Horizon Scanning Technology. Prioritising Summary. LifePort. ® kidney transporter: A portable donor kidney transporter/ perfuser. November 24 – What to do after pumping begins. 28 – Removing a kidney from LifePort Kidney Transporter; removing used Perfusion Circuit after a case. 34 – 45 . The LifePort Kidney Transporter is a revolutionary method of transporting kidneys for transplantation: it is a portable, insulated perfusion transporter with.

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The Lifeport Kidney Transporter

Results suggest that the modified HMP system may meet the demands of the flow and pressure under the hypothermic conditions that are suitable for rat liver preservation, while retaining the dependability and portability of the LifePort Kidney Transporter. OC, ATP production transported bile production were markers to assess cellular metabolic activity.

The device prolongs cold storage time from the current 18 hours to 35 hours or transportdr. In conclusion, the present study demonstrated the feasibility of a modified HMP system using a LifePort Kidney Transporter for rat liver preservation. Another poly ethylene catheter outer diameter, 3. No significant difference was observed between the two regions.

The Lifeport Kidney Transporter – INDEX: Design to Improve Life®

Finally, the samples were observed under a light microscope. Open in a separate window. Articles from Experimental and Therapeutic Medicine are provided here courtesy of Spandidos Publications. Although a number of previous clinical and experimental studies have reported that HMP may attenuate IRI in organs more effectively than cold storage 110 — 12the underlying mechanisms have transportre been clearly identified. One-year results of a prospective, randomized trial comparing two machine perfusion devices used for kidney preservation.


Subsequently, the hepatic artery was ligated and the portal vein was cannulated using a poly ethylene catheter outer diameter, 2. Moreover, the graft viability can be assessed by the perfusate tests and perfusion indexes 9.

Research and need The product addresses the serious need ttransporter donation organs.

However, endothelial cell detachment, which is a major cellular damage associated with HMP 1021did not significantly differ between the pre- and post-HMP groups Fig. Assessment of islet cell viability using fluorescent dyes. Liteport preservation of fatty liver grafts: A; Nanjing Jiancheng Bioengineering Institute according to the manufacturer’s instructions.

To overcome the shortage of brain-dead donors for liver transplantation, extended criteria donors ECDs have been used 1.


China Find articles by Yan Xiong. Received Dec 22; Accepted Jul However, the major obstacle preventing large-scale experimental application of HMP for rat livers is a lack of a portable HMP system that is compatible with the size of rat livers.

AO was used to stain viable cells a green, whereas dead cells were detected by red PI staining. Detection of endothelin was performed to determine the level of shear stress and pressure midney to the endothelial cell layer due to HMP. Combined with the results of ATP test Nowadays, it has been demonstrated that cold storage, a traditional organ preservation technique, cannot meet the demands of ECD preservation due to the reduced ischemic tolerance life;ort these marginal grafts 78.


Although the automation of this system requires further modification, the present results suggest that, using the modified system, the demands of flow and pressure during continuous HMP via the rat portal vein can be met, while the dependability and portability of the LifePort are retained. Outcome of liver transplantation using donors older than 60 years of age.

Endoplasmic and vascular surface activation during organ preservation: Fully supporting the organ with arterial flow, pressure, and pulse, Lifeport functions much like a hibernative surrogate body.

A surgical experience with five hundred thirty liver transplants in the transportre.

Similarly, histological observations indicated the general morphology of the parenchyma was preserved and sinusoidal dilatation was significantly increased in post-HMP tissues compared with pre-HMP tissues. China Find articles by Cheng Zeng. Enzymatic activities were detected using alanine aminotransferase assay kit cat no. Assessment for the liver during HMP at 0, 3 and 6 h.

Continuous HMP via the portal vein for liver preservation is capable of simulating hemodynamics of the portal vein and has been widely applied in a number of previous studies 1221 Introduction To overcome the shortage of brain-dead donors for liver transplantation, extended criteria donors ECDs have been used 1.

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