Gs. Long et al., INTERPRETING SEROLOGIC TESTS FOR HEPATITIS-C VIRUS-INFECTION - BALANCING COST AND CLARITY, Cleveland Clinic journal of medicine, 63(5), 1996, pp. 264-268
Although progress has been made toward developing a cheap and accurate
method to diagnose hepatitis C virus (HCV) infection, current screeni
ng tests have and unacceptably high false-positive rate. Newer tests a
re more accurate, but also more costly. This paper outlines an approac
h for interpreting and using these different tests. KEY POINTS The sec
ond-generation enzyme-linked immunosorbent assay (ELISA) for HCV antib
odies, the current screening test for HCV infection, has a sensitivity
of approximately 90% but a low specificity. Persons with risk factors
for HCV infection, elevated aminotransferase levels, and a positive E
LISA result most likely have HCV infection. Confirmatory testing with
a recombinant immunoblot assay adds considerably to the cost of diagno
sis and should only be used to confirm HCV infection in ELISA-positive
patients at low risk or with conditions such as hyperglobulinemia tha
t promote false-positive reactivity. Polymerase chain reaction (PCR) t
esting is the most sensitive and accurate method of diagnosing HCV inf
ection, but its cost limits its use. PCR testing should be reserved fo
r cases of diagnostic uncertainty, evaluation of possible acute hepati
tis C, patients with normal serum aminotransferase levels and anti-HCV
antibodies, and patients about undergo interferon therapy.