First report of 90-day support of 2 calves with a continuous-flow total artificial heart

被引:33
|
作者
Karimov, Jamshid H. [1 ]
Moazami, Nader [1 ,2 ]
Kobayashi, Mariko [1 ]
Sale, Shiva [3 ]
Such, Kimberly [4 ]
Byram, Nicole [1 ]
Sunagawa, Gengo [1 ]
Horvath, David [1 ]
Gao, Shengqiang [1 ]
Kuban, Barry [1 ]
Golding, Leonard A. R. [1 ]
Fukamachi, Kiyotaka [1 ]
机构
[1] Cleveland Clin, Lerner Res Inst, Dept Biomed Engn, Cleveland, OH 44195 USA
[2] Cleveland Clin, Kaufman Ctr Heart Failure Cardiac Transplantat &, Miller Family Heart & Vasc Inst, Dept Thorac & Cardiovasc Surg, Cleveland, OH 44195 USA
[3] Cleveland Clin, Inst Anesthesiol, Dept Cardiothorac Anesthesiol, Cleveland, OH 44195 USA
[4] Cleveland Clin, Lerner Res Inst, Biol Resources Unit, Cleveland, OH 44195 USA
来源
基金
美国国家卫生研究院;
关键词
total artificial heart; mechanical circulatory support; continuous flow; pumps; heart-assist; biocompatibility testing; FAILURE; PUMPS;
D O I
10.1016/j.jtcvs.2015.06.023
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: The Cleveland Clinic continuous-flow total artificial heart (CFTAH) is a compact, single-piece, valveless, pulsatile pump providing self-regulated hemodynamic output to left/right circulation. We evaluated chronic in vivo pump performance, physiologic and hemodynamic parameters, and biocompatibility of the CFTAH in a well-established calf model. Methods: CFTAH pumps have been implanted in 17 calves total. Hemodynamic parameters, pump performance, and device-related adverse events were evaluated during studies and at necropsy. Results: In vivo experiments demonstrated good hemodynamic performance (pump flow, 7.3 +/- 0.7 L/min; left atrial pressure, 16 +/- 3 mm Hg; right atrial pressure, 17 +/- 3 mm Hg; right atrial pressure-left atrial pressure difference, 1 +/- 2 mm Hg; mean arterial pressure, 103 +/- 7 mm Hg; arterial pulse pressure, 30 +/- 11 mm Hg; and pulmonary arterial pressure, 34 +/- 5 mm Hg). The CFTAH has operated within design specifications and never failed. With ever-improving pump design, the implants have shown no chronic hemolysis. Three animals with recent CFTAH implantation recovered well, with no postoperative anticoagulation, during planned in vivo durations of 30, 90, and 90 days (last 2 were intended to be 90-day studies). All these longest-surviving cases showed good biocompatibility, with no thromboembolism in organs. Conclusions: The current CFTAH has demonstrated reliable self-regulation of hemodynamic output and acceptable biocompatibility without anticoagulation throughout 90 days of chronic implantation in calves. Meeting these milestones is in accord with our strategy to achieve transfer of this unique technology to human surgical practice, thus filling the urgent need for cardiac replacement devices as destination therapy.
引用
收藏
页码:687 / +
页数:8
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