The most common insult to donor kidneys destined for transplantation is Acute Tubular Necrosis (ATN). The extent of ATN will affect post-transplant function and is a significant risk factor for long-term graft function and survival. Optical Coherence Tomography (OCT) is a rapidly emerging imaging modality that can function as a type of "optical biopsy", providing non-invasive images of tissue morphology in situ and in real-time. In this paper, we review studies that support the use of OCT and Doppler based OCT (i.e., DOCT) to image the renal microstructure and blood flow of human donor kidneys. We conclude that OCT/DOCT imaging of donor kidneys prior to and following transplantation can provide transplant surgeons with a means for predicting ATN and post-transplant renal function.
Imaging Donor Kidneys to Determine their StatusEnd-stage Renal Disease (ESRD) is associated with both high mortality rates and an enormous economic burden [1]. The preferred treatment option for ESRD that can extend patients' lives and improves their quality of life is kidney transplantation. However, ischemic insult suffered by kidneys awaiting transplantation frequently causes acute tubular necrosis (ATN) that leads to varying degrees of delayed graft function (DGF) after transplantation. Also, ATN represents a significant risk for eventual graft and patient survival [2,3], and can be difficult to discern from rejection. In present clinical practice, there is no reliable real-time test to determine the viability of donor kidneys and whether or not donor kidneys might exhibit ATN. Therefore, there is a critical need for objective and reliable real-time tests to predict ATN to use these organs safely and utilize the donor pool optimally.Previously it has been shown that the non-invasive imaging techniques (i.e., tandem scanning confocal microscopy-TSCM) could be used to determine the degree of ATN by analyzing the superficial nephrons of living kidneys in animal models and that these observations correlate with post-transplant renal function [4,5]. This is not surprising in that the status of superficial proximal convoluted tubules is indicative of the status of proximal convoluted throughout the entire kidney cortex. Non-invasive microscopic techniques are necessary for this determination because conventional microscopy results in artifacts that are difficult to distinguish from ATN [6]. Other investigators have also used near-infrared confocal microscopy [7] and multi-photon microscopy (MPM) [8][9][10] to demonstrate the ability to perform non-invasive imaging of kidney structure and function in animal models. However, the maximum penetration depth of those techniques for kidney imaging is very limited (≈100 µm for TSCM, and ≈200-300 µm for MPM), which makes it difficult to impossible to nondestructively image the human kidney, especially if an intact human renal capsule surrounds it. Indeed, in a previous clinical trial, we found that the limited penetrating ability of TSCM precluded us from imaging human donor kidneys even...