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Case Reports
. 2022 Jun 21;3(3):e210.
doi: 10.1097/PG9.0000000000000210. eCollection 2022 Aug.

Secondary Ammonia Scavenge With Glycerol Phenylbutyrate Improves Hyperammonemia Following Portosystemic Shunting

Affiliations
Case Reports

Secondary Ammonia Scavenge With Glycerol Phenylbutyrate Improves Hyperammonemia Following Portosystemic Shunting

Simone Kortbeek et al. JPGN Rep. .

Abstract

Portosystemic shunts are used to treat portal hypertension arising from extrahepatic portal venous obstruction. They decompress the portal system by allowing intestinal blood to bypass the liver and enter directly into the systemic circulation. These shunts increase the risk of minimal hepatic encephalopathy and altered neurodevelopmental outcomes in affected children. Treatment options are limited and have been extrapolated from those used in cirrhosis. We describe the use of glycerol phenylbutyrate as an alternate management strategy. A 3-year-old boy underwent distal splenorenal shunt for refractory variceal bleeding secondary to portal hypertension. He had neurologic deterioration and hyperammonemia refractory to traditional management strategies. Glycerol phenylbutyrate was initiated and resulted in a sustained improvement in ammonia levels, behavior, and school performance. This case illustrates the successful use of glycerol phenylbutyrate in a noncirrhotic patient with Portosystemic shunt and minimal hepatic encephalopathy refractory to conventional management strategies.

Keywords: hepatic encephalopathy; minimal hepatic encephalopathy.

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Conflict of interest statement

The authors report no conflicts of interest.

Figures

FIGURE 1.
FIGURE 1.
Box plot demonstrating median ammonia values and interquartile ranges before and following initiation of glycerol phenylbutyrate. A) including spurious ammonia values exceeding 100 µmol/L on three occasions post glycerol phenylbutyrate. B) excluding spurious ammonia values exceeding 100 µmol/L on 3 occasions post glycerol phenylbutyrate.

References

    1. Srivastava A, Yadav SK, Lal R, et al. . Effect of surgical portosystemic shunt on prevalence of minimal hepatic encephalopathy in children with extrahepatic portal venous obstruction: assessment by magnetic resonance imaging and psychometry. J Pediatr Gastroenterol Nutr. 2010;51:766–772. - PubMed
    1. Vilstrup H, Wong P. Hepatic encephalopathy in chronic liver disease: 2014 practice guideline by AASLD and EASL. J Hepatol. 2014;60:715–735. - PubMed
    1. Khanna R, Sarin SK. Noncirrhotic portal hypertension: current and emerging perspectives. Clin Liver Dis. 2019;23:781–807. - PubMed
    1. Said VJ, Garcia-Trujillo E. Beyond lactulose: treatment options for hepatic encephalopathy. Gastroenterol Nurs. 2019;42:277–285. - PubMed
    1. Rockey DC, Vierling JM, Mantry P, et al. ; HALT-HE Study Group. Randomized, double-blind, controlled study of glycerol phenylbutyrate in hepatic encephalopathy. Hepatology. 2014;59:1073–1083. - PMC - PubMed

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