Iyer Arjun, Chew Hong Chee, Gao Ling, Villanueva Jeanette, Hicks Mark, Doyle Aoife, Kumarasinghe Gayathri, Jabbour Andrew, Jansz Paul Cassius, Feneley Michael P, Harvey Richard P, Graham Robert M, Dhital Kumud K, Macdonald Peter S
1 The Victor Chang Cardiac Research Institute, Sydney, Australia. 2 Heart & Lung Transplant Unit, St Vincent's Hospital, Darlinghurst, Australia. 3 Department of Cardiothoracic Surgery, St Vincent's Hospital, Darlinghurst, Australia. 4 Department of Clinical Pharmacology, St Vincent's Hospital, Darlinghurst, Australia. 5 Department of Physiology and Pharmacology, University of New South Wales, Randwick, Australia. 6 Department of Cardiology, St Vincent's Hospital, Darlinghurst, Australia. 7 St. Vincent's Clinical School, Faculty of Medicine, University of New South Wales, Kensington, Australia. 8 School of Biotechnology and Biomolecular Science, Faculty of Science, University of New South Wales, Kensington, Australia.
Transplantation. 2016 Dec;100(12):2621-2629. doi: 10.1097/TP.0000000000001396.
Donation after circulatory death (DCD) provides an alternative pathway to deceased organ transplantation. Although clinical DCD lung, liver, and kidney transplantation are well established, transplantation of hearts retrieved from DCD donors has reached clinical translation only recently. Progress has been limited by concern regarding the viability of DCD hearts. The aim of this study was to document the pathophysiological changes that occur in the heart and circulation during withdrawal of life (WLS) support.
In a porcine asphyxia model, we characterized the hemodynamic, volumetric, metabolic, biochemical, and endocrine changes after WLS for up to 40 minutes. Times to circulatory arrest and electrical asystole were recorded.
After WLS, there was rapid onset of profound hypoxemia resulting in acute pulmonary hypertension and right ventricular distension. Concurrently, progressive systemic hypotension occurred with a fall in left atrial pressure and little change in left ventricular volume. Mean times to circulatory arrest and electrical asystole were 8 ± 1 and 16 ± 2 minutes, respectively. Hemodynamic changes were accompanied by a rapid fall in pH, and rise in blood lactate, troponin-T, and potassium. Plasma noradrenaline and adrenaline levels rose rapidly with dramatic increases in coronary sinus levels indicative of myocardial release.
These findings provide insight into the nature and tempo of the damaging events that occur in the heart and in particular the right ventricle during WLS, and give an indication of the limited timeframe for the implementation of potential postmortem interventions that could be applied to improve organ viability.
心脏死亡后器官捐献(DCD)为 deceased 器官移植提供了一条替代途径。尽管临床 DCD 肺、肝和肾移植已很成熟,但从 DCD 供体获取的心脏移植直到最近才实现临床转化。进展一直受到对 DCD 心脏存活能力担忧的限制。本研究的目的是记录撤除生命支持(WLS)期间心脏和循环中发生的病理生理变化。
在猪窒息模型中,我们对 WLS 长达 40 分钟后的血流动力学、容积、代谢、生化和内分泌变化进行了特征描述。记录循环停止和心电静止的时间。
WLS 后,迅速出现严重低氧血症,导致急性肺动脉高压和右心室扩张。同时,出现进行性全身低血压,左心房压力下降,左心室容积变化不大。循环停止和心电静止的平均时间分别为 8±1 分钟和 16±2 分钟。血流动力学变化伴随着 pH 值迅速下降,血乳酸、肌钙蛋白 -T 和钾升高。血浆去甲肾上腺素和肾上腺素水平迅速升高,冠状窦水平显著增加,表明心肌释放。
这些发现深入了解了 WLS 期间心脏尤其是右心室中发生的损伤事件的性质和节奏,并表明实施可能用于提高器官存活能力的潜在死后干预措施的时间框架有限。