Chronic ketamine use resulting in a reversible cholangiopathy: A case series from a single Canadian centre and review of the literature.

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A Canadian case series describes three patients with chronic ketamine use presenting as reversible cholangiopathy, highlighting that liver enzyme elevation and biliary dilation may resolve upon cessation of the drug.

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Abstract

BackgroundKetamine-related cholangiopathy is increasingly being described in America, Europe, and Asia, paralleling increases in ketamine use globally. However, ketamine-related cholangiopathy has not been described in Canada previously. We report three cases of ketamine-related cholangiopathy in Calgary, Alberta.ResultsBetween May 2024 and April 2025, three patients were assessed by the University of Calgary Liver Unit in Calgary, Alberta, Canada. Case 1 was a 28-year-old female referred for elevated liver enzymes and features concerning for sclerosing cholangitis identified on magnetic resonance cholangiopancreatography. Case 2 was a 40-year-old male referred due to features of sclerosing cholangitis identified on magnetic resonance cholangiopancreatography. Case 3 was a 33-year-old female referred for elevated liver enzymes with biliary dilation on abdominal CT scan. In all cases, a history of chronic ketamine use and a negative comprehensive workup for other etiologies strongly suggested ketamine as the cause of their presentations. Case 1 had normalization of liver enzymes and marked improvement of radiographic biliary changes at 3-month follow-up after complete cessation of ketamine. Case 2 reduced ketamine use by 50% and experienced similar clinical improvement at 3-month follow-up. Case 3 continued using ketamine, resulting in worsening liver enzyme elevations and persistent biliary tree imaging abnormalities.ConclusionsChronic ketamine use should be considered in patients presenting with liver enzyme elevation and/or imaging evidence of biliary dilation. Increased awareness in Canada is essential to ensuring health care providers consider ketamine-related cholangiopathy in patients presenting with these clinical findings, as with ketamine cessation liver injury and biliary abnormalities are potentially reversible.

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SciLite annotations

chemicals 19
ketamine ketamine ketamine ketamine ketamine ketamine ketamine ketamine ketamine ketamine ketamine ketamine tetrahydrofolyl glutamate ketamine cocaine lisdexamfetamine pantoprazole 6-{3-[(progesterone-4-yl)thiopropionyl]amino}hexanoic acid ursodeoxycholic acid
organisms 2
severe acute respiratory syndrome coronavirus 2 rabbits

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europepmc
last seen: 2026-09-13T09:25:22.628771+00:00
scilite
last seen: 2026-08-23T10:03:07.687773+00:00