. Predictors and non invasive identification of severe liver fibrosis in patients with chronic hepatitis C
• 2007
Publication Information
Authors
Metwally MA, Zein CO, Zein NN
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publication.type
International
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Abstract
Diagnosis of severe fibrosis (stages III and IV)
in hepatitis C has clinical implications. Our objective was
to distinguish independent predictors of severe fibrosis and
use them to identify patients with severe fibrosis without a
liver biopsy. One hundred ninety-nine hepatitis C patients
were included in the initial analysis to identify predictors of
severe fibrosis. Univariate and multivariate analyses of 26
predetermined variables for significance in predicting severe
fibrosis were performed. Based on the coefficient regression
and P values, a scoring system was developed and applied
to a second independent cohort (137 patients) for validation.
In multivariate analysis, low platelet count, low albumin,
aspartate transaminase level, history of blood transfusion,
and hepatitis B core antibody were significant independent
predictors of severe fibrosis. A scoring system (range, 0–9)
was developed from the three variables with the lowest P
values (platelet count, aspartate transaminase, and albumin).
A cutoff point of 4 had 99% specificity and 94% positive
predictive value. A cutoff point of 2 had 87% sensitivity
and 95% negative predictive value. We conclude that severe
fibrosis in hepatitis C may potentially be identified with a
high degree of certainty in a substantial number of patients
with a simple noninvasive scoring system.
in hepatitis C has clinical implications. Our objective was
to distinguish independent predictors of severe fibrosis and
use them to identify patients with severe fibrosis without a
liver biopsy. One hundred ninety-nine hepatitis C patients
were included in the initial analysis to identify predictors of
severe fibrosis. Univariate and multivariate analyses of 26
predetermined variables for significance in predicting severe
fibrosis were performed. Based on the coefficient regression
and P values, a scoring system was developed and applied
to a second independent cohort (137 patients) for validation.
In multivariate analysis, low platelet count, low albumin,
aspartate transaminase level, history of blood transfusion,
and hepatitis B core antibody were significant independent
predictors of severe fibrosis. A scoring system (range, 0–9)
was developed from the three variables with the lowest P
values (platelet count, aspartate transaminase, and albumin).
A cutoff point of 4 had 99% specificity and 94% positive
predictive value. A cutoff point of 2 had 87% sensitivity
and 95% negative predictive value. We conclude that severe
fibrosis in hepatitis C may potentially be identified with a
high degree of certainty in a substantial number of patients
with a simple noninvasive scoring system.
Staff Members - Benha University