L-Ornithine-L-Aspartate and Intermittent Renal Replacement Therapy in Fulminant Hepatitis A: A Case Report

Main Article Content

Nourhane J. Obeid
Khaled H. Soukarieh
Jessy G. Fadel
Rayyan M. Wazzi-Mkahal
Marianne A. Alwan
Jessica J. Fakhir
Paul W. Rassam
Najat I. Joubran
Mona H. Hallak

Keywords

fulminant hepatitis, hepatitis A, L-ornithine-L-aspartate, intermittent renal replacement therapy, continuous renal replacement therapy, a case report

Abstract

Hepatitis A is a common viral infection worldwide that is transmitted via the fecal-oral route. Since the introduction of an efficient vaccine, the incidence of infection has decreased but the number of cases has risen due to widespread community outbreaks among unimmunized individuals. Classic symptoms include fever, malaise, dark urine, and jaundice, and are more common in older children and adults. People are often most infectious 14 days prior to and 7 days following the onset of jaundice. We will discuss the case of a young male patient, diagnosed with acute hepatitis A, leading to fulminant hepatitis refractory to conventional therapy and the development of subsequent kidney injury. The medical treatment through the course of hospitalization was challenging and included the use of L-ornithine-L-aspartate and prolonged intermittent hemodialysis, leading to a remarkable outcome. Hepatitis A is usually self-limited and vaccine-preventable; supportive care is often sufficient for treatment, and chronic infection or chronic liver disease rarely develops. However, fulminant hepatitis, although rare, can be very challenging to manage as in the case of our patient.

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References

1. Abutaleb A, Kottilil S. Hepatitis A. Gastroenterol Clin N Am. 2020;49(2):191–9. 10.1016/j.gtc.2020.01.002

2. Jeong S-H, Lee H-S. Hepatitis A: Clinical manifestations and management. Intervirology. 2010;53(1):15–9. 10.1159/000252779

3. Iorio N, John S. Hepatitis A. Treasure Island, FL: StatPearls Publishing; 2022.

4. Bernal W, Hyyrylainen A, Gera A, Audimoolam VK, McPhail MJ, Auzinger G, et al. Lessons from look-back in acute liver failure? A single centre experience of 3300 patients. J Hepatol. 2013;59(1):74–80. 10.1016/j.jhep.2013.02.010

5. Shammout R, Alhassoun T, Rayya F. Acute liver failure due to hepatitis A virus. Case Rep Gastroenterol. 2021;15(3):927–32. 10.1159/000514393

6. Jain A, Sharma BC, Mahajan B, Srivastava S, Kumar A, Sachdeva S, et al. L-ornithine L-aspartate in acute treatment of severe hepatic encephalopathy: A double-blind randomized controlled trial. Hepatology. 2021;75(5):1194–203. 10.1002/hep.32255

7. Butterworth RF. L-Ornithine L-aspartate (LOLA) for the treatment of hepatic encephalopathy in cirrhosis: Novel insights and translation to the clinic. Drugs. 2019;79(S1):1–3. 10.1007/s40265-018-1021-4

8. Butterworth RF, Kircheis G, Hilger N, McPhail MJW. Efficacy of L-ornithine L-aspartate for the treatment of hepatic encephalopathy and hyperammonemia in cirrhosis: Systematic review and meta-analysis of randomized controlled trials. J Clin Exp Hepatol. 2018;8(3):301–13. 10.1016/j.jceh.2018.05.004

9. Kircheis G, Lüth S. Pharmacokinetic and pharmacodynamic properties of L-Ornithine L-aspartate (LOLA) in hepatic encephalopathy. Drugs. 2019;79(S1):23–9. 10.1007/s40265-018-1023-2

10. Mokhtari V, Afsharian P, Shahhoseini M, Kalantar SM, Moini A. A review on various uses of N-acetyl cysteine. Cell J. 2017;19(1):11–7. 10.22074/cellj.2016.4872

11. Walayat S. Role of N-acetylcysteine in non-acetaminophen-related acute liver failure: An updated meta-analysis and systematic review. Ann Gastroenterol. 2021;34(2):235–240. 10.20524/aog.2021.0571

12. Oe S. Hepatitis A complicated with acute renal failure and high hepatocyte growth factor: A case report. World J Gastroenterol. 2015;21(32):9671. 10.3748/wjg.v21.i32.9671

13. Gupta S, Fenves AZ, Hootkins R. The role of RRT in hyperammonemic patients. Clin J Am Soc Nephrol. 2016;11(10):1872–78. 10.2215/cjn.01320216

14. Cohen PG. The hypokalemic, bowel, bladder, headache relationship; a new syndrome. the role of the potassium ammonia Axis. Med Hypotheses. 1984;15(2):135–40. 10.1016/0306-9877(84)90118-x

15. Kamboj M, Kazory A. Expanding the boundaries of combined renal replacement therapy for non-renal indications. Blood Purific. 2018;47(1–3):69–72. 10.1159/000493179

16. Alfadhel M, Mutairi FA, Makhseed N, Jasmi FA, Al-Thihli K, Al-Jishi E, et al. “Guidelines for acute management of hyperammonemia in the Middle East region.” Ther Clin Risk Manag 2016; 12: 479–87. 10.2147/TCRM.S93144

17. Cardoso F S, Gottfried M, Tujjos S, Olson JC, Karvellas CJ, US Acute Liver Failure Study Group. “Continuous renal replacement therapy is associated with reduced serum ammonia levels and mortality in acute liver failure.” Hepatology. 2018;67(2): 711–20. 10.1002/hep.29488