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Fulminate Hepatic Failure in a 5 Year Old Female after Inappropriate Acetaminophen Treatment

BACKGROUND: Acetaminophen is a drug widely used in children because of its safety and efficacy. Although the risk of its toxicity is lower in children such reactions occur in pediatric patients from intentional overdoses and less frequently attributable to unintended inappropriate dosing. The aim of...

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Autores principales: Kasmi, Irena, Sallabanda, Sashenka, Kasmi, Gentian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Institute of Immunobiology and Human Genetics 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4877837/
https://www.ncbi.nlm.nih.gov/pubmed/27275268
http://dx.doi.org/10.3889/oamjms.2015.080
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author Kasmi, Irena
Sallabanda, Sashenka
Kasmi, Gentian
author_facet Kasmi, Irena
Sallabanda, Sashenka
Kasmi, Gentian
author_sort Kasmi, Irena
collection PubMed
description BACKGROUND: Acetaminophen is a drug widely used in children because of its safety and efficacy. Although the risk of its toxicity is lower in children such reactions occur in pediatric patients from intentional overdoses and less frequently attributable to unintended inappropriate dosing. The aim of reporting this case is to attract the attention to the risk of the acetaminophen toxicity when administered in high doses. CASE PRESENTATION: We report here a 5 year old girl who developed fulminate liver failure with renal impairment and acute pancreatitis, as a result of acetaminophen toxicity caused from unintentional repeated supratherapeutic ingestion, with a total administered dose of 4800 mg in three consecutive days, 1600 mg/day, approximately 90 mg/kg/day. The blood level of acetaminophen after 10 hours of the last administered dose was 32 mg/l. The patient presented with high fever, jaundice, lethargic, agitating with abdominal pain accompanied by encephalopathy. The liver function test revealed with high level of alanine aminotransferase 5794 UI/l and aspartate aminotransferase 6000 UI/l. Early initiation of oral N-acetylcysteine (NAC) after biochemical evidence of liver toxicity was beneficial with rapid improvement of liver enzymes, hepatic function and encephalopathy. During the course of the illness the child developed acute pancreatitis with hyperamylasemia 255 UI/L and hyperlypasemia 514 UI/L. Patient totally recovered within 29 days. CONCLUSION: Healthcare providers should considered probable acetaminophen toxicity in any child who has received the drug and presented with liver failure. When there is a high index of suspicion of acetaminophen toxicity NAC should be initiated and continued until there are no signs of hepatic dysfunction.
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spelling pubmed-48778372016-06-06 Fulminate Hepatic Failure in a 5 Year Old Female after Inappropriate Acetaminophen Treatment Kasmi, Irena Sallabanda, Sashenka Kasmi, Gentian Open Access Maced J Med Sci Case Report BACKGROUND: Acetaminophen is a drug widely used in children because of its safety and efficacy. Although the risk of its toxicity is lower in children such reactions occur in pediatric patients from intentional overdoses and less frequently attributable to unintended inappropriate dosing. The aim of reporting this case is to attract the attention to the risk of the acetaminophen toxicity when administered in high doses. CASE PRESENTATION: We report here a 5 year old girl who developed fulminate liver failure with renal impairment and acute pancreatitis, as a result of acetaminophen toxicity caused from unintentional repeated supratherapeutic ingestion, with a total administered dose of 4800 mg in three consecutive days, 1600 mg/day, approximately 90 mg/kg/day. The blood level of acetaminophen after 10 hours of the last administered dose was 32 mg/l. The patient presented with high fever, jaundice, lethargic, agitating with abdominal pain accompanied by encephalopathy. The liver function test revealed with high level of alanine aminotransferase 5794 UI/l and aspartate aminotransferase 6000 UI/l. Early initiation of oral N-acetylcysteine (NAC) after biochemical evidence of liver toxicity was beneficial with rapid improvement of liver enzymes, hepatic function and encephalopathy. During the course of the illness the child developed acute pancreatitis with hyperamylasemia 255 UI/L and hyperlypasemia 514 UI/L. Patient totally recovered within 29 days. CONCLUSION: Healthcare providers should considered probable acetaminophen toxicity in any child who has received the drug and presented with liver failure. When there is a high index of suspicion of acetaminophen toxicity NAC should be initiated and continued until there are no signs of hepatic dysfunction. Institute of Immunobiology and Human Genetics 2015-09-15 2015-09-08 /pmc/articles/PMC4877837/ /pubmed/27275268 http://dx.doi.org/10.3889/oamjms.2015.080 Text en Copyright: © 2015 Irena Kasmi, Sashenka Sallabanda, Gentian Kasmi. http://creativecommons.org/licenses/by/2.5/ This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Case Report
Kasmi, Irena
Sallabanda, Sashenka
Kasmi, Gentian
Fulminate Hepatic Failure in a 5 Year Old Female after Inappropriate Acetaminophen Treatment
title Fulminate Hepatic Failure in a 5 Year Old Female after Inappropriate Acetaminophen Treatment
title_full Fulminate Hepatic Failure in a 5 Year Old Female after Inappropriate Acetaminophen Treatment
title_fullStr Fulminate Hepatic Failure in a 5 Year Old Female after Inappropriate Acetaminophen Treatment
title_full_unstemmed Fulminate Hepatic Failure in a 5 Year Old Female after Inappropriate Acetaminophen Treatment
title_short Fulminate Hepatic Failure in a 5 Year Old Female after Inappropriate Acetaminophen Treatment
title_sort fulminate hepatic failure in a 5 year old female after inappropriate acetaminophen treatment
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4877837/
https://www.ncbi.nlm.nih.gov/pubmed/27275268
http://dx.doi.org/10.3889/oamjms.2015.080
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