Bile Biochemistry Following Liver Reperfusion in the Recipient and Its Association With Cholangiopathy. Issue 8 (21st July 2020)

• Record Type: Journal Article
• Authors: Gaurav, Rohit; Atulugama, Niroshan; Swift, Lisa; Butler, Andrew J.; Upponi, Sara; Brais, Rebecca; Allison, Michael; Watson, Christopher J. E.
• Is Part Of: Liver transplantation. Volume 26:Issue 8(2020)
• Page Start: 1000
• Page End: 1009
• Publication Date: 2020-07-21
• Subjects: Liver -- Transplantation -- Periodicals; Liver -- Diseases -- Periodicals; Liver Transplantation -- Periodicals; Foie -- Greffe -- Périodiques; 617.5560592
• DOI: 10.1002/lt.25738
• Languages: English
• ISSNs: 1527-6465

Abstract

Abstract : Cholangiocytes secrete bicarbonate and absorb glucose, producing bile with alkaline pH and low glucose content. These functions of cholangiocytes have been suggested as a marker of bile duct viability during normothermic ex situ liver perfusion, and they are now monitored routinely after reperfusion in our center. In this study, we reviewed the composition of bile immediately after reperfusion in liver transplant recipients to determine normal posttransplant parameters and the predictive value of bile biochemistry for the later development of cholangiopathy. After reperfusion of the liver graft, a cannula was placed in the bile duct to collect bile over a median 44‐minute time period. The bile produced was analyzed using a point‐of‐care blood gas analyzer (Cobas b221, Roche Diagnostics, Indianapolis, IN). A total of 100 liver transplants (35 from donation after circulatory death and 65 from donation after brain death) were studied. Median bile pH was 7.82 (interquartile range [IQR], 7.67‐7.98); median bile glucose was 2.1 (1.4‐3.7) mmol/L; median blood‐bile‐blood pH difference was 0.50 (0.37‐0.62); and median blood‐bile glucose difference was 7.1 (5.6‐9.1) mmol/L. There were 12 recipients who developed cholangiopathy over a median follow‐up of 15 months (IQR, 11‐20 months). Bile sodium (142 versus 147 mmol/L; P = 0.02) and blood‐bile glucose concentration differences (5.2 versus 7.6 mmol/L; P = 0.001) were significantly lower and were associated with ischemic cholangiopathy. In conclusion, bile biochemistry may provide useful insights into cholangiocyte function and, hence, bile duct viability. Our results suggest bile glucose is the most sensitive predictor of cholangiopathy.