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Severe Hepatocellular Injury After Hematopoietic Cell Transplant: Incidence, Etiology, and Outcome

Hepatic complications of transplant are a common cause of mortality. While mild elevations of serum aminotransferase enzymes (AST, ALT) do not carry an adverse prognosis, this is not the case with severe hepatocellular injury. We reviewed 6,225 consecutive recipients to determine the incidence and o...

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Autores principales: Sakai, Miwa, Strasser, Simone I., Shulman, Howard M., McDonald, Scott J., Schoch, H. Gary, McDonald, George B.
Formato: Texto
Lenguaje:English
Publicado: 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2762005/
https://www.ncbi.nlm.nih.gov/pubmed/19308033
http://dx.doi.org/10.1038/bmt.2009.56
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author Sakai, Miwa
Strasser, Simone I.
Shulman, Howard M.
McDonald, Scott J.
Schoch, H. Gary
McDonald, George B.
author_facet Sakai, Miwa
Strasser, Simone I.
Shulman, Howard M.
McDonald, Scott J.
Schoch, H. Gary
McDonald, George B.
author_sort Sakai, Miwa
collection PubMed
description Hepatic complications of transplant are a common cause of mortality. While mild elevations of serum aminotransferase enzymes (AST, ALT) do not carry an adverse prognosis, this is not the case with severe hepatocellular injury. We reviewed 6,225 consecutive recipients to determine the incidence and outcomes of severe hepatocellular injury (AST >1500 U/L) before day 100, which occurred in 88 patients. Causes were Sinusoidal Obstruction Syndrome (SOS) (n=46), hypoxic hepatitis (n=33), Varicella Zoster Virus (VZV) hepatitis (n=4), drug-liver injury (N=2), and Unknown (n=3). The incidence declined from 1.9% in the 1990s to 1.1% recently (due to a 5-fold decline in SOS and disappearance of VZV hepatitis). In hypoxic hepatitis, peak serum AST was 3545 U/L (range 1380-25246) within days of shock or prolonged hypoxemia; case fatality rate was 88%. In SOS, AST increases occurred 2-6 weeks after diagnosis; peak AST was 2252 U/L (range 1437-8281); case fatality rate was 76%, with only serum bilirubin able to distinguish survivors (2.7 mg/dL vs. 11.3 mg/dL, p=0.0009). We conclude that circulatory insults (sinusoidal injury, hypotension, hypoxemia) and not infection are the most common cause of severe hepatocellular injury, whose frequency has declined because of a falling incidence of SOS and VZV hepatitis.
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spelling pubmed-27620052010-04-01 Severe Hepatocellular Injury After Hematopoietic Cell Transplant: Incidence, Etiology, and Outcome Sakai, Miwa Strasser, Simone I. Shulman, Howard M. McDonald, Scott J. Schoch, H. Gary McDonald, George B. Bone Marrow Transplant Article Hepatic complications of transplant are a common cause of mortality. While mild elevations of serum aminotransferase enzymes (AST, ALT) do not carry an adverse prognosis, this is not the case with severe hepatocellular injury. We reviewed 6,225 consecutive recipients to determine the incidence and outcomes of severe hepatocellular injury (AST >1500 U/L) before day 100, which occurred in 88 patients. Causes were Sinusoidal Obstruction Syndrome (SOS) (n=46), hypoxic hepatitis (n=33), Varicella Zoster Virus (VZV) hepatitis (n=4), drug-liver injury (N=2), and Unknown (n=3). The incidence declined from 1.9% in the 1990s to 1.1% recently (due to a 5-fold decline in SOS and disappearance of VZV hepatitis). In hypoxic hepatitis, peak serum AST was 3545 U/L (range 1380-25246) within days of shock or prolonged hypoxemia; case fatality rate was 88%. In SOS, AST increases occurred 2-6 weeks after diagnosis; peak AST was 2252 U/L (range 1437-8281); case fatality rate was 76%, with only serum bilirubin able to distinguish survivors (2.7 mg/dL vs. 11.3 mg/dL, p=0.0009). We conclude that circulatory insults (sinusoidal injury, hypotension, hypoxemia) and not infection are the most common cause of severe hepatocellular injury, whose frequency has declined because of a falling incidence of SOS and VZV hepatitis. 2009-03-23 2009-10 /pmc/articles/PMC2762005/ /pubmed/19308033 http://dx.doi.org/10.1038/bmt.2009.56 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Sakai, Miwa
Strasser, Simone I.
Shulman, Howard M.
McDonald, Scott J.
Schoch, H. Gary
McDonald, George B.
Severe Hepatocellular Injury After Hematopoietic Cell Transplant: Incidence, Etiology, and Outcome
title Severe Hepatocellular Injury After Hematopoietic Cell Transplant: Incidence, Etiology, and Outcome
title_full Severe Hepatocellular Injury After Hematopoietic Cell Transplant: Incidence, Etiology, and Outcome
title_fullStr Severe Hepatocellular Injury After Hematopoietic Cell Transplant: Incidence, Etiology, and Outcome
title_full_unstemmed Severe Hepatocellular Injury After Hematopoietic Cell Transplant: Incidence, Etiology, and Outcome
title_short Severe Hepatocellular Injury After Hematopoietic Cell Transplant: Incidence, Etiology, and Outcome
title_sort severe hepatocellular injury after hematopoietic cell transplant: incidence, etiology, and outcome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2762005/
https://www.ncbi.nlm.nih.gov/pubmed/19308033
http://dx.doi.org/10.1038/bmt.2009.56
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