用于转化应用的血液循环确定死亡后捐赠的临床前模型的发展。

Transplantation research Pub Date : 2014-06-14 eCollection Date: 2014-01-01 DOI:10.1186/2047-1440-3-13
Géraldine Allain, Thomas Kerforne, Rodolphe Thuret, Pierre-Olivier Delpech, Thibaut Saint-Yves, Michel Pinsard, Thierry Hauet, Sébastien Giraud, Christophe Jayle, Benoît Barrou
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引用次数: 8

摘要

背景:体外膜性氧合被提议用于循环测定死亡(DCD)后捐赠的腹部器官获取。在法国,国家生物医学机构监督从DCD采购肾脏,指定耐受热缺血和冷缺血的持续时间。然而,目前还没有研究确定这种技术的最佳条件。这项工作的目的是利用腹部恒温氧合再循环(ANOR)建立DCD的临床前模型。简而言之,我们的目标是描述ANOR所涉及的机制及其对腹部器官的影响。方法:选用体重45 ~ 55 kg的大型白猪。钾诱导心脏骤停30分钟后,夹住胸降主动脉,在下腔静脉和腹主动脉之间设置ANOR,持续4小时。采集血液动力学、呼吸及生化指标。在ANOR过程中进行血气测定和生化分析。结果:进行了6次ANOR手术。手术过程描述和术中参数和生物学数据提出。泵流量在2.5 ~ 3l /min之间。血液动力学、呼吸和生化指标在可重复性条件下达到。有趣的是,动物在靶向方案下保持血流动力学稳定。动脉pH值得到控制,钠血症和肾功能在手术开始后4小时保持稳定。手术后,血红蛋白和血清蛋白水平降低,同时乳酸脱氢酶活性升高。由于体外循环循环,血钾水平升高。结论:我们的ANOR模型最接近文献中报道的临床情况,并允许研究该技术对全身和腹部器官的影响。猪的翻译相关性将允许确定新的生物标志物和方案,以改善DCD供体管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Development of a preclinical model of donation after circulatory determination of death for translational application.

Development of a preclinical model of donation after circulatory determination of death for translational application.

Development of a preclinical model of donation after circulatory determination of death for translational application.

Development of a preclinical model of donation after circulatory determination of death for translational application.

Background: Extracorporeal membranous oxygenation is proposed for abdominal organ procurement from donation after circulatory determination of death (DCD). In France, the national Agency of Biomedicine supervises the procurement of kidneys from DCD, specifying the durations of tolerated warm and cold ischemia. However, no study has determined the optimal conditions of this technique. The aim of this work was to develop a preclinical model of DCD using abdominal normothermic oxygenated recirculation (ANOR). In short, our objectives are to characterize the mechanisms involved during ANOR and its impact on abdominal organs.

Methods: We used Large White pigs weighing between 45 and 55 kg. After 30 minutes of potassium-induced cardiac arrest, the descending thoracic aorta was clamped and ANOR set up between the inferior vena cava and the abdominal aorta for 4 hours. Hemodynamic, respiratory and biochemical parameters were collected. Blood gasometry and biochemistry analysis were performed during the ANOR procedure.

Results: Six ANOR procedures were performed. The surgical procedure is described and intraoperative parameters and biological data are presented. Pump flow rates were between 2.5 and 3 l/min. Hemodynamic, respiratory, and biochemical objectives were achieved under reproducible conditions. Interestingly, animals remained hemodynamically stable following the targeted protocol. Arterial pH was controlled, and natremia and renal function remained stable 4 hours after the procedure was started. Decreased hemoglobin and serum proteins levels, concomitant with increased lactate dehydrogenase activity, were observed as a consequence of the surgery. The serum potassium level was increased, owing to the extracorporeal circulation circuit.

Conclusions: Our ANOR model is the closest to clinical conditions reported in the literature and will allow the study of the systemic and abdominal organ impact of this technique. The translational relevance of the pig will permit the determination of new biomarkers and protocols to improve DCD donor management.

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