共 18 条
Rapid sampling microdialysis as a novel tool for parenchyma assessment during static cold storage and hypothermic machine perfusion in a translational ex vivo porcine kidney model
被引:23
|作者:
Hamaoui, Karim
[1
]
Gowers, Sally
[2
]
Damji, Samir
[1
]
Rogers, Michelle
[2
]
Leong, Chi Leng
[2
]
Hanna, George
[1
]
Darzi, Ara
[1
]
Boutelle, Martyn
[2
]
Papalois, Vassilios
[1
,3
]
机构:
[1] Univ London Imperial Coll Sci Technol & Med, Dept Surg, London SW7 2AZ, England
[2] Univ London Imperial Coll Sci Technol & Med, Dept Bioengn, London SW7 2AZ, England
[3] Imperial Coll Healthcare NHS Trust, Hammersmith Hosp, Imperial Coll Renal & Transplant Ctr, London, England
关键词:
Tissue viability;
Micro-dialysis;
Preservation;
Metabolism;
Machine perfusion;
Ischaemia;
DELAYED GRAFT FUNCTION;
ONLINE MICRODIALYSIS;
TRANSPLANT OUTCOMES;
BRAIN METABOLISM;
CONTROLLED-TRIAL;
RENAL ISCHEMIA;
CARDIAC DEATH;
LIVER GRAFTS;
PRESERVATION;
ALLOGRAFT;
D O I:
10.1016/j.jss.2015.07.004
中图分类号:
R61 [外科手术学];
学科分类号:
摘要:
Background: Viability assessment during preservation is imperative to avoid unnecessary discard of marginal organs maximizing graft outcomes in kidney transplantation. To address this need, we have developed a novel system based on a rapid sampling micro-dialysis (rsMD) analyzer allowing continuous tissue monitoring and measurement of metabolic markers of cell damage. Our aim was to develop a tool that allows for accurate assessment of tissue metabolism and organ viability in the preservation period. Methods: Twenty-two porcine kidneys subjected to 15 min of warm ischemia underwent either 24 h of static cold storage (SCS) or 10 h of hypothermic machine perfusion (HMP). After preservation, tissue temperature was allowed to passively increase to ambient temperature as an ischemic challenge. Cortical and medullary metabolism was monitored throughout with online measurements of lactate concentrations made every 60 s. Results: On commencement of monitoring, lactate concentrations were successfully detected within 15 mins. During the initial 1.5 h, lactate concentrations were similar during SCS (65 mu M) and HMP (124 mu M, P > 0.05) but lower after 10 h of SCS (SCS: 68 mu M versus HMP: 230 mu M, P < 0.001). Warming data suggest a resilience of HMP kidneys to subsequent temperature induced ischemia compared to SCS kidneys. Conclusions: This preliminary study provides the baseline ischemic profile for porcine kidneys while validating the technique of rsMD as a tool for organ viability assessment during preservation. The data characterize metabolic differences between SCS and HMP preserved allografts and can help elucidate why HMP is clinically superior to SCS allowing development of interventions to augment these benefits. (C) 2016 Elsevier Inc. All rights reserved.
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页码:332 / 345
页数:14
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