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Contrast‐enhanced computed tomography for ex vivo assessment of human kidneys: A proof‐of‐concept study.

Authors :
Feizi, Alborz
DiRito, Jenna R.
Richfield, Owen
Stendahl, John C.
Harris, Matthew
Spindler, Susann
Edwards, Christopher M.
Lysyy, Taras
Lee, Shin Rong
Boutagy, Nabil E.
Feher, Attila
Yoo, Peter
Hosgood, Sarah A.
Mulligan, David C.
Nicholson, Michael L.
Sinusas, Albert J.
Haakinson, Danielle J.
Tietjen, Gregory T.
Source :
Artificial Organs. Aug2024, p1. 13p. 6 Illustrations.
Publication Year :
2024

Abstract

Background Methods Results Conclusions Ex vivo perfusion of transplant‐declined human organs has emerged as a promising platform to study the response of an organ to novel therapeutic strategies. However, to fully realize the capability of this platform for performing translational research in human organ pathophysiology, there is a need for robust assays to assess organ function and disease. State‐of‐the‐art research methods rely on analyses of biopsies taken during perfusion, which both damages the organ and only provides localized information. Developing non‐invasive, whole organ methods of assessment is critical to the further development of this research platform.We use ex vivo cold infusion scanning (EXCIS) with contrast‐enhanced computed tomography (CT) to quantify perfusion in kidneys preserved ex vivo. EXCIS‐CT computes three complementary metrics for whole organ assessment: a dynamic assessment of contrast filling, a measure of vascular network anatomical structure, and a static assessment of perfusion heterogeneity.These metrics were applied to a series of six transplant‐declined human kidneys, which demonstrated a range of anatomies and perfusion. Lastly, two transplant‐declined human kidneys were imaged before and after a 1‐h period of ex vivo normothermic perfusion (NMP). We found variable responses to NMP, with one kidney maintaining the vascular network and hemodynamics and the other showing significant changes in vessel size and spatial perfusion profile.EXCIS‐CT provides metrics that can be used to characterize whole organ perfusion and vascular function. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
0160564X
Database :
Academic Search Index
Journal :
Artificial Organs
Publication Type :
Academic Journal
Accession number :
179252786
Full Text :
https://doi.org/10.1111/aor.14840