The natural history of acute hepatitis C: clinical presentation, laboratory findings and treatment outcomes

Aliment Pharmacol Ther 2011; 33: 559–565 Summary Background  Acute hepatitis C has variable modes of presentation and frequently results in chronic infection. Its optimal management has yet to be defined. Aim  To establish natural history and complications of treatment of acute hepatitis C. Methods ...

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Veröffentlicht in:Alimentary pharmacology & therapeutics 2011-03, Vol.33 (5), p.559-565
Hauptverfasser: Loomba, R., Rivera, M. M., McBurney, R., Park, Y., Haynes‐Williams, V., Rehermann, B., Alter, H. J., Herrine, S. K., Liang, T. J., Hoofnagle, J. H., Heller, T.
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Sprache:eng
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Zusammenfassung:Aliment Pharmacol Ther 2011; 33: 559–565 Summary Background  Acute hepatitis C has variable modes of presentation and frequently results in chronic infection. Its optimal management has yet to be defined. Aim  To establish natural history and complications of treatment of acute hepatitis C. Methods  Data from all patients presenting with acute hepatitis C to the National Institutes of Health between 1994 and 2007 were reviewed. Results  Twenty‐five patients were identified. Symptoms were reported by 80% and jaundice by 40%. Aminotransferase levels and hepatitis C virus (HCV) RNA levels fluctuated greatly; 18% of patients were intermittently negative for HCV RNA. Five patients recovered spontaneously whereas 20 developed chronicity or received interferon‐based therapy during the acute phase. Among 15 patients treated during the acute phase with peginterferon with or without ribavirin for 24 weeks, all became HCV RNA negative within 4–8 weeks, and all except two (HIV‐positive) achieved a sustained virological response. Side effects (particularly psychiatric) were common and limited treatment in 30%. Conclusions  Among 25 patients with acute HCV infection, fluctuating illness was common and spontaneous recovery occurred in only 20%. Anti‐viral treatment with a 24‐week course of peginterferon and ribavirin was highly effective, but marked by frequent and severe side effects.
ISSN:0269-2813
1365-2036
DOI:10.1111/j.1365-2036.2010.04549.x