Decompensated Cirrhosis, Hepatorenal Syndrome and End-of-Life Care
A 61-year-old man with alcohol-related cirrhosis, Child-Pugh C and MELD-Na 31, has been readmitted for the fifth time in six months with tense refractory ascites requiring large-volume paracentesis every ten days. Creatinine has risen from 96 to 236 micromol/L over five days despite diuretic withdrawal, sodium is 124 mmol/L, urine sodium is low and urinalysis is bland; ascitic fluid shows 90 neutrophils per mm3. He has been declined for transplantation because of ongoing alcohol use and frailty, and he asks you whether he is dying and whether there is anything more you can do. How do you manage him?
What the panel is testing: This tests the diagnosis and treatment of hepatorenal syndrome-AKI and refractory ascites, and equally whether the candidate can hold an honest prognostic and goals-of-care conversation with a stigmatised patient in a culture where end-of-life discussion is often avoided.
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Knowledge: The pattern of a progressive rise in creatinine over days with a bland sediment, low urinary sodium, no shock, no nephrotoxins and no response to diuretic withdrawal is characteristic of hepatorenal syndrome-AKI by the International Club of Ascites criteria, but the diagnosis requires exclusion of hypovolaemia through albumin volume expansion at 1 g/kg per day for two days, exclusion of structural kidney disease, and exclusion of spontaneous bacterial peritonitis, which his neutrophil count of 90 does not meet since the threshold is 250 per mm3.
Management: I would stop diuretics, beta-blockers if hypotensive, and any nephrotoxins, give intravenous albumin 1 g/kg per day up to 100 g for two days as a volume challenge, send blood and ascitic cultures, repeat diagnostic paracentesis and screen for infection which is the commonest precipitant.
Ethics and communication: He has asked directly whether he is dying, and I must answer honestly, at his pace, checking first what he already understands and what he wants to know, and then giving a truthful and gentle picture that his liver disease is now advanced, that transplantation is currently not available to him, and that his remaining time is likely to be short.
Likely panel follow-up questions
- Give the current International Club of Ascites diagnostic criteria for hepatorenal syndrome-AKI.
- How do you distinguish hepatorenal syndrome from acute tubular necrosis at the bedside?
- When would you offer renal replacement therapy in this patient, and when would you not?
Pitfalls in this case
- Diagnosing hepatorenal syndrome without an albumin volume challenge and exclusion of infection and structural causes
- Offering TIPS or dialysis without acknowledging futility and the absence of a transplant path
- Avoiding the prognosis question or giving false hope of transplantation
Reference: EASL Clinical Practice Guidelines for the management of patients with decompensated cirrhosis, Journal of Hepatology 2018; AASLD Practice Guidance: Diagnosis, Evaluation, and Management of Ascites, Spontaneous Bacterial Peritonitis and Hepatorenal Syndrome, Hepatology 2021