维持的平均右向左压力梯度分别为7.5和-1.4 mmHg。没有出现肺部并发症。血小板计数、纤维蛋白原浓度和血细胞比容值在20天内恢复到基线水平,而胆红素、血清谷草转氨酶、血尿素氮和肌酐水平在植入后1周内恢复正常。术后第一天后,血浆游离血红蛋白水平低于10 mg/dl表明在整个研究期间没有与装置相关的溶血。在取出时(47天的研究),病理分析显示没有肾梗死、没有组织坏死、也没有热损伤。该装置被2 - 4毫米厚的纤维结缔组织完全包裹。新设计的从有纹理到光滑表面的流入方式没有显示出血管翳生长或血栓形成并发症的迹象。这些研究表明这种TAH适合长期植入。

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Chronic in vivo evaluation of an electrohydraulic total artificial heart.电动液压全人工心脏的慢性体内评估
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