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Abstract
Background. Access to lifesaving liver transplantation is limited by a severe organ shortage. One factor contributing to the shortage is the high rate of discard in livers with histologic steatosis. Livers with <30% macrosteatosis are generally considered safe for transplant. However, histologic assessment of steatosis by a pathologist remains subjective and is often limited by image quality. Here, we address this bottleneck by creating an automated digital algorithm for calculating histologic steatosis using only images of liver biopsy histology obtained with a smartphone. Methods. Multiple images of frozen section liver histology slides were captured using a smartphone camera via the optical lens of a simple light microscope. Biopsy samples from 80 patients undergoing liver transplantation were included. An automated digital algorithm was designed to capture and count steatotic droplets in liver tissue while discounting areas of vascular lumen, white space, and processing artifacts. Pathologists of varying experience provided steatosis scores, and results were compared with the algorithm's assessment. Interobserver agreement between pathologists was also assessed. Results. Interobserver agreement between all pathologists was very low but increased with specialist training in liver pathology. A significant linear relationship was found between steatosis estimates of the algorithm compared with expert liver pathologists, though the latter had consistently higher estimates. Conclusions. This study demonstrates proof of the concept that smartphone-captured images can be used in conjunction with a digital algorithm to measure steatosis. Integration of this technology into the transplant workflow may significantly improve organ utilization rates.
Original language | English (US) |
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Pages (from-to) | E1361 |
Journal | Transplantation Direct |
Volume | 8 |
Issue number | 9 |
DOIs | |
State | Published - Aug 4 2022 |
Bibliographical note
Funding Information:S.R. and H.Y. are supported by the Massachusetts General Hospital Executive Committee on Research. This research was funded by the MIT Quest for Intelligence, the National Institutes of Diabetes and Digestive and Kidney Diseases (R01DK096075, R01DK107875, R01DK114506), and the National Science Foundation (EEC 1941543, ATP-Bio). The other authors declare no conflicts of interest.
Publisher Copyright:
© 2022 Wolters Kluwer Health. All rights reserved.
PubMed: MeSH publication types
- Journal Article
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ATP-Bio: NSF Engineering Research Center for Advanced Technologies for the Preservation of Biological Systems (ATP-Bio)
Bischof, J. C. (PI), Toner, M. (CoPI), Aguilar, G. (CoPI), Healy, K. E. (CoPI), Uygun, K. (Key Personnel), Burger, A. A. (Project Manager), Wolf, S. M. (Key Personnel), Roehrig, G. H. (Key Personnel), Heremans, C. (Coordinator), McAlpine, M. (Key Personnel), Mangolini, L. (Key Personnel), Uygun, B. E. (Key Personnel), Finger, E. B. (Key Personnel), Garwood, M. (Key Personnel), Dames, C. (Key Personnel), Powell-Palm, M. J. (Key Personnel), Franklin, R. R. (Key Personnel), Singh, B. N. (Key Personnel), Yin, Y. (Key Personnel), Usta, O. B. (Key Personnel), Rubinsky, B. (Key Personnel), Tessier, S. N. (Key Personnel), Sandlin, R. D. (Key Personnel), Kangas, J. R. (Key Personnel), Iaizzo, P. A. (Key Personnel), Irimia, D. (Key Personnel), Ogle, B. M. (Key Personnel), Stadler, B. J. (Key Personnel), Bangalore Kodandaramaiah, S. (Key Personnel), Aksan, A. (Key Personnel) & Rabin, Y. (Key Personnel)
9/1/20 → 8/31/25
Project: Research and Outreach Center