Amdisen Chris, Jespersen Bente, Møldrup Ulla, Keller Anna K
Institute of Clinical Medicine, Aarhus University Hospital, Aarhus, Denmark.
Department of Renal Medicine, Aarhus University Hospital, Aarhus, Denmark.
PLoS One. 2017 May 25;12(5):e0178301. doi: 10.1371/journal.pone.0178301. eCollection 2017.
Vascular occlusion is a rare, but serious complication after kidney transplantation often resulting in graft loss. We therefore aimed to develop an experimental porcine model for stepwise reduction of the renal venous blood flow and to compare an implantable Doppler probe and microdialysis for fast detection of vascular occlusion.
In 20 pigs, implantable Doppler probes were placed on the renal artery and vein and a microdialysis catheter was placed in the renal cortex. An arterial flowprobe served as gold standard. Following two-hour baseline measurements, the pigs were randomised to stepwise venous occlusion, complete venous occlusion, complete arterial occlusion or controls.
All parameters were stable through baseline measurements. Glutamate and lactate measured by microdialysis increased significantly (p = 0.02 and p = 0.03 respectively) 30 minutes after a 2/3 (66%) reduction in renal blood flow. The implantable Doppler probe was not able to detect flow changes until there was total venous occlusion. Microdialysis detected changes in local metabolism after both arterial and venous occlusion; the implantable Doppler probe could only detect vascular occlusions on the vessel it was placed.
We developed a new model for stepwise renal venous blood flow occlusion. Furthermore, the first comparison of the implantable Doppler probe and microdialysis for detection of renal vascular occlusions was made. The implantable Doppler probe could only detect flow changes after a complete occlusion, whereas microdialysis detected changes earlier, and could detect both arterial and venous occlusion. Based on these results, the implantable Doppler probe for early detection of vascular occlusions cannot be recommended.
血管闭塞是肾移植后一种罕见但严重的并发症,常导致移植肾丧失。因此,我们旨在建立一种实验性猪模型,用于逐步减少肾静脉血流量,并比较植入式多普勒探头和微透析技术在快速检测血管闭塞方面的效果。
对20头猪,将植入式多普勒探头置于肾动脉和静脉上,并将微透析导管置于肾皮质。动脉血流探头作为金标准。在进行两小时的基线测量后,将猪随机分为逐步静脉闭塞组、完全静脉闭塞组、完全动脉闭塞组或对照组。
在基线测量期间所有参数均稳定。在肾血流量减少2/3(66%)后30分钟,微透析测得的谷氨酸和乳酸显著增加(分别为p = 0.02和p = 0.03)。直到完全静脉闭塞时,植入式多普勒探头才能检测到血流变化。微透析在动脉和静脉闭塞后均能检测到局部代谢变化;植入式多普勒探头只能检测其所在血管的血管闭塞情况。
我们建立了一种新的逐步肾静脉血流闭塞模型。此外,首次比较了植入式多普勒探头和微透析技术在检测肾血管闭塞方面的效果。植入式多普勒探头只有在完全闭塞后才能检测到血流变化,而微透析能更早检测到变化,且能检测动脉和静脉闭塞。基于这些结果,不推荐使用植入式多普勒探头进行血管闭塞的早期检测。